Göteborg: Analytical Scientist

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Publicerad: 2022-05-23 // Varaktighet: Heltid

About the position
Do you have an interest in analytical chemist? Would you like to work in a cross-functional environment using state of the art technology? Then you might be our next member in the Separation Science Laboratory team!

We’re looking for a talented and motivated analytical chemist to join our Separation Science Laboratory team within the Pharmaceutical Science function at AstraZeneca in Gothenburg.
The vision for Pharmaceutical Sciences is to deliver the therapies of the future through scientific leadership in drug delivery, design of synthetic routes and manufacturing of Active Pharmaceutical Ingredients (API). Our portfolio of projects spans traditional small molecules to nucleotide-based therapies and nanomedicines across AstraZeneca’s therapy areas.

Responsibilities
You will join a highly competent team and collaboratively drive the delivery of pure compounds to our early portfolio. We use modern chromatographic instrumentation including LC and SFC in both analytical and preparative scale and a high degree of automation.
To be successful in this role you will need a problem-solving attitude and strong delivery focus. It is essential with good communication skills and ability to engage and collaborate across boundaries. You are expected to:

• Be laboratory based and work collaboratively with colleagues
• Run chromatographic equipment as well as liquid handling robotics
• Effectively operate with scientists from other functions in a highly cross-disciplinary environment

Your profile
Essential requirements
• Scientific knowledge within analytical chemistry
• Technical skills and experience to use and maintain chromatographic equipment
• Excellent problem-solving skills
• Excellent English, both spoken and written
• Work collaboratively, prioritise your own work and act decisively

About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg for one year. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

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 unleash 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.

Alla platsannonser →

Andra jobb i Göteborg som Forskare, farmakologi

Nedan visas andra jobb i Göteborg som Forskare, farmakologi.

Clinical Supply Associate

Läs mer Apr 16
About the position
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 are opening new ways to work, pioneering ground-breaking methods, and bringing unexpected teams together. Interested? Come and join our journey.

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.

In Pharmaceutical Technology and Development (PT&D) we are the bridge which turns forward-thinking science into actual medicines that help 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.

The Clinical Supply Associate (CSA) supports Global Clinical Supply Chain (GCSC) to ensure the delivery of clinical material and associated information to meet the agreed clinical demand. This role is a great opportunity for someone who thrives working in a task based, agile and global environment.

Responsibilities
What you'll do
The CSA supports GCSC teams with task-based activities that include:

• Timely management of temperature excursion assessment affecting clinical trial material.
• Coordination of the country release requests of study labelled material.
• Electronic document archiving and quality control.
• User Acceptance Testing of digital systems.
• Support the coordination of the purchase and delivery of External Commercial Products.
• Facilitation of documentation activities ensuring inspection readiness to meet international GMP standards.
• Documentation and coordination of product complaints and GMP deviations.
• Utilising Supply Chain Management systems to support agile ways of working.
• Continually improving the Clinical Supply Chain processes through visual management, problem solving, global standardisation and process confirmation.

In this role you will have the opportunity to develop leadership skills and enterprise acumen, quickly becoming a Super User within a core role and/or leading improvement initiatives. You will work with multiple customers and partners internally and externally across all phases of the drug development lifecycle, covering small and large molecule drug products. You will follow SHE and GMP standards and will be personally accountable for these areas within your own work plans.

Your profile
• Excellent communication skills.
• A scientific / business / supply chain ambition.
• Organised and structured with an excellent aptitude for digital systems.
• Thrives in a process orientated workplace, on task-based activities and with a focus on the customer/patient.
• Team player with a problem-solving mindset and a focus on quality.
• Comfortable in a high paced and agile environment.
• Ability to reflect, see the bigger picture, whilst also having a focus on the detail.

About the organisation
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

Working as a consultant suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique 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.

Ansök nu

Scientist In vivo Bioscience

Läs mer Apr 10
About the position
We are now looking for a Scientist to join the In vivo Bioscience team within Research and Early Development, Respiratory & Immunology in Gothenburg, Sweden.

Respiratory & Immunology is one of AstraZeneca’s main therapy areas. From a research perspective we work to understand, treat, modify and ultimately cure respiratory and autoimmune diseases. In this role, you will focus on mouse models of inflammatory bowel disease (IBD).

