Hays AB jobb i Göteborg

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Formulation/Analytical Scientist

Molekylärbiolog
Läs mer Feb 4
Formulation/Analytical Scientist - AstraZeneca - Gothenburg - 12-month consultancy assignment

Formulation/Analytical Scientist, Pharmaceutical Sciences

At AstraZeneca, we turn ideas into life-changing medicines and strive to continuously meet the unmet needs of patients worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you're our kind of person.

Pharmaceutical Sciences at AstraZeneca deliver the therapies of the future through scientific leadership in drug delivery, design of synthetic routes, and manufacturing of Active Pharmaceutical Ingredients (API) across all the AstraZeneca therapy areas.
Our vision is to be "pharmaceutical science leaders, creating innovative and cost-effective solutions, shaping the diverse therapies of the future".

Are you an enthusiastic, innovative, and motivated Formulation/Analytical Scientist seeking a unique opportunity? Join our small molecule formulation team in Advanced Drug Delivery at AstraZeneca's vibrant R&D site in Gothenburg, Sweden. We offer the experience to collaborate with dedicated team members and to work closely with other skill experts delivering AstraZeneca's early portfolio.

Responsibilities:
This is a lab-based role where you will support several drug project teams and provide your technical and scientific expertise in formulation development. You will develop and deliver different formulation systems for oral, inhaled and parenteral use, with a focus on liquid formulations. You will also perform essential characterisation work e.g. content, stability, homogeneity, impurity, pH, and particle size measurements, supporting projects in the discovery and preclinical development phase. The role requires close collaboration with other internal functions to further build our capabilities within advanced drug delivery.

You are expected to perform lab-based experimental work in accordance to project timelines, appropriate Safety, Health & Environment (SHE), quality and compliance standards, and in close collaboration with other formulators and analysts, as well as other skill experts (solid state and biopharmaceutical experts). The work should be documented carefully and to the right quality and standard, and clearly communicated to your project team.

Requirements:

* MSc degree in a scientific discipline relevant to analytical and formulation science (e.g., chemistry, pharmaceutical technology, or equivalent qualifications).
* Basic understanding of liquid formulations and basic knowledge of analytical methodologies such as spectrometry and separation science (U/HPLC).
* Genuine interest in experimental work and hands-on problem-solving.
* Delivery focused with the ability to utilise scientific and innovative thinking.
* Great communication skills in English, both orally and in writing.

Desirable skills/experience:
* Technical competence in the field of drug product formulation development for oral and/or parenteral delivery.
* Experience in working with formulation development or similar product development, or other laboratory skills of relevance.
* Good understanding of suitable quality standards and regulatory frameworks

If your passion is science, and you want to be part of a team that makes a bigger impact on patients' lives, then there's no better place to be. Join us at AstraZeneca, where we truly understand science and apply it every day to strengthen and grow our pipeline.

What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

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Solid State Scientist

Molekylärbiolog
Läs mer Feb 4
Solid State Scientist - AstraZeneca - Gothenburg - 10-month consultancy assignment

Scientist Pharmaceutical Sci - Solid State

Do you have knowledge in the area of solid-state development for drug products, characterisation techniques and an understanding of solid-state properties? Would you like to apply your expertise to make an impact in a company that follows the science and turns ideas into life-changing medicines? Then AstraZeneca might be the place for you!

AstraZeneca is a global, innovation-driven biopharmaceutical business that focusses on the discovery, development and commercialisation of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. We are currently looking for a solid-state scientist to join our team in Global Product Development (GPD) in Gothenburg, Sweden, a subdivision of Pharmaceutical Technology and Development (PT&D). We believe that you have fundamental scientific knowledge and hands-on experience in the solid-state characterisation techniques, e.g. X-ray diffraction techniques, thermal analysis, moisture sorption analysis, etc. Basic understanding of pharmaceutical development is an additional advantage.

In PT&D, we are the bridge between brilliant science and innovative medicines that help millions of people. We work across the entire value chain, designing and delivering active ingredients, formulations and devices required to support new medicines - from supplies for use in early toxicology studies and clinical trials to developing the technology to ensure drugs can be scaled up for commercial manufacture.

At GPD, we focus on the fields of Oral, Inhaled and Parenteral Drug products. We work on the next generation of medicines and play a key role in the development of new medicinal products.

What you'll do:
The role is laboratory based, and you will work in cross-functional, cross-skilled pharmaceutical development project teams and be an integral part of sub-teams to deliver key results to support pharmaceutical project activities relating to the solid state of materials.

In this role you will:
* Analyse drug substances and drug products using solid state characterisation methods.
* Evaluate solid state properties of materials in relation to pharmaceutical formulations and processes using both experimental and computational methods to support product development.
* Contribute to developing the solid-state area as part of a global community. Develop personal performance by actively seeking feedback and support from peers.
* Contribute with scientific discussion in solid-state skill area during the different drug product development stages and in external collaborations.

The role holder will typically have:
* Hands-on experience in solid state characterisation with expertise in methodology and an enthusiasm for laboratory-based work.
* Basic knowledge of computational approaches related to solids, with a keen interest in contributing to the development of new methods that integrate computation and experimentation to enhance our capability in supporting the development of new medicines.
* Collaborative communication skills, agile mindset, and ability to adjust to dynamic changes in project demands to ensure optimal physical form assessments during development to meet project and patient needs working as a member of cross-functional teams.

Why AstraZeneca?
At AstraZeneca, we follow the science to explore and innovate. We are unlocking the power of what science can do, working towards treating, preventing, modifying and even curing some of the world's most complex diseases. If you're driven by curiosity and courage, inspired by the possibility of doing things that have never been done before, this is the place for you.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

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Associate Director Validation, site Quality

Biomedicinsk analytiker/BMA
Läs mer Feb 3
Associate Director Site Quality - AstraZeneca - Gothenburg - 12-month consultancy assignment

Associate Director Validation, site Quality

Join us in our Site Quality Team! We provide Quality oversight in the development of investigational products and have the responsibility for Licence to Operate at our development site and play an important part in the commercialisation of new medicines. Development Quality is a Global group, with teams located in Gothenburg (Sweden), Macclesfield, (UK) and Durham (North Carolina, US). With a portfolio encompassing both small and large molecules, combination products and ground breaking technologies you will be a part of providing novel life-changing medicines to our patients around the globe.

Are you ready to take the lead in ensuring patient safety and maintaining License to Operate across our Development functions? As an Associate Director in Site Quality, you will be the prime source for quality/compliance advise on validation activities and provide quality leadership to Development functions. You will interpret AZ regulatory and GMP standards into appropriate quality standards and provide guidance to ensure AstraZeneca and Regulatory requirements are met. The role requires independent operation, risk management and lean skills, and decision-making against a background of varying regulations and standards. Your responsibility will extend to internal assets and GMP compliance decisions, having a major impact on AZ's business.

Your role
As an Associate Director, you will develop and maintain in-depth knowledge of the quality regulations and guidelines applicable to your area. You will mentor and support junior colleagues, build strong customer relationships, and participate in GxP audits/initiatives. You will also be responsible for developing and approving GMP documentation and QA risk assessments, providing Quality input into business improvement projects, and be part of external Regulatory Authority GMP inspections. You will work closely with the leadership teams of our customers to set strategic direction for quality within that area, maintaining quality oversight and driving continuous improvement.
Most appreciated in the role is the ability to lead projects, to improve processes or ways of working and support different functions with your subject-matter expert knowledge. Working in a development environment makes your role versified and enables lifelong learning in everyday tasks.

Essential for the role:
* Appropriate scientific degree with extensive experience (5-10 years) of working with validation, in a pharmaceutical GMP environment, preferably within a pharmaceutical development organisation
* Extensive experience from working with all types of validation including, equipment, automation and IT systems.
* A broad and comprehensive understanding of Quality Systems and GMP and good knowledge and reputation in the QA arena and specifically in GMP matters
* A comprehensive understanding of the pharmaceutical/drug development process is essential. A detailed scientific understanding of the Product types being supported is desirable
* Experienced of leading projects, making decisions, acting courageously and communicating with conviction and inspiration and in building excellent relationships both internally and with external suppliers or service providers
* Understanding of Supply Chain processes is desirable

Soft skills:
*You thrive when you work independently, when leading projects and take pride in structuring your day, knowing that the diverse workload can change the schedule with little notice.
* You are a problem solver who can look at solutions in a pragmatic way - coming up with creative solutions whilst still following our strict regulations.
* Excellent team working and networking skills
* Demonstrates independent judgement and uses risk management in complex situations
* Capable of making decisions, acting courageously and communicating with conviction and inspiration
* Demands excellence (sets high bar) and delivers
* A good communicator with experience of interacting effectively across interfaces

Why AstraZeneca?
At AstraZeneca, we take Quality seriously. Our work is important, valued, and at the forefront of discovery, development, and commercialisation. We are always innovating, trialing the latest models and technologies to improve reliability and excellence in our processes. We are proactive, science-based, and driven by our ambition to go far. We are a team of ambitious people who want to achieve. We work together as a team, get our pipeline out to patients sustainably, reliably, and safely. We follow evidence to reach outcomes that benefit patients and AstraZeneca.
Make a difference! Apply now and join us in our journey to push the boundaries of science and make a real-life difference to patients.

About AstraZeneca Gothenburg Hub
Our stunning campus in Gothenburg is one of AstraZeneca's three strategic science centres. The site is home to over 2,500 employees, from 50 different nationalities. Gothenburg includes the complete range of functions, and as such offers plenty of development opportunities for a wide range of professionals. Our science teams in Gothenburg collaborate with academic and industry partners in Sweden and globally. And the site itself has been designed with collaboration in mind. From the Coffee Lab to exercise areas, we've built a series of environments where innovation can happen.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

Ansök nu

Separation Scientist

Molekylärbiolog
Läs mer Feb 3
Separation Scientist - AstraZeneca - Gothenburg - 6-month consultancy assignment

Separation Scientist - High Throughput & Automated Purification

Do you have hands-on experience with the purification of small molecules? Are you interested to further push the boundaries of automated analytical chemistry and separation sciences at a company where we are committed to lifelong learning, growth and development? Welcome to AstraZeneca!

We are seeking a specialised separation scientist that will play an important part in our iLAB team, focusing on the analysis and purification of chemical libraries. You'll have the opportunity to drive and extend the high-throughput purification capabilities within a pioneering automation platform at AstraZeneca in Gothenburg and directly impact drug discovery projects across various therapeutic areas.
We are a global, science-led BioPharmaceutical company and our innovative medicines are used by millions of patients worldwide. With our ground-breaking pipeline comes a bright future - a secure job, exciting opportunities, and varied work. You will be valued. Not only for your unique contribution, skills, and background, but because we recognise people are our greatest asset. Here we are dedicated to being a Great Place to Work.

What you will do:
As Separation Scientist, you will be part of a team of highly motivated scientists contributing to analysis, preparative separation, and characterisation of small molecule chemical libraries.

In this laboratory-based position, you will be specifically responsible for ensuring the delivery of automated analytical and preparative chromatography solutions to drive the delivery of pure compounds to the different projects across our therapy areas within AstraZeneca. You will get the opportunity to work with state-of-the-art chromatographic equipment and liquid handlers.

You will be expected to have effective levels of communication and scientific drive, coordinating effectively with the other members of the analytical and synthesis teams to drive sample progression.

Experience and technical knowledge of chromatographic separations within a drug discovery environment would be an advantage.

Responsibilities for the role:
* Provide hands-on separation science support to drug discovery chemistry using state-of-the art chromatographic instrumentation
* Deliver automated analysis and purification of novel compounds using Liquid chromatography-mass spectrometry (LC-MS) and High-performance liquid chromatography (HPLC)
* Ensure reliability, performance and data quality of analytical instrumentation and automation platforms
* Work within the team to suggest process and infrastructure improvements
* Contribute to a vibrant and entrepreneurial organisation focused on innovation & project delivery; collaborating closely with scientists across the discovery organisation

Why AstraZeneca Gothenburg?
With more than 2,400 employees from over than 50 countries, our vibrant Gothenburg site is a truly inspiring place to work. Here, the history and future of scientific breakthroughs come together. We believe that the diversity of our people is crucial to bringing new discoveries to life.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

Ansök nu

Quality Advisor

Biomedicinsk analytiker/BMA
Läs mer Feb 3
Quality Advisor - AstraZeneca - Gothenburg - 12-month consultancy assignment

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energised and rewarded for their ideas and creativity.

The arena
Are you interested in a challenging opportunity within the Development Quality function in one of the world's leading pharmaceutical companies?
The Development Quality function is responsible for quality oversight of the pharmaceutical development activities within AstraZeneca. We are now looking for a Quality Advisor with GMP focus for our Gothenburg team.

AstraZeneca's pharmaceutical development organisations manage all facets of the process of turning a molecule into a medicine which can be safely and effectively used by patients. The Quality Advisor role has a broad range of responsibilities to ensure all internal and external requirements are fulfilled for the AstraZeneca projects in the development phase.

We have an exciting opportunity for a 12-month temporary assignment as Quality Advisor, in the Site Quality Gothenburg team, who'll be the prime source for quality & compliance advice and providing quality support to the science functions and throughout the drug development process chain.
This is a great opportunity for you who are strong in quality and like to work close to development, Good Manufacturing Practice and making sure quality is assured when delivering new products.

The role
Working in the Site Quality team means you will work closely with the internal assets/facilities, team up with the pharmaceutical development functions and be involved in cross-business processes. To build strong relationships with these functions, knowing their business is key, to give support to projects and develop ways of working that builds for success.

The ability to interpret and trend compliance data to measure and improve quality standards is key. You will develop and maintain a knowledge of the quality regulations and guidelines applicable to your area and a deep scientific understanding of the products that you are supporting.
Whilst taking on your own specialist areas and making good quality decisions, you will be encouraged to think strategically and use your problem-solving skills to resolve any quality issues. You will participate and contribute to continuous improvement projects with the aim to standardise and simplify our internal processes.

Typical Accountabilities:
* Responsible for quality release of manufactured Drug Product, Investigational Medicinal Product for clinical trials
* Support the pharmaceutical development functions with investigations of deviations, changes and other quality and compliance decisions in the development projects related to drug products
* Providing proactive quality advice to support the development, implementation and continuous improvement of GMP quality systems across the Clinical Supply functions and support implementation of agreed global standards
* Operate as part of a global organisation with an integrated mindset to create an organisation with common processes and ways of working

Minimum requirements - Education and Experience
* MSc in pharmacy or engineering (specialising in Pharmaceuticals) with at least 3 years' experience of working within a pharmaceutical GMP environment
* Demonstrates understanding of international quality systems regulations, concepts, industry practices to adopt best in class processes
* A comprehensive understanding of GMP regulations, the pharmaceutical development process and supply chain process would be advantageous
* Experience of interacting effectively across interfaces, collaborating internally in a good communicative way
* Fluent in written and spoken English

Required soft skills:
* Ability to work in a fast-paced environment, meet deadlines, and balance multiple priorities. Independently motivated, detail-oriented, and "can-do" attitude
* Excellent team working and networking skills and encourages team effectiveness
* A good communicator with experience of interacting effectively across interfaces and collaborating internally

About AstraZeneca Gothenburg Hub
Our stunning campus in Gothenburg is one of AstraZeneca's three strategic science centers. The site is home to over 2,500 employees, from 50 different nationalities. Gothenburg includes the complete range of functions, and as such offers plenty of development opportunities for a wide range of professionals. Our science teams in Gothenburg collaborate with academic and industry partners in Sweden and globally. And the site itself has been designed with collaboration in mind. From the Coffee Lab to exercise areas, we've built a series of environments where innovation can happen.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

Ansök nu

Scientist in the Microphysiological systems (MPS) Team

Mikrobiolog
Läs mer Jan 28
Scientist in Microphysiological Systems - AstraZeneca - Gothenburg - 12 month consultancy assignment

Do you have strong experience in cell culture, and you would like to apply your expertise to a company that is accelerating innovative science and turn ideas into life-changing medicines? Join our Microphysiological systems (MPS) team to discover future preclinical models that can support development of new medications for Cardiovascular, Renal and Metabolic diseases!

