Lediga jobb som Cell- och molekylärbiologer m.fl. i Uppsala

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible. We are looking for a Senior Research Engineer to join the Viral Vector Applications R&D section in Uppsala. The team consists of approximately 20 researchers focused on the development and optimization of downstream processes for viral vectors, plasmids, and nucleic acids, including purification, filtration, and analytical workflows. The work is closely connected to product development, translating process understanding into solutions that meet customer needs. We are now seeking a new colleague who will work with downstream process development activities for viral vector manufacturing. The role focuses on developing, optimizing, and scaling purification processes, with particular emphasis on filtration and chromatography operations. The successful candidate will apply process understanding to improve productivity, robustness, scalability, and manufacturability while supporting the development of next-generation Cytiva technologies. What You'll Do: As a Senior Research Engineer, you will focus on the development, optimization, and implementation of filtration and purification processes for AAV and lentiviral vectors, including harvest and clarification of upstream material. Your work will span new product development, product care, and market support projects, always with a strong customer and process performance focus. Your responsibilities will include: Driving process development activities within filtration and downstream purification, including experimental design, method development, and method verification to ensure robust and scalable processes. Applying a holistic understanding of the end-to-end workflow (Upstream to Downstream including analytics) to design efficient, integrated process solutions and provide technically sound recommendations aligned with customer needs and regulatory requirements. Independently planning, executing, and analyzing experiments in a structured and data-driven manner, and effectively communicating results in project teams and customer interactions. Owning and maintaining process-related infrastructure by ensuring proper use, calibration, and upkeep of instrumentation, as well as developing and updating standard operating procedures (SOPs) to support reproducibility and quality. Evaluating, proposing, and implementing new technologies and technical solutions within your area, with a focus on improving process efficiency, robustness, and scalability. Contributing to scientific dissemination by preparing and delivering posters and oral presentations at conferences, translating process development outcomes into clear and impactful insights. Who you are: You hold a MSc and have at least 5 years of industrial experience in biopharmaceutical process development, particularly within harvest and downstream processing. You have hands-on experience in developing and optimizing end-to-end purification processes, with a strong understanding of critical process parameters, scalability, and process robustness. Experience with viral vectors is highly desirable. You enjoy working in the lab, bringing structure to complex tasks, and take pride in maintaining clear, accurate, and well-organized documentation. You possess strong presentation and communication skills, with the ability to translate complex process data into clear insights. You are fluent in English (spoken and written) and having working proficiency in Swedish in seen as a plus. It would be a plus if you also possess experience in: Experience working with large-scale production equipment is considered a strong advantage and demonstrates your ability to bridge process development and manufacturing. You thrive on working in cross-functional teams, where collaboration and communication are essential to drive projects forward. You enjoy working in a dynamic environment and maintain a strong focus on delivering robust, customer-oriented process solutions. Application We continuously assess candidates and invite them for interviews, so please don’t hesitate to write and send in the application. The recruitment will be completed as soon as a suitable candidate is found. We look forward to seeing your application.

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible. Background At Cytiva R&D in Uppsala, we develop Biacore™ systems that enable scientists worldwide to generate world-class, label-free interaction analysis data. For more than 35 years, Biacore technology has been a leader in biomolecular interaction analysis, helping advance drug discovery and life science research. A key part of our mission is to push the boundaries of what is possible through the development of innovative applications, methodologies, and consumables that expand the capabilities and value of Biacore systems. About the Role We are looking for a passionate and experienced Senior Research Engineer to join our Biacore Applications & Consumables team. In this role, you will have the opportunity to shape the next generation of Biacore consumables, turning new ideas into products that enable scientific breakthroughs for researchers around the globe. As part of a collaborative and highly skilled team, you will drive innovation from concept to product, combining hands-on laboratory work, scientific expertise, and creative problem-solving to develop solutions that make a real impact. You will also play an important role in supporting and continuously improving our existing consumables portfolio, ensuring that Biacore remains the trusted choice for interaction analysis. What You'll Do Drive the development of innovative Biacore consumables products from idea to launch. Design, evaluate, and optimize new consumables concepts and technologies. Solve scientific and technical challenges through experimentation and innovation. Perform hands-on laboratory work to develop and validate new products and applications. Collaborate closely with cross-functional teams to deliver customer-focused solutions. Support product care activities and contribute to the continuous improvement of our consumables portfolio. Who You Are MSc or similar in relevant life science discipline. Experience working with SPR technology and Biacore systems. Strong laboratory skills and a genuine passion for experimental science. Knowledge of statistics and data analysis, with an interest in applying them to product development. An innovative problem-solver who enjoys turning scientific challenges into practical solutions. Strong communication and presentation skills. Fluent in Swedish and English, both written and spoken. A collaborative team player who thrives in a multidisciplinary environment. Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com.

