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:
* Have an understanding and competence in GLP and laboratory workflows.
* Perform sampling, testing, release and investigation activities associated with materials in accordance with cGMP requirements.
* Perform analytical testing including preparation and review of documentation and any investigations for in process and finished combination products in accordance with cGMP requirements.
* Perform analytical testing and any investigations with external test laboratories to ensure compliance to cGMP requirements.
* Support lab support activities (Sample Management, Chemical / Consumables management, Specification / Method management, Equipment Management) to ensure compliance with local procedures and GLP requirements.
* Contribute to department Quality Management System deliverables (Deviations, CAPAs, Change control) as required.
Required Experience:
* Minimum of 2 years experience in QC Testing Laboratory is required.
* Demonstrated understanding of pharmaceutical QC laboratory operations and GLP.
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