Manpower Join a dynamic and innovation-driven pharmaceutical environment in Visp as a QC Scientist, where you will play a key role in ensuring the quality and reliability of analytical methods. Description: Competences & Responsibilities of a QC Scientist: Responsible for project tasks in the area of method development, implementation, transfer and validation Writing test instructions, methods, plans and reports Double check and release raw data and analysis results in LIMS Specialist support for the laboratory (troubleshooting) Processing of CRs, DRs, investigations (SST, OOX, etc.) and CAPAs Independent planning, implementation, evaluation and documentation of the assigned tasks and projects Compliance with quality (ISO and GMP) and safety standards Experience: Data Review experience is important! PhD in a relevant field (biotechnology, biochemistry, pharmaceuticals, etc.), then 1 year of experience desired (no experience acceptable if necessary)or MSc in a relevant field, then at least 2 years of experience desired (whether in a laboratory or as a scientist or similar)IMPORTANT: Focus on ELISA methods (relative potency) and qPCR ? hands-on experience in the laboratory and/or in their validation/development, GMP experience also a PLUS Remote: 2 days max. Language: English mandatory / German a plus Contact: Alba Jansa alba.jansa(at)experis.ch 41 61 282 22 13 Branche: Pharma-Industrie Funktion: Personalwesen