QC Analyst
- Contract
- Good Manufacturing Practice (GMP)
- Switzerland
This vacancy has now expired. Please see similar roles below...
Are you passionate about quality and precision? Join the team as a QC Analyst and help ensure top-tier standards every day.
This role will focus on routine analytics and method development within the Quality Control Department, ensuring compliance with GMP and safety standards. This position requires proficiency in LC-MS analytics and fluency in German.
Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.
Responsibilities:
- Execute routine analytics and develop/validate methods in the Quality Control Department.
- Operate, calibrate, and maintain quality control equipment and machinery.
- Test and assess product samples to ensure they meet predefined standards.
- Aggregate test data and document results.
- Receive, store, and complete paperwork for samples submitted for testing.
- Perform routine housekeeping activities and maintain sample inventory.
- Support material release processes.
- Conduct routine maintenance and calibration checks on instruments.
- Supply materials to the QC laboratory.
- Undertake additional duties as assigned by your Supervisor/Manager.
Key Skills and Requirements:
- Lab technician qualification or equivalent, or a bachelor's degree in Chemistry/Biotechnology.
- Experience in Quality Control, ideally entry-level.
- Fluency in German; English is advantageous.
- On-site work required; remote work is not possible.
If you are having difficulty in applying or if you have any questions, please contact Ashley Bennett at a.bennett@proclinical.com.
Apply Now:
If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
Related jobs
Highly Competitive
Berne, Switzerland
Ready to use your FMEA and GMP knowledge to identify risks, strengthen processes, and make a meaningful impact in a highly regulated industry?
Highly Competitive
Paris, France
Notre client recherche un Coordinateur QHSE Prestataires pour rejoindre leur équipe et intervenir sur le site de l'un de leurs clients majeurs en pharmaceutique.
€40000 - €75000 per annum
Normandy, France
Vous parlez couramment LEAN (5S, SMED et Kaizen)? Vous avez déjà transformé un atelier plus vite qu'un café ne refroidit ? On a un poste pour vous?
Highly Competitive
Basel, Switzerland
Join a high performing CMO where your quality expertise keeps site operations running with precision, efficiency, and flawless coordination.
US$20 - US$24 per hour + Highly Competitive Salary
Hoover, USA
Ready to grow your career in sterile compounding? Looking to join a thriving pharmaceutical operation and help deliver exceptional standards of quality and compliance.
Highly Competitive
Philadelphia, USA
Play a crucial role in advancing life-changing cell and gene therapies by ensuring GMP production environments remain audit-ready and contamination-free.
Highly Competitive
Bristol, USA
Join a team transforming the future of medicine through cutting-edge bioconjugation and gene therapy manufacturing.