Civilingenjör, bioteknik

Job description Senior Specialist, Regulatory Drug Project Delivery is a pivotal operational and strategic role within the Global Regulatory Affairs department. The primary mission of this role is to lead and project-manage the end-to-end delivery of regulatory submissions (like clinical trial applications, marketing authorizations, and variations) to health authorities globally (e.g., FDA, EMA, MPA) to get life-changing medicines to patients. This is a consulting assignment with Randstad Life Sciences. Randstad Life Sciences is specialized in competences within Life Science. As a consultant with us, you get a competitive salary, benefits and collective agreements. Your consultant manager is always there for you and ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities. Responsibilities In this role, you will experience the full drug development pipeline through three high-impact rotations within Respiratory & Immunology: Rotation 1: Genome Engineering (Early Discovery) Focus on cutting-edge biotechnology by conducting independent research on novel gene-editing projects. In this lab-based role, you will execute experimental protocols, analyze complex data sets, and collaborate with senior scientists to support high-profile scientific publications. Rotation 2: Early Clinical Development Shift from the lab bench to clinical trials by supporting the design and execution of a Phase 2 trial for Crohn’s disease. You will partner with Clinical Scientists and Study Physicians on medical monitoring, data review, and protocol amendments. You will also manage site communications (including urgent medical queries) and author key pediatric strategy documents and investigator meeting materials. Rotation 3: Patient Centered Science Bridge the gap between clinical data and the human experience by researching patients’ lived experiences to develop and validate Patient-Reported Outcome (PRO) measures. Qualifications You are essentially the "controller" and operational execution lead for a drug project’s regulatory journey. While the Regulatory Director focuses on the long-term scientific and political strategy with health authorities, the Senior Specialist focuses on how that strategy gets built, managed, and successfully submitted. You work in a matrix environment, bridging the gap between scientists, clinical teams, medical writers, and publishing teams. About the company Randstad På Randstad vet vi att alla människor har en plats på arbetsmarknaden. Med verksamhet över hela landet och inom alla kompetensområden hjälper vi människor att hitta ett jobb som känns bra, och där de får möjlighet att växa, utvecklas och uppnå sin fulla potential. Med närmare 600 000 anställda i 38 länder är Randstad världsledande inom HR-tjänster, med målsättningen att bli världens främsta och mest uppskattade partner på arbetsmarknaden. Genom att kombinera vår passion för människor med kraften i dagens teknologi hjälper vi människor och företag att uppnå deras fulla potential. Vi kallar det Human Forward.

Job description Senior Specialist, Regulatory Drug Project Delivery is a pivotal operational and strategic role within the Global Regulatory Affairs department. The primary mission of this role is to lead and project-manage the end-to-end delivery of regulatory submissions (like clinical trial applications, marketing authorizations, and variations) to health authorities globally (e.g., FDA, EMA, MPA) to get life-changing medicines to patients. This is a consulting assignment with Randstad Life Sciences. Randstad Life Sciences is specialized in competences within Life Science. As a consultant with us, you get a competitive salary, benefits and collective agreements. Your consultant manager is always there for you and ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities. Responsibilities In this role, you will experience the full drug development pipeline through three high-impact rotations within Respiratory & Immunology: Rotation 1: Genome Engineering (Early Discovery) Focus on cutting-edge biotechnology by conducting independent research on novel gene-editing projects. In this lab-based role, you will execute experimental protocols, analyze complex data sets, and collaborate with senior scientists to support high-profile scientific publications. Rotation 2: Early Clinical Development Shift from the lab bench to clinical trials by supporting the design and execution of a Phase 2 trial for Crohn’s disease. You will partner with Clinical Scientists and Study Physicians on medical monitoring, data review, and protocol amendments. You will also manage site communications (including urgent medical queries) and author key pediatric strategy documents and investigator meeting materials. Rotation 3: Patient Centered Science Bridge the gap between clinical data and the human experience by researching patients’ lived experiences to develop and validate Patient-Reported Outcome (PRO) measures. Qualifications You are essentially the "controller" and operational execution lead for a drug project’s regulatory journey. While the Regulatory Director focuses on the long-term scientific and political strategy with health authorities, the Senior Specialist focuses on how that strategy gets built, managed, and successfully submitted. You work in a matrix environment, bridging the gap between scientists, clinical teams, medical writers, and publishing teams. About the company Randstad På Randstad vet vi att alla människor har en plats på arbetsmarknaden. Med verksamhet över hela landet och inom alla kompetensområden hjälper vi människor att hitta ett jobb som känns bra, och där de får möjlighet att växa, utvecklas och uppnå sin fulla potential. Med närmare 600 000 anställda i 38 länder är Randstad världsledande inom HR-tjänster, med målsättningen att bli världens främsta och mest uppskattade partner på arbetsmarknaden. Genom att kombinera vår passion för människor med kraften i dagens teknologi hjälper vi människor och företag att uppnå deras fulla potential. Vi kallar det Human Forward.

