Who we are Olink, part of Thermo Fisher Scientific, is transforming the understanding of human diseases through advanced proteomics. We are driven by a commitment to innovation, quality, and transparency, providing exceptional solutions and support for human protein biomarker discovery. For many years, the critical role of proteins in human biology has been recognized, but technological constraints limited comprehensive research into their potential across various biological processes and diseases. With our innovative Olink solutions, scientists can now measure thousands of human proteins simultaneously using just a few microliters of blood. Our highly specific and validated assays cover a wide dynamic range, empowering groundbreaking research. Our services include flexible protein biomarker solutions, with a robust library of thoroughly validated assays covering ~5000 proteins. As we expand globally, we continue to play a pivotal role in shaping the future of scientific discovery. To learn more, visit www.olink.com. Position Description As Development Engineer within the Affinity Department, R&D Proteomics Sciences Division, you will participate in research and early product development, in a culture of creativity and inclusion. The position is focused on the characterization and analysis of affinity proteins and with hands-on wet-lab work. You will work in a skilled team of ~ 8 experts in proteomics and antibody development and collaborate with colleagues within and across R&D teams on activities to efficiently meet company objectives. We are looking for a team player who can continue to grow our protein characterization team, ensuring we continue to develop our products with desired antibodies and antigens. Primary Responsibilities Plan and perform laboratory work in accordance with set project plans and work schedules, with active collaboration and communication with the team. Evaluate, report and document results from the laboratory work. Actively participate in the development of the group's and department's activities and participate in improvement projects. Investigate and solve arising problems within the area. Comply with company policy, instructions and routines. Qualifications University degree in Biotechnology, Biomedicine, Biochemistry, Molecular Biology or similar. Documented lab experience in a biochemistry/biology setting. Experience from protein characterization methods such as mass spectrometry, binding kinetics using SPR and sandwich ELISA is advantageous. Scientific understanding of the field of proteomics and protein sciences. Data analysis tools e.g. R/Python, including essential statistics and experimental design. Strong communication and writing skills. Fluent in English. Soft Skills At Thermo Fisher Scientific, we value innovation, collaboration, and professional growth. We offer a supportive environment where you can make a significant impact and drive the future of technology and product development. If you want to help deepen the understanding of real-time human biology and are looking for an exciting new challenge, we encourage you to apply. The last day for applying is on 2025-04-20 but please submit your application as soon as possible. PLEASE NOTE: We would like to kindly ask you to send in an anonymous CV without name, email address, picture or any other personal information on the CV. Thank you!

Who we are Olink, part of Thermo Fisher Scientific, is transforming the understanding of human diseases through advanced proteomics. We are driven by a commitment to innovation, quality, and transparency, providing exceptional solutions and support for human protein biomarker discovery. For many years, the critical role of proteins in human biology has been recognized, but technological constraints limited comprehensive research into their potential across various biological processes and diseases. With our innovative Olink solutions, scientists can now measure thousands of human proteins simultaneously using just a few microliters of blood. Our highly specific and validated assays cover a wide dynamic range, empowering groundbreaking research. Our services include flexible protein biomarker solutions, with a robust library of thoroughly validated assays covering ~5000 proteins. As we expand globally, we continue to play a pivotal role in shaping the future of scientific discovery. To learn more, visit www.olink.com. Position Description We are looking to hire a Development engineer, who will act as a sub-project leader, to join the Design transfer team within the Engineering department, Technical Operations. The department’s main responsibility is to lead the industrialization of the kit manufacturing processes within the Supply Chain organization and ensuring equipment control and business continuity in the premises of our Uppsala office. The department currently consists of a total of 22 employees divided into the three individual teams: 1) Design transfer, 2) Process development & Validation and 3) Equipment & Maintenance. In this position you will act as a sub-project leader responsible for coordinating design transfer activities of new products from R&D to Supply Chain, to ensure producibility of the kit components. You will coordinate complex transfer activities and sometimes also be operational in all necessary design transfer activities such as process development, qualification and validation, manufacturing methods and article structures (BOMs etc.). You will also coordinate changes of existing products. The position is based in Uppsala and reports to Manager Design Transfer. Primary responsibilities As a Development Engineer Design Transfer your primary responsibilities includes, but is not limited to: Lead and coordinate design transfer activities in NPI and development projects according to internal quality processes. Act