Job description:Join Our Team as an Associate II Quality Control Sample Management & LogisticsLocation: Solothurn, SwitzerlandAbout the RoleAre you looking to advance your career in Quality Control within a dynamic and innovative biotech environment? We are seeking a dedicated and detail-oriented Associate II for our Quality Control (QC) Sample Management & Logistics team at a state-of-the-art manufacturing facility in Solothurn, Switzerland. In this role, you will play a crucial part in managing QC test, stability, and retain samples while ensuring full GMP compliance.Key ResponsibilitiesOversee the preparation, movement, and shipping of QC test, stability, and retain samples, ensuring compliance with GMP and trade regulations.Organize and coordinate sample shipments for raw materials, manufacturing science, analytical development, and partner organizations.Conduct aliquotation and sub-sampling of drug substance bags for QC analysis.Support day-to-day operations in Central and WIP laboratories, including managing QC-related non-analytical testing equipment (e.g., freezers).Manage and distribute QC reagents and consumables across laboratories and oversee QC labware.Prepare solutions such as liquid chromatography buffers and TOC testing solutions.Order and manage reference standards and qualified materials in collaboration with the global QC reference group.Assess and process GMP-relevant alerts via the Quality Review Manager (QRM).Author, review, and approve complex GMP documentation, including plans, protocols, procedures, specifications, CAPAs, and deviations.Who You AreYou are an organized and proactive professional with experience in pharmaceutical or biotech manufacturing environments. Your background in GMP Quality Control, along with knowledge of Microbiology and Chemistry, equips you to excel in this role. You thrive in a fast-paced, regulated setting and are comfortable working both independently and collaboratively.Qualifications & SkillsAssociate's Degree, technical degree (1-2 years), or Bachelor's Degree.Prior experience in GMP Quality Control within the pharmaceutical or biotech sector.Basic knowledge of Microbiology and Chemistry; experience with buffer and solution preparation preferred.Familiarity with aseptic working environments.Strong organizational and time-management skills.Excellent communication skills across all levels, including management, peers, and external partners.Proficiency in Microsoft Office (Word, Excel, Outlook).Preferred experience with LabWare LIMS and Oracle systems.Dual language proficiency (German & English) preferred (minimum level B1).Why Join Us?We offer a collaborative and inclusive work environment, competitive benefits, and career growth opportunities. If you are ready to make a meaningful impact in the biotech industry, we encourage you to apply!Apply now and be part of our innovative team in Solothurn! jidfb17bb6a jit0313a jiy25a