Job description The overall purpose of the role is to support pilot plant activities connected to clinical & stability batches, laboratory work, process development and documentation in a GMP-regulated environment. Essential duties and responsibilities: • Support preparation and execution of clinical, pilot and development batches in accordance with established instructions and procedures. • Perform hands-on laboratory and pilot plant work, including material handling, sample preparation and documentation. • Support process development, technical evaluations and troubleshooting activities. • Document work in protocols, batch records, reports and/or relevant quality systems. • Collaborate with R&D, Quality, QC, Production and other internal functions. • Participate in investigations, deviation handling and improvement activities when relevant. Responsibilities Essential knowledge and skills: Basic understanding of laboratory work, structured documentation and working according to established procedures. Interest in GMP-regulated environments, pharmaceutical manufacturing, process development and technical problem-solving. Core competencies required for this role: • Strong analytical, communication and collaboration skills. • Structured and quality-conscious way of working. • Independent thinking and good planning/prioritization skills. • Highly motivated self-starter who takes accountability for assigned tasks. • High degree of accuracy, quality and attention to detail. Qualifications Requested skills Must have: Relevant Life Science / Engineering Education Ongoing or completed university education within pharmacy, biotechnology, chemical engineering, or similar. Must have: Laboratory Experience / Hands-on Practical Work Experience from laboratory work, sample handling, experimental work, preparation of materials or other practical technical/scientific tasks. Must have: Quality Mindset & Attention to Detail Structured and accurate way of working, with an understanding of the importance of quality, traceability and documentation in regulated environments. Must have: Problem-Solving & Analytical Skills Interest in understanding technical processes, evaluating results and contributing to practical solutions and continuous improvements. Must have: Swedish and English Language Skills Good communication skills in Swedish and English, both written and spoken. Good to have: GMP / QA / QC Understanding Experience or understanding of GMP, quality assurance, quality control, deviation handling, regulated documentation or quality systems. Good to have: Pharmaceutical / Biotech / Medtech Environment Exposure Previous exposure to pharmaceutical, biotech, medtech, laboratory, pharmacy or other regulated life science environments. Good to have: Analytical Methods / Sample Handling Experience from analytical laboratory work, sample preparation, material handling, material characterisation such particle size distribution, morphology, flowability, disintegration, viscosity etc. Good to have: Process Development / Process Workflow Interest Interest in process understanding, troubleshooting, process improvement or working close to the transition between development and production. Good to have: Independent & Collaborative Work Style Ability to take responsibility for assigned tasks, work proactively and collaborate with different internal functions. About the company Randstad På Randstad vet vi att alla människor har en plats på arbetsmarknaden. Med verksamhet över hela landet och inom alla kompetensområden hjälper vi människor att hitta ett jobb som känns bra, och där de får möjlighet att växa, utvecklas och uppnå sin fulla potential. Med närmare 600 000 anställda i 38 länder är Randstad världsledande inom HR-tjänster, med målsättningen att bli världens främsta och mest uppskattade partner på arbetsmarknaden. Genom att kombinera vår passion för människor med kraften i dagens teknologi hjälper vi människor och företag att uppnå deras fulla potential. Vi kallar det Human Forward.

