Expert Microbiology in Quality Control

Location:

Basel or Kaiseraugst

Contract duration: 1 year

• Processing and conceptual oversight of complex microbiological specialist topics in the field of product analysis (e.g. endotoxin, sterility, bioburden), contamination control/aseptic assurance and environmental monitoring
• Technical support and consulting of various interfaces (including production plants [DP, DS, Biologics, Synthetics], QA, registration) in a central SME function
• Representation in official inspections and audits
• Participation in regulatory approval reports
• Matrix lead/collaboration in changing cross-functional projects both locally and in the global network, including supervision of interns
• Implementation of new technologies in the field of pharmaceutical microbiology
• Processing of deviations, changes and other GMP-relevant documentation (e.g. regulations, planning and documentation of studies, preparation of rationales)

• Master's or PhD Degree in a scientific background.
• Min. 1 year of experience in pharmaceutical microbiology.
• Experience with GMP (documentation) and its systems, e.g. Veeva (Change, Deviation, Quality Docs) is an advantage.
• Excellent communication skills in German (C2) and English (oral and written).