Responsibilities
As part of the team, you will plan, execute and analyse ex vivo samples generated from in vivo studies to progress our drug discovery projects and generate publishable scientific insights. You will actively take part in scientific discussions to add valuable inputs in experimental design and data interpretation.

This is a mainly lab-based role where you will be involved in ongoing projects focusing on pre-clinical experiments.

What you’ll do:

• As a Scientist you will be a vital member of the in vivo community and will contribute to the development and characterization of pre-clinical models of IBD to discover novel therapeutics.
• You will contribute to the analysis of in vivo studies with a specific focus on FACS analysis.

Your profile
• At last 5 years of experience with regular FACS analysis of mouse samples (organ processing and digestion, cell staining, antibody panel set up, proficient in the use of BD FACS DIVA machines and Flowjo).
• Ability to organize, execute and interpret the results from in vivo studies according to study plans in agreement with the team leader or other colleagues.
• Experience with other in vitro methodology in addition to FACS (ELISA/MSD and/or qRT-PCR) to analyze ex vivo samples generated from in vivo studies.
• Experience of maintaining the highest standards of welfare and ethical compliance and ensuring the integrity of the 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.
• Valid education required for compliance to work with live animals in Sweden.
• Excellent English written and oral communication skills, including presentation skills.

Desirable for the role:

• Degree in immunology (master or PHD) and understanding of autoimmune diseases with a specific focus on gut immunology.
• Several years of hands-on experience with rodents including live animal handling, drug administration through different routes (i.v, i.p., p.o.), blood and organ sampling and processing (colon, small intestine, spleen, lymph nodes).
• Experience with animal models of inflammatory bowel disease (IBD) and in vivo PK/PD relationships.

About the organisation
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

Working as a consultant suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique 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.

Ansök nu

Scientist In vivo Bioscience at AZ Gothenburg

Läs mer Apr 10
Scientist In vivo Bioscience at AstraZeneca Gothenburg!

We are now looking for a Scientist to join the In vivo Bioscience team within Research and Early Development, Respiratory & Immunology at AstraZeneca in Gothenburg, Sweden. Respiratory & Immunology is one of AstraZeneca´s main therapy areas. From a research perspective we work to understand, treat, modify and ultimately cure respiratory and autoimmune diseases. In this role, you will focus on mouse models of inflammatory bowel disease (IBD)

Purpose, Offer and Benefits

This is a 9-month consulting assignment starting in May. You will be employed by TNG during the assignment period. Please note that the selection process is ongoing.

At AstraZeneca we´re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash 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.

Your Responsibilities

As part of the team, you will plan, execute and analyse ex vivo samples generated from in vivo studies to progress our drug discovery projects and generate publishable scientific insights. You will actively take part in scientific discussions to add valuable inputs in experimental design and data interpretation.

• You will be a vital member of the in vivo community and will contribute to the development and characterization of pre-clinical models of IBD to discover novel therapeutics.
• You will contribute to the analysis of in vivo studies with a specific focus on FACS analysis.

The Bigger Picture

This is a mainly lab-based role where you will be involved in ongoing projects focusing on pre-clinical experiments.

 

Our Expectations

• At last 5 years of experience with regular FACS analysis of mouse samples (organ processing and digestion, cell staining, antibody panel set up, proficient in the use of BD FACS DIVA machines and Flowjo).
• Ability to organize, execute and interpret the results from in vivo studies according to study plans in agreement with the team leader or other colleagues.
• Experience with other in vitro methodology in addition to FACS (ELISA/MSD and/or qRT-PCR) to analyze ex vivo samples generated from in vivo studies.
• Experience of maintaining the highest standards of welfare and ethical compliance and ensuring the integrity of the 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.
• Valid education required for compliance to work with live animals in Sweden.
• Excellent English written and oral communication skills, including presentation skills.

Desirable for the role:

• Degree in immunology (master or PHD) and understanding of autoimmune diseases with a specific focus on gut immunology.
• Several years of hands-on experience with rodents including live animal handling, drug administration through different routes (i.v, i.p., p.o.), blood and organ sampling and processing (colon, small intestine, spleen, lymph nodes).
• Experience with animal models of inflammatory bowel disease (IBD) and in vivo PK/PD relationships.