Job description Scientist Safety Science, Clinical Pharmacology Make a more meaningful impact to patients’ lives around the globe  Here you’ll have the opportunity to make a meaningful difference to patients’ lives. With science at its heart, this is the place where breakthroughs born in the lab become transformative medicines – for the world’s most complex diseases. Answer unmet medical needs by pioneering the next wave of science, focusing on outcomes and shaping the patient ecosystem.  Join a key international site for AstraZeneca. Discover countless opportunities to grow and develop your personal career, experience and skills.  Always advancing our scientific knowledge and helping to shape the future of healthcare for the greatest and swiftest impact on disease.  We are seeking highly motivated, skilled Scientists with experience in Cell Biology, Automation and human advanced cell models.  You will perform in vitro investigative studies in advanced human cell models to seek a mechanistic understanding of toxicities from projects developing novel medicines, building new in vitro methods predictive of undesired in vivo effects.  You will have the opportunity to work closely with a team of Scientists to apply ground-breaking Imaging and Omics technologies and push the boundaries of predictive safety science with our vision in mind: to deliver innovative safety science to help restore patient's lives.  This is a consulting assignment with Randstad Life Sciences. Randstad Life Sciences is specialized in competences within Life Science. As a consultant with us, you get a competitive salary, benefits and collective agreements. Your consultant manager is always there for you and ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities. Responsibilities What you will be doing:   You will be a member of the Safety Omics team within the Clinical Pharmacology and Safety Sciences department. Together with other hands-on lab scientists you will apply primary human 2D in vitro and 3D advanced systems to the discovery and development of safe and effective candidate drugs.   Specifically, you will:   Work in close collaboration with Biologists, Omics experts, Computational and AI scientists and other team members to set and answer critical project safety questions  Actively contribute to the experimental design, practical delivery and interpretation of data  Apply your expert knowledge and address capability gaps by contributing to the further development of advanced cell models (kidney, lung)    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.  Qualifications We are looking for a highly motivated scientist to work within a vibrant group at the leading edge of their field to support drug safety assessments, a critical component of the drug discovery and development process.   About the company Randstad På Randstad vet vi att alla människor har en plats på arbetsmarknaden. Med verksamhet över hela landet och inom alla kompetensområden hjälper vi människor att hitta ett jobb som känns bra, och där de får möjlighet att växa, utvecklas och uppnå sin fulla potential. Med närmare 600 000 anställda i 38 länder är Randstad världsledande inom HR-tjänster, med målsättningen att bli världens främsta och mest uppskattade partner på arbetsmarknaden. Genom att kombinera vår passion för människor med kraften i dagens teknologi hjälper vi människor och företag att uppnå deras fulla potential. Vi kallar det Human Forward.

