Method, Validation, or Tech Transfer Specialist

About the Position Experienced Method Specialist – Method Development, Validation & Tech Transfer – Stockholm/Uppsala We are building the future in Qualification, Automation & Validation (QAV) – Are you the next star in our team? About the Position – We are seeking a specialist We are looking for an experienced and driven specialist in Method Development, Method Validation, and/or Tech Transfer within the Life Science sector. We are currently expanding our QAV (Qualification, Automation & Validation) project team and seeking committed employees for independent consulting assignments with our partners and to join our own Statement of Work (SOW) project groups in Stockholm County. Your expertise is crucial when our partners face implementation of new analytical methods, validation for regulatory approvals, or large-scale technology transfer from R&D to production. By joining QRIOS, you'll have the opportunity to tackle these critical challenges in some of Sweden's most innovative companies. Format: Proactive application/Expression of Interest – we will match you with upcoming assignments/projects. Full-time (100%) or by agreement. Stockholm/Uppsala Application Deadline: We process applications on an ongoing basis, submit your interest today! Primary Work Tasks Your focus competence areas depending on the project nature and your specialty will include: • Leading or participating in method validation projects according to applicable guidelines (e.g., GMP), including planning, execution, and reporting. • Driving Tech Transfer initiatives for analytical methods (e.g., from R&D to QA/QC or between production sites). • Developing and optimizing new analytical methods in chemistry, biology, or cell and gene therapies (ATMP). • Writing and reviewing GxP documentation related to methods, validation, and equipment qualification. • Acting as Subject Matter Expert (SME) and providing advice on regulatory matters related to your specialist areas. • Working independently on consulting assignments or as part of an SOW project group delivering a specific result. Who Are You? The expert we are seeking: You are a specialist who takes initiative, has a strong quality focus, and thrives at the intersection of science, technology, and regulatory requirements. You see yourself as a key player who can contribute both theoretical knowledge and practical implementation skills. You have: • Academic degree (MSc or PhD is meritorious) in Analytical Chemistry, Molecular Biology, Biotechnology, Pharmacy, or similar field. • At least 5 years of relevant experience in Life Science, Pharmaceuticals, or Medtech – specifically in Method Development, Validation, or Tech Transfer. • Deep expertise in at least one of the following areas: - Analytical Chemistry: HPLC, GC, Mass Spectrometry, Dissolution, etc. - Molecular Biology/Cell Therapy: qPCR, ELISA, Flow Cytometry, Potency Assays (especially ATMP). - Microbiology: Sterility Tests, Bioburden, Endotoxin. • Solid knowledge of GxP and regulatory requirements (e.g., EMA, FDA). • Ability to lead projects or sub-projects and influence cross-functional teams. • Excellent communication skills in Swedish and English. About the Company QRIOS is your career partner for specialist roles in Life Science and Engineering. We offer you the opportunity to quickly develop your expertise through varied assignments and projects. As a consultant with us, you will get: Security in employment combined with the variation of a consulting life. Opportunity to be part of our QAV network for knowledge exchange and professional development. Access to SOW projects where we as a company take total responsibility for delivery. Together we drive innovation and contribute to a better future – MINDS GO FURTHER.