Olink Proteomics AB jobb

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 currently seeking a Laboratory Coordinator for our Analysis Service (AS) department in Uppsala. Analysis Service is our service laboratory, analyzing customer samples using Olink products in compliance with applicable GXP requirements (e.g. GCP) and ISO17025. AS consists of three units: The Laboratory unit, the Laboratory Operations unit and the Quality unit. The role as Laboratory Coordinator belongs to Laboratory Operations unit. The main task as the role of Laboratory Coordinator is to prepare and coordinate various activities within the department, e.g. purchasing, logistics, supply and reagents. You will work in close communication with both the Laboratory unit and the functions that exist in its surroundings. You will strive to minimize the laboratory downtime and improve the laboratory’s work environment, and act as an important point of contact for the laboratory and other departments. Primary Responsibilities: Control of reagents and supply, orders, and forecasting of consumables and reagents. Coordinate activities concerning e.g. reagents, supplies and logistics with other departments, such as Analysis Service US, Supply Chain, Facility, Finance and IT. Support the Analysis Service team to work efficiently, safely and with the highest possible quality. Coordinate Access management within Analysis service, e.g. train staff who need access to our facilities. Independent work according to Olink QMS instructions. Work independently within the Analysis Service team and collaborate effectively with other teams to ensure alignment of global Olink processes. Qualifications/Skills: BSc within the Life Science field or similar. 3+ years of experience working in a laboratory setting with customer deliveries (internal or external) and the ability to meet strict deadlines. Familiarity with GCP regulations in laboratory work. Experience with LIMS or similar systems is an advantage. Experience with ERP or similar systems is an advantage. Experience with logistics work is and advantage. Fluent verbal and written communications skills in English. We are looking for a meticulous and quality-focused professional who enjoys driving their own daily tasks as well as coordinating communication and activities between different functions within the department/company. You are pro-active, flexible, and capable of adjusting your priorities in a fast-paced and dynamic environment. You are a team player with strong communication skills and a positive, solution-oriented mindset. Please note that you should already be eligible to work in Sweden and should be able to come into our Uppsala office daily. 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 the 19th of June 2025. If this sounds interesting, please send us your application, and come join Olink!

Vilka vi är Olink, en del av Thermo Fisher Scientific, förändrar förståelsen för mänskliga sjukdomar genom avancerad proteomik. Vi drivs av ett engagemang för innovation, kvalitet och transparens, och tillhandahåller exceptionella lösningar för upptäckt av biomarkörer för mänskliga proteiner. Proteiners avgörande roll för att förstå mänsklig biologi har varit känd i många decennier men tekniska begränsningar försvårade en omfattande undersökning av det enorma antalet proteiner som kan vara viktiga i olika biologiska processer och sjukdomar. Med våra innovativa Olink-lösningar kan forskare nu mäta tusentals mänskliga proteiner samtidigt med bara några mikroliter blod. Våra mycket specifika och validerade analyser täcker ett brett dynamiskt område, vilket möjliggör banbrytande forskning. Våra tjänster inkluderar flexibla proteinbiomarkörlösningar, med ett robust bibliotek med noggrant validerade analyser som täcker ~5000 proteiner. När vi expanderar globalt fortsätter vi att spela en avgörande roll i att forma framtiden för vetenskapliga upptäckter. För mer information, besök www.olink.com. Om Rollen Vi söker ännu en driven och engagerad medarbetare till Avdelningen Quality & Regulatory. Avdelningen består av 19 personer och är fördelat på två team: Quality Asssurance (QA) & Quality Systems (QS). Tjänsten är placerad inom QA som idag består av 9 personer. Rollen innebär att tillsammans med QA-teamet kvalitetssäkra utveckling och tillverkning av Olink’s biomarkörpaneler samt analys av kundprover. Som Quality Assurance Manager rapporterar du till Head of Quality Assurance. Vänligen notera att det här är ett föräldravikariat från 2025.09.01 till 2026.10.31. Huvudsakliga arbetsuppgifter Medverka i att kontinuerligt utveckla och förbättra Olinks kvalitetsprocesser, så som Avvikelsehantering (NC), CAPA, Change Control, Product Release, Reklamationshantering, Riskhantering, Leverantörstyrning, Product Life Cycle Management m.m. Stötta hela organisationen i QA frågor och praktiskt kvalitetsarbete