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

Join us in shaping the future of cell therapy Do you bring experience in clinical study feasibility, patient recruitment, and study delivery? Are you motivated by the opportunity to help shape innovative studies from the earliest planning stages and work with people across functions to make a real difference for patients? We are now recruiting a Local Study Associate Director, Feasibility Lead to join our team in Stockholm. This is a chance to play an important role in our cell therapy portfolio, using your operational insight, strategic thinking, and collaborative approach to help set studies up for success. About AstraZeneca At AstraZeneca, we are driven by science and inspired by the difference we can make for patients. Across our business, we bring together deep scientific expertise, innovation, and collaboration to discover, develop, and deliver medicines that address some of the world's most serious diseases. Within Oncology, we are advancing a bold pipeline, including cell therapy, with the ambition to transform outcomes for people living with cancer. It is a place where you can contribute to meaningful work, grow your career, and be part of a team that values curiosity, ownership, and partnership. About the role As Local Study Associate Director, Feasibility Lead, you will be at the heart of country-level feasibility for AstraZeneca's internally delivered cell therapy studies. You will help shape key decisions on study design, site selection, recruitment forecasting, and retention planning, ensuring that local insight translates into strong, realistic study plans. You will also play an important role in local study delivery, leading cross-functional collaboration to ensure studies are progressed in line with timelines, quality expectations, and compliance requirements. You will work closely with colleagues across Feasibility, Global Project Teams, Medical Affairs, Site Management & Monitoring, Site Partnerships, Patient Operations, and Study Management, as well as with investigators and site personnel externally. Your ability to build relationships, influence decisions, and bring people together around shared goals will be central to success in this role. This is an exciting opportunity for someone who enjoys combining strategy and delivery, and who wants to contribute to innovative clinical development in a highly collaborative environment. What you will do Lead Local Study Teams to deliver study commitments to agreed timelines, quality, and compliance standards Support country start-up and study oversight, including site identification, qualification, and essential document readiness Maintain compliance and inspection readiness in line with AstraZeneca standards, ICH-GCP, and local regulations Contribute to continuous improvement in feasibility, recruitment, and retention practices Lead country feasibility activities for assigned cell therapy studies Provide local insight to support study design, site selection, country allocation, and recruitment planning Develop recruitment and retention strategies based on feasibility findings and delivery insights Partner with local and global stakeholders to align on priorities, risks, and opportunities Essential Requirements Bachelor's degree in a relevant field such as life sciences, business management, or project management, or equivalent project management certification Significant experience in the pharmaceutical industry, including drug development processes Minimum 1 year of experience in clinical study feasibility Experience developing and delivering study delivery strategies and tactical or operational plans Experience in patient and investigator recruitment and retention Proven project and budget management skills, with the ability to manage multiple priorities and deliver high-quality work Strong stakeholder management, communication, collaboration, and negotiation skills in complex environments Good knowledge of ICH-GCP, basic knowledge of GMP/GDP, and good understanding of local regulations and clinical study management Good medical knowledge in relevant AstraZeneca therapeutic areas Strong analytical, problem-solving, prioritisation, and digital skills Desirable requirements Experience in cell therapy Experience working with CROs, AROs, or external partners Experience in new product development within the pharmaceutical industry Experience developing study delivery strategies aligned to local regulatory objectives Experience managing complex or cross-border projects Ability to work effectively with remote collaborators, adapt positively to change, and influence stakeholders A process innovation mindset, including the ability to identify opportunities for AI or digital tools to improve efficiency, quality, or innovation Why join us? This role offers the opportunity to make a visible contribution in an innovative and fast-moving area of clinical development. You will help shape how studies are planned and delivered locally, work with experienced colleagues across a broad network, and contribute to work that has the potential to change patients' lives. What's next? Ready to take the next step? We'd love to hear from you. Please submit your CV and cover letter, no later than September 16th, 2026 . To help us review your application smoothly, please combine your CV and cover letter into one document before uploading. Öppen för alla Vi fokuserar på din kompetens, inte dina övriga förutsättningar. Vi är öppna för att anpassa rollen eller arbetsplatsen efter dina behov.

