The posting
Salary: up to $7000 + 0.5m completion bonus Duration: 6 months renewable
Working Days & Hours: Mon-Fri Office Hours
Location: Tuas (islandwide company pickup)
Job Description:
* Lead and manage end-to-end manufacturing deviation investigations within a GMP-regulated biopharmaceutical manufacturing environment.
* Act as the deviation owner, driving investigations from initiation through root cause determination, CAPA development and closure.
* Conduct Root Cause Analysis (RCA) using structured investigation methodologies such as 5 Whys, Fishbone/Ishikawa and other relevant tools.
* Facilitate and lead cross-functional investigation meetings involving Manufacturing, QA, QC, MSAT, Engineering and other relevant stakeholders.
* Assess manufacturing deviations, process discrepancies and potential product quality impacts to support timely batch disposition and release.
* Develop, implement and monitor Corrective and Preventive Actions (CAPAs), including effectiveness checks to prevent recurrence.
* Prepare comprehensive deviation investigation reports, technical assessments and supporting GMP documentation.
* Monitor investigation timelines, manage outstanding actions and ensure timely closure of deviations and CAPAs.
* Support deviation trending, recurring issue investigations and continuous improvement initiatives.
* Ensure all investigation activities comply with GMP requirements, internal SOPs and applicable regulatory standards.
Job Requirements: Min Degree in Life Sciences or similar w min 5 yrs of relevant experience & QA ops in pharmaceutical industry
Interested candidates, please submit your resume to: [email protected]
Ally Audrey Lok Xin Woon
Recruit Express Pte Ltd (Healthcare & Lifescience)
Company EA Licence number : 99C4599
Personnel EA License: R21102307



