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

PPD (Thermo Fisher)

Swindon, United Kingdom
Not specified; not specified; not specified
3 years qa experience in sterile manufacturing
Adherence to gmp and cgmp standards
Cleanroom gowning and safety protocols
This role offers the opportunity to join a top-tier manufacturing team at the Swindon, UK site specializing in sterile pharmaceutical production

Job Summary

  • This role offers the opportunity to join a top-tier manufacturing team at the Swindon, UK site specializing in sterile pharmaceutical production.
  • You will ensure high-quality production by proactively identifying operational issues and driving continuous improvement in a fast-paced environment.
  • The position involves hands-on quality assurance oversight including reviewing sterilization cycles, managing logbooks, and conducting cleanroom physical checks.

Matching Summary

This role offers the opportunity to join a top-tier manufacturing team at the Swindon, UK site specializing in sterile pharmaceutical production.

Salary

Not specified; Not specified; Not specified

Skills & Requirements

Must-have

  • 3 years QA experience in sterile manufacturing
  • Adherence to GMP and cGMP standards
  • Cleanroom gowning and safety protocols
  • Batch record review and LIMS/SAP usage
  • Sterilization cycle and FMS system knowledge

Nice-to-have

  • Proactive continuous improvement mindset
  • Strong interpersonal communication skills
  • Experience with CAPA and DR generation
  • Ability to challenge behaviors confidently

Key Requirements

  • Minimum 3 years of QA experience
  • Previous sterile aseptic pharmaceutical manufacturing experience
  • Knowledge of MHRA and FDA regulatory standards

Work Rights

Not specified

Tailored Resume

Cover Letter