Interested?
This is a staffing assignment which means that you are employed by TNG, but work for one of our customers. If you are interested in this position, apply right now! The selection process is ongoing and the position can be filled before the last apply-date. If you have any questions, please contact the recruiter.

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Biologics Translational PKPD Modeling & DMPK Expert

Läs mer Mar 12
Do you have a passion for PKPD modelling of antibody-based therapeutics and expertise in respiratory and immunology? Would you like to apply your knowledge in a global company that follows the science and turns ideas into life-changing medicines? Then you could be the new colleague we are looking for!



We currently have an exciting opportunity for a passionate PKPD modelling and DMPK Scientist to join our DMPK department as a Biologics Translational PKPD Modeling & DMPK Specialist within Early Respiratory and Immunology (R&I). The R&I DMPK department provides drug metabolism and pharmacokinetic, as well as translational PKPD modeling & simulation support to our portfolio. This position is located at AstraZeneca's vibrant R&D site in Gothenburg, Sweden.



At AstraZeneca Early Respiratory & Immunology (R&I), we're proud to have an outstanding workplace culture that encourages innovation and teamwork. We are united by our vision to push the boundaries of DMPK science to transform ideas into medicines for R&I patients. Employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.



What you'll do?
As a Biologics Translational PKPD Modelling & DMPK Specialist (Principal Scientist) you will have the opportunity to drive strategy and provide global leadership in PKPD science across our diverse portfolio, and act as role model, mentoring and guiding less experienced members of the team. You have in-depth knowledge of biologics drug discovery and a keen interest in understanding the translational PKPD of antibody-based therapeutics.

In the role you would provide projects with specialist modeling input into exploring PK/PD/Efficacy in pre-clinical models and use them to guide an understanding of the dosing across different patient populations.



Main Duties and Responsibilities:

*

Be the key link between the leadership team and department in driving the translational PKPD strategy and leveraging modeling approaches in discovery projects towards human dose predictions
*

Drive and embed strategic direction by developing and implementing best practices in supporting projects and share insight across the department
*

Able to handle and balance the workload of multiple projects and efficiently manage your time and submit pragmatic solutions/strategies to ensure effective support of your projects
*

Represent early R&I DMPK in projects and providing overall scientific leadership for cross functional collaborations involving DMPK
*

Exploring the effects on target and pathway to understand the requirements for efficacy and set a candidate drug target profile (CDTP)
*

Ensuring that translational PKPD approaches are embedded at the heart of project strategy and used to support design of appropriate experiments that are aligned to the strategy underpinning human dose prediction and providing input into exposure and pharmacodynamic (PD) biomarker based decision criteria
*

Identify, champion and develop new ideas
*

Offer a breadth of influence and impact across AstraZeneca DMPK
*

Leading scientific discipline networks and acting as a focus for debate within the AstraZeneca scientific community
*

Develop excellent working relations with key stakeholders within both DMPK and in the project teams, to ensure strategic alignment, strong cross discipline collaboration and communication.



Essential for the role

*

PhD (or equivalent industrial experience) in a relevant field e.g. pharmacokinetics, pharmacology, biopharmaceutics etc.
*

7 years of industry experience in Modeling & Simulation, ideally in preclinical/translational setting with a focus on biologics
*

In-depth knowledge of therapeutic antibody drug discovery (incl. complex biologics, cell therapies, ADCs) and a keen interest in understanding the translational PKPD of antibody based molecules
*

Experience of DMPK project facing role in pharmaceutical R&D with a variety of therapeutic antibody formats (e.g. mAbs, Fabs, bispecifics, ADCs etc).
*

Track record of supporting PK, PKPD and TKPD aspects of projects, with a delivery focus and ability to meet timelines to pre-specified quality and cost
*

Excellent interpersonal skills, and ability to work in cross-functional teams as well as strong scientific leadership skills
*

Experience in defining quantitative modeling strategies across several therapeutic modalities (e.g. small molecules, oligonucleotides, peptides, proteins, antibodies)
*

Hands on experience of using specialist tools such as WinNonLin/Phoenix, MATLAB, R, Berkely Madonna or similar



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 unleash 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.



