Process Engineer (C&Q)
Location: Singapore
Duration: 6 month renewable contract
Start Date: May 2026
Role:
Overview We are supporting a GMP pharmaceutical manufacturing site in Singapore that is entering late-stage commissioning. An experienced Process C&Q Engineer is required to support the transition from IQ into OQ and PQ, working hands-on on the shop floor alongside Manufacturing, Engineering, Automation, and Quality teams. This is an execution-focused role, ideal for candidates with strong on-site commissioning and qualification experience. Key
Responsibilities
- Execute commissioning activities following completion of IQ.
- Lead and support OQ and PQ for process equipment and systems.
- Perform hands-on testing, challenge testing, and operational verification.
- Support system walkdowns, readiness checks, and engineering handover.
- Work closely with Manufacturing, Engineering, Automation, and QA during execution.
- Support start-up, trial runs, and performance runs.
- Assist with deviations, investigations, and troubleshooting during OQ/PQ.
- Execute qualification activities in line with GMP, GAMP 5, and site SOPs.
- Contribute to final qualification reports and inspection readiness
Required Experience
- 510+ years experience in Process Commissioning & Qualification within pharma or biopharma.
- Proven hands-on OQ and PQ execution experience.
- Strong process or plant background (e.g. upstream, downstream, formulation, fill-finish, utilities, packaging).
- Experience working on-site in live GMP manufacturing environments.
- Good understanding of GMP, GAMP 5, and the validation lifecycle.