Join RISE Processum and help shape the future of strain development. As an Automation Specialist, you will support cutting-edge biotechnology research by building and maintaining high-throughput laboratory workflows in close collaboration with scientists and engineers. About us RISE is Sweden’s research institute and innovation partner. Through collaboration with industry, academia, and the public sector, we contribute to a competitive and sustainable society. RISE Processum is part of RISE and is a key player in the development of biobased processes and products. At our research facility in Örnsköldsvik, we work closely with industry partners and research organizations within one of Sweden’s strongest biotechnology and biorefinery clusters. Our Biotechnology group manages a growing portfolio of projects focusing on bioprocesses, chemical and biotechnological analysis, method development, and sustainable materials. We are now building a new Strain Development team and are looking for an Automation Specialist who wants to join us on this exciting journey. The role As an automation specialist at RISE within our new strain development team, you will mainly work on R&D projects and contract research targeting applications such as biochemicals, biofuels, biomaterials, proteins & enzymes, and food & feed. You will play a central role in ensuring reliable and scalable, high-throughput workflows, collaborating closely with other scientists and engineers in the team. Your responsibilities will include: • Operate and maintain our automation equipment for high-throughput screening, including liquid handling, colony picking and arraying, imaging, analytics, and robotic integration. • Develop and maintain scripts and methods for instrument control, data capture, and workflow automation, both independently and in close collaboration with other team members. • Troubleshoot and resolve technical issues and handle routine maintenance and updates, to improve equipment availability and ensure timely data delivery. • Maintain and extend our Docker-based solutions for remote processing and transfer of data. • Onboard new team members by introducing them to the equipment, scripts, and automated workflows. • Contribute to continuous improvement by identifying bottlenecks, optimizing protocols, and helping shape new projects, including grant applications. Location: On site in Örnsköldsvik, Sweden. Who are you? We are looking for a person who can bridge laboratory automation and strain development workflows. Requirements: • BSc or MSc in engineering, biotechnology, automation or a related field. • Hands-on experience operating and maintaining laboratory automation systems. • Proficiency in programming automation equipment using standard vendor software (e.g., method and script development for liquid handlers and integrated platforms). • Demonstrated ability to integrate automation hardware and software into standardized, reliable workflows in a laboratory environment. • Independent troubleshooting and sound technical judgment to diagnose and resolve issues across hardware and software. • Excellent communication skills and the ability to work effectively in different research teams. • Working proficiency in English, both spoken and written. Meritorious: • Experience in a biotech, pharma, or academic R&D environment, ideally involving microbial strain development. • Familiarity with common automation and scheduling platforms, such as Tecan FluentControl and Thermo Scientific Momentum. • Python programming skills, along with familiarity with Docker, Linux, version control (Git), and basic data pipelines. • Knowledge of LIMS/ELN systems and laboratory data management practices. • Experience with AI/ML methods for workflow optimization, image analysis, or data quality assurance. • Experience specifying, procuring, and commissioning laboratory equipment. • Swedish language skills As a person, you are a collaborative problem solver who enjoys working closely with colleagues and external partners. You are curious and motivated by finding innovative solutions to complex challenges. You have strong communication skills, and the ability to drive your work independently while contributing to the success of the team. You are also eager to share knowledge and help build a strong and supportive team. You have an interest in sustainability and the circular bioeconomy, and how R&D translates into applications in bio-based chemicals, materials, or food. Our offer We offer a workplace with strong development potential and a growing portfolio of research projects. With us, you will have a varied and stimulating role, working closely with advanced instrumentation and dedicated colleagues. You will become part of an organization that values curiosity, skills development, and long-term thinking, where your expertise truly makes a difference for the sustainable processes of the future. We look forward to receiving your application! If you have any questions regarding the position, you are welcome to contact Gunnar Westin, Group Manager, +46 70 260 46 23. The application deadline is July 12, 2026. Union representatives: Frida Sandberg +46 10 516 67 79 ([email protected]), Verónica Benavente +46 10 516 67 51 ([email protected]). SACO representative: Johanna Källman +46 10 516 60 10 ([email protected]).

