Validation Engineer (MNC/pharmaceutical)

Key Responsibilities

• Execute CQV activities for GMP-regulated pharmaceutical and biopharmaceutical facilities.
• Prepare and review validation documents, including plans, IQ/OQ/PQ protocols, test scripts, and reports.
• Support validation of equipment, utilities, facilities, and computerized systems in compliance with GMP, GAMP 5, and 21 CFR Part 11.
• Coordinate with Engineering, QA, clients, and vendors on validation activities.
• Conduct risk/impact assessments, deviation investigations, and CAPA.
• Support FAT, SAT, commissioning, and qualification of new equipment and systems.
• Maintain accurate validation records and data integrity.

Requirements

• Bachelor’s Degree in Engineering, Life Sciences, Pharmaceutical Sciences, or related field.
• 3–5 years of CQV/validation experience in pharmaceutical or biopharmaceutical industries.
• Strong documentation, analytical, problem-solving, and communication skills.
• Experience with equipment, utilities, cleanrooms, HVAC, water systems, or CSV is preferred.
• Knowledge of FDA 21 CFR Part 11, EU GMP, GMP, GAMP 5, and data integrity.

For interested applicant, kindly send your resume in Word/PDF format, include the following informations:

1. Current Salary

2. Expected Salary

3. Availability

4. Reason for leaving

Thank you for your application and we regret that only shortlisted applicants will be notified

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RRECRUITER INT PTE. LTD. | 22C1414