
Regulatory Compliance Specialist
1 day ago
About the Role
This exciting opportunity is open to experienced validators who want to take their career to the next level.
Key Responsibilities
- Site Master Validation Plan Development
- Develop and execute site master validation plans as per approved and scheduled planning.
- Qualification and Validation Monitoring
- Monitor and maintain the qualification and validation status of facilities, utilities, HVAC, equipment, processes, methods, and computer systems.
- Protocol Preparation and Authorization
- Prepare and obtain authorization for qualification and validation protocols as per applicable regulatory and cGMP requirements.
Why Choose Us?
At Pharmatec, we offer a dynamic and supportive work environment, collaborative teams, and opportunities for growth and development.
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