At AstraZeneca, we are harnessing advanced cell models, microfluidic chip technologies, multi-omics screens, and mathematical modelling to help us achieve the next wave of breakthroughs - here we do things that have never been done before. Are you excited to contribute, then you might be the person we are looking for!

This role will be based in the MPS team at the Early Cardiovascular, Renal and Metabolism (CVRM) department in our dynamic R&D site in Gothenburg, Sweden. The MPS team establishes and applies state-of-the-art MPS platforms to support the CVRM portfolio with emerging therapeutic area needs and new drug modalities. Our mission is to improve translatability from in vitro models to humans and accelerate drug discovery and development.

What you'll do:
You will execute and provide input into the practical delivery of MPS studies and support the development, characterisation, and optimisation of new models.

Responsibilities include:
* Take part in the design, conduct, interpretation and reporting of studies with advanced cell models and MPS.
* Carry out various downstream analyses from the cell culture samples with versatile in-vitro analytical methods such as, but not limited to, ELISA's, qPCR, staining and imaging.
* Join further model development activities to support drug projects with MPS data for resolving mechanisms of action, target identification, and candidate drug evaluation.
* Effectively communicate and collaborate across the Early CVRM and with the key stakeholders in other functions.



Requirements for the role:
* Master's degree + 2 years of relevant experience.
* Background in Pharmacy, Biology, Biotechnology, Biochemistry, Medical Biosciences, Bioengineering or similar
* Strong hands-on cell culture experience
* Experience with primary cells or hPSCs
* Versatile in-vitro analytical methods (e.g., qPCR, staining and high-content imaging, plate-based assays e.g., ELISAs)
* Independent study design, laboratory work, and data analysis
* Data visualisation and statistical analysis
* Excellent interpersonal skills and excellent communication skills in English, both verbal and in writing
* Strong ability to engage and collaborate across boundaries with a problem-solving attitude and focus on delivery

Desired for the role:
* Experience in 3D cell culture, i.e., spheroids, organoids, or multicellular co-cultures
* Experience with one or more of cell models for liver, kidney, cardiac, pancreas, or adipose tissue
* Experience of culturing immune cells
* Handling microfluidic chips
* RNA-Seq and proteomics
* Workflow automation e.g. robotic liquid handling
* Experience of the pharmaceutical industry

Why AstraZeneca?
At AstraZeneca, we follow the science to explore and innovate. We are unlocking the power of what science can do, working towards treating, preventing, modifying and even curing some of the world's most complex diseases. If you're driven by curiosity and courage, inspired by the possibility of doing things that have never been done before, this is the place for you.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

Ansök nu

Senior Scientist in the Microphysiological Systems (MPS) team

Mikrobiolog
Läs mer Jan 28
Senior Scientist in Microphysiological Systems - AstraZeneca - Gothenburg - 12 month consultancy assignment

Flow cytometry Senior Scientist in the Microphysiological Systems (MPS)

Do you have experience in flow cytometry and versatile knowledge in cell culture, and are you eager to apply your expertise in a company that accelerates innovative science to turn ideas into life-changing medicines? Join our Microphysiological Systems (MPS) team and contribute to the discovery of future preclinical models that support the development of new medications for Cardiovascular, Renal, and Metabolic (CVRM) diseases!

At AstraZeneca, we are harnessing advanced cell models, microfluidic chip technologies, multi-omics screens, flow cytometry, and mathematical modelling to achieve the next wave of breakthroughs - here we do things that have never been done before. Are you excited to contribute? Then you might be the person we are looking for!

This role is based in the MPS team at the Early CVRM department in our dynamic R&D site in Gothenburg, Sweden. The MPS team establishes and applies state-of-the-art MPS platforms to support the CVRM portfolio with emerging therapeutic area needs and new drug modalities. Our mission is to improve translatability from in vitro models to humans and accelerate drug discovery and development.

What you'll do:
You will execute and provide input into the practical delivery of MPS studies while also serving as a flow cytometry (FACS) scientist. You will support the development, characterisation, and optimisation of advanced cell models and flow cytometry-based assays. We'll look to you as an expert in cell and molecular biology techniques, and you will independently carry out various downstream in-vitro analytical methods.

Responsibilities include:
* Develop and execute flow cytometry-based assays for cell characterisation and functional analysis, including panel design.
* Take part in the design, conduct, interpretation, and reporting of studies with advanced cell models and MPS.
* Carry out various downstream analyses from cell culture samples with versatile in-vitro analytical methods such as, but not limited to, ELISA, qPCR, staining, and imaging.
* Join further model development activities to support drug projects with MPS and flow cytometry data for resolving mechanisms of action, target identification, and candidate drug evaluation.
* Effectively communicate and collaborate across the Early CVRM department and with key stakeholders in other functions.



Requirements for the role:
* Master's degree + 4 years of relevant experience.
* Background in Pharmacy, Biology, Biotechnology, Biochemistry, Medical Biosciences, Bioengineering, or similar.
* Proficiency in flow cytometry, including assay development, troubleshooting, and data interpretation.
* Strong hands-on cell culture experience.
* Versatile in-vitro analytical methods (e.g., qPCR, staining and high-content imaging, plate-based assays such as ELISAs).
* Independent study design, laboratory work, and data analysis.
* Data visualisation and statistical analysis.
* Strong interpersonal and communication skills in English, both verbal and written.
* Strong ability to engage and collaborate across boundaries with a problem-solving attitude and focus on delivery.

Desired for the role:
* Experience in 3D cell culture, i.e., spheroids, organoids, or multicellular co-cultures.
* Experience with one or more of the following cell models: liver, kidney, cardiac, pancreas, or adipose tissue.
* Experience in culturing immune cells.
* Handling microfluidic chips.
* Workflow automation, e.g., robotic liquid handling.
* Experience of the pharmaceutical industry.

Why AstraZeneca?
At AstraZeneca, we follow the science to explore and innovate. We are unlocking the power of what science can do, working towards treating, preventing, modifying and even curing some of the world's most complex diseases. If you're driven by curiosity and courage, inspired by the possibility of doing things that have never been done before, this is the place for you.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

Ansök nu

Operational Technologist/Associate Scientist

Laboratorieassistent
Läs mer Jan 13
Operational Technologist-Associate Scientist - AstraZeneca - Gothenburg - 6 month assignment

Consultancy role for AstraZeneca.

Operational Technologist/Associate Scientist - Early Product Development and Manufacturing

At AstraZeneca, we unlock the power of What Science Can Do. Empowered to explore, every day we work towards our ultimate aim - treating, preventing, modifying and even curing complex diseases. Be part of the team where you are empowered to follow the science!

Pharmaceutical Sciences is responsible for the design and development of synthetic routes, preclinical and phase I/II formulations, encompassing both small molecules and new modalities such as mRNA and oligonucleotides, across the whole range of AstraZeneca's therapeutic areas.

The manufacturing unit within Early Product Development and Manufacture (EPDM) in Gothenburg is accountable for the manufacture of early investigational medicinal products (oral solutions/suspensions, parenteral solutions, capsules, tablets and inhalers), mainly for clinical Phase I and II studies.

We are now looking for an Operational Technologist/Associate Scientist starting as soon as possible with the location Gothenburg, Sweden.

What you will do
You will have a great opportunity to learn more about pharmaceutical development working with experienced operators. This role contributes to the manufacturing of drug products in the development phase for clinical studies. All the activities below will have an impact on the speed, quality and cost of the AZ development portfolio.

As part of the EPDM manufacturing unit, your work will focus on the manufacturing of drug products. You will perform practical hands-on work in our Good Manufacturing Practice (GMP) facilities with dedicated tasks in close collaboration and to support EPDM Scientist/Senior Scientist e.g. assisting GMP operators with:

* Preparation of process rooms before and after clinical manufacture
* Assembly/disassembly and cleaning of equipment
* Dispensing of API (Active Pharmaceutical Ingredients) and excipients (inactive pharmaceutical ingredients)
* Bulk packing
* Visual inspection of drug products
* Metal check of drug products
* Check of log books
* Working according to SHE (Safety Health and environment) and GMP standards

The role is intended to be used in a flexible way to resolve short-term bottlenecks. The role holder will not become fully qualified as a GMP operator but will be able to carry out much of the work expected from operators under supervision.

Why AstraZeneca
At AstraZeneca, we follow the science to explore and innovate. We are unlocking the power of what science can do, working towards treating, preventing, modifying and even curing some of the world's most complex diseases. If you're driven by curiosity and courage, inspired by the possibility of doing things that have never been done before, this is the place for you.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

Ansök nu

Scientist - EPDM

Biomedicinsk analytiker/BMA
Läs mer Jan 13
Scientist EPDM - AstraZeneca - Gothenburg - 6 month assignment

Hays is currently recruiting a scientist for a consultancy role for AstraZeneca.

Scientist - Early Product Development and Manufacturing

Are you ready to make a significant impact on the development of new medicines? Join us at AstraZeneca's Early Product Development and Manufacture (EPDM) unit in Gothenburg, Sweden. We are accountable for delivering a vast portfolio of early investigational medicinal products, supplying different types of clinical trial material to studies across the globe. This is your chance to explore and innovate in our dynamic environment!

This is an exciting opportunity to join our Pharmaceutical Sciences department, which is accountable for the design and development of synthetic routes, preclinical and phase I/II formulations, encompassing both small molecules and new modalities such as mRNA and oligonucleotides, across the whole range of AstraZeneca's therapeutic areas. The role will be offered at Scientist level.

What you will do:
As part of the EPDM manufacturing unit, you will work in a GMP (Good Manufacturing Practice) environment, contributing to the delivery of clinical results. Your role will focus on the manufacturing of drug products, with responsibilities including timely manufacture of various drug products, working with practical hands-on processes in our GMP facilities, monitoring regulatory requirements, supporting documentation activities, and driving initiatives to improve flexibility and productivity. As we are investing in innovative technology, amongst others within Continuous manufacturing, we need to expand knowledge and competence in this area. Depending on prior experience and interest, this role could be more adapted to this area.

Accountabilities include:
* Work with practical hands-on processes in our GMP facilities following manufacturing batch records and performing transactions in material management systems.
* Assume responsibilities toward timely manufacture of various drug products in line with the plans agreed within EPDM and surrounding stakeholders.
* Monitor, secure and follow up on other regulatory requirements according to GMP through associated IT-systems.
* Rapidly develop strong competence within relevant process technologies and build credibility and the ability to drive and secure product establishment, scale-up and clinical manufactures.
* Support documentation activities, e.g. by authoring manufacturing batch records, taking part in deviation investigations, authoring SOPs, and other guidance documents, change control processes etc.
* Assess records and report manufacturing and validation data accurately according to GMP.
* Ensure that SHE (Safety Health and Environment) and GMP standards are upheld and ensure AZ Policies and Standards are understood and followed.
* Be entrepreneurial and drive initiatives to further improve flexibility and productivity, resulting in shorter lead times or increased value for our customers and patients.

Why AstraZeneca?
At AstraZeneca, we follow the science to explore and innovate. We are unlocking the power of what science can do, working towards treating, preventing, modifying and even curing some of the world's most complex diseases. If you're driven by curiosity and courage, inspired by the possibility of doing things that have never been done before, this is the place for you.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

Ansök nu

Analytical Scientist

Biomedicinsk analytiker/BMA
Läs mer Dec 3
Analytical Scientist - AstraZeneca - 12 month consultancy assignment - Gothenburg

We are currently recruiting two Analytical Scientists for a consultancy assignment for AstraZeneca.

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives- and are made to feel valued, energised and rewarded for their ideas and creativity. At AstraZeneca, we set pride to drive development in a sustainable way, in all areas of our business, from influencing our suppliers through development to commercial products.

Tasks and responsibilities/The role:
We are looking for a scientist in Analytical Chemistry who can provide input in the area of analytical science during the development of drug products, and can work together with us to determine the quality attributes during the development of the formulations. The work includes analytical testing, documentation, and attending and presenting at project team meetings. The role is primarily laboratory based.

Requirements:
* BSc or MSc typically from pharmaceutics, chemistry, or analytical science, but also other disciplines with relevant skills.
* Good knowledge of written and spoken Swedish and/or English is necessary.
* Scientific knowledge within analytical science.
* Laboratory experience including working with computerised systems and chromatography techniques (e.g. UPLC) for detection of small molecules.

Desirable:
* Experience from working within the pharmaceutical industry.
* Well organised, analytical, flexible and accurate.
* Good team working skills are also important, together with the ability to operate independently.
* Good communication skills linked to the ability to work to tight timelines are highly valued.
* If you have experience from working in a GMP environment or the pharmaceutical industry, this will be an advantage.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

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Operations Regulatory CMC - Specialist

Hälsovårdsinspektör
Läs mer Dec 3
Operations Regulatory CMC Specialist - AstraZeneca - 7 month consultancy assignment - Gothenburg

We are currently recruiting an Operations Regulatory CMC - Specialist for a consultancy assignment for AstraZeneca.

Do you have expertise in regulatory and overall understanding of GxP requirements? Are you highly collaborative and like contributing to clear instructions and implementing process improvements? This opportunity as Processes Specialist in the Regulatory Process and Compliance team might be the right opportunity for you.

At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means putting patients first, doing the right thing and working together to make the impossible a reality. If you are swift to action, willing to collaborate, and curious about what science can do, then you're our kind of person.

Global Regulatory Excellence's vision is to Leading enterprise-wide regulatory strategies, policy and delivery - so that no patient waits. In the Regulatory Process and Compliance team, we network collaboratively to enable our customer groups to operate efficient processes in a compliant manner.

What you'll do
As a Processes Specialist in the Regulatory Process and Compliance team, you will be working with the Process team members and taking responsibility for the management of assigned tasks related to procedural document management. You will act as technical writer and reviewer, and support project management to ongoing procedural document update program.
You will be accountable for executing the delivery of the authoring and lifecycle management of current procedural documents. We hope that you have the drive to establish a culture of continuous improvement, high performance, flexibility and quality, emphasising a "can do" attitude and ensuring high standards of quality in all outputs.

Other key responsibilities in this position:
* Identify opportunities for and drive the enhancement of existing processes and procedural documents
* Using understanding of regulatory processes and regulations to provide support to the regulatory process team
* Identify opportunities to improve and simplify the methodology in processes and guidance, provide practical solutions
* Review and verify documents and data for accuracy and completeness
* Collaborate with team members to ensure high standards of quality in all outputs
* Contribute to communication and change management activities associated with process initiatives



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

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Associate Scientist/Operational Technologist

Kemist
Läs mer Nov 25
Associate Scientist/Operational Technologist - AstraZeneca - 4 month consultancy assignment

Associate Scientist/Operational Technologist - Drug Product Delivery

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energised and rewarded for their ideas and creativity.

We are curious, creative, and open to new ideas and ways of working. Above all, we are passionate about science and driven to always put patients first. Join AstraZeneca and apply your expertise to a company that is following science and turning ideas into life-changing medicines. We have an exciting opportunity for a talented Drug Product Delivery (DPD) Associate Scientist/Operational Technologist to be based in Gothenburg, Sweden.

Pharmaceutical Technology and Development (PT&D) is the organisation that turns brilliant science into actual medicines that helps millions of people. We work across the entire value chain, designing and delivering active ingredients, formulations and devices for new medicines and providing expert technical support to all AstraZeneca's commercial drug substances and products to ensure we successfully supply medicines to patients.
Drug Product Delivery (DPD) within PT&D is the sole internal AstraZeneca department that packs, labels and distributes investigational medicinal products to clinical trial patients. We support launched, pre-launched and products under development within all our therapeutic areas. We work in a fast-paced environment where flexibility, agility and teamwork enable us to deliver high value to clinical trials.

We are now looking for one Associate Scientist/Operational Technologists starting as soon as possible with the location Gothenburg, Sweden.

