Jobdescription
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.