What's next!
If you are ready to make a difference - apply today, and we'll make it happen together! We welcome your application until March 31, 2024.

For more information about the position, please contact recruiting manager Nina Lawrence at Nina.Lawrence@astrazeneca.com

Ansök nu

Scientist/Senior Scientist - Early Product Dev and Mfg

Läs mer Mar 22
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 or Senior Scientist level, depending on your background and experience.





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 product, 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.





Accountabilities include:



*

Work with practical hands-on processes in our GMP facilities following manufacturing batch records and perform 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 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.





Essential requirements

*

MSc or BSc in pharmacy/engineering or extensive GMP-manufacturing experience from the pharmaceutical industry
*

Excellent collaboration, communication, and planning skills
*

Strong sense of responsibility, teamwork and delivery focus
*

Strong verbal and documentation skills in English
*

Keen interest to learn and operate complex manufacturing equipment





Desirable for the role

*

Experience from pharmaceutical development or working in a manufacturing or supply chain organisation
*

Experience from sterile manufacture
*

Experience with material management systems
*

Ability to author manufacturing batch records, SOPs, and other guidance documents
*

Experience with deviation investigations and change control processes
*

Familiarity with SHE standards





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.





So, what's next? We welcome your application (including CV and cover letter), no later than April 7th, 2024.





Additional information
Our Gothenburg site: https://www.astrazeneca.com/our-science/gothenburg.html
About BioPharmaceuticals R&D: https://www.astrazeneca.com/r-d.html

Ansök nu

Andra jobb i Göteborg från QRIOS Minds AB

Nedan visas andra jobb i Göteborg från QRIOS Minds AB .

Clinical Supply Associate

Forskare, farmakologi
Läs mer Apr 16
About the position
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 are opening new ways to work, pioneering ground-breaking methods, and bringing unexpected teams together. Interested? Come and join our journey.

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.

In Pharmaceutical Technology and Development (PT&D) we are the bridge which turns forward-thinking science into actual medicines that help 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.

The Clinical Supply Associate (CSA) supports Global Clinical Supply Chain (GCSC) to ensure the delivery of clinical material and associated information to meet the agreed clinical demand. This role is a great opportunity for someone who thrives working in a task based, agile and global environment.

Responsibilities
What you'll do
The CSA supports GCSC teams with task-based activities that include:

• Timely management of temperature excursion assessment affecting clinical trial material.
• Coordination of the country release requests of study labelled material.
• Electronic document archiving and quality control.
• User Acceptance Testing of digital systems.
• Support the coordination of the purchase and delivery of External Commercial Products.
• Facilitation of documentation activities ensuring inspection readiness to meet international GMP standards.
• Documentation and coordination of product complaints and GMP deviations.
• Utilising Supply Chain Management systems to support agile ways of working.
• Continually improving the Clinical Supply Chain processes through visual management, problem solving, global standardisation and process confirmation.

In this role you will have the opportunity to develop leadership skills and enterprise acumen, quickly becoming a Super User within a core role and/or leading improvement initiatives. You will work with multiple customers and partners internally and externally across all phases of the drug development lifecycle, covering small and large molecule drug products. You will follow SHE and GMP standards and will be personally accountable for these areas within your own work plans.

Your profile
• Excellent communication skills.
• A scientific / business / supply chain ambition.
• Organised and structured with an excellent aptitude for digital systems.
• Thrives in a process orientated workplace, on task-based activities and with a focus on the customer/patient.
• Team player with a problem-solving mindset and a focus on quality.
• Comfortable in a high paced and agile environment.
• Ability to reflect, see the bigger picture, whilst also having a focus on the detail.

About the organisation
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

Working as a consultant suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique 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.

Ansök nu

Scientist In vivo Bioscience

Forskare, farmakologi
Läs mer Apr 10
About the position
We are now looking for a Scientist to join the In vivo Bioscience team within Research and Early Development, Respiratory & Immunology in Gothenburg, Sweden.

Respiratory & Immunology is one of AstraZeneca’s main therapy areas. From a research perspective we work to understand, treat, modify and ultimately cure respiratory and autoimmune diseases. In this role, you will focus on mouse models of inflammatory bowel disease (IBD).