The role
You will have a great opportunity to learn more about pharmaceutical development working with experienced operators. This role contributes to the packaging of drug products in development phase for clinical studies. All the activities below will have an impact on the speed, quality and cost of the AZ development portfolio.
Practical hands-on work in our Good Manufacturing Practice (GMP) facilities with dedicated tasks in close collaboration and to support DPD Scientist/Senior Scientist e.g. assisting GMP operators with:
-Preparation of process rooms and equipment before and after clinical manufacture
-Assembly/disassembly and cleaning of equipment
-Primary packing, i.e. packing of tablets/capsules in bottles (manually or automated)
-Secondary packing, i.e. labelling of study materials (manually or automated)
-Working according to SHE (Safety Health and environment) and GMP standards

The role is intended to be used in a flexible way to resolve short-term bottle necks. The role holder will not become fully qualified as a GMP operator but will be able to carry out much of the work expected from operators under supervision.

Preferred experience/requirements
- You must have completed your studies at upper secondary school level e.g. in natural/technical sciences
-It is essential that you follow written procedures carefully and document executed tasks.
-GMP knowledge is desirable
-Interest in technique and manufacturing equipment and practical hands-on work is desirable
-You need to be flexible with good team-working skills.
-Good knowledge of oral and written English is a requirement.

AstraZeneca is one of the world's most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

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Solid State Scientist/Senior Scientist

Kemist
Läs mer Nov 18
Solid State Scientist/Senior Scientist - AstraZeneca - Gothenburg

We are currently recruiting a Solid State Scientist/Senior Scientist to AstraZeneca for a 6-month assignment, with the possibility of extension.

At AstraZeneca, we turn ideas into life-changing medicines and strive to continuously meet the unmet needs of patients worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you're our kind of person.

Pharmaceutical Sciences at AstraZeneca deliver the therapies of the future through scientific leadership in drug delivery, design of synthetic routes, and manufacturing of Active Pharmaceutical Ingredients (API) across all the AstraZeneca therapy areas.
Our vision is to be "pharmaceutical science leaders, creating innovative and cost-effective solutions, shaping the diverse therapies of the future".
We're looking for talented and motivated solid-state scientists to join our solid state and automation team within Early Product Development and Manufacturing (EPDM) in Gothenburg.

You would join a highly collaborative team and help us deliver the solid-state science to product development within the early portfolio from discovery up to phase II.
To be successful in this role, you will need a strong scientific background with good skills in written and verbal communication and the ability to engage and collaborate across boundaries with a positive problem-solving attitude and delivery focus.
The successful applicant will become a core member of the global Solid-state skill area which is responsible for ensuring suitable physical form screening, selection and control within drug substances and products. You will get the opportunity to apply your excellent crystallography and solid-state expertise to the drug projects you are working in, contributing to the progression of these projects and drive the scientific development within the field of solid-state science at AstraZeneca.

Accountabilities/Responsibilities

* Deliver solid state characterisation data in our state of the art laboratory using techniques like TGA, DSC, XRPD and DVS.
* Responsible for ensuring suitable physical form screening, characterisation, form selection and control within drug substance and product.
* Drive solid state skill area in projects and work closely with analytical, formulation, and biopharmaceutics scientists to drive science and innovation.
* Plan and conduct lab-based experimental work in accordance with project timelines.
* Run and develop solid state workflows on automation equipment such as weighting robots and liquid handling systems
We are working towards treating, preventing, modifying and even curing some of the world's most complex diseases. Here we have the potential to grow our pipeline and positively impact the lives of billions of patients around the world. With more than 2,400 employees from over 50 countries, our vibrant Gothenburg site is a truly inspiring place to work. Here, the history and future of scientific breakthroughs come together. We believe that the diversity of our people is crucial to bringing new discoveries to life.

What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

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Analytical Chemist Early Product Development and Manufacturing

Biomedicinsk analytiker/BMA
Läs mer Nov 20
Analytical Chemist - AstraZeneca - Gothenburg

Hays is currently recruiting for an Analytical Chemist for a 12-month consultancy assignment.

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energised and rewarded for their ideas and creativity.

Pharmaceutical Sciences at AstraZeneca deliver the therapies of the future through scientific leadership in drug delivery, design of synthetic routes, manufacturing of Active Pharmaceutical Ingredients (API) and Investigational Medicinal Product (IMP) across all the AstraZeneca therapy areas. Our vision is to be "pharmaceutical science leaders, creating innovative and cost-effective solutions, shaping the diverse therapies of the future".

We're looking for a talented and motivated Analytical Chemist (Scientist/Senior Scientist) to join our analytical characterisation team within Early Product Development and Manufacturing (EPDM) in Gothenburg, Sweden.



What you'll do:
In the role as Scientist/Senior Scientist, you would join a highly collaborative team, and together we will deliver the analytical science to drug product development within the early portfolio up to phase II. To be successful in this role you will need a strong scientific background with good skills in written and verbal communication and the ability to engage and collaborate across boundaries with a positive problem-solving attitude and delivery focus. This is a lab-based role where you will work collaboratively with colleagues, documenting your experiments carefully and to the right quality, as well as contributing to regulatory clinical trial applications (CTA). You will get the opportunity to apply your excellent analytical expertise in the drug product projects you will be working in. You will contribute to the progress of drug product development, getting new medicines for patients and driving the scientific development within the field of analytical science at AstraZeneca.

Essential requirements:
- University degree (MSc, PhD) in relevant discipline, preferable with industry experience
- Scientific knowledge within analytical science and technically skilled to use chromatography with relevant detection techniques for small molecules
- Broad industry experience of pharmaceutical development including oral solid dosage form development
- Experience of CMC regulatory submissions and work according to GMP
- In-depth skills in specific analytical techniques for small molecules, e.g. mass spectrometry, NMR, dissolution etc.
- Excellent written and oral communication skills in English are a must
- Experience, knowledge and keen interest in the field of automation, AI and digitalisation would be advantageous
- Proven track record in publications related to analytical science or characterisation of pharmaceuticals is desirable

Soft skills:
You are a driven experimentalist, with a passion to deliver highly relevant and reliable data and with the ability to be influential in discussions in a wide set of communities and multi-disciplinary project teams in accordance with project timelines.
You keep abreast with the scientific discipline and the ability to drive and lead science and innovation personally, within the department and manage external collaborations to meet future needs.
You have excellent communication, collaboration, networking and leadership skills & the ability to lead and inspire colleagues.

At AstraZeneca, we are committed to making a difference. We have built our business around our passion for science. Now we are fusing data and technology with the latest scientific innovations to achieve the next wave of breakthroughs. Here, we think holistically about patients and are always learning from those living with diseases. We harness digital, data science & AI to fast-forward our research, ensuring that work born in a lab can make a real difference. Every day, we impact patients' lives across the world.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

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Scientist in Vivo

Laborant, biologi
Läs mer Nov 19
In Vivo Scientist - AstraZeneca - Gothenburg

Hays is now recruiting an In Vivo Scientist for AstraZeneca for a 12-month consultancy assignment.

Are you an experienced scientist ready to apply your skills in a diverse and dynamic organisation? If you can envision providing scientific expertise in a role that can impact patients' lives - join us now!

At AstraZeneca, we believe in the potential of our people, and you'll develop beyond what you thought possible. We make the most of your skills and passion by actively supporting you to see what you can achieve, no matter where you start with us.
We are now looking to recruit an In Vivo Scientist with excellent laboratory skills and a drive for innovation to join the Bioscience in vivo department within the Early Respiratory and Immunology (eR&I) R&D unit located in Gothenburg, Sweden.

Respiratory and immunology are two of AstraZeneca's main therapy areas. From a research perspective, we work to understand, treat, modify, and ultimately cure respiratory disease with an emphasis on four respiratory diseases with significant unmet medical need: asthma, COPD, Idiopathic Pulmonary Fibrosis (IPF) and Chronic Cough. In addition, we also focus on immunology-driven disease areas including rheumatology, dermatology, gastrointestinal and inflammatory diseases driven by eosinophilic immune dysfunction.

The successful candidate will join a highly motivated team that works closely together with other departments focusing on target identification, drug formulation, translational science, in vitro assay development and drug metabolism/pharmacokinetics to support discovery projects and to drive exciting new research. Are you ready to join us?

What you'll do:
As a vital member of our in vivo team, you will contribute to progress in our drug discovery projects. Your role will be mainly lab-based in which you will be actively involved and responsible to coordinate, perform and analyse in vivo studies. While we expect you to be independent, we are also looking for someone that thrives in a team setting and contributes to the success of others.

At AstraZeneca, when we see an opportunity for change, we seize it and make it happen, because any opportunity, no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognising their potential. Join us on our journey of building a new kind of organisation to reset expectations of what a bio-pharmaceutical company can be. This means we're opening new ways to work, pioneering groundbreaking methods, and bringing unexpected teams together. Interested? Come and join our journey.



Requirements for the role:
? B.Sc. or M.Sc. degree in relevant subjects or equivalent level of understanding developed through experience in drug discovery or early development.
? Excellent technical and experimental In vivo experience and skills, including rodent handling, drug administration and collection of biological samples. Ability to coordinate and perform respiratory disease and mechanistic models.
? Valid certificates to work with live animals in Sweden.
? Excellent written and oral communication skills in English.
? Maintain the highest standards of animal welfare and ethical compliance and ensure integrity of generated data. Familiar with using Good Statistical Practice in animal research and applying the 3R's (reduction, refinement, and replacement) across the full range of studies.
? Good generic computer proficiency including Microsoft Office.

Desirable for the role:
? Experience in basic cellular and molecular biology techniques (e.g. ELISA, western blot, FACS, Meso Scale Discovery (MSD) technology platform), and gene expression analyses (qPCR)).
? Good written and oral communication skills in Swedish and experience in writing ethical applications for animal work in Sweden.
? Good understanding of pharmacology, physiology, immunology, respiratory diseases (COPD, asthma, cough, IPF) and PKPD relationships.

So, what's next!

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

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Formulation Scientist

Laborant, biologi
Läs mer Nov 11
Formulation Scientist - AstraZeneca - 12 month assignment - Gothenburg

Consultancy role for AstraZeneca.

At AstraZeneca, we turn ideas into life-changing medicines and strive to continuously meet the unmet needs of patients worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you're our kind of person.

Pharmaceutical Sciences at AstraZeneca deliver the therapies of the future through scientific leadership in drug delivery, design of synthetic routes, and manufacturing of Active Pharmaceutical Ingredients (API) across all the AstraZeneca therapy areas.
Our vision is to be "pharmaceutical science leaders, creating innovative and cost-effective solutions, shaping the diverse therapies of the future".
Are you an enthusiastic, innovative, and motivated Formulation Scientist seeking a unique opportunity? Join one of our small molecule formulation teams in Pharmaceutical Sciences at AstraZeneca's vibrant R&D site in Gothenburg, Sweden. Collaborate with dedicated teams and work closely with other skill experts in our common effort to drive AstraZeneca's pipeline forward.

Responsibilities
This is a lab based role where you will support project teams and provide your technical and scientific expertise into formulation development. You will develop and deliver different formulation systems for oral and parenteral use, with focus on liquid formulations, supporting projects in preclinical and clinical phase. You will also perform essential characterisation work.
This requires a tight collaboration with other internal functions and external partners to build our capabilities in drug delivery as well as engaging with customers in the development of solutions by applying a broader perspective.

You are expected to perform lab-based experimental work in accordance with project timelines, in close collaboration with other formulators, analysts, solid state and biopharmaceutical experts. The work should be documented carefully and to the right quality.

Essential requirements:
* MSc degree in a discipline relevant to formulation science, pharmaceutical technology, chemical engineering or equivalent qualifications.
* Experience in working with formulation development or similar product development, or other laboratory skills of relevance.
* Technical competence in the field of drug product formulation development for oral and/or parenteral delivery is desirable
* Good understanding of suitable quality standards and regulatory frameworks is desirable

Soft skills:
* Delivery focused with the ability to utilise scientific and innovative thinking.
* Genuine interest in experimental work and hands-on problem-solving.
* Great communication skills in English, both orally and in writing.

If your passion is science, and you want to be part of a team that makes a bigger impact on patients' lives, then there's no better place to be. Join us at AstraZeneca, where we truly understand science and apply it every day to strengthen and grow our pipeline.

AstraZeneca is one of the world's most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

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Material Management and Distribution Operator

Laborant, biologi
Läs mer Okt 29
Material Management and Distribution Operator - AstraZeneca - 9 month assignment - Gothenburg

Consultancy role for AstraZeneca.

About AstraZeneca
AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialisation of prescription medicines for some of the world's most serious diseases. At AstraZeneca, we are proud to have a unique workplace culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives and are made to feel valued, energised and rewarded for their ideas and creativity.

We are curious, creative, and open to new ideas and ways of working. Above all, we are passionate about science and driven to always put patients first. Join AstraZeneca and apply your expertise in a company that is following science and turn ideas into life-changing medicines. We have an exciting opportunity for talented DPD Operators to be based in Gothenburg, Sweden.

About the role:
Drug Product Delivery (DPD) within Pharmaceutical Technology & Development is the sole internal AstraZeneca department that packs, labels and distributes investigational medicinal products to clinical trial patients. We support launched, pre-launched and products under development within all our therapeutic areas. We work in a fast-paced environment where flexibility and agility enable us to deliver high value to early phase clinical trials.

The DPD Operator role will be an operational role within Distribution or Material Management of two Drug Product Deliveries in three operational skill areas: Material Management, Pack Label and Distribution. We work in an environment where flexibility and agility enable us to deliver high value in early phase clinical trials. To complement our existing team, candidates with the following experience are of interest:

- Distribution experience from a complex supply chain organisation
- Drug Product Knowledge including management of Item/article and lot/batch management to ensure traceability of items/articles in a patient kit, including a drug product, packaging material and patient labels from the pharmaceutical industry.

Main Duties and Responsibilities
The role holder will contribute to the DPD organisation applying their expertise in the complex and regulated GMP environment. The work is focused on operational within Distribution or Material Management. As a DPD operator, you will perform and document all the operational work according to written procedures. Be engaged in the development and improvement of internal processes and managing deviations. Be responsible for writing of GMP and SHE procedures within own skill areas and will be responsible for related training and compliance activities. As required, maintain defined facilities or equipment according to GMP standards and be proactive to contribute to projects/activities through applying specialist knowledge within appropriate areas.

Responsibilities example:
Preparing documentation, receiving and packing of investigational medicinal products to clinical trials. Being the main point of contact when it comes to distribution questions for a number of studies.

Essential requirements and skills
* BSc/MSc in chemistry/pharmacy/engineering/logistics or equivalent experience. Preferably 2 years experience within pharmaceutical development.
* Demonstrated ability to work with teams in a culturally diverse, complex and changing environment most internally but to some extent externally.
* Good written and verbal English communication and understanding.

Beneficial requirements and skills:
* Understanding of principles, applications and management of SHE and GMP in an R&D environment.
* Understanding the disciplines in Drug Product Delivery, Supply Chain and Pharmaceutical development in order to contribute to an effective Supply Chain organisation.

Soft skills:
* Curious and innovative mindset with problem-solving ability - solving issues with minimal guidance

AstraZeneca is one of the world's most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

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Personal Assistant/Personal Administrator

Laboratorieassistent
Läs mer Okt 29
Personal Assistant/Personal Administrator - AstraZeneca Group - 18 months assignment - Gothenburg

Consultancy role for an 18-month assignment.

Evinova is an innovative health-tech business with the ambition to deliver industry-leading digital health solutions to the wider healthcare community, to improve patient experience and outcomes. It is an independent company, part of the AstraZeneca group.

Do you have an impressive track record as a Personal Assistant or Senior Administrator, outstanding organisational skills and the ability to multitask effortlessly? We are now looking for an 18-month maternity replacement in Evinova Gothenburg. This is an exciting opportunity to take on a challenging and varied role within our team.

Your focus will be on providing high quality professional PA support to the Head of Digital Patient & Site Products and the Executive Director of Digital Respiratory & Inflammation. You will also participate in building the Evinova community in Gothenburg. As the successful candidate, you will be an individual with high standards, enthusiasm and a passion for learning, together with excellent communication skills, a proactive approach and the confidence to act independently.

Attention to detail and strong organisational skills will be the key to success in this role as you will be required to action on portfolio and stakeholder management specific tasks, manage complex calendars, coordinate internal and external meetings, process expenses, manage complex travel arrangements including travel visas, as well as organising and preparing materials for key meetings, events, and communications.

