Sr Document Control Administrator
Thermo Fisher Scientific · Grand Island, NY
QualityFull timeCompany career page
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Role summary
Senior Document Control Administrator position at Thermo Fisher Scientific in Grand Island, New York. Manages documentation processes and ensures GMP compliance across operations, coordinating change control procedures and supporting quality assurance initiatives.
What they're looking for
- Minimum 2 years document control or quality systems experience in regulated environment
- Proficiency in document management systems (Agile, SAP, OCPLM, TrackWise, E1)
- Strong working knowledge of GMP requirements and documentation practices
- Advanced Microsoft Office skills, particularly Excel and Word
- Experience with change control procedures and quality management systems
- Excellent written and verbal communication skills
- Ability to manage multiple priorities and meet deadlines
What you'll be doing
- Manage and optimize document control processes supporting GMP-compliant operations
- Coordinate change control procedures for critical documentation
- Ensure compliance with GMP standards across cross-functional teams
- Review batch records and maintain documentation accuracy
- Support quality assurance of products and services
Compensation$19.83–$29.74 hourly
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.