Kvalitetssäkring inom produktutvecklingsprojekt Design Transfer Ansvara för Product Release samt hantering av NC och CC Skriva instruktioner och andra styrande dokument Utforma och leda kvalitetsutbildningar i organisationen Kvalifikationer Högskoleexamen inom lämpligt naturvetenskapligt ämnesområde, tex bioteknik, biologi eller kemi Erfarenhet av kvalitetsinriktat arbete inom företrädelsevis Life Science, har du arbetat i en roll inom QA är det meriterande Erfarenhet av systematiskt kvalitetsarbete baserat på en etablerad kvalitetsstandard, t ex ISO 9001, ISO13485, ISO 17025 eller GxP är meriterande God förmåga att kommunicera på svenska och engelska i tal och skrift Som person är du engagerad, driven och trivs i en dynamisk miljö med högt tempo. Du är pragmatisk och noggrann när det behövs och kan tänka och arbeta långsiktigt. Slutligen är Du en lagspelare som är bra på att kommunicera och som kan se saker ur olika perspektiv. Vi lägger stor vikt vid dina personliga egenskaper. Detta är en unik möjlighet att vara med på resan att fortsätta etablera och stärka upp Olink’s kvalitetsledningssystem & organisation. Det är ett expansivt bolag som nu är en del av en större organisation, Thermo Fisher Scientific. Din ansökan med CV och personligt brev önskar vi snarast dock senast den 2025.06.25. Urval och intervjuer kommer göras löpande under ansökningstiden och tjänsten kan komma att tillsättas före sista annonseringsdag. Varmt välkommen med din ansökan!

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 The Quality unit, a part of the Analysis Service department, is looking to hire a Quality Engineer. At Analysis Service, protein expression analyses are performed for various customers in academia and the Life Science industry to identify biomarkers. We read out the expression with qPCR or with NGS methodology. The Quality unit is responsible for ensuring quality and that samples, analyses and data are handled in accordance with applicable laws and regulations as well as for managing our quality management system. In this role, you will support the business by maintaining quality throughout the work flow by, for example, reviewing and releasing results to customers and managing governing documentation, SOPs, etc. and being responsible for instrument documentation.  As Quality Engineer, you will also be responsible for managing deviations within the department, participating in customer audits and handle other quality-related issues from our customers. You will report to the Quality Manager at Analysis Service and be located at the head office in Uppsala. Primary Responsibilities Responsible for CAPA, CC, deviations and risk management within the department. Evaluate the effectiveness of the quality management system and investigate trends. Manage, organize and archive controlled documents. Write, update and review SOP/instructions/reports in collaboration with others. Approve data to be delivered to customers. Plan, implement and document quality training for staff. Be supportive in quality issues regarding equipment (qualification, maintenance and control). Represent Analys services at internal as well as customer audits. Qualifications Bachelor's degree or equivalent in the Life Science field. Experience working with quality in a contract laboratory or QC laboratory with a QMS based on ISO17025 or GCP is a strong merit. Experience with LIMS and/or document management systems. Good oral and written communication skills in English are a requirement, good knowledge of Swedish is an advantage. Soft Skills As a person, you are committed, independent and you thrive in a dynamic, fast-paced environment. You are a meticulous problem solver and have a sense of quality, and you can be pragmatic when needed. Finally, you are a team player who is good at communicating and can see things from different perspectives. We place great importance on your personal qualities. The application deadline is 2025.05.11. The role may be filled before the application deadline. If you have experience in ensuring quality assurance systems for production within Life Science or laboratory work, GLP/GMP/GCP/similar and thrive in a fast-paced, dynamic work environment, please do not hesitate 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 The QC team, which today consists of 14 people, is divided into two sub-teams: One with a focus on checking raw materials, components and finished products and one where the focus is on receiving and implementing new QC methods from RnD/ the Design Transfer process. The main purpose of this position is to be responsible for transfer of methods from RnD to Quality Control. The position is based in our Uppsala headquarters and reports to Head of Quality Control. This is a temporary position (from May 2025 to September 2026) to cover for a parental leave.  