Main Responsibilities:
·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
Qualifications and Experience:
·Relevant working/residency permit or Swiss/EU-Citizenship required
·PhD in a relevant field (biotechnology, biochemistry, pharmaceuticals, etc.), then 1 year of experience desired (no experience is also acceptable if other things are matching) or MSc in a relevant field, then at least 2 years of experience is desired (whether in a laboratory or as a scientist or similar)
·Data Review experience is 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
·Language: English mandatory, German a plus