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CQV Engineer
Job Description
We're Hiring: CQV Engineer
We are looking for Commissioning, Qualification and Validation (CQV) Engineers to join our pharmaceutical and life sciences clients in Singapore.
Location: Singapore
Key Responsibilities
- Prepare, execute and review CQV documentation
- Support commissioning and qualification activities for equipment, utilities and facilities
- Ensure work meets GMP and regulatory requirements
- Work closely with engineering, quality and vendor teams
- Maintain accurate, audit-ready records
Requirements
- Experience in CQV within a GMP-regulated environment
- Knowledge of GMP and validation practices
- Good documentation and communication skills
- Eligibility to work in Singapore
All experience levels are welcome to apply.
How to Apply
Send your CV to [Confidential Information] or apply directly via the link below. Only shortlisted candidates will be contacted.
#Hiring #CQV #Pharma #Validation #GMP #SingaporeJobs
More Info
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Key Skills
About Company
Skills:
Validation Lifecycle, Equipment Qualification, Documentation, CQV, Gmp, Temperature Mapping, Technical Writing
Skills:
IQ OQ PQ, Technical Writing, Documentation, CQV, temperature mapping, Gmp, Change Controls
Skills:
cleanroom systems, process equipment, GAMP 5, Hvac, ISPE Baseline Guides, CQV, clean steam, WFI, Gmp
Skills:
Commissioning, PQ, Validation, OQ, Sat, CQV, IQ, Gmp, Qualification, DQ, URS, FAT
Skills:
ISPE Baseline Guides, HEPA integrity testing, change controls, CQV, smoke studies, particle monitoring, requalification, airflow and velocity testing, Grade C D cleanrooms, FAT SAT commissioning, temperature humidity mapping, ductwork, air change calculations, ISO 14644, EU GMP Annex 1, Hvac, Good Documentation Practices, GMP-regulated facilities, deviation management, environmental controls, AHUs, pressurization checks, HEPA filtration