Göteborg: Scientist In vivo Bioscience

About the position
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.

Research Scientist position – in vitro cellular profiling
We are looking for a passionate Research Scientist to join our Mechanistic and Structural Biology department within the Discovery Sciences organization in Gothenburg, Sweden. You will apply your proven cell biology expertise to in vitro cellular assays. Routine profiling will be combined with tailored mechanism of action studies in cellular models across a multitude of different drug discovery projects. You will build a detailed understanding of the impact of treatment by multiple drug modalities, including small molecules, PROTACS and therapeutic oligonucleotides.
You will demonstrate a passion for applied science, combined with a strong emphasis on team work. 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.

Responsibilities
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.

Your profile
Essential to the role and desirable skills:

-MSc or PhD within a relevant scientific discipline or demonstrated relevant experience in the Life Science industry.
-Proven track record of cellular biology techniques and pharmacology studies.
-Compound profiling in a screening environment using microtiter plates and automation as well as experience in the design, development and validation of biological test assays for compound profiling.
-Practical knowledge of high-resolution MS for targeted or global proteomics analysis and several technology platforms such as imaging, flow cytometry and LC-MS
-Good knowledge of oral and written English is a requirement

Soft skills:
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.

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.

About the position
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 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.

Responsibilities
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.

Your profile
• Bachelor’s Degree in a scientific or supply chain subject area – equivalent experience will be considered.
• Experience within a supply chain management environment with a holistic knowledge of end-to-end supply chain activities
• Experience of demand planning and forecasting and risk identification and management
• Experience in running projects and in?uencing customer demands.
• Strong in?uencing, negotiating and problem-solving skills, across geographical and cultural boundaries
• Excellent English written and verbal communication skills.
• Proficient IT skills with an ability to adapt and operate in bespoke multiple systems.

Desirable for the role
• Awareness of GMP (Good Manufacturing Practise) and GCP (Good Clinical Practice)
• Knowledge of clinical development processes relevant to the supply of clinical materials
• Lean knowledge and understanding
• Experienced in handling Quality Events (Deviations, Change Controls, Complaints)

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.

About the position
APNC is an expanding company specializing in providing statistical solutions for life science research. Our clients are primarily medical researchers in academia, and pharmaceutical and medical technology companies. With a diversified client base, we offer stability and ample opportunities for growth. At APNC Sweden, each individual shapes the company as delegated responsibilities and leadership create the most favorable work environment. Our goal is to be as attractive employer as possible, both to attract and retain the very best employees and to contribute to their well-being and satisfaction. We offer benefits such as bonuses, flexible working hours and part-time options, opportunities for remote work, maximum health support, as well as healthcare and pension insurance. Our ambition is to promote continuous learning through various lectures, courses, and other skill development opportunities.

Responsibilities
We are currently seeking a Senior Statistician to join our growing team, which currently consists of 7 individuals with diverse backgrounds in statistics, biostatistics and programming. Our office is located in Mölndal, within the new, ever-growing life science cluster GoCo Health Innovation City. We are looking for an experienced statistician with a strong passion for medical research and the ability to collaborate and lead a team. Personality is key to meeting our clients and driving the continued development of the company.

Responsibilities:
• Planning and designing clinical studies
• Leading statistical analysis and programming
• Reporting and interpretation of results (study reports/publications)
• Collaboration with various roles, such as programmers, project managers, medical specialists, and regulatory experts
• Team leadership


Your profile
• University degree in statistics, mathematical statistics, or mathematics
• At least 5 years of experience working with statistics in medical research
• Solid experience in SAS/R/python
• Positive and problem-solving attitude
• Excellent communication and collaboration skills
• Experience in leading a team

About the organisation
We are collaborating with QRIOS Life Science & Engineering regarding this recruitment. The selection is ongoing, so be sure to send in your application today!

About the position
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 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.

Responsibilities
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.

Your profile
• Bachelor’s Degree in a scientific or supply chain subject area – equivalent experience will be considered.
• Experience within a supply chain management environment with a holistic knowledge of end-to-end supply chain activities
• Experience of demand planning and forecasting and risk identification and management
• Experience in running projects and in?uencing customer demands.
• Strong in?uencing, negotiating and problem-solving skills, across geographical and cultural boundaries
• Excellent English written and verbal communication skills.
• Proficient IT skills with an ability to adapt and operate in bespoke multiple systems.

Desirable for the role
• Awareness of GMP (Good Manufacturing Practise) and GCP (Good Clinical Practice)
• Knowledge of clinical development processes relevant to the supply of clinical materials
• Lean knowledge and understanding
• Experienced in handling Quality Events (Deviations, Change Controls, Complaints)

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 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.