as change control responsible or owner by coordinating activities between other teams and departments. Lead continuous improvements and develop and improve work processes within the area. Take responsibility of identifying and implementing improvements of work processes that are connected to design transfer in NPI projects. Actively participate and contribute to performance of risk assessments of projects, processes and products. Be accountable for reporting status timely to manager and stakeholders in progress of the above. Qualifications BSc or MSc in Life Science or equivalent. Experience from a leading role in a manufacturing environment, preferably within Life science (e.g. as production preparation engineer, project manager/ activity leader). Experience from design transfer, alternatively product development, where design/ tech transfer has been included. At least 3 years relevant work experience after relevant degrees. Very good communication skills in both English and Swedish. As a person, you should have a genuine technical interest but also enjoy driving and leading projects toward challenging goals. To succeed in this role, you should have strong communication skills, be curious and creative with a proactive mindset. Finding the best solution sometimes requires being flexible and pragmatic, without loosing sight of the most important details. We are looking for a team player that always wants to find the best way of working with the aim to find the most efficient paths to deliver and reach goals. The selection process is on-going, and the position might get filled before the last day of application so please apply as soon as possible, however no later than 2025.04.06. If you want to help to deepen the understanding of real-time human biology and are looking for an exciting new challenge, we encourage you to apply!

Who we are Olink, part of Thermo Fisher Scientific, is transforming the understanding of human diseases through advanced proteomics. We are driven by a commitment to innovation, quality, and transparency, providing exceptional solutions and support for human protein biomarker discovery. For many years, the critical role of proteins in human biology has been recognized, but technological constraints limited comprehensive research into their potential across various biological processes and diseases. With our innovative Olink solutions, scientists can now measure thousands of human proteins simultaneously using just a few microliters of blood. Our highly specific and validated assays cover a wide dynamic range, empowering groundbreaking research. Our services include flexible protein biomarker solutions, with a robust library of thoroughly validated assays covering ~5000 proteins. As we expand globally, we continue to play a pivotal role in shaping the future of scientific discovery. To learn more, visit www.olink.com. Position Description We are seeking a highly motivated and experienced Scientist to join our Affinity Evaluation qPCR Section within the Highplex Department, enabling the development of new highplex products. As Scientist you will participate in research and development of product ideas and products as well as routine screening in accordance with project plans and work schedules. The position involves laboratory work, analysis and documentation. In this role you would report to the Section Manager Affinity Evaluation qPCR and be based in our Uppsala headquarters. Primary Responsibilities Actively lead and/or participate in section-, project- and department activities, and the development of product concepts and ideas. Participate as project member in meetings and project planning. Independently plan and execute laboratory work in accordance with set project plans and work schedules as well as evaluating and documenting results. Handle and prepare antibodies, antigens and biological samples for experiments. Perform PEA-experiments, mainly using qPCR as a readout. Develop new and continuously improve existing procedures, protocols and analysis methods. Perform verification studies and contribute to analyzing data shared with customers. Qualifications Ph.D. in a relevant life sciences field (e.g., Molecular Biology, Biochemistry, Biotechnology, Immunotechnology) or equivalent experience. Two or more years of working experience from an industry setting. Documented lab experience. Extensive scientific and technical knowledge in molecular biology, proteomics and biochemistry. Experience with assay development of antibody-based test methods as well as working with and optimizing PCR/qPCR and DNA sequencing (NGS). Experience of lab automation, pipetting robots and different conjugation chemistries is advantageous. Proven experience of data analysis. Experience with R and handling of large data sets is a preferable. Good general computer skills and expert level knowledge of Excel. Experience of working in, and driving projects. Good communication skills in written and spoken English, Swedish skills is a plus. Soft Skills As a person youare a team player who treats people with respect and finds it easy to communicate with others, both within the team and cross-functionally. You love to solve problems by thinking outside the box and drive development initiatives forward in cooperation with others. Finally, you are a positive person who is flexible in terms of your daily tasks. If you are a driven scientist with a passion for developing innovative protein assays and want to be part of a team at the forefront of biotechnology, we encourage you to apply. Please submit your resume and a cover letter detailing your relevant experience and why you are the ideal candidate for this position. The last application date is on the 30th of March. The selection process is ongoing and the position could get filled before the last application date.