Primary Responsibilities Be responsible for driving the QC preparation tasks in the Design transfer process, according to internal procedures and routines and act as the Quality Control Preparation Engineer. Write and review instructions and methods. Actively participate as core team member in Product Development projects (NPI). Manage and drive product care activities within Supply Chain including improvements, non-conformities, CAPAs and Change Control activities. Actively participate in the business development of the department, i.e. create and improve work processes and routines. Qualifications MSs within Biotechnology/ Molecular Biology or similar. At least 2 years’ experience from a role as development engineer or similar within Life Science. Experience from a similar role as PM/Member/ Production Preparation Engineer of various Product Development Projects. Experience/ knowledge with ERP systems. Experience from ISO13485 certified or IVD/MD regulated business is highly beneficial. Fluent in (speaking/reading/writing) both Swedish and English is mandatory and necessary to be successful in this role. Soft Skills As a person, you are meticulous and used to following instructions. You are able to see the bigger picture and make suggestions for improvements where needed. You are a solution oriented team player with integrity who can be pragmatic when needed. You are also open towards changes and is motivated by driving improvements together with others. 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! The last day of application is on the 8th of May 2025.

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 we continue to scale, we are now looking to hire a PPI Lead, to be based in our Uppsala headquarters, reporting to our Vice President Operations. The role of the PPI Lead is to set the structure and foundation for, as well as establishing, the Thermo Fisher Scientific’s Continuous Improvement Business System (PPI) for the entire Proteomics Sciences division from the ground up as well as implementing it and owning it over time. In this role, you will work closely with the global PPI business network, business leadership and steering committee to establish and mature the Lean Management System (tiered daily management systems, Gemba walks, and leader standard work) and other coaching tools to facilitate the cultural transformation and achieve site goals and objectives. Primary Responsibilities PPI Business System: Work with the leadership team to identify transformational opportunities for business improvements and establish a Continuous Improvement Business System. Engagement: Drive a culture of continuous improvements in the areas of productivity, customer, finance, people and quality by implementing KPIs. Lean Support: Provide ongoing Lean support to the business in general and Operations, Commercial and RnD in particular. Work with the expanded team to develop/promote/standardize the Business System further. PPI Steering Committee: Prioritize improvement opportunities and develop site deployment plan. Lead/work with functional teams to streamline processes to improve customer experience, enable profitable growth and become more efficient. PPI Maturity Health Assessment: Conduct PPI Maturity Health Assessments on site involving all functions on a yearly basis. Safety: Work closely with EHS team to establish a Safety-First / zero accident culture and Environmental stewardship Qualifications Bachelor’s degree in engineering, science, operations or business, with evidence of operational, leadership, or professional experience. Master’s degree preferred. A Lean Expert with significant experience (7+ years) and a ‘hands-on’ track record of implementing successful TPS-based business systems including elements such as: Lean Leadership (Daily Management, Leader Standard Work, and Gemba Walks). Strategy Deployment and Value-stream mapping. Kaizen events, cell design, process and product 3P, Value-Analysis/Value Engineering, Heijunka, and Kanban. Expertise in problem-solving utilizing a formal program/process. Proven track record of developing, training, and coaching teams. Broad knowledge of multi-functional, multi-site, global organizational processes and financial business methods. Fluent in English and preferably proficient in Swedish. Operational Management experience is beneficial. To be successful in this role, you should have a passion for driving improvements and leading change in a complex, global environment. You are a self-directed leader with a proven ability to connect with leadership and manage/influence across all levels of the organization. Finally, you are able to drive strategic thinking and continuous improvement to improve efficiency along the extended value streams. Why Join Us? 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. 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 the 11th of May 2025.

