Similar posts
QC Associate
- Contract
- Good Manufacturing Practice (GMP)
- Switzerland
This vacancy has now expired. Please see similar roles below...
Join a dynamic team at a leading Contract Manufacturing Organisation (CMO) and contribute to groundbreaking projects and cutting-edge solutions.
Proclinical is seeking a QC Associate to join the Bioanalytics Microbial Team, focusing on the release analytics of biopharmaceutical substances for clinical and commercial use. This role requires adherence to GMP and safety guidelines, with an emphasis on quality and timely completion of assigned tasks.
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:
- Plan and co-manage the execution of release analytics.
- Implement, optimize, transfer, and validate analytical methods, particularly in biochemical analysis such as SDS-PAGE, qPCR, ELISA, and plate assays.
- Provide expertise in technical and analytical inquiries.
- Extract, evaluate analytical data, and prepare reports and presentations.
- Handle change requests and deviations under GMP.
- Create, review, and approve documents to ensure compliance with regulatory guidelines.
- Collaborate closely with other QC groups, research, production, and quality assurance teams.
Key Skills and Requirements:
- Proficiency in biochemical analytical techniques.
- Strong analytical and problem-solving skills.
- Ability to work independently and manage projects.
- Excellent communication and collaboration abilities.
- Familiarity with GMP regulations and documentation processes.
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 applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists 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.
By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.proclinical.com/privacy-policy
Related jobs
US$140000 - US$160000 per annum
Newark, USA
Are you passionate about GMP quality assurance and CMC Operations? Join our client and help ensure top-tier standards every day.
Highly Competitive
Newark, USA
Lead quality with confidence-shape the future of innovative therapies while ensuring the highest standards of GMP compliance.
Highly Competitive
Waterford, Republic of Ireland
Are you ready to safeguard quality, ensure compliance, and make a real impact in a GMP-driven environment?
Highly Competitive
Boston, USA
Ensuring compliant product release while strengthening quality systems across the manufacturing lifecycle.
Highly Competitive
Clayton, USA
Be the backbone of innovation and join a leading pharmaceutical company to help keep life-changing science moving forward!
Highly Competitive
Berne, Switzerland
Ready to safeguard quality at the heart of aseptic manufacturing and make a real impact in a cutting-edge pharmaceutical environment?
Highly Competitive
Cologne, Deutschland
Be the guardian of quality on the shopfloor, ensuring every batch meets world‑class GMP standards.
Highly Competitive
Brussels, België
Step into a leadership role where your expertise in evidence quality supports innovation, compliance, and successful global product launches.