Responsibilities
As part of the team, you will plan, execute and analyse ex vivo samples generated from in vivo studies to progress our drug discovery projects and generate publishable scientific insights. You will actively take part in scientific discussions to add valuable inputs in experimental design and data interpretation.

This is a mainly lab-based role where you will be involved in ongoing projects focusing on pre-clinical experiments.

What you’ll do:

• As a Scientist you will be a vital member of the in vivo community and will contribute to the development and characterization of pre-clinical models of IBD to discover novel therapeutics.
• You will contribute to the analysis of in vivo studies with a specific focus on FACS analysis.

Your profile
• At last 5 years of experience with regular FACS analysis of mouse samples (organ processing and digestion, cell staining, antibody panel set up, proficient in the use of BD FACS DIVA machines and Flowjo).
• Ability to organize, execute and interpret the results from in vivo studies according to study plans in agreement with the team leader or other colleagues.
• Experience with other in vitro methodology in addition to FACS (ELISA/MSD and/or qRT-PCR) to analyze ex vivo samples generated from in vivo studies.
• Experience of maintaining the highest standards of welfare and ethical compliance and ensuring the integrity of the 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.
• Valid education required for compliance to work with live animals in Sweden.
• Excellent English written and oral communication skills, including presentation skills.

Desirable for the role:

• Degree in immunology (master or PHD) and understanding of autoimmune diseases with a specific focus on gut immunology.
• Several years of hands-on experience with rodents including live animal handling, drug administration through different routes (i.v, i.p., p.o.), blood and organ sampling and processing (colon, small intestine, spleen, lymph nodes).
• Experience with animal models of inflammatory bowel disease (IBD) and in vivo PK/PD relationships.

About the organisation
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

Working as a consultant suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique 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.

Ansök nu

Erfaren geotekniker till SGI

Geotekniker
Läs mer Mar 22
Ansök via denna länk
https://recruit.visma.com/spa/sv/public/apply?guidAssignment=ea846e08-0025-496c-87bf-ee7987077ce5&description=True&forcelocale=true
Om Arbetsplatsen
Statens geotekniska institut (SGI) är en expertmyndighet som arbetar för ett säkert, effektivt och hållbart byggande och ett hållbart användande av mark och naturresurser. I våra uppgifter ingår att förebygga jordskred, ras och stranderosion. SGI arbetar också med att ta fram nya metoder för att sanera förorenade områden. SGI tillhör Klimat- och näringslivsdepartementet och har totalt cirka 100 medarbetare. Huvudkontoret ligger i Linköping och kontor finns i Stockholm, Göteborg och Malmö.
Göta älvdalen är Sveriges mest skredbenägna region och samtidigt det område som bedöms påverkas mest av klimatförändringen framöver. Framtida skred skulle påverka både samhällsviktiga funktioner, riksintressen, Natura2000-områden och inte minst många som bor i Göta älvdalen.
Som geotekniker i sekretariatet för Göta älv får du möjlighet att minska riskerna i denna region du kan göra skillnad, som är till nytta för hela samhället!
Arbetsuppgifter
Det är ett välfinansierat regeringsuppdrag som möjliggör att SGI kan arbeta enligt nya utredningsmetoder med projekt från behovsanalys och fram till färdig åtgärd, optimerad enligt den senaste kunskapen. Här blir du del av en engagerad och prestigelös projektgrupp som drivs av att förbättra förutsättningarna för de som bor och verkar längs Göta älv och samtidigt fördjupa sin kunskap inom geotekniska frågeställningar.

Våra medarbetare är den viktigaste tillgången vi har! För att på bästa sätt utföra samhällsuppdraget, behöver vi kunniga och engagerade människor som arbetar hos oss. Vi behöver också dra nytta av våra olikheter i bakgrund, erfarenhet och kompetens.

Istället för att jobba med små enskilda uppdrag får du möjlighet att jobba med helheten. Vi ser hela Göta älv från Vänersborg till Göteborg som ett stort projekt. Sekretariatet har tillgång till en stor mängd undersökningsresultat. Såväl geotekniska beräkningsverktyg som GIS-program används i hög grad. I vårt arbete får vi en bra överblick av allt underlag med hjälp av GIS. Vi behöver en person med god erfarenhet av att genomföra geotekniska utredningar och att medverka vid åtgärder i lös lera.
Du kommer att leda stabilitetsutredningar samt stötta våra kommuner i deras projektering och under åtgärdsfasen med stöd från kompetenta kollegor.