We are now looking for a Scientist or Engineer who wants to contribute to cutting-edge biotechnology research. In this role, you will work at the intersection of science and industry, developing microbial strains for sustainable biobased solutions together with highly skilled colleagues in a dynamic research environment. About us RISE is Sweden’s research institute and innovation partner. Through collaboration with industry, academia, and the public sector, we contribute to a competitive and sustainable society. RISE Processum is part of RISE and a key player in the development of biobased processes and products. At our research facility in Örnsköldsvik, we work closely with industry partners and research organizations within one of Sweden’s strongest biotechnology and biorefinery clusters. Our Biotechnology group manages a growing portfolio of projects focusing on bioprocesses, chemical and biotechnological analysis, method development, and sustainable materials. We are now building a new Strain Development team and are looking for a scientist or engineer who want to join us on this exciting journey. The role As a Scientist or Engineer within Strain Development, you will play an important role in our newly established team in Örnsköldsvik. You will primarily work with R&D projects and contract research focused on strain development targeting various applications such as biochemicals, biofuels, biomaterials, proteins & enzymes, food & feed etc. In this role, you will collaborate with researchers and specialists across RISE, as well as with professionals from companies, universities, and other R&D organizations. You will be expected to plan and execute experiments, as well as analyze and interpret results. You will contribute to the development of new projects, including grant applications and contract research for clients. At RISE, you will have access to state-of-the-art research infrastructure, including a high-throughput facility for strain development, pilot-scale fermentation facilities with bioreactors up to 10,000 liters, and downstream processing capabilities. Biotechnology is a strategically prioritized area within RISE and is expected to grow significantly in the coming years, making this an excellent opportunity to help shape the future of sustainable biotechnology. Location: On site in Örnsköldsvik, Sweden. Travel may occur in connection with research collaborations, customer meetings, and conferences. Who are you? Requirements: • Academic degree (PhD, MSc, BSc) in molecular biology, biotechnology, biochemistry • Extensive expertise in metabolic engineering, gene editing, and strain optimization, with a broad understanding of various host organisms (yeast, bacteria, filamentous fungi) and their industrial applications. • Strong competence in genome analysis, NGS, bioinformatics, and data analysis. • Experience in high-throughput screening, including automation and robotics. • Solid hands-on experience in strain engineering, with the ability to identify bottlenecks and plan the competencies and resources required to drive operations forward. • Your personal qualities are of great importance, and we would like you to be a cooperative problem solver. • Working proficiency in English, both spoken and written. Meritorious: • Fluent in Swedish • Experience in writing grant applications • Experience in applied research with industrial needs and requirements As a person, you are a collaborative problem solver who enjoys working closely with colleagues and external partners. You have a structured way of working and the ability to drive your work independently while contributing to the success of the team. You are also eager to share knowledge and help build a strong and supportive research environment. Our offer We offer a workplace with strong development potential and a growing portfolio of research projects. With us, you will have a varied and stimulating role, working closely with advanced instrumentation and dedicated colleagues. You will become part of an organization that values curiosity, skills development, and long-term thinking, where your expertise truly makes a difference for the sustainable processes of the future. We look forward to receiving your application! If you have any questions regarding the position, you are welcome to contact Gunnar Westin, Group Manager, +46 70 260 46 23. The application deadline is July 12, 2026. Union representatives: Frida Sandberg +46 10 516 67 79 ([email protected]), Verónica Benavente +46 10 516 67 51 ([email protected]). SACO representative: Johanna Källman +46 10 516 60 10 ([email protected]).

