Qa Officer (gmp Environment) - (2 Positions Available)

Thermo Fisher Scientific UK

Covingham, United Kingdom
**
Gmp environment adherence
Sterile pharmaceutical production
Cleanroom operations and gowning
** Thermo Fisher Scientific is seeking two QA Officers to join their team in Covingham, UK, focusing on quality assurance within a sterile pharmaceutical manufacturing environment. Candidates should have at least three years of experience in a related field and be prepared for rotational shifts in a cleanroom setting. **

Job Summary

  • As a member of our Quality Assurance team, you'll help enable our mission of making the world healthier, cleaner and safer through quality oversight of pharmaceutical manufacturing operations.
  • This is a hands-on, high-impact role for candidates with at least 3 years of experience in sterile manufacturing or a related pharmaceutical environment.
  • You will ensure high-quality production, proactively identify and resolve operational issues, and help drive continuous improvement in a fast-paced, innovative setting.

Matching Summary

Match Score: 75

** Thermo Fisher Scientific is seeking two QA Officers to join their team in Covingham, UK, focusing on quality assurance within a sterile pharmaceutical manufacturing environment. Candidates should have at least three years of experience in a related field and be prepared for rotational shifts in a cleanroom setting. **

Skills & Requirements

Must-have

  • GMP environment adherence
  • Sterile pharmaceutical production
  • Cleanroom operations and gowning
  • Review sterilization cycles and controls
  • Online batch record review
  • Standard Operating Procedures maintenance
  • Cleanroom physical checks

Nice-to-have

  • Continuous improvement and problem-solving
  • Effective communication and collaboration
  • Mentoring and training staff

Key Requirements

  • Minimum 3 years of experience in a QA position
  • Previous experience in sterile, aseptic pharmaceutical manufacturing or related controlled, GMP environments is essential
  • Strong knowledge of cGMP and regulatory requirements
  • Experience with clean room operations and gowning procedures preferred

Work Rights

Not specified

Tailored Resume

Cover Letter