Do you have deep expertise in fluidics and flow-cell design for analytical instrumentation? Are you excited by the opportunity to drive development from early concepts to production and product care? Join Moleculent and play a key role in developing a cutting-edge life science instrumentation! Moleculent is on a mission to build products that yield new insights into the molecular foundation of human biology. This is a chance to join a focused and dedicated team with extensive experience building successful life-science companies and products. This is a permanent position based in Solna, Stockholm. The position is full-time and based at Moleculent’s headquarters in Solna, Stockholm. Please don’t wait to submit your application. We review candidates on an ongoing basis, and the position may be filled before the final application deadline. Applicants must be eligible to work in Sweden without sponsorship. JOB DESCRIPTION As a Senior Systems Engineer – Fluidics at Moleculent, you will be responsible for flow cells and fluidics design throughout the entire product development life cycle – from concept development and prototyping to design transfer and product care. You will work closely with cross-functional teams and external partners to develop robust and scalable solutions for advanced analytical instrumentation. You will combine hands-on laboratory work with system-level thinking and project leadership responsibilities. Key responsibilities include: * Lead flow cell and fluidics design activities, including design, testing, troubleshooting, and verification * Drive development of new flow cell concepts and consumable designs * Support flow cell production engineering and production troubleshooting * Ensure production equipment is maintained, supported, and qualified * Participate in and drive instrument-level testing and verification activities * Lead or contribute to throughput improvement initiatives * Manage system-related project activities and integration work * Contribute to early-stage conceptual development for future instrument generations * Collaborate closely with R&D, Operations, Product Management, Biochemistry teams, suppliers, and contract manufacturers QUALIFICATIONS To fit the role, you most likely hold an MSc in Technical Biology, Molecular Biotechnology, Material Science, Mechanical Engineering, or a related field. A PhD within a relevant discipline is considered a strong advantage. Fluent written and spoken English is required. You have several years of experience working with fluidics and flow cell development in analytical or life science instrumentation environments. You are comfortable moving between development, testing, production support, and cross-functional collaboration. We believe you have: * Experience with fluidics design in analytical systems * Experience with consumable prototyping, product development, and transfer to manufacturing * Knowledge of plastics and adhesives commonly used in life science or medical technology products * Experience from product development of instrumentation within Life Science * Hands-on laboratory experience and practical troubleshooting skills * Project management or project leadership experience * Experience with testing, verification, and troubleshooting activities * Good understanding of integrated hardware/software instrumentation systems Nice to have: * Experience with flow simulations * Experience with requirements engineering and formal verification methodologies * Experience working with analytical instruments, in vitro diagnostics systems, or medical devices * Experience writing test specifications and verification documentation * Swedish language skills You are hands-on, analytical, and solution-oriented, with a strong ability to navigate complex technical challenges. You enjoy working closely with both development and production teams and thrive in collaborative environments where innovation and quality are central. You are structured in your approach while remaining pragmatic and adaptable in a fast-moving environment. You take ownership of your work and enjoy driving projects forward together with others. MOLECULENT We believe innovative biotechnology has enabled massive leaps forward in understanding the composition of tissues and organs. However, the functional understanding of how cells communicate in their native context and form these complex systems has just begun. We develop technology designed to uncover radical new insights into the cellular level of human biology by mapping the communication between cells in human tissue and providing meaningful data. https://www.moleculent.com/ Please note that Moleculent manages the recruitment process for this position. External recruitment agencies are requested to refrain from direct contact with us in this regard.       *

Computational Staff Scientist - shared between 2 labs - in spatial and single cell omics vid Karolinska Institutet. Ansök senast 2026-09-15.

Postdoctoral studies in Human Tumor Immunology and T-cell Biology (scholarship) vid Karolinska Institutet. Ansök senast 2026-09-22.

