About the Role

We are seeking a CQV Engineer to support the commissioning, qualification, and validation of pharmaceutical and biotechnology manufacturing facilities. The successful candidate will work closely with engineering, project, and quality teams to ensure systems, utilities, and equipment are commissioned and validated in compliance with GMP and regulatory requirements, enabling successful operational readiness.

Responsibilities

• Plan, coordinate, and execute commissioning, qualification, and validation (CQV) activities for pharmaceutical and biotechnology facilities, utilities, and process equipment.
• Prepare, review, and execute IQ, OQ, and PQ protocols and reports in accordance with GMP, GAMP 5, company procedures, and regulatory requirements.
• Work closely with engineering, project, quality, and construction teams to ensure CQV activities are completed according to project schedules.
• Investigate, troublesho...