Scientist - QC Microbiology Lead

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.

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.