Assoc. Scientist - Technical Development
- Contract
- Good Manufacturing Practice (GMP)
- Switzerland
Proclinical is seeking a Quality Control Specialist to support the release and stability strategy, method validation, and transfer activities for biologics. The successful candidate will manage GMP testing operations for clinical drug substances and products, ensuring documentation meets timelines and standards.
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:
- Deliver work packages for GMP testing of biologics for release, stability, validation, and transfer.
- Author and review technical documents for global submissions.
- Review CMC documentation for health authority submissions.
- Conduct instrument qualification and decommissioning as a System Owner.
- Support shipment desk as a Sample Management Officer.
Key Skills and Requirements:
- Strong planning, organizational, problem-solving, and interpersonal skills.
- Effective communication with a collaborative, patient-focused approach.
- Proficient in computer and IT systems.
- Science degree in Chemistry, Pharmacy, Biochemistry, Molecular Biology, Biotechnology, Biology, or equivalent.
- Experience in Quality Control within a GMP environment or pharmaceutical industry.
- Technical and scientific knowledge of pharmaceutical development and analytical sciences.
- Understanding of health authority regulations.
- Ability to critically evaluate data from various scientific disciplines.
- Proficient in English; additional languages are a plus.
If you are having difficulty in applying or if you have any questions, please contact Emile De Beer at e.debeer@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
Visp, Switzerland
Proclinical is seeking a CQV Engineer to join our client's team on a contract basis.
Highly Competitive
Cambridge, USA
Proclinical is working alongside a pharmaceutical company seeking a Quality Assurance Specialist to join their team.
Highly Competitive
Visp, Switzerland
Proclinical is currently working alongside a contract manufacturing organisation to recruit for a QC Analyst. This is a temporary contract position based in Visp, Switzerland.
Highly Competitive
Visp, Schweiz
Proclinical is seeking a QA Operations Specialist to join our client's team in Visp.
Highly Competitive
Visp, Schweiz
Proclinical is seeking a QA Specialist to join our client's team in Visp, Switzerland. This is a contract role.
Highly Competitive
Neuchâtel, Switzerland
Proclinical is currently working alongside a pharmaceutical company seeking a QA Expert Senior to join the QA Team.
£45000 - £50000 per annum
Windsor and Maidenhead, England
Proclinical is currently working alongside a pharmaceutical company to recruit for a QA Manager, GMP. This is a permanent position based in Surrey, UK or Lyon, France.
Highly Competitive
Visp, Switzerland
Proclinical is seeking a Quality Engineering Specialist to join our client's team in Visp, Switzerland.
Highly Competitive
Neuchâtel, Switzerland
Proclinical is currently working alongside a pharmaceutical company seeking a QC Associate Scientist to join their team on a contract basis.
Highly Competitive
Visp, Switzerland
Proclinical is seeking a QA Specialist to join our client's team on a contract basis.