Who we are Olink, part of Thermo Fisher Scientific, is transforming the understanding of human diseases through advanced proteomics. We are driven by a commitment to innovation, quality, and transparency, providing exceptional solutions and support for human protein biomarker discovery. For many years, the critical role of proteins in human biology has been recognized, but technological constraints limited comprehensive research into their potential across various biological processes and diseases. With our innovative Olink solutions, scientists can now measure thousands of human proteins simultaneously using just a few microliters of blood. Our highly specific and validated assays cover a wide dynamic range, empowering groundbreaking research. Our services include flexible protein biomarker solutions, with a robust library of thoroughly validated assays covering ~5000 proteins. As we expand globally, we continue to play a pivotal role in shaping the future of scientific discovery. To learn more, visit www.olink.com. Position Description We are on an exciting growth trajectory, and we are thrilled to announce an opportunity for a passionate and skilled Project Manager to join our Project Management Office (PMO). Our PMO, a dedicated team of 8 project managers, spearheads the most strategic and impactful projects aligned with our visionary goals. As a Project Manager at Olink, part of Thermo Fisher Scientific, you will be at the forefront of innovation in proteomics, driving a variety of projects including New Product Introductions (NPI) and diverse business initiatives. Your role will be pivotal in ensuring the continued success and advancement of our cutting-edge products. This position is based at our Uppsala office and reports directly to the Head of PMO. If you are ready to make a significant impact and contribute to the future of proteomics, we would love to hear from you! Primary Responsibilities As Project Manager you will be responsible for leading and delivering strategic projects according to set timeframe and budget. This could include, but is not limited to, the following tasks: Develop a timetable for the projects according to set goals. Lead projects towards agreed goals according to set schedule, quality and budget. Collaborate with project stakeholders internally and externally. Responsible for communication with the Steering Committee. Continually work to improve, educate and lead within Olink's project processes. Develop, manage and drive improvements through engagement, support teamwork and apply structured models in project management. Qualifications/skills Relevant degree in a related field (Bsc, MSc, PhD in Engineering, Life Sciences) Certification in Project Management (e.g PMP, IPMA etc) is highly beneficial. At least a few years of experience in project management or product management within the Life Science industry. Experience of NPI projects is highly advantageous. Professional proficiency in both Swedish and English is mandatory and necessary to be successful in this role. As a person you are responsive, curious and committed. You are a solution-focused leader who thrives in a dynamic and fast-paced environment. Furthermore, you are a team player who is good at communicating with different stakeholders and who can see things from different perspectives. To be successful in this role you should also be pragmatic and meticulous when needed and be able to see things from a long-term, strategic perspective. The selection process is on-going, and the position might get filled before the last day of application so please apply as soon as possible, however no later than 2025.03.30. If you want to help to deepen the understanding of real-time human biology and are looking for an exciting new challenge, we encourage you to apply!

Who we are Olink, part of Thermo Fisher Scientific, is transforming the understanding of human diseases through advanced proteomics. We are driven by a commitment to innovation, quality, and transparency, providing exceptional solutions and support for human protein biomarker discovery. For many years, the critical role of proteins in human biology has been recognized, but technological constraints limited comprehensive research into their potential across various biological processes and diseases. With our innovative Olink solutions, scientists can now measure thousands of human proteins simultaneously using just a few microliters of blood. Our highly specific and validated assays cover a wide dynamic range, empowering groundbreaking research. Our services include flexible protein biomarker solutions, with a robust library of thoroughly validated assays covering ~5000 proteins. As we expand globally, we continue to play a pivotal role in shaping the future of scientific discovery. To learn more, visit www.olink.com. Position Description We are now looking for a Development Engineer to join the Assay Development NGS team within the Highplex department, RnD. If you want to work with a world-leading technology that contributes to the development of precision medicine, you might be the person we are looking for. Assay Development NGS has the main responsibility to develop immunoassays for the Olink Highplex products and to evaluate assay performance throughput development projects. This includes performing verification experiments and generating assay performance data for website. Product development is carried out in projects with members from other departments. Further more, Assay Development NGS also contributes to research and development of product concepts and ideas. Assay Development NGS currently consists of 10 people, but since the company is