Slough

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Job Description

Are you passionate about quality and compliance in the pharmaceutical space? We’re hiring a QA Associate to join a high-performing team at one of the world’s leading pharmaceutical organizations. This is a fantastic opportunity to contribute to life-changing products while growing your career in a dynamic, regulated environment.


Key Responsibilities

  • Perform batch record reviews and support lot disposition for clinical and commercial products
  • Review and approve deviations, CAPAs, change controls, and other quality documentation
  • Support internal and external audits, including inspection readiness and follow-up
  • Collaborate with cross-functional teams including manufacturing, QC, and regulatory affairs
  • Maintain and improve Quality Management Systems (QMS) in compliance with GMP standards
  • Author and revise SOPs, work instructions, and quality agreements


Required Knowledge, Skills, and Abilities