You will need to have strong influencing skills with the ability to engage relevant people and develop solutions; your patience and flexibility will be advantageous in securing this challenging but interesting role. Often working independently, you must be able to respond to changes in customer and stakeholder demands with the flexibility to adapt to changing situations.

What you'll do

* Proactive diary management
* Extensive and proactive planning of travel arrangements, including flights, accommodation, airport transportation, car bookings, trains etc. (preparing travel packs / itineraries)
* Internal/external meeting arrangements and support
* Facilitating contracting: Statement of Work, purchase order creation, invoice resolution and other financial administration
* Onboard new starters (ordering IT equipment, setting up key meetings, assigning a buddy etc)
* Support preparation of presentation materials for department head and prepare agendas and minutes for specific meetings
* Working collaboratively with the wider Digital Health PA/admin team to provide specialist project-based administrative support when required
* Maintain databases and distribution lists

Why Evinova?

Evinova draws on AstraZeneca's deep experience developing novel therapeutics, informed by insights from thousands of patients and clinical researchers. Together, we can accelerate the delivery of life-changing medicines, improve the design and delivery of clinical trials for better patient experiences and outcomes, and think more holistically about patient care before, during, and after treatment. We know that regulators, healthcare professionals, and care teams at clinical trial sites do not want a fragmented approach. They do not want a future where every pharmaceutical company provides its own, different digital solutions.
They want solutions that work across the sector, simplify their workload, and benefit patients broadly. By bringing our solutions to the wider healthcare community, we can help build more unified approaches to how we all develop and deploy digital technologies, better serving our teams, physicians, and ultimately, patients. Evinova represents a unique opportunity to deliver meaningful outcomes with digital and AI to serve the wider



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

Ansök nu

Senior Scientist, SPR & Biophysics

Molekylärbiolog
Läs mer Okt 21
Senior Scientist, SPR & Biophysics - Protein Science, Structural Biology and Biophysics - AstraZeneca - Gothenburg - 12 month assignment

Consultancy role for AstraZeneca

Are you a scientist with expertise and enthusiasm for applying Surface Plasmon Resonance (SPR) and other biophysical tools to uncover molecular interactions and advance drug discovery? Do you want to leverage your skills to broaden the application of SPR and related techniques in impactful drug discovery projects, while growing your career within a company that values science and transforms ideas into life-changing treatments? AstraZeneca has an exciting opportunity for you!

AstraZeneca is committed to the development of the next generation of innovative medicines. To help us with this, we are looking for a scientist with passion, expertise and experience to join our Protein Science, Structural Biology and Biophysics department as a lab-based Senior Scientist on a one-year contract basis within the Biophysics team. The team is based in our vibrant R&D site in Gothenburg, Sweden and applies biophysical technologies across a range of different modalities to support drug discovery from target validation to drug candidate. You will be part of a team of enthusiastic scientists that deliver deep technical and scientific expertise by applying molecular biophysical methods, including SPR, NMR, ITC, DSF, HDX-MS and single molecule approaches. This is a unique opportunity to contribute to the development and execution of research strategies for the discovery of new medicines - and be focused on the field of Biophysics.

What you will do:

The role of Senior Scientist is a laboratory-based position supporting the characterisation of molecular interactions in drug discovery, with a focus on Surface Plasmon Resonance (SPR) and other biophysical techniques. We are seeking a highly skilled and motivated biophysicist with deep expertise in SPR assay development, method optimisation, and screening to join our team on a one-year contract basis. The ideal candidate will have a strong theoretical and practical background in biophysical techniques, particularly SPR, along with experience in protein-ligand interactions. This role is crucial in advancing our research and development projects across various therapeutic areas.

You will have significant control and influence over project direction, allowing you to shape experimental strategies and outcomes. Additionally, you will have opportunities to learn new techniques and develop your leadership skills. Working in a collaborative and innovative environment, you will engage with scientists from diverse disciplines. This position offers a unique chance for professional development in an industrial setting, helping you gain valuable experience and build a strong foundation for future career growth.

You will be responsible for designing and implementing advanced SPR assays, tailored to specific research needs, as well as larger screening activities. You will conduct intricate experiments aimed at understanding binding kinetics, affinity, and thermodynamics, ensuring accurate and precise data collection and reporting. Your expertise will be crucial in analysing SPR data, interpreting results, and integrating findings with other research data to provide comprehensive insights into drug mechanisms of action. You will collaborate closely with multidisciplinary teams, contributing to the integration of SPR and biophysical findings into broader research objectives. Additionally, you will keep abreast of the latest advancements in SPR and biophysics, continuously applying this knowledge to enhance our research capabilities.

You will document and present your results in both internal and external meetings, playing a vital role in driving our scientific endeavours forward. Finally, to be successful in this role, we see that you have good social and communication skills, are collaborative and a strong team player. You should also be able to work independently and have a positive, goal-oriented and problem-solving attitude.

Why AstraZeneca?

When we see an opportunity for change, we seize it and make it happen, because any opportunity can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognising their potential. Join us on our journey in finding new ways to work, pioneering cutting-edge methods and bringing unexpected teams together!

Does this sound like your next challenge and place to work? We look forward to your application.

Ansök nu

Senior Research Scientist - Cellular assay development

Molekylärbiolog
Läs mer Okt 2
Senior Research Scientist - AstraZeneca - 8 month assignment - Gothenburg

Consultancy role for AstraZeneca.

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energised and rewarded for their ideas and creativity.

The arena:
We are looking for a motivated and engaged Senior Scientist to join our Oligo Cell Assay Development team at AstraZeneca in Gothenburg for an 8-month fixed-term contract (maternity replacement). As a Senior Scientist in oligo cellular assay development, you will use your knowledge of cells and assay technologies to develop state-of-the-art cell-based assays for screening and profiling of potential therapeutic oligos such as antisense oligonucleotides or siRNA, with the aim of identifying lead molecules. You will contribute to the progression of drug projects by bringing novel ideas and scientific strategies. You will work within Discovery Sciences, part of AstraZeneca's BioPharmaceuticals organisation, with a focus on scientific advances in drug discovery across therapeutic areas including, respiratory and inflammation (R&I), cardiovascular, renal and metabolism (CVRM) and rare disease (Alexion).

Tasks and responsibilities/The role:
This is an exciting opportunity for you to join us as a lab-based scientist to develop cell assays for discovery of novel oligonucleotide-based therapies. The assays you develop will be used in projects in all phases of AstraZeneca's drug discovery pipeline. You will work closely with our colleagues in the Cell engineering and Cell banking teams, screening scientists in the oligo profiling team, and the rest of the AstraZeneca therapeutic oligo platform.
We believe that our new colleague is a highly motivated scientist with a keen interest in technological and scientific advances. Along with this we see you as a person who enjoys collaboration, who holds networking skills with experience of interacting effectively across functions and disciplines. This goes hand in hand with your problem-solving skills, great goal focus and enthusiasm for science.
You will be strongly encouraged and supported to think creatively in our dynamic environment. Here, we are free from fear of failure, free to ask the right questions, and make bold decisions.

Essential requirements:
* PhD in Biology, Pharmacology, Cell biology or a related discipline or a BSc/MSc degree with significant relevant experience, preferably in the pharmaceutical or biotechnology industry.
* Highly skilled in cellular biology techniques applied to develop cell-based assays.
* Extensive experience in the development and application of assays for quantitative measurements of RNA transcripts.
* Experience with therapeutic oligonucleotides (e.g. ASOs or siRNAs).
* Experienced working with many and diverse cell models.
* First-rate analysis and decision-making skills, coupled with a tenacity to see decisions through, even in situations of ambiguity.

Desirable in the role:
- Expertise in a range of cell biology techniques, including cloning, transfection methods, and gene expression knock-down (RNAi or other).
* Experience in the design, development and validation of cellular assays for compound screening and /or profiling.
* Cellular imaging and image analysis experience.
* Experience with automation for cell assays.

Why AstraZeneca?
Thrive in a place where the brightest and most curious minds seamlessly come together in our inclusive environment. This is the place to go beyond discovery - we think holistically about patients and are always learning from those living with diseases.
AstraZeneca is one of the world's most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

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IT Manager

Chief Information Officer/CIO/IT-chef
Läs mer Sep 25
IT Manager in the Digital Marketing domain - Göteborg

IT Manager, Digital Customer Experience

Essity is a leading global hygiene and healthcare company. They are committed to improving the quality of life through high-quality hygiene and healthcare solutions. They sell their products and solutions in around 150 countries under many strong brands, including the global market leaders TENA and Tork, as well as well-known brands such as Jobst, Leukoplast, Libero, Libresse, Lotus, Nosotras, Saba, Tempo, Vinda and Zewa.

About The Role
As an IT Manager in the Digital Marketing domain, you will be reporting to the Senior IT Manager Digital Marketing and will be at the forefront of delivering and supporting a robust and comprehensive application portfolio. You will play a pivotal role in ensuring the seamless functionality and continuous improvement of digital marketing applications, contributing to the success of customer experience and brand awareness strategies. The ideal candidate will possess a deep understanding of digital marketing technologies, a proven track record in delivering and supporting web applications, and strong leadership skills.

We're looking for people who aren't afraid to challenge, innovate, experiment, and move at a fast pace.

What You Will Do

* Application Portfolio Management: Develop and execute a strategic roadmap for a product line within a digital marketing application portfolio, aligning it with business goals and marketing strategies. Evaluate, select, and implement new applications to enhance the digital marketing technology stack.
* Delivery and Implementation: Lead the planning, development, and implementation of custom-built digital marketing applications, ensuring timely and successful delivery. Collaborate with cross-functional teams, including marketing, IT, and external vendors, to achieve project objectives.
* Support and Maintenance: Establish and oversee effective support and maintenance processes for a product line in the digital marketing application portfolio. Coordinate troubleshooting efforts and resolve application-related issues to minimise downtime and disruptions.
* Team Leadership and Development: Manage a Full Stack team of IT professionals responsible for the delivery and support of digital marketing applications. Foster a culture of innovation, collaboration, and continuous improvement within the team.
* Vendor Management: Collaborate with vendors to ensure the effective delivery of application solutions and services. Negotiate contracts, manage vendor relationships, and ensure adherence to service level agreements (SLAs).
* Performance Monitoring and Optimisation: Implement monitoring tools to track the performance and efficiency of digital marketing applications. Analyse data to identify areas for optimisation and enhancement, ensuring optimal functionality.
* Compliance and Security: Ensure that digital marketing applications comply with relevant data protection regulations and industry standards. Implement security measures to safeguard application data and user information.

Who You Are

* Education and Experience: Bachelor's degree in Information Technology, Computer Science, or a related field. Master's degree is preferred. 4 years of experience in IT management, with focus on Marketing Technology and digital customer experience solutions.
* Technical Skills: Proficiency in web development technologies, e-commerce platforms, and content management systems. Familiarity with MACH architecture principles.
* Leadership and Management: Proven experience leading and managing a team of IT professionals. Strong project management and SDLC skills with a track record of delivering agile projects on time and within budget.
* Strategic Thinking: Demonstrated ability to develop and execute a strategic roadmap for digital marketing technology initiatives. Strong analytical and problem-solving skills with a strategic mindset.
* Communication Skills: Excellent written and verbal communication skills in English. Ability to communicate complex technical concepts to non-technical stakeholders.
* Collaboration and Teamwork: Ability to foster a collaborative and inclusive team environment. Proven experience collaborating with cross-functional teams to achieve common goals.
* Location and Travel: This position is offered with a hybrid working pattern (3 days in office and 2 days from home). The position is based in Munich or Gothenburg. Ability to travel is up to 15%.

What's next? If this sounds like a good opportunity to you - welcome to apply!

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R&D Director of Procurement

Biomedicinsk analytiker/BMA
Läs mer Sep 13
R&D Director of Procurement - AstraZeneca - 12-month assignment - Gothenburg

Consultancy role for AstraZeneca.

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies!

AstraZeneca is now recruiting a Director to join R&D Procurement. This position is located at one of AstraZeneca's vibrant strategic R&D sites in Gothenburg, Sweden. AstraZeneca has a single R&D Procurement group which supports the two integrated R&D science units - Oncology and Biopharmaceuticals (Respiratory, CVRM and INA). These units have responsibility for the value chain from discovery through to late-stage development, enabling rapid acceleration of promising early-stage assets and life-cycle management programs. The R&D structure is designed to help us build on this proud legacy of scientific contribution, and ensure we are positioned to continue to translate our innovative science into even more life-changing medicines for patients.

Your role
Join our diverse community and contribute to our truly global Procurement team, which reflects the full diversity of the people we serve. In this procurement leadership role, you will be accountable for the overall management of a cluster of categories, or a complex category within R&D Procurement and it may also include managing activities of a group of Global Procurement Associate Directors. You are expected to lead, coach and develop non-direct report team members to achieve set goals. You will do this by acting as a role model for our AstraZeneca Values and Behaviours. The role reports to the Senior Director of Procurement R&D Lab Equipment, Services and Supplies. Other parts of your role:

Strategy:
Accountable for designing, and implementation of global categories that include region or market strategies to optimise business efficiency
Accountable for ongoing global category management including strategic sourcing, supplier collaboration and innovation, contract and risk management
Accountable for developing and maintaining expert knowledge of respective global supply markets, competitors and product innovations
Accountable to understand the global spend and identify ongoing opportunities to increase quality and improve value for money. Facilitate implementation of procurement change initiatives within categories to improve business performance

Business & Supplier Engagement:
Develop an extensive understanding of customer needs and the business environment and translate this into meaningful Procurement projects
Builds strong relationships with stakeholders and ensure customer satisfaction
Responsible for Category level sustainability actions, ensuring our suppliers are aligned and delivering in line with our sustainability goals
For Procurement owned suppliers accountable for all aspects of supplier relationship management
Instil the highest standards of compliance and ethics consistently across AZ

Essentials for the role
- Degree level qualification or relevant experience
- Thorough knowledge of the pharmaceutical industry (or other industry), specifically Lab equipment, services and supplies
- Expertise in at least one area of Procurement or relevant R&D experience
- Proven leadership experience
- Communication skills and ability to influence others
- Comfort with risk and ambiguous situations

Why AstraZeneca
At AstraZeneca, we're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and fuel your entrepreneurial spirit. There's no better place to make a difference to medicine, patients, and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth, and development.

Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available, and we hope it's yours.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

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Animal Technician

Zoolog
Läs mer Sep 9
Consultancy role for AstraZeneca

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energised and rewarded for their ideas and creativity.

The arena:
AstraZeneca is a global, innovation-driven biopharmaceutical company that focusses on the discovery, development and commercialisation of prescription medicines for some of the world's most serious diseases. We are proud to have a unique workplace culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energised and rewarded for their ideas and creativity.

The Animal Science and Technologies (AST) is a global department that delivers in vivo studies, animal care, and welfare that is compliant to internal standards and external regulations. Principles of the 3Rs are applied to all aspects of animal care and study conduction.

The role:
*Performs daily animal husbandry tasks for rodents and pigs to ensure the highest standards of animal care & welfare.
*Responsibilities may include breeding and maintenance of transgenic mice.
*Responsibilities may include technical procedures such as collecting biological samples, weighing and administering medicines/compounds.
*Maintains daily record keeping for animals and the environment.
*Responsibilities may include routine facility operations tasks, dish and maintenance on racks and caging equipment.
*Is required to work flexibly across different areas and participate in provision of weekend and out of hours support.
*Ensures that work is performed in accordance with appropriate Safety, Health & Environment (SHE), quality and compliance standards, e.g. General Laboratory Standard (GLS).

AstraZeneca is one of the world's most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

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Quality Assurance Advisor

Biomedicinsk analytiker/BMA
Läs mer Sep 5
Consultancy role for AstraZeneca.

AstraZeneca is a global, innovation-driven biopharmaceutical business that focusses on the discovery, development, and commercialisation of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. At AstraZeneca, we're proud to have a unique workplace culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energised and rewarded for their ideas and creativity.

