For one of our clients, a world leader in the CDMO industry and biotechnology, we are currently looking for a Scientist - QC Microbiology Lead.
General Information:
- Start date: 01.12.2025
- Duration: until 31.08.2026
- Workplace: Visp
- Workload: 100%
- Remote/Home Office: possible, max 2 days, 100 % on-site preferred
- Working hours: Standard
Tasks & Responsibilities:
- Technical representation of the QC Microbiology department internally and at customer meetings/audits/visits as well as during inspections within the projects assigned.
- Scientific SME for project-specific analyses and other microbial analyses in QC Microbiology: Monitoring, evaluating and, if necessary, coordinating the implementation of current improvements.
- Coordinate and ensure the timely completion of individual work packages assigned to specific business units (BUs), while facilitate effective communication within interdisciplinary overarching teams (e.g., studies, validation/verification, deviations, and transfers).
- Collect and evaluate verification data to identify weak points and implement corrective measures. You will define cGMP examinations in the event of deviations, ensuring strict compliance and operational excellence.
- Support other departments with Quality Assurance tasks, drive process improvements, and contribute to various projects across the Visp site.
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Requirements:
- Degree in Pharmaceutical Sciences, Microbiology, Biology, or equivalent experience (MSc preferred).
- Min. 2 years experience in GMP environment, ideally in QC Microbiology.
- Proven work experience in pharmaceutical Quality Control, particularly with endotoxin and/or bioburden analysis is highly desirable.
- Proficiency in English and German skills are nice to have.
Application Submission Deadline: 24.11.2025
Sounds interesting? Apply Now! We look forward to receiving your application.
