BMR Reviewer Specialist
Thermo Fisher Scientific · Wiltshire, UK
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
Thermo Fisher Scientific seeks Batch Record Reviewer Specialists to support GMP-regulated manufacturing operations in Swindon. The role involves reviewing batch manufacturing records for compliance, providing documentation feedback to production teams, and driving continuous improvement in a 24/7 rotating shift environment.
What they're looking for
- Proven knowledge of Good Manufacturing Practice (GMP) principles and guidelines
- Experience in pharmaceutical, biopharmaceutical, or medical device manufacturing
- Experience reviewing or completing controlled manufacturing documentation
- Strong attention to detail and ability to identify compliance risks
- Excellent written and verbal communication skills
- Proficiency in Microsoft Office and general computer literacy
- Ability to work 24/7 rotating shifts including nights, weekends, and holidays
What you'll be doing
- Review Batch Manufacturing Records for accuracy, completeness, and GMP compliance
- Identify documentation errors and trends, providing coaching to production operators
- Track batch record review progress and ensure timely completion within SAP
- Draft and maintain manufacturing documentation including SOPs and Master Batch Records
- Support deviation investigations, change controls, and CAPA implementation
Privacy & handoff
This role links to Thermo Fisher Scientific's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.