Quality System Coordinator
3 days ago
Quality Document Administrator
Job Summary
Serve as a key member of the Document Control team at Almac Group, playing a crucial role in maintaining the company's Quality system. The post holder will be responsible for managing the compilation, issuance, and review of GMP documentation, generating various documents in approved formats, and ensuring the organization of Document Control storage areas.
Key Responsibilities
- Manage the compilation, issuance, and review of GMP documentation
- Generate various GMP documents, such as Manufacturing and Packaging Specifications, SOPs, and validation documentation
- Issue batch records, circulate quality system-related documentation, and manage controlled documents
- Collaborate with different departments to retrieve and distribute GMP documentation, maintain quality system indexes, and participate in data collation for QA reports and investigations
- Participate in investigations, trending quality performance indicators, and tracking GMP-associated documentation to support continuous improvement initiatives
Requirements
- Previous experience within a quality system or manufacturing environment
- Eligibility to work in the UK or possess a valid work permit
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