Position Details
About this role
Provide quality oversight for computer system validation and data management activities at a pharmaceutical manufacturing site, ensuring compliance with GMP and regulatory standards.
Key Responsibilities
- Oversee computer system validation
- Ensure data integrity and management
- Support GMP manufacturing
- Prepare for regulatory inspections
- Mentor data and QA teams
Technical Overview
Validation of computer systems, data integrity and management, GMP compliance, regulatory inspection readiness, data governance.
Ideal Candidate
The ideal candidate is a senior QA professional with 5+ years experience in computer system validation, data integrity, and GMP within pharmaceutical manufacturing, capable of leading validation and data oversight activities.
Must-Have Skills
Nice-to-Have Skills
Tools & Platforms
Required Skills
Hard Skills
Soft Skills
Industry & Role
Keywords for Your Resume
Deal Breakers
Lack of experience with computer system validation, No pharmaceutical or GMP background, No data integrity expertise, No leadership or mentoring experience
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