growing rapidly with very exciting things going on, the group needs to be expanded with additional members. Primary Responsibilities As a Development Engineer in the group, your duties will vary across project phases. It will consist of both laboratory work, but also data analysis and logging of information. The main tasks will be to: Perform experiments using Olinks PEA (Proximity Extension Assay) with NGS as a readout platform. Plan and perform laboratory work in accordance with set project plans and work schedules. Evaluate, report and document results from the laboratory work according to existing procedures. Handle and register data for large amounts of antibodies, antigens and biological samples. Actively participate in the development of the group's and department's activities and participate in improvement projects. Qualifications/skills Master’s degree in life sciences or corresponding education. Documented lab experience and a few years of working experience from the industry. Experience in pipetting small volumes and of using pipetting robots is advantageous. Experience with antibody-based test methods as well as with PCR and NGS. Experience with handling and characterizing biological samples, with a focus on plasma and serum is advantageous. Good computer skills in general and good knowledge of Excel. Experience of using python or R-scripts are advantageous. Experience of working in projects. Fluent in spoken and written English, Swedish is a plus. As a person you are responsible, driven, proactive and solution oriented. As we handle large amounts of reagents and data, we value that you are thorough and structured. You are a team player who finds it easy to communicate and interact with others both within the group and with those who work in other departments and functions. It is important that you have a positive attitude and can adapt to changing circumstances. The selection process is on-going, and the position might get filled before the last day of application so please apply as soon as possible, however no later than 2025.03.23.. If you want to help to deepen the understanding of real-time human biology and are looking for an exciting new challenge, we encourage you to apply!

Who we are Olink, part of Thermo Fisher Scientific, is transforming the understanding of human diseases through advanced proteomics. We are driven by a commitment to innovation, quality, and transparency, providing exceptional solutions and support for human protein biomarker discovery. For many years, the critical role of proteins in human biology has been recognized, but technological constraints limited comprehensive research into their potential across various biological processes and diseases. With our innovative Olink solutions, scientists can now measure thousands of human proteins simultaneously using just a few microliters of blood. Our highly specific and validated assays cover a wide dynamic range, empowering groundbreaking research. Our services include flexible protein biomarker solutions, with a robust library of thoroughly validated assays covering ~5000 proteins. As we expand globally, we continue to play a pivotal role in shaping the future of scientific discovery. To learn more, visit www.olink.com. Position Description We are seeking a highly motivated and driven Development Engineer to join our Midplex team within R&D, responsible for the development of our Midplex products. In the Midplex product area, we are focusing on products that via qPCR-based quantification measure up to 100 proteins simultaneously. In this role, you will take an active part in research and development projects, developing and optimizing new assays and actively contributing to development of product concept and ideas. You will have the opportunity to work on new and exciting projects, collaborate with cross-functional teams, and contribute to the development of future innovative products. The position will be based in our Uppsala headquarters. Primary Responsibilities Actively participate in development of product concepts and ideas within the area of the Midplex product portfolio. Plan and design laboratory experiments to validate and optimize protocols and technical solutions. Evaluate, report and document results in technical reports and presenting results. Analysis of data sets, applying statistical methods as needed to interpret data and draw conclusions. Develop and improve existing and new procedures, protocols and analysis methods. Collaborate closely with cross-functional teams to translate customer needs into product specifications. Qualifications University degree in life sciences (e.g., Biochemistry, Molecular Biology, Immunology) or corresponding education. At least a couple of years of experience in development work within the field. Documented skills and experience in laboratory work (e.g., DNA sequencing techniques such as PCR, qPCR and NGS). Experienced in the development of protein assays, such as PEA, ELISA or other relevant techniques. Familiarity with relevant software and data analysis tools. Fluent in English, Swedish is a plus. We believe that you are inclusive, driven and pragmatic. You enjoy working in a team and communicating with lots of different people. You have an analytical mindset and you are motivated by solving all kinds of problems and you pay attention to details. It’s also important that you are adaptable and enjoy a high work pace. The last day for applying is on the 23.03.2025 but please submit your application as soon as possible. If you want to help to deepen the understanding of real-time human biology and are looking for an exciting new challenge, we encourage you to apply!

