The role focuses on developing and executing validation strategies to ensure compliance with regulatory standards in pharmaceutical environments
Job Summary
The role focuses on developing and executing validation strategies to ensure compliance with regulatory standards in pharmaceutical environments.
Candidates will be responsible for investigating deviations, implementing corrective actions, and supporting global packaging changes as a subject matter expert.
The company offers a generous leave policy, comprehensive health coverage, and opportunities for professional development within an inclusive culture.
Matching Summary
Match Score: 75
The role focuses on developing and executing validation strategies to ensure compliance with regulatory standards in pharmaceutical environments.
Skills & Requirements
Must-have
4 years pharmaceutical manufacturing experience
2 years validation protocol creation
GMP compliance knowledge
IQ OQ PQ execution
Deviation investigation and CAPA
Nice-to-have
Packaging validation experience
Labeling review expertise
Risk assessment skills
Cross-functional collaboration
Vendor management capabilities
Key Requirements
Minimum 4 years pharmaceutical or medical device experience
At least 2 years creating or approving validation protocols
Experience with GMP compliance and deviation management