The arena
Are you interested in a challenging opportunity within the Development Quality function in one of the world's leading pharmaceutical companies?
The Development Quality function is responsible for quality oversight of the pharmaceutical development activities in AstraZeneca. We are now looking for a Quality Advisor with GMP focus to our Gothenburg team. AstraZeneca's pharmaceutical development organisations manage all facets of the process of turning a molecule into a medicine which can be safely and effectively used by patients. The Quality Advisor role has a broad range of responsibilities to ensure all internal and external requirements are fulfilled for the AstraZeneca projects in the development phase.
The role
As a Quality Advisor, you will work with early product development manufacturing and packaging teams and be responsible for Development Quality release of externally manufactured Drug Product and Investigational Medicinal Product for clinical trials. You are expected to assure that activities and processes across the development chain are delivered to appropriate standards to meet regulatory expectations and assure product integrity and acceptability. You will develop and maintain a knowledge of the quality regulations and guidelines applicable to your area and a deep scientific understanding of the products that you are supporting. In your role, you will have interactions with internal and external stakeholders.

Typical Accountabilities:

* Responsible for quality Release of manufactured Drug Product, Investigational Medicinal Product for clinical trials.
* Providing quality input to Manufacturing, Packaging, Labelling & Distribution activities.
* Providing proactive quality advice to support the development, implementation, and continuous improvement of GMP quality systems across the Clinical Supply functions and supporting implementation of agreed global standards.
* Support the pharmaceutical development functions with investigations of deviations, changes and other quality and compliance decisions in the development projects.
* Provide appropriate Quality Assurance input for business improvement projects.
* Operate as part of a global organisation with an integrated mindset to create an organisation with common processes and ways of working.

Requirements:

* Degree in pharmacy or engineering (specialising in Pharmaceuticals)
* 2-3 years' experience of working within a pharmaceutical GMP environment.
* Understanding of Quality Systems and GMP and related activities to Investigational Medicinal Product (IMP).
* Experience of documentation, deviations, changes, and other quality and compliance decisions in the development projects.
* Experience preferably within a pharmaceutical manufacturing organisation is desirable
* Understanding of Project Management processes is desirable
* Fluent in written and spoken English.


Desirable:

* Experience preferably within a pharmaceutical manufacturing organisation.
* Understanding of Project Management processes.
* Good team work and networking skills.
* Capable of making effective decisions.
* Demonstrate drive and energy in the role to make a difference.
* Demonstrate a high degree of personal credibility.
* Comprehensive understanding of the pharmaceutical/drug development process.
* Good communicator with experience of interacting effectively across interfaces.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

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Research Scientist Biosamples, Biobank Scientist

Biokemist
Läs mer Aug 26
Research Scientist Biosamples, Biobank Scientist - Consultancy role for AstraZeneca

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. However, as a company we are more than one of the world's leading pharmaceutical companies, we are proud to have a unique workplace culture that inspires innovation and collaboration. AstraZeneca employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.

The arena:
Biobank scientists are responsible for the storage and timely supply of human biological samples (HBS) to AZ research projects. HBS are received from e.g. clinical studies or academic collaborations, stored in local biobanks and distributed to projects. The group primarily supports the Sweden Region but partners with other Biobank groups within AZ globally to provide efficient support across AZ and our partner organisations.

The Biobank group works collaboratively to provide support within agreed service levels with a strong focus on our customers. We strive hard to understand what fits their needs best and to add value through our services. With an increased focus on the value and use of biobank samples we actively seek ways to improve our process or exploit new technology to build a cutting-edge facility.

Tasks and responsibilities/The role:
We are currently recruiting for a Biobank Scientist in the AZ Gothenburg Biobank group within the global Precision Medicine and Biosamples organization. This position will provide the opportunity to work in a dynamic and enthusiastic environment whilst supplying a critical service to drug discovery projects. The work is highly collaborative with the team having a collective responsibility for the overall delivery.

The role is focused on supporting drug discovery projects within R&D Gothenburg by maintaining high quality handling and storage of HBS and support projects with requested samples in a timely manner.

As a Biobank Research Scientist you will be expected to:
-Work as part of the team rotating between the following typical tasks
-Receive and register incoming HBS
-Process requests for HBS to customers, including using automated liquid handler
-Manage customer orders using specialized informatics systems as well as databases
-Respond to customer queries via mail or telephone
-Partner with Biobank groups globally as well as internal and external customers
-Work closely with other groups in the organization
-Act upon day-to-day issues that occur whilst processing HBS samples to ensure continuous improvement
-Identify initiatives to improve efficiency or quality.

The group has a strong emphasis on continuous improvement which takes the form of individual and group projects within the team, the department and across Biobank groups within AZ.

The biobank team is a highly collaborative group working to tight delivery schedules so the ability to be comfortable working at a fast pace with a goal orientated and team focussed attitude is essential. Excellent communication skills with a proactive and service minded approach is key.

AstraZeneca is one of the world's most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

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Quality Assurance Specialist

Biomedicinsk analytiker/BMA
Läs mer Aug 5
Consultancy role for AstraZeneca.

AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development, and commercialisation of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. At AstraZeneca, we're proud to have a unique workplace culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energised and rewarded for their ideas and creativity.

The arena
Are you interested in a challenging opportunity within the Development Quality function in one of the world's leading pharmaceutical companies?
The Development Quality function is responsible for quality oversight of the pharmaceutical development activities in AstraZeneca. We are now looking for a Quality Advisor with GMP focus to our Gothenburg team. AstraZeneca's pharmaceutical development organisations manage all facets of the process of turning a molecule into a medicine which can be safely and effectively used by patients. The Quality Advisor role has a broad range of responsibilities to ensure all internal and external requirements are fulfilled for the AstraZeneca projects in the development phase.
The role
As a Quality Advisor, you will work with early product development manufacturing and packaging teams and be responsible for Development Quality release of externally manufactured Drug Product and Investigational Medicinal Product for clinical trials. You are expected to assure that activities and processes across the development chain are delivered to appropriate standards to meet regulatory expectations and assure product integrity and acceptability. You will develop and maintain a knowledge of the quality regulations and guidelines applicable to your area and a deep scientific understanding of the products that you are supporting. In your role, you will have interactions with internal and external stakeholders.

Typical Accountabilities:

* Responsible for quality Release of manufactured Drug Product, Investigational Medicinal Product for clinical trials.
* Providing quality input to Manufacturing, Packaging, Labelling & Distribution activities.
* Providing proactive quality advice to support the development, implementation, and continuous improvement of GMP quality systems across the Clinical Supply functions and support implementation of agreed global standards.
* Support the pharmaceutical development functions with investigations of deviations, changes and other quality and compliance decisions in the development projects.
* Provide appropriate Quality Assurance input to business improvement projects.
* Operate as part of a global organisation with an integrated mindset to create an organisation with common processes and ways of working.

Requirements:

* Degree in pharmacy or engineering (specialising in Pharmaceuticals)
* 3 years' experience of working within a pharmaceutical GMP environment.
* Broad understanding of Quality Systems and GMP and related activities to Investigational Medicinal Product (IMP).
* Experience of documentation, deviations, changes, and other quality and compliance decisions in the development projects.
* Fluent in written and spoken English.

Desirable:
* Experience preferably within a pharmaceutical manufacturing organisation.
* Understanding of Project Management processes.
* Good team work and networking skills.
* Capable of making effective decisions.
* Demonstrate drive and energy in the role to make a difference.
* Demonstrate a high degree of personal credibility.
* Comprehensive understanding of the pharmaceutical/drug development process.
* Good communicator with experience of interacting effectively across interfaces.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

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Analytical Scientist

Laborant, biologi
Läs mer Aug 5
Consultancy role for AstraZeneca

Inhalation Product Development (IPD) at AstraZeneca is a multinational organisation that combines decades of experience in inhalation technology, whether it is nebulisation, pMDI or DPI. Our vision is to develop and provide to patients best-in-class, innovative and sustainable products to deliver medicine via inhalation.

We are now seeking an Analytical Scientist to join our dynamic Analytical Sciences team, focusing on the characterisation of inhaled molecules within Inhalation Product Development in Gothenburg. This is a unique opportunity to play a pivotal role in the development of inhaled products for AstraZeneca. You will be part of a highly collaborative team of analytical experts within the inhalation area, contributing to analytical development and characterisation of inhaled products.

This job includes lab-based responsibilities, where you are expected to work collaboratively with colleagues in daily analytical deliveries, documenting your experiments carefully and to the right quality, utilising both manual and automated analytical techniques to develop and deliver innovative inhaled medicines to patients.

To be successful in this role you will need an analytical background combined with excellent communication skills and the ability to engage and collaborate cross-functionally. We are looking for a candidate that possesses a fair understanding of the overall drug development process and has an enthusiasm for laboratory-based work as well as solving technical challenges and problems.

Essential qualifications for the role:

* BSc or MSc degree in Analytical Chemistry or other relevant scientific discipline (Biochemistry, Biotechnology.).
* Scientific knowledge within analytical sciences and technically skilled with analytical separation techniques such as liquid chromatography (UPLC).
* Strong scientific interest and ambition to develop yourself in the analytical sciences area as well as learning analytical techniques used for inhaled products.
* Excellent communication skills in English, both oral and written.
* Understanding the principles and applications of GMP.

Desirable skills:

* Experience in aerosol characterisation techniques used for inhaled products, such as impactor analysis.
* Experience of working in a GMP environment.
* Experience with method development and validation.
* Experience with solving technical challenges and problems.
* Experience of analysis of small molecules.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

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Senior research scientist

Molekylärbiolog
Läs mer Aug 8
Consultancy role for AstraZeneca.

Here at AstraZeneca, we are working towards turning novel state-of-art technologies into effective and safe medicines for severe genetic disease. Do you want to be part of this effort? Welcome to join our exciting journey!

As our new Senior Research Scientist, you will be a part of the Therapeutic Editing team in the Department of Genome Engineering. The role is based in Gothenburg, Sweden, where you will join an international team that develops novel genome engineering technologies and applies these technologies for the generation of therapeutic agents. We provide a stimulating environment for innovation and translational application of genome engineering tools, to turn them into effective and safe medicines.

We continually push the boundaries of science to deliver medicines that treat diseases across our main therapy areas. We expand the limits of scientific research to better understand diseases and to discover new life-changing treatments for them.

What you will do:
You will bring your expertise in molecular biology or screening sciences to develop novel genome editing approaches that can potentially lead to therapies. You will be a key member of cross-functional therapeutic editing project teams with various backgrounds and expertise, where you will be responsible for establishing screening capabilities and running the screens for therapeutic editing projects.

Accountabilities will include screening and optimisation of genome engineering technologies to facilitate effective gene editing in target cell & tissue types, analysing gene editing outcomes, documenting, interpreting, and communicating results to appropriate partners. You will collaborate with other functions to develop and test novel CRISPR delivery strategies - and to develop high throughput next generation sequencing approaches to analyse gene editing outcomes.

We also believe that our new colleague is a person who thinks outside the box and finds innovative approaches to scientific problems. You hold enthusiasm and curiosity towards scientific questions and learning new skills. You can work in an independent and goal-oriented way, but you also enjoy team work and have the ability to communicate and collaborate in a global setting with cross-functional groups.

Why AstraZeneca?

If you are passionate about translating scientific advances into real next generation medicines, AstraZeneca is the right place for you. Join the team to unlock the power of what science can do. You have the potential to grow yourself, our pipeline, and positively impact the lives of billions of patients around the world.

What's next? If this sounds like a good opportunity to you - welcome to apply!

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Senior Research Scientist High-throughput synthesis

Molekylärbiolog
Läs mer Jul 16
Senior Research Scientist - High-throughput synthesis - Consultancy role for AstraZeneca

Do you have organic synthesis expertise? Are you interested in becoming part of an impactful team, passionate for science and technology, and focusing on chemistry automation to accelerate drug discovery? Would you like to become part of a company where we are committed to lifelong learning, growth, and development? This might be your next challenge!

We are looking for an Organic Chemist who will play an important part in our interdisciplinary team, implementing state-of-the-art chemistry automation technologies for the high-throughput synthesis of new molecules for projects.

Join our team at AstraZeneca in Gothenburg, Sweden. Thrive in a place where the brightest and most curious minds seamlessly come together in our inclusive environment.

What you will do:
By using chemistry automation technologies, you will contribute to the optimisation and synthesis of libraries of screening compounds (including traditional small molecules and small molecules degraders) on nanomol and micromol scale to progress projects. You will collaborate with experts in a variety of disciplines, including medicinal chemistry and artificial intelligence, to maximise the impact of our capabilities. You will contribute to the evaluation and development of automation-friendly synthetic methods to access optimal synthetic pathways for the synthesis of desired libraries and make a significant contribution to the team delivery.
You will have access to the best internal and external science and enhance business reputation internally and externally through peer-reviewed publications and oral/poster presentations.

Requirements:
* You're a chemist with a track record of applying innovative chemistry solutions, with resulting impact on project delivery.
* Ph.D. in organic chemistry, or a Master degree in chemistry with minimum of 5 years' experience in synthetic organic chemistry
* Experience of planning and executing chemistry experiments in parallel and adapting existing protocols to new applications
* Expertise in organic synthesis, retrosynthesis, compound route design, purification, and analytical chemistry
* Experience in chemistry automation and plate chemistry would be desirable

The successful candidate should encourage innovation and be motivated to work effectively in a team having strong communication and collaboration skills. The ideal candidate should demonstrate ability to work across scientific fields, possess a curious mind and a long-term commitment to advancing chemistry automation as an innovative tool in drug discovery.

Why AstraZeneca Gothenburg?
With more than 2,800 employees from more than 70 different countries, our vibrant Gothenburg site is a truly inspiring place to work. Here, the history and future of scientific breakthrough come together. We believe that the diversity of our people is crucial to bringing new discoveries to life. Thrive in a place where the brightest and most curious minds seamlessly come together in our inclusive environment.

So, what's next? If this sounds like your next challenge - welcome to apply today!

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Scientist (in vitro)

Kemist
Läs mer Jul 1
Consultancy role for AstraZeneca - Research Scientist position - in vitro compound profiling

We are looking for a Research Scientist to join our Mechanistic Biology & Profiling function within the Discovery Sciences organisation in Gothenburg, Sweden. You will apply proven biochemistry and cell biology expertise to perform in vitro assays, including independent planning, analysis and reporting. Routine profiling will be combined with tailored mechanism of action studies in support of chemistry optimisation across different drug discovery projects.

As an individual you are passionate about laboratory work and want to apply this in a setting where team work and flexibility is critical. You will join a team whose remit is to support our drug discovery projects globally with early DMPK assessment, SAR profiling and detailed mechanism of action data. We offer a highly rewarding scientific environment with ample learning opportunities.

You will be strongly encouraged and supported to think creatively in our dynamic environment. Here, we are free from fear of failure, free to ask the right questions and make bold decisions.

What you will do:

This is a lab-based role focused on generating routine screening data and bespoke in vitro pharmacology studies in support of drug discovery projects. The work includes independent troubleshooting and timely reporting of data according to agreed timelines. All work is conducted in close dialog with project teams, specifically in support of the Cardiovascular, Renal and Metabolism as well as Respiratory & Immunology disease area organisations locally in Gothenburg.

Requirements:

* A strong passion for laboratory work.
* MSc or PhD within a relevant scientific discipline or demonstrated relevant experience in the Life Science industry.
* Proven track record of in vitro pharmacology studies.
* Excellent communication skills and an ability to operate effectively in a multi-disciplinary research environment.
* Independent analysis and evaluation of complex data and delivery of data to agreed timelines.
* First-rate decision-making skills, coupled with tenacity to see decisions through, even in situations of ambiguity.
Desirable in the role:
* Compound profiling in a screening environment using microtiter plates and automation.
* Experience with either enzymology studies or mechnistic cell-based studies.

Why AstraZeneca in Gothenburg?

You can ask anybody who has ever set foot here - our Gothenburg site has a vibrant culture that pulls you in! It is a mix of both local and international talent. We welcome the contribution of people from all backgrounds, beliefs and walks of life.

So, what's next? If this sounds like your next challenge - please apply today!

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

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Analytical Senior Scientist

Biomedicinsk analytiker/BMA
Läs mer Jun 5
Consultancy role for AstraZeneca for a 6-month assignment.

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energised and rewarded for their ideas and creativity.

