Job Description
Join a leading pharmaceutical manufacturing company as they look to expand their Quality Control Team. This is the perfect opportunity for someone looking to progress their career.
Responsibilities:
The QC Analyst will be responsible for coordinating and/or performing all laboratory activities including but not limited to
1. Have an understanding and competence in GLP and laboratory workflows.
2. Perform sampling, testing, release and investigation activities associated with materials in accordance with cGMP requirements.
3. Perform analytical testing including preparation and review of documentation and any investigations for in process and finished combination products in accordance with cGMP requirements.
4. Perform analytical testing and any investigations with external test laboratories to ensure compliance to cGMP requirements.
5. Support lab support activities (Sample Management, Chemical / Consumables management, Specification / Method management, Equipment Management) to ensure compliance with local procedures and GLP requirements.
6. Contribute to department Quality Management System deliverables (Deviations, CAPAs, Change control) as required.
Required Experience:
7. Level 8 qualification in scientific discipline
8. Minimum of 2 years experience in QC Testing Laboratory is required
9. Demonstrated understanding of pharmaceutical QC laboratory operations and GLP
Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.
BY APPLYING FOR THIS ROLE YOU ARE AGREEING TO OUR TERMS OF SERVICE WHICH TOGETHER WITH OUR PRIVACY STATEMENT GOVERN YOUR USE OF MORGAN MCKINLEY SERVICES.
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