Job Description
CQV Engineer | Pharmaceutical & Biopharmaceutical Projects | Singapore
Looking for your next CQV opportunity
We're looking to connect with CQV Engineers in Singapore who are open to exploring opportunities within the Life Sciences industry.
What you'll be doing
• Supporting Commissioning, Qualification & Validation activities for pharmaceutical/biopharmaceutical facilities, equipment and systems
• Preparing and executing URS, FAT, SAT, DQ, IQ, OQ and PQ documentation
• Supporting equipment start-up, commissioning and qualification activities
• Working closely with Engineering, QA, Automation and Project teams
• Reviewing technical documentation, drawings and vendor documentation
• Supporting deviations, change controls and other CQV-related activities
• Ensuring activities are carried out in line with GMP and project requirements
What we're looking for
• Degree/Diploma in Engineering, Life Sciences, Biotechnology, Chemistry or a related discipline
• Experience in CQV / C&Q / Commissioning / Qualification / Validation
• Experience within pharmaceutical, biopharmaceutical or other GMP environments
• Familiarity with IQ/OQ/PQ, FAT/SAT, URS and validation documentation
• Good communication and documentation skills
Fresh graduates with relevant internship/project experience may also be considered for junior opportunities.
If you're interested in gaining broader exposure across Life Sciences projects and developing your CQV career, apply through LinkedIn with your updated CV.
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