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.
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