Vilka vi är Olink, en del av Thermo Fisher Scientific, förändrar förståelsen för mänskliga sjukdomar genom avancerad proteomik. Vi drivs av ett engagemang för innovation, kvalitet och transparens, och tillhandahåller exceptionella lösningar för upptäckt av biomarkörer för mänskliga proteiner. Proteiners avgörande roll för att förstå mänsklig biologi har varit känd i många decennier men tekniska begränsningar försvårade en omfattande undersökning av det enorma antalet proteiner som kan vara viktiga i olika biologiska processer och sjukdomar. Med våra innovativa Olink-lösningar kan forskare nu mäta tusentals mänskliga proteiner samtidigt med bara några mikroliter blod. Våra mycket specifika och validerade analyser täcker ett brett dynamiskt område, vilket möjliggör banbrytande forskning. Våra tjänster inkluderar flexibla proteinbiomarkörlösningar, med ett robust bibliotek med noggrant validerade analyser som täcker ~5000 proteiner. När vi expanderar globalt fortsätter vi att spela en avgörande roll i att forma framtiden för vetenskapliga upptäckter. För mer information, besök www.olink.com. Rollbeskrivning  Produktionär en del av Supply Chain och ansvarar för framställning av komponenterna i Olinks produkter. För närvarande består gruppen av 10 medarbetare.Som Laboratorietekniker kommer du att få chansen attarbeta med tillverkning av komponenter till Olinkprodukter i olika steg. Tillverkningsstegen är uppdelade från råvara till färdig produkt så produktionskedjan är i vissa fall lång. Du kommer attrapportera till Head of Manufacturing i Uppsala. Huvudsakliga arbetsuppgifter Tillverkning av Olink Probe-komponenter enligt tillverkningsorder, huvudsakligen spädningar och beredningar via manuell pipettering och via olika robotlösningar Tillverkningsdokumentation ingår även i rollen med granskning och rapportering i affärssystem Samarbete med andra team (kvalitetskontroll, processutveckling, RnD) är också en del av denna tjänst Tillverkning av buffert- och bulklösningar, små- och storskalig antikropps-konjugering. En del av tillverkningen sker mot slutprodukt, andra delar sker i projektform, där projektmaterial förädlas i produktionen En stor del av tjänsten kommer omfatta hantering av våra material och råvaror, mottagning, certifikathantering, upparbetning, provuttag och analyser Kvalifikationer 3-årig universitetsutbildning inom biokemi eller molekylärbiologi alternativt erfarenhet från arbete inom bioteknikområdet med tillverkning/QC under flera år Erfarenhet av pipettering av små volymer ( 10µL) och multikanalspipettering med hög precision Erfarenhet av arbete på laboratorieverksamhet med leverans till kund (intern eller extern) och vana av att arbeta mot skarpa deadlines är också en fördel Erfarenhet av att arbeta inom GxP-reglerad laboratorieverksamhet Erfarenhet av LIMS eller liknande system är önskvärt Erfarenhet av dokumentering, granskning och rapportering i affärssystem Mycket goda kunskaper i både tal och skrift i svenska och engelska är ett krav Som person är du engagerad, strukturerad och noggrann. Det är viktigt att du har förmågan att omsätta dina erfarenheter till pratiskt utförande samt har en god kvalitétsmedvetenhet.Slutligen är du en positiv lagspelare som trivs i en omväxlande produktionsmiljö och har en stark initiativförmåga. Din ansökan med CV och personligt brev önskar vi snarast, dock senast den 2025.05.06. Urval och intervjuer kommer göras löpande under ansökningstiden och tjänsten kan komma att tillsättas före sista ansökningsdag. Varmt välkommen med din ansökan!

