Job Summary Responsible for qualification and validation activities for laboratory systems and equipment, ensuring compliance with GMP and regulatory requirements within a pharmaceutical manufacturing environment.
Key Responsibilities - Perform qualification and validation activities for laboratory systems and equipment.
- Execute and support IQ, OQ, and PQ protocols and reports.
- Support implementation, requalification, relocation, and retirement of validated systems.
- Ensure compliance with GMP, data integrity, and regulatory requirements.
- Maintain accurate validation documentation and records.
- Coordinate with cross-functional teams to support validation projects and system compliance.
Qualifications - Diploma or Bachelor's Degree in Engineering, Life Sciences, or related field.
- Minimum of 5 years of experience in a regulated pharmaceutical manufacturing environment.