Därför är detta jobb för dig Du vill vara en del av regionens främsta Life Science-konsulter. Vi bidrar gemensamt med våra kunder till att förbättra människors liv och livskvalitet genom att bland annat utveckla produktion, kvalitet och projektverksamhet. Här sätts du och din utveckling i fokus, du kommer ha en kontinuerlig dialog med din chef om utvecklingsmöjligheter framåt för att forma en plan och resa som passar dig och dina ambitioner. Som konsult på Knightec Group kommer du ha ett starkt stöd av ledare och dina kollegor där ni hjälper varandra att lyckas i uppdrag, projekt och i er utveckling. Du blir en del av vårt affärsområde inom Compliance & Management där vi stöttar en effektiv omställning till digitala, hållbara och säkra lösningar genom expertkunskap inom exempelvis kvalitet, säkerhet, hållbarhet och projektstyrning. Arbetsuppgifter Vårt team besitter en bred kunskap inom Life Science och dina uppdrag kommer att variera och kan innebära både roller i våra egna leveranser i interna team samt i våra kunders verksamheter. Du kommer arbeta inom något av nedan områden: validering/kvalificering projektledning processutveckling/produktionsutveckling QA IT Kvalifikationer För att passa i rollen vill du arbeta i komplexa produktionsmiljöer, har en förmåga att arbeta förbättringsorienterat och gillar att ha olika kontaktytor. För att lyckas i rollen har du även: Nyfikenhet på/kännedom om konsultrollen Erfarenhet av arbete inom läkemedelsindustrin eller den medicintekniska branschen God kännedom om relevanta regelverk Relevant ingenjörsexamen eller motsvarande Flytande kunskaper i svenska och engelska, i tal och skrift  En spännande resa med Knightec Group Knightec Group är idag en av Norra Europas ledande strategiska partners inom produkt- och digital tjänsteutveckling – hur häftigt är inte det? Genom att förena ingenjörskompetens, digital expertis och affärsförståelse hjälper vi våra kunder att omvandla ny teknik till verkliga lösningar som skapar värde. Vi arbetar i skärningspunkten mellan affärsstrategi och teknikutveckling och stöttar våra kunder genom hela resan – från de första idéerna till utveckling, implementering och vidare utveckling. På Knightec Group samlas människor med olika perspektiv, erfarenheter och specialistområden. Tillsammans skapar vi innovation som gör verklig skillnad – för företag, människor och samhället i stort. För våra medarbetare innebär det stora möjligheter att vara med och forma framtidens lösningar genom meningsfulla projekt i teknikens absoluta framkant. Här får du inte bara utvecklas och växa i din roll – du blir också en del av ett team där nyfikenhet, samarbete och modet att utmana driver oss framåt. Låter det som platsen för dig? Häng med på vår fortsatta resa! Praktisk information Detta är en tjänst placerad på vårt kontor i Södertälje, Storgatan 41C. Resor i tjänsten kan förekomma till våra kunder. Startdatum är enligt överenskommelse. Skicka in din ansökan så snart som möjligt, men senast 2026-06-28. Om du har några frågor om tjänsten är du välkommen att kontakta Kicki Björ, Talent Acquisition Specialist. Vi hanterar alla ansökningar via vår karriärsida för att säkerställa en trygg och säker hantering av dina personuppgifter i enlighet med GDPR. Vi ser fram emot att höra från dig!

Därför är detta jobb för dig Du vill vara en del av regionens främsta Life Science-konsulter. Vi bidrar gemensamt med våra kunder till att förbättra människors liv och livskvalitet genom att bland annat utveckla produktion, kvalitet och projektverksamhet. Här sätts du och din utveckling i fokus, du kommer ha en kontinuerlig dialog med din chef om utvecklingsmöjligheter framåt för att forma en plan och resa som passar dig och dina ambitioner. Som konsult på Knightec Group kommer du ha ett starkt stöd av ledare och dina kollegor där ni hjälper varandra att lyckas i uppdrag, projekt och i er utveckling. Du blir en del av vårt affärsområde inom Compliance & Management där vi stöttar en effektiv omställning till digitala, hållbara och säkra lösningar genom expertkunskap inom exempelvis kvalitet, säkerhet, hållbarhet och projektstyrning. Arbetsuppgifter Vårt team besitter en bred kunskap inom Life Science och dina uppdrag kommer att variera och kan innebära både roller i våra egna leveranser i interna team samt i våra kunders verksamheter. Du kommer arbeta inom något av nedan områden: validering/kvalificering projektledning