* Life Sciences - Quality Management * Wallis * Contracting * Vollzeit * 02/02/2026 - 01/08/2026 *, LIMS, QC, GMP, qPCR, ELISA Your Tasks: * Analytical Method Lifecycle * Lead and execute project tasks related to method development, implementation, transfer, and validation. * Prepare and maintain test instructions, analytical methods, study plans, and technical reports according to internal quality standards. Data Review & Documentation * Perform double-check and release of raw data and analytical results in LIMS. * Ensure data integrity and compliance in accordance with ISO and GMP requirements. Laboratory Support * Provide expert technical support to the QC laboratory, including troubleshooting of analytical issues. * Independently plan, execute, evaluate, and document assigned tasks and projects. Quality & Compliance * Manage and support Change Requests (CRs), Deviations (DRs), investigations (SST, OOX, etc.) and CAPAs. * Ensure full adherence to quality, safety, ISO, and GMP standards in all work processes. Your Profile: Education * PhD in Biotechnology, Biochemistry, Pharmaceuticals, or a related field * *1 year of relevant experience preferred (entry-level considered)* * or MSc in a relevant scientific field * *Minimum 2 years of relevant experience required (laboratory or scientist roles)* Technical Skills * Hands-on experience with ELISA (focus on relative potency) * Hands-on experience with qPCR, including method development and/or validation * Data Review experience is important and strongly preferred * GMP experience is a plus Other Requirements * * Strong understanding of laboratory best practices and data integrity principles * Ability to work both independently and collaboratively in cross-functional environments * Excellent communication skills, with English mandatory; German is an advantage * Ability to work on-site with a maximum of 2 remote days per week