I arbetet ingår att vara en del av SGI:s beredskapsorganisation som geotekniskt stöd till framför allt räddningstjänsten i händelse av eller vid tidiga indikationer på ras eller skred.
Kvalifikationer
Tjänsten kräver universitets- eller högskoleutbildning: civilingenjör (exempelvis väg och vatten eller samhällsbyggnad) eller liknande utbildning som av arbetsgivaren bedöms vara lämplig för tjänsten. För arbetet krävs goda geotekniska kunskaper, särskilt inom området släntstabilitet. Du bör ha erfarenhet av geotekniskt utredningsarbete samt projektering.

Arbetet innebär många kontakter, både internt och externt, och du behöver därför vara utåtriktad och lyhörd. Vi löser våra uppdrag tillsammans, vilket innebär att du bör tycka om att jobba i grupp/team och att dela med dig av erfarenheter. Du ska kunna uttrycka dig väl i tal och skrift. Du har mycket god datavana och arbetar väl i Microsoft- Officepaket.

Vid urvalet kommer det att läggas stor vikt vid din personliga lämplighet. För att kunna arbeta hos oss ska du dela statens gemensamma värdegrund, http://www.sgi.se/sv/om-sgi/sa-arbetar-vi/vardegrund-och-kompass/

Vi erbjuder
om en statlig myndighet är de flesta av våra anställningsvillkor kopplade till det centrala statliga avtalet men vi har också en del av mer specifika anställningsvillkor. Vi erbjuder dig ett samhällsviktigt uppdrag, spännande och utvecklande arbetsuppgifter med generös syn på kompetensutveckling samt en trevlig arbetsplats med medarbetare i fokus med stort engagemang och arbetsglädje. Vi har generöst med semesterdagar, möjlighet att till viss del arbeta på distans, individuell lön, flexibel arbetstid, ett generöst friskvårdsbidrag, mm.
Vid urvalet kommer det att läggas stor vikt vid din personliga lämplighet.
Fackliga företrädare: Martin Holmén SACO tel. 013-20 18 15, Eva Albin ST tel. 013-20 18 29
Tjänsten är placerad vid Sekretariatet för Göta älv i Göteborg och är en tillsvidareanställning på 100%. Tillträde snarast enligt överenskommelse.

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Handläggare Badvatten

Ekolog
Läs mer Mar 21
Jag söker efter en konsult för ett heltidsuppdrag hos en myndighet i Göteborg under perioden 2024-06-24 fram till 2024-08-09.
Konsulten kommer att omfattas av bestämmelserna i offentlighets- och sekretesslagen (2009:400), OSL. Konsulten kommer att få skriva under en sekretesserinran innan uppdraget påbörjas.

Dina arbetsuppgifter i huvudsak
Myndigheten vägleder kommunerna om skötsel av EU-bad i Sverige, rapporterar badvattendirektivet till Europeiska kommissionen och är värd för webbplatsen Badplatsen.

Under sommaren behöver myndigheten förstärka personalstyrkan och söker efter en sommararbetare som har en naturvetenskaplig bakgrund samt erfarenhet av att jobba serviceinriktat.
Uppdraget pågår upp till 7 veckors heltidsarbete förlagda över kontorstid: måndag till fredag. Trycket på arbetsuppgifterna varierar beroende av väder och badvilja. Huvudsakligen görs vägledningen via mejl, men sker också över telefon.

• Löpande ge vägledning runt badvatten till kommuner och allmänhet
• Löpande följa upp rapportering till webbplatsen Badplatsen
• Löpande hantera användarkonton för webbplatsen Badplatsen
• Löpande bidra till arbetet med utredningar och sammanställningar kring badvattenfrågor som uppkommer under
badsäsongen.

Du utför uppdraget i nära samarbete med medarbetare i myndighetens badvattengrupp, och interna beställare.

Vem är du?
• Högskole- eller universitetsexamen om minst 3 år med inriktning på akvatisk ekologi eller vattenvård.
• Andra möjliga inriktningar på utbildning är miljövetarprogrammet, samhällsvetenskapligt miljövetarprogram och biologiprogrammet.

