GMP QA Officer β€” Documentation & QMS Specialist in Essex

GMP QA Officer β€” Documentation & QMS Specialist in Essex

Essex Full-Time 30000 - 40000 Β£ / year (est.) No working from home possible
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At a Glance

  • Tasks: Manage controlled documentation and support quality audits in a GMP environment.
  • Company: Leading pharmaceutical organisation in Essex with a focus on quality assurance.
  • Benefits: Opportunity for career advancement and contribution to quality initiatives.
  • Other info: Great chance to grow your career in a regulated industry.
  • Why this job: Join a dynamic team and make a real impact in the pharmaceutical sector.
  • Qualifications: Experience in pharmaceuticals or biotechnology and knowledge of electronic QMS systems.

The predicted salary is between 30000 - 40000 Β£ per year.

CY Partners is recruiting for a Pharmaceutical QA Officer to join a leading pharmaceutical organization in Essex.

This role requires managing controlled documentation, supporting quality audits, and maintaining quality records within a GMP-regulated manufacturing environment.

The ideal candidate should have experience in the pharmaceutical or biotechnology sector and be skilled in using electronic QMS systems.

This is an excellent opportunity to advance your career while contributing to quality assurance initiatives.

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Contact Details:

CY Partners Recruitment Team

We think you need these skills to ace GMP QA Officer β€” Documentation & QMS Specialist in Essex

GMP Knowledge
Quality Assurance
Controlled Documentation Management
Quality Audits Support
Quality Records Maintenance
Experience in Pharmaceutical Sector
Experience in Biotechnology Sector