Thermo Fisher Scientific·17 days ago
17 days ago
Manager, Document Control - Quality Systems & Compliance
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About this role
Seeking a leader to oversee document control and training compliance for a large sterile injectable pharmaceutical manufacturing site. Drive governance of electronic document management systems, ensure compliance with cGMP and regulatory standards, and lead a high-performing compliance team. Ideal for experienced professionals in GMP environments with strong leadership and technical expertise.
Skills
- gmp document control
- training compliance
- electronic document management systems
- records management
- learning management systems
- quality systems governance
- cgmp
- good documentation practices
- regulatory inspections
- audit readiness
- capa implementation
- change control
- version control
- access control
- traceability
- archival practices
- continuous improvement
- lean manufacturing
- six sigma
- instructional design
- training lifecycle management
- data integrity
- sterile manufacturing
- aseptic processing
- pharmaceutical quality systems
- cross-functional leadership
- team development
- change management
- problem solving
- analytical skills
Company
Thermo Fisher Scientific
Greenville, United States of America
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