Are you passionate about transforming complex spatial biology data into actionable insights? Do you thrive in a cross-functional environment bridging experimental and computational teams? Moleculent is looking for an experienced Computational Biology Scientist with Immunology knowledge to drive and evolve our Applications and Fee-for-Service (FFS) initiatives. Join us to contribute to cutting-edge technology that unveils new perspectives on human biology! Moleculent is on an exciting mission to map cell communication at the molecular level in tissue, aiming to unlock radical new insights into human biology. This is a chance to join a focused and dedicated team with extensive experience in building successful life science companies and products. This is a permanent position based in Solna, Stockholm, with the possibility to work remotely. We welcome your application, but please note that interviews will be conducted in August! JOB DESCRIPTION As a Computational Biology Scientist, you will play a key role in driving data analysis workflows for customer and internal validation projects. You will take ownership of project design, biological interpretation, and stakeholder communication, working closely with wet-lab scientists, the Applications Team Lead, and R&D to ensure high-quality, reliable data insights. Key responsibilities: * Design and interpret analysis strategies to support application development and pilot studies. * Execute image preprocessing, cell segmentation, and spatial metrics extraction using established pipelines. * Compile and visualize results into standardized reports for internal use and customer delivery. * Collaborate on refining methods, troubleshooting, and prototyping new analysis metrics. * Ensure data traceability and compliance with Moleculent's data packaging standards.  QUALIFICATIONS To fit this role well, you should hold an MSc or PhD in computational biology, bioinformatics, image analysis, spatial omics, or a related field. It’s a strong advantage if you have done a postdoc in a relevant field. Fluency in both written and spoken English, along with strong computer skills, is essential. Experience in clearly and effectively presenting data—both in writing and in oral presentations—is a key requirement. * Proficiency in Python and spatial single-cell analysis, with the ability to design, execute, and interpret analysis workflows for complex datasets. * A solid understanding of immunology is important, as our data closely relates to immune cell populations, marker panels, and tissue-based immune profiling. * Experience working directly with customers—whether through pilot studies, fee-for-service delivery, or technical support—is highly valued in this role. * Experience working across R&D, product, and commercial functions is a plus. * Skilled in summarizing insights for cross-functional teams.  MOLECULENT We believe that our understanding of the molecular basis of human biology, in health and disease will increase radically in the coming ten years. This will lead to a vast improvement in therapies, and diagnostics, and a new, fundamental understanding of our own biology. Moleculent is on a mission to develop technology-enabled products that leverage new insights into the molecular foundation of human biology. https://www.moleculent.com/

LAB TECHNICIAN WITH EXPERIENCE IN HISTOLOGY Do you have hands-on laboratory experience and a passion for generating high-quality scientific data? Do you enjoy structured experimental workflows, precision, and attention to detail, and want to play a key role in supporting innovative applications and customer projects? Join Moleculent and contribute to the successful execution of our Applications and Fee-for-Service operations! Moleculent is on an exciting mission to map cell communication at the molecular level in tissue, aiming to unlock radical new insights into human biology. This is a chance to join a focused and dedicated team with extensive experience in building successful life science companies and products. This is a permanent position based in Solna, Stockholm. We will review the applications after the vacation period. Applicants must be eligible to work in Sweden without sponsorship. JOB DESCRIPTION As a Lab Technician, Applications and Fee-for-Service at Moleculent, you will play an important role in supporting customer projects and internal application development studies. Working primarily in the laboratory, you will be responsible for sample handling, assay execution, quality control, and laboratory operations to ensure reliable, reproducible, high-quality data. Over time, you will take on increasing responsibility for independently managing Fee-for-service project workflows and supporting the scale-up of our service operations. Key responsibilities: * Prepare for experiments by organizing workspaces, confirming sample lists, and ensuring required consumables and equipment are available. * Receive, handle, track, label, and store FFPE tissue samples according to established SOPs. * Perform experimental workflows using prepared assay kits and standardized protocols. * Execute tissue staining and multiplex in situ assay workflows under established procedures. * Perform assay quality control checks and review imaging results for completeness and consistency. * Accurately document experimental procedures, reagents, conditions, and results to ensure full traceability. * Support troubleshooting activities and contribute to workflow optimization together with Applications and R&D teams. * Maintain laboratory readiness through