The arena:
At AstraZeneca, we turn ideas into life-changing medicines and strive to continuously meet the unmet needs of patients worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you're our kind of person.

Inhalation Product Development (IPD) at AstraZeneca is a multinational organisation that combines decades of experience in inhalation technology, whether it is nebulisation, pMDI or DPI. Our vision is to develop and provide to patients best-in-class, innovative and sustainable products to deliver medicine via inhalation.

Tasks and responsibilities:
We are seeking an Analytical Scientist to join our dynamic Analytical Sciences team, focusing on the characterisation of inhaled molecules within Inhalation Product Development in Gothenburg. This is a unique opportunity to play a pivotal role in the development of inhaled products for AstraZeneca. You will be part of a highly collaborative team of analytical experts within the inhalation area, contributing to analytical development and characterisation of both small and large molecules.
Responsibilities:
This job includes lab-based responsibilities, where you are expected to work collaboratively with colleagues in daily analytical deliveries, utilising both manual and automated analytical techniques to develop and deliver innovative inhaled medicines to patients.
You will apply your analytical expertise with large and/or small molecules to specific drug projects, contributing to the analytical development and strategy within the inhaled project.
You will be contributing significantly to Chemistry, Manufacturing, Control (CMC) aspects of the project, working closely with formulation scientists, device engineers, biopharmaceuticals and process engineers at IPD Gothenburg as well as globally with colleagues at IPD North Carolina.
To be successful in this role, you will need a strong analytical background in working with different types of molecules combined with excellent communication skills and the ability to engage and collaborate cross-functionally. We are looking for a candidate that possesses a fair understanding of the overall drug development process and has an enthusiasm for laboratory-based work as well as solving technical challenges and problems.

Essential requirements:
-Degree in Analytical Chemistry or other relevant scientific discipline (Biochemistry, Biotechnology). (PhD or Bsc/Msc with extensive experience).
-Experience with analytical separation techniques such as liquid chromatography (UPLC) for large and/or small molecules. Experience with large molecules would also be beneficial. Proficiency in method development and validation of analytical methods. Experience with analytical methodologies for oligonucleotides, peptide and protein characterisation (e.g., capillary electrophoresis, ion-exchange chromatography, ELISA, SDS-PAGE) is highly desirable.
-Strong data analysis skills, with the ability to interpret results and communicate findings effectively to stakeholders, along with a proven ability to solve technical challenges and problems. Insights into the use of statistical analysis software would be great. Familiarity with working and communicating within a global, cross-functional project environment is desirable. Understanding of analytical development work and CMC delivery projects.
Experience working in a GMP environment and knowledge of corresponding instrument/equipment maintenance procedures as well as knowledge of the overall drug development process from discovery through to launch would be beneficial. Experience in aerosol characterisation techniques used for inhaled products, such as impactor analysis, would be a bonus.
-Excellent communication skills in English, both oral and written.

AstraZeneca is one of the world's most exciting biopharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

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Senior Scientist NMR spectroscopy

Molekylärbiolog
Läs mer Jun 3
Senior Scientist NMR spectroscopy - consultancy role for 12 months for AstraZeneca

Are you a scientist with expertise in, and passion for, the application of NMR to understand and determine the dynamics and structure of therapeutically relevant target proteins? Would you like to apply your expertise to impact and expand the use of NMR in drug discovery projects whilst being presented with a professional development opportunity within a company that follows science and turns ideas into life changing medicines? Then AstraZeneca has a challenge for you!

AstraZeneca is committed to the development of the next generation of innovative medicines and is focused on expanding the use of small molecules to treat dyslipidaemia and familial hypercholesterolaemia. The company currently exploits new avenues for lowering LDL cholesterol in patients at risk of cardiovascular disease in order to provide additional disease treatment opportunities. To help us with this, we are looking for a scientist with passion, expertise and experience to join our Mechanistic and Structural Biology Department (MSB) as a lab-based Senior Scientist on a one-year contract basis within the Biophysics group in Gothenburg, which is part of the global Discovery Sciences area in AstraZeneca's BioPharmaceuticals organisation.

The MSB department has leading capabilities in biophysics, crystallography, cryo-EM, enzymology and cellular pharmacology. The Biophysics team has specific expertise in molecular biophysics methods, including SPR, NMR, ITC, DSF, HDX-MS, nMS and single molecule approaches. We apply biophysics across a range of different modalities to support drug discovery from target validation to drug candidate.

What you will do:

The role as Senior Research Scientist is a laboratory-based position supporting the structure determination of protein-drug complexes in solution utilising NMR spectroscopy. For this we are seeking a highly skilled and motivated NMR spectroscopist to join our Biophysics team on a one-year contract basis. The ideal candidate will have a strong theoretical and practical background in pulse sequences for solution-state NMR, along with extensive experience in the assignment and determination of protein structures using NMR techniques. This role is crucial for advancing our research and development projects in dyslipidaemia and familial hypercholesterolaemia.

You will have a high level of control and influence over the project, allowing you to shape its direction and outcomes significantly. Additionally, you will have ample opportunities to learn new technical skills and develop leadership abilities. Our collaborative and innovative work environment enables you to work alongside scientists and postdocs from various disciplines, both within and across the global AstraZeneca community. This role offers a unique opportunity for professional development in an industrial setting, providing you with a valuable experience and additional skills and helping you build a strong foundation for your future endeavours.

You will be responsible for designing and implementing advanced pulse sequences for solution-state NMR, tailored to our specific research needs. You will perform intricate NMR experiments aimed at the assignment and structural determination of proteins, ensuring precise and accurate data collection. Your expertise will be crucial in analysing NMR data, interpreting results, and integrating these findings with other research data to provide comprehensive insights into the drug mechanism of action. You will collaborate with multidisciplinary teams, contributing to the synthesis of NMR findings with the broader research objectives of this project. Additionally, you will stay abreast of the latest advancements in NMR spectroscopy and protein structure determination, continuously applying this knowledge to enhance our research capabilities.

Your findings will not only support the ongoing project but will also constitute an important part of our publication strategy, aiming for high-impact journal publications. You will document and present your results in both internal and external meetings, playing a vital role in driving our scientific endeavours forward.

Finally, to be successful in this role, we see that you have good social and communication skills, are collaborative and a strong team player. You should also be able to work independently and have a positive, goal-oriented and problem-solving attitude.

Why AstraZeneca Gothenburg?

With more than 2,400 employees from over 50 countries, our vibrant Gothenburg site is a truly inspiring place to work. Here, the history and future of scientific breakthroughs come together. We believe that the diversity of our people is crucial to bringing new discoveries to life.

Does this sound like your next challenge? Apply today!

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Discovery Safety Scientist/Senior Scientist In Vitro Biology

Molekylärbiolog
Läs mer Maj 30
Consultant role for AstraZeneca.

Are you a motivated cell biologist with experience of in vitro work in molecular biology, omics and oligonucleotides? Do you also enjoy working hands-on in the lab with a great group of colleagues by your side? If yes, this might be the next position for you!

Right now, we are looking for a highly engaged and enthusiastic cell biologist to join us as a Discovery Safety Scientist and complement us in our In Vitro Safety group at AstraZeneca in Gothenburg, Sweden. The ideal candidate will have a passion for in vitro lab based experimentation and analysis and value the utility of early drug safety investigations. We are looking for someone with a strong communication and collaboration drive, who can adopt a brave and forward-thinking approach to drive our predictive in vitro safety assay design to support drug discovery and development projects.

What you'll do:

Working in an industry-leading in vitro safety lab, you will work with internal research groups to identify potential off-target risks for siRNA/antisense oligonucleotide (ASO) projects. Develop in vitro assays to explore those potential off targets in a variety of different mammalian cell types via gene expression analysis. You will also be required to summarise safety related literature relating to modulation of off-target genes to help inform decisions and support the development of safer oligonucleotide-based drug products.

Why AstraZeneca?

We are working towards treating, preventing, modifying and even curing some of the world's most complex diseases. Here we have the potential to grow our pipeline and positively impact the lives of billions of patients around the world. With more than 2,400 employees from over 50 countries, our vibrant Gothenburg site is a truly inspiring place to work. Here, the history and future of scientific breakthroughs come together. We believe that the diversity of our people is crucial to bringing new discoveries to life.

Does this sound like your next challenge? Apply today!



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

Ansök nu

Scientist - Bioscience COPD/IPF

Molekylärbiolog
Läs mer Maj 28
Consultancy role for AstraZeneca.

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energised and rewarded for their ideas and creativity.

We are currently looking for a laboratory skilled Scientist to join the Bioscience COPD IPF Department within Early Respiratory and Immunology (R&I). This role is located in Gothenburg, Sweden.
The Bioscience COPD/IPF department consists of 7 teams spread across Sweden, UK and the US and our focus is primarily to progress projects within our portfolio, but it also includes work to increase our knowledge of COPD and IPF and to support target identification for new projects.

What you'll do:
As a Scientist you will plan, optimise, and execute in vitro experiments as well as support analysis from both in vitro and in vivo studies to progress our drug discovery projects and generate publishable scientific insights. You are expected to actively take part in scientific discussions and to add valuable input in experiment design and data interpretation to drive projects and techniques.
This is a lab-based role where you will be involved in multiple ongoing projects with responsibility to perform experiments from various cells and tissues for both in vitro-, in vivo- and patient studies. This role will give you the opportunity to support, design, develop and conduct experiments supporting the identification of new drug targets and the progression of drug discovery projects.
For this role, we are looking for someone with experience in modern cell biology and molecular analysis techniques that can rapidly become an integrated project member and deliver key data.

We will rely on you to:
* Execute in vitro/ex vivo experiments according to study plans
* Contribute to the interpretation of experimental data and play an important role in the planning of further experiments
* Effectively communicate results to other members of the project, team or to departments as required
* Be an effective team member in supporting projects to meet their objectives
* To conduct where appropriate in parallel more than one area of work to agreed timelines
* Possess a range of practical skills and demonstrate flexibility within and across teams

Essential requirements:
-A relevant science degree (MSc or BSc) (e.g. Molecular/Cell Biology, Pharmacy, Biotechnology)
-Practical experience running in vitro assays and cell culturing
Relevant experimental experience in cell and molecular biology methods, immunoassays, protein and RNA analysis
-Isolation, culturing and analysis of primary cell cultures along with experience in the use of biological dose response assays is desirable. Experience in immunological methods (ELISA, MSD), protein analysis (western blot) and RNA analysis (qPCR) plus handling and evaluation of pharmacological drug substances would also be beneficial.
- Excellent written and oral communication skills in English is a must

Soft skills:
You also possess great problem-solving skills. You have a positive and goal-oriented attitude, and you are a team player, but are also able to take your own initiatives. You are organised and incorporate the views of others in your communication and collaboration.

AstraZeneca is one of the world's most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.



What you need to do now



If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

Ansök nu

Scientist in Genome Medicines

Molekylärbiolog
Läs mer Maj 28
Consultancy role for AstraZeneca

We are developing state-of-the-art technologies and models to advance gene and cell therapy approaches. AstraZeneca's Genome Editing Team in Gothenburg, Sweden, is now looking for a passionate Scientist to innovate in the field of Therapeutic Genome Editing. If you are looking for a fast-paced environment where your scientific insights can translate into meaningful impacts on patient lives, this is the position for you!

Meet us:
As a Scientist in the Genome Editing Team, you will join an international group of energetic researchers of various backgrounds who are excited about science and challenge its dogmas. We create a supportive and inclusive environment, and a fun atmosphere for everyone, independent of their preferences, experiences and beliefs. Our work focusses on basic yet translational research that is designed to reach the clinics. Especially, we are passionate about modifying genomes at will for therapeutic purposes.

Our successful candidate needs the ability to communicate, interact and collaborate with other team members, as well as across our AZ global functions and fields. Alongside this, our ideal candidate enjoys working in an innovative, proactive, forward-thinking, project-focused and goal-oriented way and shares our excitement about the latest gene-editing techniques.



Essential for the role:
- The detailed knowledge of Therapeutic Genome Editing - literature, technologies, competitive landscape
- Multidisciplinary laboratory experience and meticulous scientific knowledge in cell biology, molecular biology and genetics
- Cell culture work and cell biology (genome engineering, immunofluorescence, FACS)
- Molecular biology (DNA extraction, PCR, Amplicon-sequencing, Western blot)

Why AstraZeneca?
We are working towards treating, preventing, modifying and even curing some of the world's most complex diseases. Here we have the potential to grow our pipeline and positively impact the lives of billions of patients around the world.



What you need to do now



If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

Ansök nu

Senior Scientist - Bioscience COPD/IPF

Molekylärbiolog
Läs mer Maj 28
This is a consultancy role for AstraZeneca.

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energised and rewarded for their ideas and creativity.

We are currently looking for a laboratory skilled Scientist to join the Bioscience COPD IPF Department within Early Respiratory and Immunology (R&I). This role is located in Gothenburg, Sweden.
The Bioscience COPD/IPF department consists of 7 teams spread across Sweden, UK and the US and our focus is primarily to progress projects within our portfolio, but it also includes work to increase our knowledge of COPD and IPF and to support target identification for new projects.

What you'll do:
As a Senior Scientist you will plan, optimise, and execute in vitro experiments as well as support analysis from both in vitro and in vivo studies to progress our drug discovery projects and generate publishable scientific insights. You are expected to actively take part in scientific discussions and to add valuable input in experiment design and data interpretation to drive projects and techniques.
This is a lab-based role where you will be involved in multiple ongoing projects with responsibility to perform experiments from various cells and tissues for both in vitro-, in vivo- and patient studies. This role will give you the opportunity to support, design, develop and conduct experiments supporting the identification of new drug targets and the progression of drug discovery projects.
For this role, we are looking for someone with experience in modern cell biology and molecular analysis techniques that can rapidly become an integrated project member and deliver key data.

We will rely on you to:
* Execute in vitro/ex vivo experiments according to study plans
* Contribute to the interpretation of experimental data and play an important role in the planning of further experiments
* Effectively communicate results to other members of the project, team or to departments as required
* Be an effective team member in supporting projects to meet their objectives
* To conduct where appropriate, in parallel more than one area of work to agreed timelines
* Possess a range of practical skills and demonstrate flexibility within and across teams

Essential requirements:
-A relevant science degree (PhD) (e.g. Molecular/Cell Biology, Pharmacy, Biotechnology)
-Practical experience running in vitro assays and cell culturing
-Relevant experimental experience in cell and molecular biology methods, immunoassays, protein and RNA analysis
-Isolation, culturing and analysis of primary cell cultures along with experience in the use of biological dose response assays is desirable. Experience in immunological methods (ELISA, MSD), protein analysis (western blot) and RNA analysis (qPCR) plus handling and evaluation of pharmacological drug substances would also be beneficial.
Experience in lung research is desirable
- Excellent written and oral communication skills in English is a must

Soft skills:
You also possess great problem-solving skills. You have a positive and goal-oriented attitude, and you are a team player, but are also able to take your own initiatives. You are organised and incorporate the views of others in your communication and collaboration.

AstraZeneca is one of the world's most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.



What you need to do now



If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

Ansök nu

Separation Scientist

Kemist
Läs mer Maj 27
Consultancy role for AstraZeneca on a 12-month contract.



Do you have hands-on experience with the purification of small molecules? Are you interested to further push the boundaries of automated analytical chemistry and separation sciences at a company where we are committed to lifelong learning, growth and development? Welcome to AstraZeneca!

We are seeking a specialised separation scientist that will play an important part in our iLAB team, focusing on the analysis and purification of chemical libraries. You'll have the opportunity to drive and extend the high-throughput purification capabilities within a pioneering automation platform at AstraZeneca in Gothenburg and directly impact drug discovery projects across various therapeutic areas.

We are a global, science-led BioPharmaceutical company and our innovative medicines are used by millions of patients worldwide. With our ground-breaking pipeline comes a bright future - a secure job, exciting opportunities, and varied work. You will be valued. Not only for your unique contribution, skills, and background, but because we recognise people are our greatest asset. Here we are dedicated to being a Great Place to Work.

What you will do:

As Separation Scientist, you will be part of a team of highly motivated scientists contributing to analysis, preparative separation, and characterisation of small molecule chemical libraries.