• Du får gärna ha relevant erfarenhet inom t.ex. vattenförvaltning, miljökommunikation, miljöövervakning, digitalisering, arbete inom databaser, relevanta mikrobiologiska analyser, föroreningar av ytvatten, algblomning.

• God kommunikationsförmåga, serviceinriktad, självständig, stresstålig, lättlärd.

About the organisation
Detta är ett konsultuppdrag under perioden 2024-06-24 fram till 2024-08-09.
Under tiden som uppdraget är, så kommer du vara anställd av QRIOS.

Urval och intervjuer kommer ske löpande. Vänligen sök snarast.

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Konsulter sökes till Engineering uppdrag

Civilingenjör, kvalitet, elektronik
Läs mer Feb 22
QRIOS Life Science & Engineering är i behov av kompetenta medarbetare för flera spännande konsultuppdrag. Vi välkomnar sökande med minst tre års erfarenhet inom områdena Mechanics & Cabling samt Electronics.
Mechanics & Cabling
Vi letar efter kandidater med erfarenhet inom följande områden:

Miljökrav -Maritima, markbaserade och luftburna domäner


Kunskap inom mikrovågsteknik


Expertis inom kraftelektronik


Hantering av äldre teknik på grund av långa produktlivscykler


Erfarenhet av Chrome 6


Användning av Creo (Mech Solid modellering + cabling)


Färdigheter inom Visio (cabling)


Användning av PDM System (IFS)


Electronics
Vi söker individer med erfarenhet inom följande områden:

RF/Mikrovågsdesign


Digital design


PCB-design



Dessa tjänster är konsultuppdrag hos vår kund i Göteborg. Under denna tid kommer du att vara anställd av QRIOS Life Science & Engineering.
QRIOS anställer nyfikna experter inom IT, Life Science och Engineering. Vi vill fortsätta att attrahera de bästa medarbetarna för att kunna stödja våra partners med de viktiga kompetenser de behöver. Vi är ett rekryterings- och konsultföretag som starkt inspireras av dem som aldrig slutar söka efter nya lösningar. Som vi säger, QRIOS MINDS GO FURTHER.

#LI-HF3

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External Supply Co-ordinator

Forskare, farmakologi
Läs mer Mar 18
About the position
Do you have an interest in clinical supply chain and working with external vendors and are you a person who would like to be part of a truly global team and play a key role in getting medicines to patient – then join us!

Pharmaceutical Technology and Development (PT&D) apply science and technology that turns concepts into actual medicines which 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 toxicology studies and clinical trials to developing the technology to ensure drugs can be scaled up for commercial manufacture.

Clinical Manufacture & Supply (C&MS;) within PT&D provides an agile and flexible end-to-end Clinical Supply Chain that manufactures, outsources and delivers supplies and services to hundreds of thousands of patients across the globe.

Responsibilities
CM&S are now looking for an External Supply Co-ordinator to join our global External Commercial Product Team in Oncology Therapy Area on a 12 month contract. We are seeking those who embrace change, show great initiative, flexibility, and a willingness to learn. As External Supply Co-ordinator, you will establish relationships with external suppliers and collaborate in teams of internal experts (e.g., Technical, Quality Assurance, Procurement) in the sourcing of services and goods required by CM&S from external suppliers in support of global projects for AstraZeneca. This role will have a specific focus on sourcing the goods and services required for sourcing commercially available product for use in AstraZeneca sponsored Clinical Trials. We would ideally like to receive applications from people with clinical supply chain and supplier management experience.

Your profile
Requirements for the role:

• BSc level education in a relevant discipline.
• Minimum 5 years’ experience of working within a Research & Development or Procurement environment and working with external providers.
• Appropriate depth of technical knowledge for the activity being sourced, to be able to fully understand any risks to delivery and make the best use of the technical experts on the team to make effective decisions.
• Experience of data analysis

Desirable for the role:

• Supplier Relationship Management skills
• Understanding quality principles and GMP requirements
• Project Management experience.
• Networking skills
• Good communication skills
• A high degree of personal credibility when interfacing with organisations internal and external to AZ.

About the organisation
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

Working as a consultant suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique 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.

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