Quality Assurance Documentation Specialist

hace 7 días

Cartagena, Murcia, España beBee Careers A tiempo parcial

Job Title: Quality Assurance Documentation Specialist

Salary and Benefits

We offer a competitive salary and a comprehensive benefits package, including up to 25 days annual leave (pro-rata) and the opportunity to purchase additional holiday time.

Job Description

This role involves managing and maintaining quality-critical documents, ensuring compliance with current Good Manufacturing Practices (cGMP), regulatory requirements, and company policies.

  • Create, review, and issue quality-critical documents such as SOPs, Work Instructions, specifications, and logbooks.
  • Maintain compliance of documentation processes with internal procedures and external regulatory requirements.
  • Manage document archiving in line with company record retention schedules.
  • Generate and manage manual Certificates of Analysis (CofAs).
  • Issue and verify batch documentation for accuracy and compliance.
Responsibilities and Requirements

The ideal candidate will possess excellent communication skills, be highly organized, and have experience working in a Quality Systems/Pharmaceutical environment. They should also have knowledge of data integrity principles, electronic document management systems, and tools such as DocuSign.

  • Educated to A-Level standard or equivalent.
  • Minimum 1-2 years' experience working in a Quality Systems/Pharmaceutical environment.
  • Familiarity with Microsoft Office software.
  • Experience with electronic document management systems and tools.
About This Role

This is an on-site position at our Romford location. The successful candidate will work independently and collaboratively, managing multiple priorities and meeting deadlines.

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