CQV Engineer: GMP-Ready Pharma Facility Validation

MORIMATSU PHARMADULE (SINGAPORE) PTE. LTD.; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

MORIMATSU PHARMADULE (SINGAPORE) PTE. LTD. is seeking a CQV (Commissioning, Qualification & Validation) Engineer to support the validation of pharmaceutical/Biotech manufacturing facilities. Responsibilities include managing CQV activities and ensuring compliance with regulatory requirements.

The ideal candidate will have a Bachelor's degree in Engineering or Life Sciences and 2–5 years of related experience. Familiarity with GMP and hands-on experience with utilities or cleanroom systems is highly preferred.

Qualifications

• 2–5 years of experience in commissioning/qualification/validation in pharmaceutical or biotech industries.
• Familiar with GMP, GAMP 5, ISPE Baseline Guides, and pharmaceutical regulations.
• Hands-on experience with utilities and process equipment preferred.

Responsibilities

• Plan, execute, and manage commissioning, qualification, and validation activities.
• Develop and review CQV protocols and reports.
• Coordinate with engineering, project, and quality teams.

Skills

Project coordination

GMP compliance

Troubleshooting

Communication skills

Education

Bachelor’s degree in Engineering or Life Sciences

Job description

MORIMATSU PHARMADULE (SINGAPORE) PTE. LTD. is seeking a CQV (Commissioning, Qualification & Validation) Engineer to support the validation of pharmaceutical/Biotech manufacturing facilities. Responsibilities include managing CQV activities and ensuring compliance with regulatory requirements.

The ideal candidate will have a Bachelor's degree in Engineering or Life Sciences and 2–5 years of related experience. Familiarity with GMP and hands-on experience with utilities or cleanroom systems is highly preferred.