About the role
We are working with one of our clients in the pharmaceutical space, and they are recruiting for a CQV Engineer. The candidate is responsible to ensure all systems meet GMP compliance and are ready for commercial production in plant projects.
Job Responsibilities
- Execute commissioning, qualification, and validation (CQV) activities for pharmaceutical/biotech facilities and equipment.
- Prepare and review IQ/OQ/PQ protocols and reports in compliance with GMP and GAMP 5.
- Collaborate with engineering, project, and quality teams to deliver CQV activities on schedule.
- Troubleshoot validation issues and ensure compliance with FDA, EMA, PIC/S, and other regulatory requirements.
- Support FAT, SAT, risk assessments, and project activities from design through operational readiness.
Job Requirements
- Degree in Engineering, Life Sciences, or a related field.
- 2–5 years' CQV experience in the pharmaceutical or biotech industry.
- Good knowledge of GMP, GAMP 5, ISPE, and pharmaceutical regulations.
- Experience with pharmaceutical utilities (WFI, clean steam, HVAC), process equipment, or cleanroom systems is an advantage.
How to Apply:
- Interested applicants may apply by sending in your updated résumé (in MS Word format) to my email or apply directly:
- Consultant: Tan Wei Xiang
- EA personnel reg. no.- R1658660
- EA License No. 17C8502
Millions of jobs, with real people getting hired every day
Questions, answered
Click "Apply with JobAssist" – we tailor your resume and application to this role and submit it for your approval.
Yes. This role at Integrity was screened before publishing – we confirmed the employer before listing it.
The employer didn't disclose a salary range for this listing. JobAssist shows pay whenever it's available.
This position can be done from anywhere, with no in-office requirement.
Yes – every application is tailored from your profile and this job's requirements, and you can review and edit before it's sent.