CIP Engineer (CQV)

We are partnering with a premier, global bio-pharmaceutical engineering consultancy to secure a Process / CQV Engineer specialized in automated cleaning systems for a flagship multi-million dollar facility expansion in Singapore.

In this role, you won't just be pushing paper, you will own the technical crossover between engineering design review and validation lifecycle execution.

What the role is about:

• Engineering Review: Evaluating system blueprints (P&IDs), fluid transfer pathways, and spray mechanics to ensure cleanability and eliminate risk areas.
• C&Q Lifecycle Execution: Generating, managing, and executing comprehensive IQ/OQ/PQ protocols for complex processing units, chromatography skids, and purification networks.
• The Validation Science: Partnering with QA teams to execute cleaning validation metrics (swab/rinse sampling) to ensure flawless adherence to strict sterile manufacturing parameters (including EU GMP Annex 1).
• Automation Crossover: Reviewing automated cleaning sequences and phase recipes (DeltaV / Siemens frameworks) to ensure optimal system cycling.

What we are looking for:

• A degree in Mechanical, Chemical, Bioprocess, or Biomedical Engineering.
• 5+ years of practical track record within a cGMP Biologics or high-purity API facility.
• Direct, hands-on experience handling the qualification, troubleshooting, or parameter optimization of Clean-in-Place (CIP) systems and clean utilities (WFI, Purified Water).
• Familiarity with digital validation tools (e.g., Kneat) is a massive advantage but not a dealbreaker.
• Strong communication skills—you must be comfortable stepping up as a technical point-of-contact in front of project stakeholders and external vendors.

Only shortlisted candidates will be notified

EnviroDynamics Solutions Pte Ltd I EA License No.: 12C6285

Ng Chin Shen I Reg. No: R25127347

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