equipment upkeep, reagent inventory management, and general lab organization. * Contribute to the expansion and standardization of Fee-for-Service operations . QUALIFICATIONS To fit the role, you hold a BSc in Molecular Biology, Biotechnology, Biomedical Sciences, or a related life sciences field. Equivalent relevant work experience will also be considered. Fluent written and spoken English is required. You have experience working in a molecular biology, histology, or related laboratory environment. Experience with FFPE sample handling, immunofluorescence (IF), immunohistochemistry (IHC), or similar workflows is highly valuable. You are comfortable working according to structured SOPs and understand the importance of quality documentation and reproducible laboratory processes. Technical skills: * Hands-on experience with tissue preparation, staining, microscopy, and reagent preparation. * Familiarity with laboratory imaging systems and basic image data handling. * Experience with quality control procedures and experimental documentation. * Knowledge of laboratory organization, equipment maintenance, and chemical safety practices. * Ability to follow version-controlled protocols and standardized workflows. As a person, you are highly organized, detail-oriented, and committed to delivering high-quality results. You enjoy practical laboratory work and are motivated by contributing to scientific excellence. You are proactive, reliable, and capable of working independently once trained, while also collaborating effectively with colleagues across scientific and operational teams. An adaptable mindset and eagerness to learn new technologies and workflows are important for success in this role. MOLECULENT We believe that our understanding of the molecular basis of human biology, in health and disease will increase radically in the coming ten years. This will lead to a vast improvement in therapies, and diagnostics, and a new, fundamental understanding of our own biology. Moleculent is on a mission to develop technology-enabled products that leverage new insights into the molecular foundation of human biology. https://www.moleculent.com/ Please note that Moleculent manages the recruitment process for this position. External recruitment agencies are requested to refrain from contacting us directly in this regard.

RF ENGINEER – RADIO TESTING & INTEGRATION We are looking for a skilled RF Engineer with solid experience in RF testing, integration, and troubleshooting. This role involves working with lab-based radio systems, test equipment, and network validation. Candidates with more than 5 years of experience are welcome, though we strongly prefer profiles with 8–10+ years of deep, hands-on RF experience. You should be able to work independently and feel confident managing test setups and technical analysis. Experience with Ericsson products is a plus but not mandatory. Key Responsibilities: * Configure and integrate RF products in lab/test environments * Validate node configurations based on cell and frequency planning * Create and manage cell/frequency plans for lab setups * Conduct passive RF component testing and EMF measurements * Analyze and troubleshoot RF interference issues * Verify all RF connections in test environments * Operate test equipment: Spectrum Analyzers, Network Analyzers, Signal Generators * Document technical setups and maintain lab records * Handle support requests and incidents via Jira * Collaborate with cross-functional teams and support knowledge sharing * Provide training on CCN functionalities and RF procedures Requirements: * Minimum 5 years of hands-on experience in RF Engineering * Preferred: 8–10+ years in RF integration, test environments, and troubleshooting * Strong understanding of RF systems, RF leakage, interference, and wireless technologies (2G/3G/LTE/NR) * Familiarity with frequency and PCI planning * Basic scripting skills (MOSHELL/Shell) for RF operations * Experience working with test environments and lab validation setups * Proficiency with RF test tools and analysis * Strong communication and documentation skills Advantages: * Experience with Ericsson radio products and RAN architecture * Exposure to Ericsson tools and systems * Experience in EMF measurement and radio test configuration What we offer: * Health insurance and wellness benefits * Regular team-building activities and seasonal events (summer & Christmas parties) * A supportive, technically strong team environment * Market-aligned salary (negotiable) * Visa sponsorship and full relocation support (If needed) * Assistance with visa extensions (If applicable) WHY K TWO? At K Two, our consultants are known for their strong technical and social competence, deep industry experience, responsiveness, and winning attitude. We value not just skilled developers, technicians, and team leads—but also true consultants who thrive on delivering value. We're in the business of assembling winners. Join us, and discover that working with and for K Two is more than just a job—it's a genuinely rewarding experience. Sounds interesting? Apply Now If you're a capable RF Engineer who thrives on solving real-world radio network challenges and enjoys working hands-on with advanced RF systems, we’d love to hear from you. Whether you're currently based in Sweden or planning an international move, we’re here to support you every step of the way—with visa sponsorship, relocation assistance, and a welcoming team environment. Join us in shaping the future of radio technology—apply today and become part of something rewarding.

