
Equipment Validation Specialist
3 days ago
About the Role:
As an Equipment Validation Specialist at GlaxoSmithKline, you will play a critical role in ensuring the compliance of our equipment and systems with regulatory requirements. This includes validation of SAT, DQ/EDR, IQ, OQ processes to guarantee quality management system (QMS) adherence.
Your Key Responsibilities:
- Ensure Computerized System Validation at site including Kneat, CSQMS and Periodic Compliance Review.
- Prepare and perform Periodic Compliance Review and Periodic Validation Review of all GxP equipment and utility systems.
- Update validation tracker and keep validation activities on track as per SVMP schedule.
- Lead New Validation which includes URS, SIA, RTM, DQ/DR, CVP/IOQ protocol and Validation Report.
- Track and inform Site Engineering Lead that all facilities, equipment, and operations are in line with regulatory and corporate requirements.
- Maintain complete documentation and record keeping of Validation and CSV documents.
Why this Role?
This is a fantastic opportunity to contribute to a leading biopharma company like GlaxoSmithKline, where science, technology, and talent come together to tackle disease.
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