GE HealthCare·19 days ago
19 days ago
Director, Central Quality Audit, Pharmacovigilance
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About this role
Become part of our team as Director, Central Quality Audit, Pharmacovigilance, leading the development and execution of global audit strategies to ensure compliance with regulatory standards. Oversee audit operations and collaborate with cross-functional teams. Ideal for experienced pharmacovigilance professionals with strong leadership and regulatory expertise.
Skills
- pharmacovigilance audit
- pharmacovigilance program management
- qualified lead auditor certification
- pharmaceutical quality management system
- cgmp compliance
- gdp compliance
- gpvp compliance
- gcp compliance
- glp compliance
- audit operations
- team leadership
- fda regulatory compliance
- ema regulatory compliance
- mhra regulatory compliance
- pmda regulatory compliance
- risk identification
- performance management
- cross-functional collaboration
- medical device qms
- fda cfr 21 820
- iso 13485
- veeva
- trackwise
- irca certification
- asq certification
- lean certification
- six sigma
- dfr
Company
GE HealthCare
99999, United States of America
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