In this laboratory-based position, you will be specifically responsible for ensuring the delivery of automated analytical and preparative chromatography solutions to drive the delivery of pure compounds to the different projects across our therapy areas within AstraZeneca. You will get the opportunity to work with state-of-the-art chromatographic equipment and liquid handlers.

You will be expected to have effective levels of communication and scientific drive, coordinating effectively with the other members of the analytical and synthesis teams to drive sample progression.

Experience and technical knowledge of chromatographic separations within a drug discovery environment would be an advantage.

Responsibilities for the role:

* Provide hands-on separation science support for drug discovery chemistry using state-of-the art chromatographic instrumentation
* Deliver automated analysis and purification of novel compounds using Liquid chromatography-mass spectrometry (LC-MS) and High-performance liquid chromatography (HPLC)
* Ensure reliability, performance and data quality of analytical instrumentation and automation platforms
* Work within the team to suggest process and infrastructure improvements
* Contribute to a vibrant and entrepreneurial organisation focused on innovation & project delivery; collaborating closely with scientists across the discovery organisation

Why AstraZeneca Gothenburg?

With more than 2,400 employees from over than 50 countries, our vibrant Gothenburg site is a truly inspiring place to work. Here, the history and future of scientific breakthroughs come together. We believe that the diversity of our people is crucial to bringing new discoveries to life.

Does this sound like your next challenge? Apply today!

Ansök nu

Quality Advisor

Miljöinspektör
Läs mer Maj 20
Quality Advisor - AstraZeneca - Gothenburg - 18-month assignment

Quality Advisor

AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialisation of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. At AstraZeneca, we're proud to have a unique workplace culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energised and rewarded for their ideas and creativity.

The arena
Are you interested in a challenging opportunity within the Development Quality function in one of the world's leading pharmaceutical companies?

The Development Quality function is responsible for quality oversight of the pharmaceutical development activities within AstraZeneca. We are now looking for a Quality Advisor with GMP focus to our Gothenburg team. AstraZeneca's pharmaceutical development organisations manage all facets of the process of turning a molecule into a medicine which can be safely and effectively used by patients. The Quality Advisor role has a broad range of responsibilities to ensure all internal and external requirements are fulfilled for the AstraZeneca projects in the development phase.
We have an exciting opportunity for an 18-month temporary assignment as Quality Advisor, in the Site Quality Gothenburg team, who'll be the prime source for quality & compliance advice and providing quality support to the science functions and throughout the drug development process chains.

This is a great opportunity for you who are strong in quality and like to work close to development, Good Manufacturing Practice and making sure quality is assured when delivering new products

The role
Working in the Site Quality team means you will work closely with the internal assets/facilities, teaming up with the pharmaceutical development functions and be involved in cross-business processes. To build strong relationships with these functions, knowing their business is key, to give support to projects and develop ways of working that builds for success.
The ability to interpret and trend compliance data to measure and improve quality standards is key. You will develop and maintain a knowledge of the quality regulations and guidelines applicable to your area and a deep scientific understanding of the products that you are supporting.
Whilst taking on your own specialist areas and making good quality decisions, you will be encouraged to think strategically and use your problem-solving skills to resolve any quality issues. You will participate and contribute to continuous improvement projects with the aim of standardising and simplifying our internal processes.

Typical Accountabilities:
- Responsible for quality release of manufactured Drug Product, Investigational Medicinal Product for clinical trials
- Support the pharmaceutical development functions with investigations of deviations, changes and other quality and compliance decisions in the development projects related to drug products
- Providing quality advice and approval of documentation related to equipment, facilities, IT systems and instruments e.g. maintenance, calibration, validation and change control
- Providing proactive quality advice to support the development, implementation and continuous improvement of GMP quality systems across the Clinical Supply functions and support implementation of agreed global standards
- Operate as part of a global organisation with an integrated mindset to create an organisation with common processes and ways of working

Minimum requirements - Education and Experience
-MSc in pharmacy or engineering (specialising in Pharmaceuticals) with at least 3 years' experience of working within a pharmaceutical GMP environment
-Demonstrates understanding of international quality systems regulations, concepts, industry practices to adopt best in class processes
-A comprehensive understanding of GMP regulations, the pharmaceutical development process and supply chain process would be advantageous.
-Experience of interacting effectively across interfaces and collaborating internally. Working in a fast-paced environment, meeting deadlines and balance multiple priorities. You are used to team work, networking and an experienced communicator, effectively interacting across interfaces and collaborations.
-Fluent in written and spoken English

As a person, you should have the ability to work in a fast-paced environment, meet deadlines, and balance multiple priorities. Independently motivated, detail-oriented, and "can-do" attitude as well as Excellent team-working and networking skills and encouraging team effectiveness are skills that you possess. We also believe you are a good communicator with experience of interacting effectively across interfaces collaborating internally.

About AstraZeneca Gothenburg Hub, Our stunning campus in Gothenburg is one of AstraZeneca's three strategic science centres. The site is home to over 2,500 employees, from 50 different nationalities. Gothenburg includes the complete range of functions, and as such offers plenty of development opportunities for a wide range of professionals. Our science teams in Gothenburg collaborate with academic and industry partners in Sweden and globally. And the site itself has been designed with collaboration in mind. From the Coffee Lab to exercise areas, we've built a series of environments where innovation can happen.



What you need to do now



If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

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Analytical Scientist to Oral Product Development Department

Analytisk kemist
Läs mer Maj 14
Hays Life Science is now looking for an analytical chemist for a four month long assignment at AstraZeneca!

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives- and are made to feel valued, energized and rewarded for their ideas and creativity. In AstraZeneca we set pride to drive the development in a sustainable way, in all areas of our business from influencing our suppliers through development to commercial products.

The arena:
We now have the opportunity for a consultant to join our team in the roles as Analytical Scientists (Career Level C) within the Analytical Science Unit in the department Oral Product Development at AstraZeneca Gothenburg.

Tasks and responsibilities/The role:
We are looking for a scientist in Analytical Chemistry who can provide input in the area of analytical science during the development of drug products and can work together with us determining the quality attributes during the development of the formulations. The work includes analytical testing, documentation, and attending and presenting in project team meetings. The role is primarily laboratory based.

Essential for the role:
- BSc or MSc typically from pharmaceutics, chemistry or analytical science, but also other disciplines with relevant skills.
- Scientific knowledge within analytical science, laboratory experience including working with computerized systems and chromatography techniques (e.g. UPLC) for detection of small molecules.
- Experience from working within the pharmaceutical industry is an advantage.
- If you have experience from working in a GMP environment or worked in AstraZeneca or pharmaceutical industry, this will be an advantage.
- Good knowledge in written and spoken Swedish and/or English is necessary

As a person, you should be well organized, analytical, flexible and accurate.
Good team working skills are also important, together with the ability to operate independently.
Good communication skills linked to the ability to work to tight timelines are highly valued.

AstraZeneca is one of the world's most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.

Ansök nu

Formulation Scientist/Product Developer

Analytisk kemist
Läs mer Maj 14
Formulation Scientist/Product Developer - Konsultroll för AstraZeneca
AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives- and are made to feel valued, energized and rewarded for their ideas and creativity. In AstraZeneca we set pride to drive the development in a sustainable way, in all areas of our business from influencing our suppliers through development to commercial products.

The arena:
We now have the opportunity for one or several consultants to join our team in the role as Formulation Scientist/Product Developer within the department Oral Product Development at AstraZeneca in Gothenburg. The assignment is on a temporary basis.

Tasks and responsibilities/The role:
We are looking for a formulation scientist who can work together with us with generating and evaluating pharmaceutical technologies and formulations. The work includes development, characterization, and documentation, mainly of solid based formulations, in order to develop drug products.

The tasks include planning and implementation of experiments with the aim of generating new formulations and optimizing processes in lab and pilot scale. We are looking for both people with and without previous experience in the area.

Essential/desirable for the role:
MSc/BSc in chemistry, pharmacy, chemical engineering, food technology or equivalent. Good knowledge in written and spoken Swedish and/or English is necessary as well as laboratory experience including working with computerized systems. If you have experience from working within the pharmaceutical industry, medical tech, or with manufacturing equipment, this will be an advantage. Solid materials/formulation experience is highly meriting.

As a person, you should be well organized, analytical, flexible and accurate. Good team working skills are also important, together with the ability to operate independently. Good communication skills linked to the ability to work to tight timelines are highly valued.

AstraZeneca is one of the world's most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.

Ansök nu

Drug Product Delivery Distribution Operator

Miljösamordnare/Miljökoordinator
Läs mer Maj 17
Drug Product Delivery Distribution Operator - AstraZeneca - Gothenburg - 1 year contract

Drug Product Delivery Distribution Operator, AstraZeneca Gothenburg

This is a consultancy role for AstraZeneca on a 1-year contract.

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energised and rewarded for their ideas and creativity.
We are curious, creative, and open to new ideas and ways of working. Above all, we are passionate about science and driven to always put patients first. Join AstraZeneca and apply your expertise in a company that is following science and turn ideas into life-changing medicines.

We now have an exciting opportunity for talented DPD Operators to be based in Gothenburg, Sweden.
Drug Product Delivery (DPD) within Pharmaceutical Technology & Development is the sole internal AstraZeneca department that packs, labels and distributes investigational medicinal products to clinical trial patients. We support launched, pre-launched and products under development within all our therapeutic areas. We work in a fast-paced environment where flexibility and agility enable us to deliver high value to early phase clinical trials.
The DPD Operator role will be an operational role within Distribution, one of Drug Product Deliveries three operational skill areas, Material Management, Pack Label and Distribution. We work in an environment where flexibility and agility enable us to deliver high value to early phase clinical trials. To complement our existing team, candidates with the following experiences are of interest:
- Distribution experience from a complex supply chain organisation
- Drug Product Knowledge including management of Item/article and lot/batch management to ensure traceability on items/articles in a patient kit including a drug product, packaging material and patient labels from the pharmaceutical industry

Main Duties and Responsibilities:
The role holder will contribute to the DPD organisation applying their expertise in the complex and regulated GMP environment. The work is focused on operations within distribution. As a DPD operator, you will perform and document all the operational work according to written procedures. Be engaged in the development and improvement of internal processes and managing deviations. Be responsible for writing of GMP and SHE procedures within own skill areas and will be responsible for related training and compliance activities. As required, maintain defined facilities or equipment according to GMP standards and be proactive to contribute to projects/activities through applying specialist knowledge within appropriate areas.
Distribution responsibilities examples:
Preparing documentation, receiving and packing of investigational medicinal products for clinical trials. Being the main point of contact when it comes to distribution questions for a number of studies.

Essential requirements:
-BSc/MSc in chemistry/pharmacy/engineering or equivalent experience. Preferably 2 years experience within pharmaceutical development
-Understanding the disciplines in Drug Product Delivery, Supply Chain and Pharmaceutical development in order to contribute to an effective Supply Chain organisation
-Understanding of principles, applications and management of SHE and GMP in an R&D environment
-Demonstrated ability to work with teams in a culturally diverse, complex and changing environment most internally but to some extent externally
-Good written and verbal English communication and understanding
-Warehouse experience is an advantage

Soft skills:
As a person, you should have a curious and innovative mindset with problem-solving ability, resolving issues with minimal guidance. The perfect candidate should show interest in working operationally to learn and quickly adapt to the new tasks with a willingness to develop within this role.

AstraZeneca is one of the world's most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

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Senior Analytical scientists to Oral Product Development

Analytisk kemist
Läs mer Maj 14
Hays Life Science is now looking for a Senior Analytical Scientist for a four month long assignment at AstraZeneca!

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives- and are made to feel valued, energized and rewarded for their ideas and creativity. In AstraZeneca we set pride to drive the development in a sustainable way, in all areas of our business from influencing our suppliers through development to commercial products.

The arena:
We now have the opportunity for a consultant to join our team in the roles as Senior Scientist Pharmaceutical/Senior Analytical scientists (Career Level D) within the Analytical Science Unit in the department Oral Product Development at AstraZeneca Gothenburg.

Tasks and responsibilities/The role:
We are looking for a senior scientist in Analytical Chemistry who can provide input in the area of analytical science during the development of drug products and can work together with us determining the quality attributes during the development of the formulations. The work includes analytical testing, documentation, and attending and presenting in project team meetings. The role is primarily laboratory based.

To be successful in this role you will need expertise in analytical chemistry and an experience from laboratory work. Excellent skills in written and verbal communication and the ability to engage and collaborate across boundaries with a positive problem-solving attitude and delivery focus.
- University degree (BSc, MSc, PhD) in relevant subject area, with industry experience
- Experience from working with chromatography and other techniques e.g. HPLC/UPLC, and dissolution, both in a GxP and a non GxP environment
- Experience of supporting clinical manufacture and working with contract manufacturing organisations
- Experience of authoring CMC content for the analytical aspects of drug product regulatory filings throughout the clinical development phase
- Experience of the analytical area such as method development and method validation.
- Experience from evaluation of stability data and assigning shelf life to drug products
- Excellent communication skills and a proven track record of working collaboratively to develop innovative solutions
- Strong leadership skills including the ability to deliver robust scientific contributions to projects and utilise risk-based approaches to project delivery
- Good knowledge in written and spoken Swedish and/or English is necessary

AstraZeneca is one of the world's most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.

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Dev Quality Consultant/Microsoft 365

Mjukvaruutvecklare
Läs mer Maj 8
Consultancy role for AstraZeneca - based in Gothenburg - 2-month assignment

Development Quality Consultant, Microsoft 365 (SharePoint/PowerApp) - Process Mapping & Doc System Interface

Description of role
The Development Quality Consultant, Microsoft 365 (SharePoint/PowerApp) - Process Mapping & Doc System Interface will lead the creation of a visually engaging "Quality Management System (QMS) House" to enable visualisation of our business processes and route the user via direct links to filtered views of our Quality Management System (EQV ECMS). The EQV Enterprise Content Management System (EQV ECMS) houses all GxP documentation and is central to our Quality Management System.
The role involves designing a user-friendly SharePoint site that allow users to visually navigate process levels and selecting impacted business areas to find procedural documents relevant to specific areas. This will make up of approximately 600 direct links to filtered views in EQV ECMS to include all available process levels and impacted business areas.
The consultant will ensure the digital interface is intuitive, user-friendly, and visually compelling and will support adoption and roll-out across various business functions by adding relevant information to the page. The page can be built with or without using the Power Apps as part of the solution. But it must be easy to maintain after implementation for updates to links and information for someone with a fundamental understanding of SharePoint.

Accountabilities/Responsibilities

* Architect and implement a visual and digital solution within SharePoint and the Power Platform to streamline document access.
* Create the filtered views in the EQV ECMS and implement to the SharePoint page.
* Ensure the digital interface is intuitive, user-friendly, and visually engaging.
* Collaborate with the Quality Systems team and internal stakeholders to ensure effective linkage to EQV ECMS.
* Design and deliver training and support materials to facilitate system adoption.
* Establish a maintenance plan for the visual QMS House to ensure long-term usability and ease of updates.

Minimum Requirements

* Proven experience with SharePoint and Power Platform design and implementation.
* Familiarity with Quality Management Systems in a pharmaceutical or similarly regulated environment.
* Understanding of document management systems and creating filtered views based on metadata.
* Ability to work independently and manage time effectively to meet project deadlines.
* Strong communication skills for collaborating with cross-functional teams and enabling system adoption.

Education and Experience

* Bachelor's degree in Quality Engineering, Information Technology, Computer Science, or a related field.
* Experience working with PowerBI and PowerApps is highly desirable.
* Previous involvement in projects at the intersection of IT and Quality within a pharmaceutical context is desirable.

Functional & Business knowledge

* Understanding of the importance of GxP documentation and regulatory requirements in the pharmaceutical industry.
* Knowledge of document control practices and the importance of accurate tagging and categorisation.

Skills and Capabilities

* Technical proficiency with SharePoint and the Power Platform, including Power BI and PowerApps.
* Strong analytical and problem-solving skills.
* Excellent interpersonal and change management skills to drive adoption of new systems.
* Ability to create user-friendly and visually appealing digital interfaces that simplify complex processes.
* Commitment to delivering high-quality work within a defined timeline.