Be part of something altogether life-changing! This is a consulting assignment until 31/3 2027, with the possibility of extension. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term. About the assignment Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics. The Manufacturing Quality Engineer at Cytiva provides technical support to improve product quality, with a focus on data analysis, issue resolution, and continuous improvement. This role is responsible for driving the non-conforming material process and supporting root cause investigations by coordinating with Production Engineers, Quality Specialists, Supplier Quality Engineers, affected project teams, and manufacturing suppliers. This position is part of the Custom Engineering Manufacturing team and located in Uppsala. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery. Who should apply for this job? Essential qualifications • Ownership of the Deviation handling process • Coordinate and document manufacturing quality issues to ensure clear ownership, effective follow-up, and timely resolution. • Coordinate resources to support problem-solving and rework activities in ongoing production for manufacturing quality-related issues. • Lead analysis of supplier deviations and quality follow up with suppliers • Collaborate with Supplier Quality, Global Sourcing, and other cross-functional teams on manufacturing quality-related topics. • Conduct root cause analysis for product quality issues, identify trends, and coordinate with Supplier Quality Engineers, Production Engineering, and Global Sourcing to drive resolution and submit improvement proposals to the Change Control Board. • Manage non-conforming material inventory to ensure accurate control, follow-up, and disposition. • Support the customer complaints team by contributing manufacturing quality expertise and follow-up as needed. Desirable qualifications Who you are: • Technical knowledge of manufacturing processes • Quality focus • Strong communication skills, verbal and written • Experience from production or design of work of products for the Biopharmaceutical industry • Bachelor Degree in Mechanical Engineering or equivalent. It would be a plus if you also possess previous experience in: • Quality management, NC/CAPA process • ISO9001:2015 At Cytiva we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, hybrid working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a hybrid work arrangement in which you can work part-time at the Company location identified above and part-time remotely from your home. Additional information about this hybrid work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Cytiva can provide. As One of Us As an employed staffing consultant at Lernia, you will always receive a competitive salary, vacation benefits, pension contributions, insurance coverage, and be part of our collective agreement. We care about your well-being, which is why we offer all our consultants wellness allowances and access to occupational health services. During your employment, you will have a dedicated consultant manager responsible for your assignment, ensuring you thrive at your workplace while supporting and developing you in your professional role. Don't wait – apply today! Welcome to apply for the job by submitting your CV and cover letter via the link. If you have any questions, please contact the responsible recruiter, Emma Rasmusson, via email: lernia.uppsala@lernia.se We work with continuous selection and may fill the position as soon as we find the right person. Therefore, please submit your application as soon as possible!

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible. The Fast Trak Operations and Training Specialist is an operations-focused role embedded within the Fast Trak labs, responsible for the end-to-end execution excellence of Fast Trak training courses and related on-site customer activities. The role acts as the primary operational interface between customers, scientists, and lab operations to ensure high-quality, safe, and efficient delivery of trainings. This position reports to the Section Manager Fast Trak and is part of Clinical Programs located in Uppsala, Sweden and will be an on-site role. What you will do: Serve as the primary point of contact for customers attending Fast Trak trainings and on-site events, ensuring an exceptional customer experience. Lead and coordinate operational aspects of training delivery in close cooperation with Fast Trak scientists, including lab and training room preparation, training materials, equipment readiness, consumables availability, and compliance with EHS requirements. Generate training quotes and support customer pre-sales discussions, ensuring operational feasibility and alignment. Support customer PD projects when needed, leveraging hands-on operational and lab knowledge. For training offerings, developing and maintaining relationships with the regional commercial and marketing teams, as well as the global Fast Trak organizations. Drive continuous improvement and DBS initiatives while contributing to a safe, compliant, and efficient laboratory environment and building strong relationships with regional commercial, marketing, and global Fast Trak teams. Who you are: MSc in biotechnology, bioprocess/biomedical engineering or related life sciences field. Life Science industry background with experience from laboratory related activities and responsibilities. Experience working with chromatographic methods (e.g., affinity chromatography, SEC, IEX) is advantageous. English as working language. It would be a plus if you also possess previous experience in: Experience from customer-facing roles. Swedish as working language. To be successful in this role, we believe that you are a person who thrives working in a flexible environment with demonstrated abilities to navigate in a collaborative, matrixed, and customer focused environment. The ideal candidate is a self-propelled and goal-oriented individual with a strong ability to spot customer needs, communicate solutions and build trust through collaboration. In addition, the candidate should have excellent analytical, planning and interpersonal skills with a demonstrated ability to establish and maintain relationship with co-workers and customers. Application We continuously assess candidates and invite them for interviews, so please don’t hesitate to write and send in the application. The recruitment will be completed as soon as a suitable candidate is found. We look forward to seeing your application.