processutveckling/produktionsutveckling QA QA IT Kvalifikationer För att passa i rollen vill du arbeta i komplexa produktionsmiljöer, har en förmåga att arbeta förbättringsorienterat och gillar att ha olika kontaktytor. För att lyckas i rollen har du även: Nyfikenhet på/kännedom om konsultrollen Erfarenhet av arbete inom läkemedelsindustrin eller den medicintekniska branschen God kännedom om relevanta regelverk Relevant ingenjörsexamen eller motsvarande Flytande kunskaper i svenska och engelska, i tal och skrift  En spännande resa med Knightec Group Knightec Group är idag en av Norra Europas ledande strategiska partners inom produkt- och digital tjänsteutveckling – hur häftigt är inte det? Genom att förena ingenjörskompetens, digital expertis och affärsförståelse hjälper vi våra kunder att omvandla ny teknik till verkliga lösningar som skapar värde. Vi arbetar i skärningspunkten mellan affärsstrategi och teknikutveckling och stöttar våra kunder genom hela resan – från de första idéerna till utveckling, implementering och vidare utveckling. På Knightec Group samlas människor med olika perspektiv, erfarenheter och specialistområden. Tillsammans skapar vi innovation som gör verklig skillnad – för företag, människor och samhället i stort. För våra medarbetare innebär det stora möjligheter att vara med och forma framtidens lösningar genom meningsfulla projekt i teknikens absoluta framkant. Här får du inte bara utvecklas och växa i din roll – du blir också en del av ett team där nyfikenhet, samarbete och modet att utmana driver oss framåt. Låter det som platsen för dig? Häng med på vår fortsatta resa! Praktisk information Detta är en tillsvidareanställning med en provanställning på sex månader, placerad på något av våra kontor i Stockholm, Hagaesplanaden 49 (Forskaren) eller Rättarvägen 3 (Solna). Resor i tjänsten kan förekomma till våra kunder. Startdatum är enligt överenskommelse. Skicka in din ansökan så snart som möjligt, men senast 2026-06-28. Om du har några frågor om tjänsten är du välkommen att kontakta Kicki Björ, Talent Acquisition Specialist. Vi hanterar alla ansökningar via vår karriärsida för att säkerställa en trygg och säker hantering av dina personuppgifter i enlighet med GDPR. Vi ser fram emot att höra från dig!

Vill du arbeta i en varierande och utvecklande roll där du får kombinera processutveckling, laboratoriearbete och problemlösning i en högteknologisk GMP-miljö? Nu söker vi en person till vår kund där man kommer arbeta i pilotanläggningen, där du blir en viktig del i arbetet med kliniska batcher, teknisk utveckling och övergången mellan R&D och produktion. Här får du möjlighet att arbeta nära flera delar av verksamheten, bidra i spännande projekt och utvecklas i en roll med stort ansvar och bred variation. Ansök redan idag - vi tillämpar löpande urval! Om tjänsten:Rollen passar dig som trivs i en praktisk och dynamisk miljö där ingen dag är den andra lik. Du kommer att arbeta nära både R&D, kvalitetsavdelning och andra interna funktioner för att säkerställa effektiva processer och hög kvalitet i verksamheten. Arbetet innebär en kombination av hands-on arbete i pilotanläggningen och mer analytiska samt koordinerande uppgifter kopplade till processer, material och dokumentation. Du blir en del av ett mindre team med stort ansvar och bred variation i arbetet. Fokus ligger på att stötta och utveckla processer kopplade till kliniska batcher, utvärdera nya material och tekniker samt bidra till att skapa en smidig och kvalitetssäkrad övergång från utveckling till produktion. Rollen innebär även ett nära samarbete med flera delar av organisationen, vilket ställer krav på struktur, noggrannhet och god kommunikationsförmåga. ARBETSUPPGIFTTER:Tillverkning och support vid kliniska batcher Processutveckling och troubleshooting Materialhantering, dokumentation och GMP-relaterat arbete Analysarbete och tekniska utvärderingar Samarbete med R&D, kvalitetsavdelning och andra interna funktioner Vi söker dig som:Har en ingenjörsutbildning inom exempelvis kemiteknik, läkemedel, biomedicin eller livsmedel Talar och skriver flytande svenska då båda språken används i det dagliga arbetet Det är inte nödvändigt, men meriterande om du har: Tidigare erfarenhet från GMP-miljö eller laboratoriearbete Vidare kommer stor vikt läggas vid personlig lämplighet. För att du skall passa in och trivas i rollen ser vi att du har ett genuint tekniskt intresse och som motiveras av att förstå