What you need to do now



If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

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Supply Chain Manager for Clinical Trial medications

Biomedicinare
Läs mer Apr 22
This is a consultancy role for AstraZeneca for 12 months.



Supply Chain Manager for Clinical Trial medications

Would you like to utilise your planning and supply chain knowledge to lead clinical supplies for your portfolio of global clinical studies? With constant new products and launches, there has never been a better time to join Global Clinical Supply Chain and shape our future with a significant contribution to life-changing medicines.

We have an exciting opportunity for talented Supply Chain Managers to join our Clinical Study Supply Chain team in Gothenburg, Sweden. This is a key role within our Clinical Manufacturing and Supply teams, and we make sure clinical trial medications are available at the right quality, in the right quantity at the right time for every patient taking part in AstraZeneca's trials all over the world. Our goal is to never miss a patient.

In Pharmaceutical Technology and Development (PT&D) we are the bridge which turns forward-thinking science into actual medicines that helps millions of people around the world. We work across the entire value chain, crafting and delivering active ingredients, formulations and devices required to support new medicines - from supplies for use in early toxicology studies and clinical trials to developing the technology to ensure drugs can be scaled up for commercial manufacture.

What you'll do:
In this role you will project manage the design, plan, and set-up of the study supply chain to ensure on-time delivery of clinical supplies. You will also lead a cross-functional team enabling continuous dialogue with both internal and external partners on study design requirements and associated changes which may impact the supply chain elements of the study.

To be successful in this role you need to be a fast learner, self-driven and comfortable working in a high pace R&D environment. You need to be a collaborative team player, flexible and have strong communication, planning and problem-solving skills.

Your main responsibilities will include:
* Project manage the delivery of clinical supplies effectively and consistently, and input to the balance of costs and any risks to supply.
* Ensure effective communication with project teams and key partners across a global network.
* Support risk management of individual studies with proactive mitigation of risks that potentially impact the quality or delivery of supplies.
* Take ownership for Inventory management including any rework and recalls, extensions of shelf life and expiry date management, or stock destruction.
* Manage the Interactive Response Technology (IRT) system to execute demand and supply planning.
* Work within GMP Quality Management Systems ensuring that you actively handle any deviations, complaints and change controls.



What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

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Quality Assurance Specialist

Kemist
Läs mer Apr 3
Your new company

Quality Assurance Advisor AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies.

At AstraZeneca, we're proud to have a unique workplace culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity. The arena Are you interested in a challenging opportunity within the Development Quality function in one of the world's leading pharmaceutical companies. The Development Quality function is responsible for quality oversight of the pharmaceutical development activities in AstraZeneca.

We are now looking for a Quality Advisor with GMP focus to our Gothenburg team. AstraZeneca's pharmaceutical development organizations manage all facets of the process of turning a molecule into a medicine which can be safely and effectively used by patients. The Quality Advisor role has a broad range of responsibilities to ensure all internal and external requirements are fulfilled for the AstraZeneca projects in the development phase.

The role

As a Quality Advisor, you will work with early product development manufacturing and packaging teams and be responsible for Development Quality release of externally manufactured Drug Product and Investigational Medicinal Product for clinical trials. You are expected to assure that activities and processes across the development chain are delivered to appropriate standards to meet regulatory expectations and assure product integrity and acceptability. You will develop and maintain a knowledge of the quality regulations and guidelines applicable to your area and a deep scientific understanding of the products that you are supporting. In your role you will have interactions with internal and external stakeholders.

Typical Accountabilities:

* Responsible for quality Release of manufactured Drug Product, Investigational Medicinal Product for clinical trials
* Providing quality input to Manufacturing, Packaging, Labelling & Distribution activities
* Providing proactive quality advice to support the development, implementation and continuous improvement of GMP quality systems across the Clinical Supply functions and support implementation of agreed global standards
* Support the pharmaceutical development functions with investigations of deviations, changes and other quality and compliance decisions in the development projects
* Provide appropriate Quality Assurance input to business improvement projects
* Operate as part of a global organisation with an integrated mindset to create an organisation with common processes and ways of working.

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Associate Scientist/Operational Technologist

Kemist
Läs mer Mar 20
AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energised and rewarded for their ideas and creativity.

We are curious, creative, and open to new ideas and ways of working. Above all, we are passionate about science and driven to always put patients first. Join AstraZeneca and apply your expertise in a company that is following the science and turn ideas into life changing medicines. We have an exciting opportunity for a talented Drug Product Delivery (DPD) Associate Scientist/Operational Technologist to be based in Gothenburg, Sweden.

Pharmaceutical Technology and Development (PT&D) is the organisation that turns brilliant science into actual medicines that helps millions of people. We work across the entire value chain, designing and delivering active ingredients, formulations and devices for new medicines and providing expert technical support to all AstraZeneca's commercial drug substances and products to ensure we successfully supply medicines to patients.

Drug Product Delivery (DPD) within PT&D is the sole internal AstraZeneca department that packs, labels and distributes investigational medicinal products to clinical trial patients. We support launched, pre-launched and products under development within all our therapeutic areas. We work in a fast-paced environment where flexibility, agility and teamwork enable us to deliver high value to clinical trials.

We are now looking for two Associate Scientists/Operational Technologists starting as soon as possible with the location of Gothenburg, Sweden. In the role you will have a great opportunity to learn more about pharmaceutical development working with experienced operators. This role contributes to the packaging of drug products in the development phase for clinical studies. All below activities will have an impact on the speed, quality and cost of the AZ development portfolio. Practical hands-on work in our Good Manufacturing Practice (GMP) facilities with dedicated tasks in close collaboration and to support DPD Scientist/Senior Scientist e.g. assisting GMP operators with:
- Preparation of process rooms and equipment before and after clinical manufacture
- Assembly/disassembly and cleaning of equipment
- Primary packing, i.e. packing of tablets/capsules in bottles (manually or automated)-Secondary packing, i.e. labelling of study material (manually or automated)
- Working according to SHE (Safety Health and environment) and GMP standards.

The role is intended to be used in a flexible way to resolve short-term bottlenecks. The role holder will not become fully qualified as a GMP operator but will be able to carry out much of the work expected from operators under supervision.

Preferred experience/requirements
- You must have completed your studies at upper secondary school level e.g. in natural/technical sciences-It is essential that you follow written procedures carefully and document executed tasks. GMP knowledge is desirable-Interest in technique and manufacturing equipment and practical hands-on work is desirable
- You need to be flexible (temporary positions) with good team working skills.
- Good knowledge of oral and written English is a requirement.

AstraZeneca is one of the world's most exciting biopharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.

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Analytical Chemist - Early Product Development

Analytisk kemist
Läs mer Mar 12
Analytical Chemists (Scientist or Senior Scientist) - Early Product Development and Manufacturing

Hays Life Science is now looking for a new consultant to become an Analytical Chemist at AstraZeneca in Gothenburg, Sweden. This is a consultant assignment for 8 months.

Analytical Chemists (Scientist or Senior Scientist) - Early Product Development and Manufacturing, AstraZeneca Gothenburg

At AstraZeneca we turn ideas into life changing medicines and strive to continuously meet the unmet needs of patients worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you're our kind of person.

Pharmaceutical Sciences at AstraZeneca deliver the therapies of the future through scientific leadership in drug delivery, design of synthetic routes, and manufacturing of Active Pharmaceutical Ingredients (API) across all the AstraZeneca therapy areas.
Our vision is to be "pharmaceutical science leaders, creating innovative and cost-effective solutions, shaping the diverse therapies of the future".
We're looking for talented and motivated analytical chemist to join one of our analytical characterization teams within Early Product Development and Manufacturing (EPDM) in Gothenburg.
You would join a highly collaborative team and together we will deliver the analytical science to product development within the early portfolio up to phase II.
To be successful in this role you will need a strong scientific background with good skills in written and verbal communication and the ability to engage and collaborate across boundaries with a positive problem-solving attitude and delivery focus.
This is a lab-based role where you will work collaboratively with colleagues, documenting your experiments carefully and to the right quality. You will get the opportunity to apply your excellent analytical expertise to the drug projects you are working in, contributing to the progression of these projects and drive the scientific development within the field of analytical science at AstraZeneca.

Required Qualifications, Skills and Experience:
-University degree (MSc, PhD) in relevant discipline, preferable with industry experience
-Scientific knowledge within analytical science and technically skilled to use chromatography with relevant detection techniques for small molecules
-You are a driven experimentalist, with a passion to deliver highly relevant and reliable data and with the ability to be influential in discussions in a wide set of communities and multi-disciplinary project teams
-Excellent communication, collaboration, networking and leadership skills & ability to lead and inspire colleagues

If you also have experience in one or more of the following areas - great!
-Industry experience of pharmaceutical development including oral solid dosage form development
-Experience of CMC submissions and work according to GMP
-Skilled in specific analytical techniques for small molecules, e.g. mass spectrometry, NMR, dissolution etc
-Track record and keen interest of driving development within analytical science including championing new technologies and solutions

AstraZeneca is one of the world's most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we're on a mission to turn ideas into life-changing medicines that improve patients' lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.

Ansök nu

Senior Specialist Programmer, Late-Stage CVRM Biometrics

Systemutvecklare/Programmerare
Läs mer Mar 11
Senior Specialist Programmer, Late-Stage CVRM Biometrics

Hays Life Science is looking for two consultants for a position of Senior Specialist Programmer, Late-Stage CVRM Biometrics at AstraZeneca in Gothenburg, Sweden. This is a consultant assignment for a year with a preferred start on 6th of May.

Are you interested in becoming part of the group of statistical programming at AstraZeneca R&D? Late-stage Cardiovascular, Renal and Metabolism Biometrics is now looking for a Senior Specialist Programmer for a contract assignment with start as soon as possible.

Join a team of statisticians and statistical programmers to provide programming expertise to the design, conduct, reporting, interpretation, documentation, and regulatory submissions of our clinical development programs. Depending on your experience, you may contribute to more strategic planning, quantitative decision making, act as expert in our contact with external providers and collaborators and be a part of the function's adaptation and development of programming tools, standards, and processes.

Requirements for the role:
* Minimum educational level is a BSc degree in a relevant subject such as statistics, biostatistics, mathematics, computer science, life science or engineering.
* Expertise in drug development and clinical data standards (CDISC)
* Expertise in ADaM (specification writing, programming, define generation and ADRG)
* Expertise in analysis output programming (Tables, Figures etc.)
* Good written and spoken English.

Desirable for the role:
* Expertise in multiple programming software such as R or Python
* Project management experience
* Good collaboration, communication and influencing skills
* Experience from regulatory submissions

Personal Qualities:
* Candidates should possess good social skills, be a strong team player and be able to work effectively in a global organization where teams often are geographically dispersed.
* You should be able to work independently, take own initiatives and have a positive, goal oriented and problem-solving attitude.
* It is essential to have good organizational and communication skills and you should be able to analyze and summarize your results and be comfortable in presenting them.
* Successful candidates will have the ability to communicate subject matter expertise to other experts, as well as an interest in the application of programming in pharmaceutical development.

Why AstraZeneca?
Join the team for unlocking the power of what science can do. You have the potential to grow yourself, our pipeline, and positively impact the lives of billions of patients around the world.

What's next? If this sounds like your next challenge - welcome to apply!

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Senior Scientist in Genome Engineering

Biomedicinsk analytiker/BMA
Läs mer Feb 28
Hays Life Science is now looking for a new consultant to become a Senior Scientist in Genome Engineering at AstraZeneca in Gothenburg, Sweden. The assignment is to start in the middle of April and will last until the end of January 2025.

Here at AstraZeneca, we are working towards turning novel state-of-art technologies into effective and safe medicines for severe genetic disease. Do you want to be part of this effort? Welcome to join our exciting journey!

We are looking for a new team member to join our Screening and Automation team in Genome Engineering Department. The role is based in Gothenburg, Sweden, where you will join an international team that develops novel genome engineering technologies and applies these technologies for generation of therapeutic agents. We provide a stimulating environment for innovation and translational application of genome engineering tools. We continually push the boundaries of science to deliver medicines that treat diseases across our main therapy areas.

What you will do:
You will bring your scientific expertise in molecular biology and innovative thinking to drive genome editing approaches that can lead to therapies. You will be a part of cross-functional project teams with various backgrounds and expertise, where you will contribute to development of gene editing strategies.

Accountabilities will include experimental optimization of genome engineering tools to facilitate efficient gene editing, developing relevant assays, analyzing gene editing outcomes, documenting, interpreting, and communicating results to relevant partners. You will collaborate with others to develop streamlined platforms for high-throughput screening and optimization of genome editing components. This is a very exciting role that will give you exceptional professional and technical development opportunities in this state-of-the art scientific discipline.

We also believe that our new colleague is a person who thinks in a creative way and find innovative approaches to scientific problems. You are enthusiastic and curiosity-driven towards finding answers to scientific questions, coming up with solutions to technical problems and learning new skills. You can work in an independent and goal-oriented way, but you also enjoy team work and have the ability to communicate and collaborate in a global setting with cross-functional groups.

Why AstraZeneca?
If you are passionate about translating scientific advances into next generation medicines, AstraZeneca is the right place for you. Join the team for unlocking the power of what science can do. You have the potential to grow yourself, our pipeline, and positively impact the lives of billions of patients around the world.

What's next? If this sounds like your next challenge - welcome to apply!

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Business Support Coordinator

Chefssekreterare
Läs mer Feb 26
Business Support Coordinator

Hays Life Science is looking for a new consultant to become a Business Support Coordinator at AstraZeneca in Gothenburg, Sweden. The assignment is one year long with a preferred start in the middle of April 2024.

Are you an experienced administrator with a can-do attitude? Do you enjoy working in a dynamic global setting? Do you enjoy interacting with people? Join our team and support the delivery of life-changing medicines for patients! At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality.

Within the Business Support Team in Late-Stage Development Cardiovascular, Renal and Metabolism (CVRM) at AstraZeneca we have a clear vision to be recognized as a global world-class support function that drives business success.

We are now looking for a service minded Business Support Coordinator to join our team in Gothenburg, Sweden.



What You'll do

You will provide PA-support to global leaders in a dynamic and complex business environment. You will also provide global operational support to staff in Late CVRM. Responsibilities will vary from traditional administrative tasks, project coordination, design and preparation of presentation materials, management of SharePoint sites, f2f/virtual meeting facilitation to diary management.



Responsibilities

* Proactive calendar management for senior leaders and line managers including travel arrangements and coordination of meetings in different time-zones. Proactively resolve calendar conflicts, prepare meeting materials and presentations as well as more hands-on meeting support.

* Independently manage the set-up and logistics for meetings, booking meeting rooms, prepare agendas, presentations and take meeting minutes as needed.

* Provide project support for various projects within Late CVRM.

* Set-up and manage documents and materials in Microsoft 365 applications.

* Manage and create purchase orders in Coupa. Travel bookings and expense reports in Concur.

* Resolve complex queries and issues to meet stakeholder and business requirements.



Who we think you are

We believe that you are enthusiastic, highly flexible, open to change, goal-oriented and understand the value of putting customers first. You can self-lead and proactively identify opportunities within our business where you can add value. You have excellent technical skills and excellent knowledge of Microsoft 365. You have experience from PA-support and working in a multicultural global setting. You feel comfortable with multiple priorities and changing agendas. You have a sense of flexibility as no two days are alike.



Essentials for the role

* Excellent interpersonal and communication skills

* Experience of diary management

* Tech-savvy, proficient in Microsoft 365 and virtual meeting technologies

* Resourceful with ability to anticipate needs, manage multiple priorities with tight deadlines.

* Strong self-starter, independent and pro-active with ability to work well in a team environment.

* Relevant administrative experience with senior stakeholders

Desirable for the role

* Relevant professional administration qualification

* Highly skilled expert user of relevant IT-systems

* Good knowledge and skills in graphic design and presentation design

So, what's next?

Do you value giving outstanding service and support to the business and love working in a fast-paced environment? Do you enjoy continuously growing and developing your skills in the areas of administration, support, and project coordination? Are you ready to bring innovative ideas and fresh thinking to the table? Perfect! We have one seat available, and we hope it's yours.

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