Institutionen för farmaci vid Uppsala universitet har en interdisciplinär miljö som är central inom läkemedelsområdet. Med forskning i frontlinjen, utbildning i toppklass och omfattande samverkan med det omgivande samhället utgör vi en viktig motor i utvecklingen av det farmaceutiska området. I den här inspirerande miljön sker forskning av internationellt hög klass med stor betydelse. Bland våra centrala kompetenser är farmakokinetik-farmakodynamik, in vitro ADME modeller, avancerade in vivo-metoder, modellering och simulering, biologiska läkemedel, liksom patientrelaterade och samhälleliga aspekter på allt från individens läkemedelsanvändning till läkemedelspolitik. Våra vetenskapliga fokusområden i urval Farmakokinetik & Farmakodynamik • Farmakometri • Klinisk farmaci & Farmakoterapi • Avancerad läkemedelsformulering • Molekylär galenisk farmaci • Biologiska läkemedel • Läkemedelsepidemiologi • Samhällsfarmaci Mer information www.farmaci.uu.se   Arbetsuppgifter Laborativ och analytisk forskning inom riktad läkemedelsleverans med mRNA/lipidnanopartikelformulering. Kvalifikationskrav Master eller motsvarande kompetens inom biomedicin, bioteknologi eller en farmaceutisk utbildning med dokumenterad genomgången kurs inom biologiska läkemedel (minst 7.5hp).  Sökande ska ha dokumenterad erfarenhet och förståelse av arbete med antikroppsderivat och T cell receptorer.  Sökande ska även ha arbetat med en eller flera metoder så som cellodlingsbaserade assays, antikroppsbaserade laborativa assays (t.ex.flödescytometri och/eller ELISA och även ha erfarenhet av molekylärbaserade metoder. Vänligen tydliggör i er ansökan (personligt brev och CV) att ni har dokumenterad genomgången kurs eller andra erfarenheter inom dessa områden.   Önskvärt/meriterande i övrigt Erfarenhet examensarbete eller tidigare anställning inom området. Dokumenterad förmåga att ta till sig nya relevanta laboratorietekniker inom området. Erfarenhet inom fältet avancerade läkemedel/cell-terapier och metodutveckling informerat från sekvenseringsdata. Meriterande är analyser av data i FlowJo, Kaluza och GraphPad samt en erfarenhet av hög standard för hur man dokumenterar laboratorieaktiviteter. Om anställningen Anställningen är tidsbegränsad, 12 månader. Omfattningen är heltid/100 %. Tillträde 1 oktober 2026 eller enligt överenskommelse. Placeringsort: Uppsala Upplysningar om anställningen lämnas av: Professor Sara Mangsbo (sara.mangsbo@uu.se), 073-933 92 05 I denna rekrytering har vi ersatt det personliga brevet med frågor som du besvarar i samband med din ansökan. Svaren kommer att användas som en del i urvalsprocessen. Välkommen med din ansökan senast den 23 september 2026, UFV-PA 2026/2661. Uppsala universitet är ett brett forskningsuniversitet med stark internationell ställning. Det yttersta målet är att bedriva utbildning och forskning av högsta kvalitet och relevans för att göra skillnad i samhället. Vår viktigaste tillgång är alla 7 500 anställda och 53 000 studenter som med nyfikenhet och engagemang gör Uppsala universitet till en av landets mest spännande arbetsplatser. Läs mer om våra förmåner och hur det är att jobba inom Uppsala universitet https://uu.se/om-uu/jobba-hos-oss/ Anställningen kan komma att säkerhetsprövas. Vid säkerhetsprövning är en förutsättning för anställning att sökande blir godkänd. Vi undanber oss erbjudanden om rekryterings- och annonseringshjälp. Ansökan tas emot i Uppsala universitets rekryteringssystem. Fackliga företrädare: Saco-S - saco-s@uu.se, Seko - seko@uadm.uu.se, ST (OFR/S) - ofr@uu.se