Legatus Formworks Pte Ltd is seeking a Senior Quality Validation Specialist to oversee qualification and validation activities for laboratory systems and equipment within a pharmaceutical manufacturing environment. The ideal candidate should have extensive experience in a regulated setting, with specific knowledge in validation protocols and compliance requirements
Job Summary
Responsible for qualification and validation activities for laboratory systems and equipment within a pharmaceutical manufacturing environment.
Ensure strict compliance with GMP, data integrity, and regulatory requirements while maintaining accurate validation documentation.
Coordinate with cross-functional teams to support validation projects and ensure operational excellence.
Matching Summary
Match Score: 85
Legatus Formworks Pte Ltd is seeking a Senior Quality Validation Specialist to oversee qualification and validation activities for laboratory systems and equipment within a pharmaceutical manufacturing environment. The ideal candidate should have extensive experience in a regulated setting, with specific knowledge in validation protocols and compliance requirements.
Skills & Requirements
Must-have
IQ OQ PQ protocol execution
GMP regulatory compliance
Data integrity requirements
Validated laboratory systems
Automated system support
Nice-to-have
Cross-functional team coordination
Strong analytical documentation skills
System relocation and retirement experience
Key Requirements
Minimum of 5 years in regulated pharmaceutical manufacturing
At least 3 years hands-on experience in validated laboratory systems
Diploma or Bachelor's Degree in Engineering or Life Sciences