Responsible for qualification and validation activities for laboratory systems and equipment, ensuring compliance with GMP and regulatory requirements within a pharmaceutical manufacturing environment.

• 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.

• Diploma or Bachelor's Degree in Engineering, Life Sciences, or related field.
• Minimum of 5 years of experience in a regulated pharmaceutical manufacturing environment.