Public Relations

• Technical supervision of microbiological contract analyses in the areas of pharmaceuticals, medical devices, and microbial identification
• Preparation of test reports and quotations in compliance with internal and regulatory requirements (GMP, DIN EN ISO 17025)
• Preparation and processing of results, including plausibility checks
• Processing and maintenance of documents as part of quality assurance
• Supporting the department head in managing and advising national and international clients
• Contributing to the optimization of laboratory processes/organization and interfaces to upstream and downstream processes following thorough onboarding

Microbiology Team Leader, Pharmaceuticals

Audit Assistant m/f/d

Audit Assistant