processer på djupet. Du trivs med att arbeta både praktiskt och analytiskt, tar ansvar för ditt arbete och uppskattar en roll där du får möjlighet att utvecklas över tid. Övrig info:Omfattning: Heltid Start: Mitten av augusti Placering: Helsingborg Rekryteringsansvarig: Vanessa Henrysson Roqueta, [email protected] Lön: Marknadsmässig Ansök genom att klicka på länken nedan. Kom ihåg att vara snabb med din ansökan då vi gör löpande urval av kandidater och att annonsen kan stängs ner innan tjänsten är tillsatt om vi gått över till urvals och intervjufasen. Om Friday: På Friday brinner vi för att ge dig som Tech-talang en riktigt bra start på karriären. Genom att lyssna på vad just du vill och drivs av, matchar vi dig med företag och möjligheter som får dig att se fram emot att gå till jobbet. Vi värderar ambition och potential högt och arbetar aktivt för en fördomsfri rekrytering, där alla ges samma chans att lyckas. Vi finns i Stockholm, Göteborg, Malmö, Linköping och Örebro. Varje år genomför vi över 5 000 karriärmöten och matchar kandidater med allt från globala företag till innovativa startups.

Location/Division Specific Information: Olink, part of Thermo Fisher Scientific, is dedicated to advancing the understanding of human disease through proteomics. Olink panels provide innovative, high-quality solutions for human protein biomarker discovery, enabling researchers to measure thousands of proteins simultaneously from just a few microliters of blood. Using highly specific and thoroughly validated assays with a wide dynamic range, Olink’s technology overcomes traditional limitations in protein analysis and supports deeper insights into human biology and disease. Job Description Join us as a Quality Assurance Manager at Agrisera in Umeå, where you'll play a critical role in building and strengthening our quality infrastructure. You'll establish and lead the batch release process for antibodies and hyboligos, while enhancing core quality processes including Non-Conformance, CAPA, Document Control, and Change Control. As a key strategic partner, you'll collaborate closely with headquarters in Uppsala to align quality management systems across sites and with Thermo Fisher, ensuring seamless integration and operational excellence. This position reports to the Head of Quality Assurance at PSX in Uppsala. A Day in the Life: Your impact will extend across the organization as you develop and implement procedures. Contribute to establish a Design Transfer processes from R&D to Supply Chain. Support critical product development initiatives. Provide quality metrics, drive process improvements, and support the implementation of an electronic Quality Management System (eQMS). Working with the Supplier Quality process and aligning standards across sites, you'll be instrumental in reducing lead times, mitigating risks, and enabling efficient operations that directly impact customer satisfaction and business success. Technical Qualifications University degree in Life Science related field, for instance biotechnology, biology, or chemistry. Several years' experience of working with quality related tasks within Life Science. Experience of systematic quality work based on an established quality standard, e.g., ISO 9001, ISO 13485, ISO 17025 or GxP. Strong understanding of quality systems including document control, change control, deviations, CAPA. Knowledge of risk management tools and continuous improvement methodologies. Full working proficiency in both Swedish and English. Proficiency with quality systems software (TrackWise, document management systems) Soft skills Advanced problem-solving and root cause analysis skills. Strong written and verbal communication skills, including technical writing. Participate in external and internal audits. Demonstrated ability to guide and foster quality culture across organizations. Why Join Us? At Olink, Thermo Fisher Scientific, you will be part of a nurturing team that values integrity, innovation, and involvement. We offer an encouraging environment where your diverse experiences and perspectives are appreciated, enabling you to thrive and excel in your career. Come aboard and contribute significantly to global health and safety! If you believe you’re the right fit for this role, we encourage you to submit your resume along with a cover letter highlighting your relevant experience. The last day for applications is on the 31st of May 2026.