Join Our Team as a Process Engineer We are currently seeking experienced and motivated Process Engineers to join our dynamic team. As a pivotal part of our operations, the Process Engineer will play a crucial role in ensuring the efficiency and effectiveness of our processes. If you have a passion for technology and a keen eye for detail, we encourage you to apply. About the RoleAs a Process Engineer, you will be involved in the manufacturing of ATMP products, to be used in clinical trials. The role at Anocca is suited to experienced and motivated professionals with a drive to lead and execute by action. Experience in aseptic work, including processing of ATMPs, as well as in electronic batch management systems would be a significant asset. You should have high-quality relevant experience, excellent English communication skills, knowledge of aseptic manufacturing techniques, and be securely anchored in GMP regulations. You must be capable of working as part of a team but should also demonstrate initiative to drive projects forward. What We're Looking For: Manufacturing experience in the cell therapy or ATMP space Significant and relevant experience in cell processing equipment and validation Good grasp of the underlying biology, preferably experience in T-cell immunology Fluent written and spoken English Why Join Us? Our company is at the forefront of technological innovation, striving to make a difference in the industry. We offer a dynamic working environment where talent and ambition are recognized and rewarded. Join us, and be part of a team that values growth, collaboration, and the pursuit of excellence. We Offer: Competitive salary and benefits package. Opportunities for professional development and career advancement. A collaborative and supportive work culture. State-of-the-art facilities and resources. How to Apply: If this Process Engineer position resonates with you, we would love to hear from you. Submit your application, including your CV and a cover letter, through our careers portal. Join us in making a difference, apply now! We ensure unbiased recruitment by hiding your personal information such as name, email, etc. and photos from the recruiter during the screening process. We may use background checks in the recruiting process.

We are a young, fast-growing company with an agile, cross-functional work environment. We promise you open, respectful, and prestige-free colleagues and a leadership team believing in our ability to grow together. Come and contribute with your experience in product development and make our journey yours. Your Role Our products are based on the superRCA technology, which offers ultra-high sensitivity detection of multiple mutation targets simultaneously in liquid biopsies. We have developed mutation targets for both Leukemia as well as solid tumors, and are currently offering standard research kits, custom products, and research analysis services. We are now transitioning from a start-up phase to a scale-up phase and require further focus on verification and validation of our products. You will lead verification studies and analytical performance evaluations, for our research-use and diagnostic products. You will set the requirements, refine and further develop the protocols, and ensure that the documentation is accurate and fit for purpose. We are a small team, and you will collaborate cross-functionally within the company with the aim of translating research into scalable, market-ready products. Your main responsibilities will include: Designing and leading verification and validation studies, including analytical performance evaluations, for research-use and diagnostic products. Define performance requirements, refine existing protocols and define new, when needed, as well as ensure that the documentation is accurate and fit for purpose. Preparing documentation to support in vitro diagnostic device (IVD) registration in compliance with applicable regulations and guidelines, in collaboration with the RA/QA and Product Development manager. Assist in areas such as requirement management, change management, and risk management. In collaboration with statistical expertise and R&D colleagues, evaluate performance studies and reports. You will report to the Product Development Manager and be part of our core team, playing a critical role in making our liquid biopsy and mutation detection technology accessible to clinicians and researchers. We mentioned that we are on a start-up journey, meaning we adapt quickly, so your tasks may evolve as we grow. We are located in Uppsala Science Park, where we have gathered all our business functions. Your Profile We’re looking for a structured, goal-oriented individual committed to making a difference. You should have experience of leading activities, planning effectively, and delivering results independently. We also hope you are a collaborative team player who strives for unified success, but most importantly, we hope you are yourself. We are a team of individuals, and our differences are what make us a dream team. Qualifications: A university degree in Molecular/Cell Biology, Biotechnology, Biochemistry, or a related field. 3-5years of experience in product development, particularly in verification and validation within a regulated environment. Proficiency in report writing and familiarity with statistical methods and data analysis. Experience collaborating with statistical experts and designing performance studies according to standards and guidelines, such as the CLSI guidelines or similar. Professional fluency in English, both written and verbal. Experience from flow cytometry and molecular biology techniques, including PCR and other DNA amplification methods is a plus. Application Join us and be part of a transformative journey in healthcare! We are accepting applications until the 6nd ofFebruary. If you have any questions regarding the position, please do not hesitate to reach out to Sandra Bydell Sveder, Recruitment Consultant ([email protected] or 076-319 96 88).