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 seeking a Scientist to join our R&D team in Uppsala with a focus on activities related to automation of sample preparation and sequencing. The position is within the Systems and Automation team that is responsible for product engineering and improvement projects for our instrumentation product lines; and for automation and readout of Olink products using commercially available solutions. You will work with improvements and development as well as testing and validation related to automation, and readout of Olink products using qPCR and latest NGS sequencing, this work is typically performed in collaboration with other members of R&D and sometimes in external collaborations. You will also be involved in other R&D activities, primarily related to the processing of samples in Olink products, using latest advances in automation and integration. The work is expected to include both molecular biology lab work and data analysis using R and Python. The work is often carried out in multi-functional projects, with both internal and external stakeholders, where several projects are run in parallel - a collaborative approach is a key for success. Are you passionate about technology and eager to take part in innovative projects? Join us at Olink, part of Thermo Fisher Scientific, where you'll participate in advancing our products using the latest technologies. We are looking for energetic individuals who can take initiative, inspire their teammates, and thrive in a fast-paced, technology-driven environment. Primary Responsibilities As an employee in the group, your duties will vary across project phases. The main tasks will be to: Development, validation and otherwise testing related to automation and readout instruments for Olink products. Processing sequencing data using validated software tools performing statistical calculations and compiling reports. Plan and conduct laboratory work in accordance with set project plans and work schedules. Documentation in technical reports and presenting results at meetings. Collaborate cross-functionally with members of other sections. Actively participate in project work and other development activities. Qualifications/skills PhD degree in biology or bioinformatics, working with large sets of sequencing data as well as molecular biology lab work; or comparable experience. Minimum 5 years experience of working with product development and/or design control. Good computer skills in general. Strong analytical and problem-solving skills. Strong team player with excellent communication skills in English. Swedish skills are a plus but not required. Ability to handle multiple projects, prioritize and meet deadlines. We believe that you are inclusive, driven and pragmatic. You have an analytical mindset, are structured, and pay attention to details. It’s important that you are adaptable and enjoy a high work pace. Please submit your resume and a cover letter detailing your relevant experience and why you are the ideal candidate for this position. The last day for applying is on the 21st of April 2025 but please submit your application as soon as possible.

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 a Scientist within the Affinity Department, R&D Proteomics Sciences Division, you will contribute to research and early product development in a culture that values creativity and inclusion. This role is centered on LC-MS methods for protein characterization and involves hands-on wet-lab work. You will be part of a skilled team of approximately eight experts specializing in proteomics and antibody development. Additionally, you will collaborate with colleagues across R&D teams to achieve company objectives effectively. The role focuses on method development, troubleshooting, and benchmarking of both new and existing protein binders. This position offers the opportunity to tackle challenging projects, engage with cross-functional teams, and contribute to the development of innovative new products based on Olink’s Proximity Extension Assay (PEA) technology. Primary Responsibilities Develop and implement mass spectrometry methods for protein characterization in both purified and complex samples, leveraging advanced LC-MS techniques to support the sustainability and expansion of Olink products Work independently in the Protein Characterization team with active communication across internal and external interfaces Lead and have accountability for ongoing internal or external projects Plan, execute, report, and scientifically communicate outcomes of R&D studies within own area Interpret internal or external issues related to affinity reagents and recommend solutions, based on data driven insight Independently support colleagues in development or research activities Work in accordance with Olink’s quality system and relevant instructions for laboratory work Comply with company instructions and routines including environmental health and safety Qualifications/skills Ph.D. in a relevant life sciences field (e.g., Analytical Chemistry, Biochemistry, Biotechnology) or equivalent experience. At least three years industrial or equivalent R&D experience as an independent scientist using LC-MS methods for protein analysis Knowledge of single and multiplex immunoassay techniques Solid theory of mass spectrometry for relative and absolute protein quantitation of proteoforms Scientific understanding of the current field of proteomics and bioinformatics Data analysis skills using R or Python for scientific validity Effective communication and writing skills for presentation and documentation in English To enjoy working in the Affinity Department and in R&D you are open-minded and inclusive. You are action-oriented and driven with critical thinking ability. Finally, you have strong problem-solving skills, using novel approaches and perspectives where needed. We offer a competitive salary, comprehensive benefits package, and a dynamic work environment. 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. 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 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!