Do you thrive in a fast-paced, regulated environment and have a passion for detail?
This is your opportunity to join a leading pharmaceutical and biotechnology company in Harwell, where you'll play a critical role in ensuring the integrity of documentation and training.
As the QA Admin - Document Control & Training, you will:
- Maintain the heart of our documentation system: You'll oversee the entire lifecycle of controlled documents, including creation, maintenance, issuance, and archival.
- Keep our systems in tip-top shape: You'll ensure smooth and efficient document workflows, manage our cGMP documentation, and assist in implementing process improvements.
- Champion training excellence: You'll manage training requirements, track completion, and provide training when needed.
- Be a champion for compliance: You'll adhere to GxP regulations, Good Documentation Practices, and Data Integrity requirements, ensuring all documentation and records are accurate and readily available for audits and inspections.
What You'll Bring:
- Experience: 3-5 years of experience in a pharmaceutical or GMP environment.
- Expertise: Strong understanding of GxP regulations and document control best practices.
- Organization: Meticulous attention to detail and excellent organizational skills.
- Collaboration: You're a team player who can effectively collaborate with cross-functional teams.
This is your chance to:
- Make a real impact: Your work will directly contribute to the success of our pharmaceutical operations.
- Gain valuable experience: You'll grow your expertise in a fast-paced, dynamic environment.
- Become part of a leading company: You'll join a team dedicated to innovation and excellence.
If interested, please contact me at 0161 250 6795 or send your updated CV at dharanikumar. b @ randstad. co. uk
Randstad Business Support is acting as an Employment Business in relation to this vacancy.
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