BioLamina is now looking for a Bioprocess Operator to join one of their production teams in Sundbyberg. This is an opportunity to take on a varied, hands-on role with responsibility for filling and labeling, while working alongside new automation technology and broadening your skills across different areas of production. The role As a Bioprocess Operator, you will work hands-on with small-scale batch manufacturing in a cleanroom environment, with particular responsibility for the filling and labeling process. While these processes have previously been performed manually, BioLamina has recently invested in a new automated filling and labeling system and your role is to be the operator and technical authority behind that equipment. You will manage day-to-day operations, troubleshoot issues, and continuously optimize the process. This is not a passive monitoring role. You will be actively engaged in the manufacturing process, combining hands-on work with technical problem-solving. While filling and labeling will be your primary focus, you will also work across other areas of production, gradually broadening your experience in protein purification and manufacturing. Production is a true team effort. You will join one of three production teams, working alongside 12 operators and engineers in a collaborative environment with a supportive and accessible manager. There is a strong sense of community across the company, with shared lunches and social activities being a natural part of your workday. BioLamina operates across three sites in Solna, Sundbyberg, and Flemingsberg. In this role, you will be based on-site in Sundbyberg, working daytime hours, Monday to Friday. Key responsibilities: Hands-on operation and optimization of the filling and labeling equipment, including control system management, troubleshooting and technical problem-solving. Hands-on batch manufacturing, while also supporting downstream processing, primarily protein purification. Ensuring quality, efficiency and traceability throughout the filling and labeling process. Proactively identifying and driving continuous improvements in processes and ways of working. Managing manufacturing documentation, such as batch records, and contributing to the handling of deviations, change controls and risk assessments in accordance with established procedures, ISO 9001 and the quality management system. Collaborating closely with operators, engineers, quality, maintenance and logistics to ensure an efficient production flow. Your profile We are looking for someone with a hands-on approach, technical curiosity, and the confidence to take ownership of complex equipment and processes. You are comfortable with technology, willing to learn new systems, and keen to actively participate in troubleshooting and problem-solving. You want to become the technical expert in your area and the person others turn to for guidance on equipment operation and troubleshooting. At the same time, collaboration comes naturally to you. You enjoy working closely with colleagues across different functions and understand the importance of contributing to the team while taking responsibility for your own part of the process. You pay attention to detail and work in a structured and quality-conscious way. Requirements: At least a couple of years of production experience within life sciences, biotech, or another regulated industry. Experience with automated filling is required, and labeling experience is an advantage. Experience working in cleanroom environments and with aseptic techniques. Comfortable operating control systems, with a willingness to troubleshoot and optimize equipment operation. Technical interest and a proactive approach to learning and problem-solving. Ability to read and communicate verbally in English. Swedish language skills are an advantage, but not a requirement. Why join? At BioLamina, you will join an international and value-driven biotech company with high ambitions and products that support the development of future cell therapies. You will work alongside dedicated colleagues in an environment where quality, collaboration and continuous improvement are central. BioLamina is a learning organization where knowledge is shared and new perspectives are encouraged. The company is committed to a positive, sustainable and safe work environment with an inclusive culture. Application Please submit your application as soon as possible, but no later than 14 September. In this recruitment, BioLamina is collaborating with SallyQ. For questions, please contact Hanna Peterson at +46 73 940 57 98 or hanna.peterson@sallyq.se About BioLamina BioLamina AB is a Swedish biotech company founded on scientific innovations at Karolinska Institutet. Their main products are recombinant laminins, human proteins used to maintain and expand pluripotent stem cells and other primary cell types for subsequent differentiation into specialized cell types. BioLamina is revolutionizing cell culture, and the products are used by researchers worldwide to develop cellular therapies and contribute to the era of regenerative medicine. For more information, please visit: https://biolamina.com