Manufacturing Deviation Investigation (Biopharma) #HMS

📍 Location: Tuas
📄 Contract Duration: 6 months, renewable / extendable
💰 Salary: Up to $7,000/month
🎁 Completion Bonus: 0.5 month upon completion
📅 Start Date: By end November 2026
👥 Vacancies: 2

Key Responsibilities

• Lead end-to-end manufacturing deviation investigations, from initiation and root cause determination through CAPA development and closure.

• Conduct Root Cause Analysis (RCA) using methodologies such as 5 Whys and Fishbone / Ishikawa.

• Facilitate cross-functional investigation meetings with Manufacturing, QA, QC, MSAT, Engineering and other stakeholders.

• Assess manufacturing deviations, process discrepancies and potential product quality impacts to support batch disposition and release.

• Develop, implement and monitor Corrective and Preventive Actions (CAPAs), including effectiveness checks.

• Prepare detailed deviation investigation reports, technical assessments and GMP documentation.

• Monitor investigation timelines and drive timely closure of deviations and CAPAs.

• Support deviation trending, recurring issue investigations and continuous improvement initiatives.

• Ensure investigation activities comply with GMP requirements, internal SOPs and applicable regulatory standards.

📩 Interested candidates, please send your updated CV to [email protected] OR Telegram @jocelynchan

Jocelyn Chan | Consultant | Recruit Express Pte Ltd (Healthcare & Lifescience)
Company EA Licence number : 99C4599
Personnel EA License: R1331820