QA Technical Specialist (6 months/PHARMA MNC) - West/up to $7k #HAO

Your tasks

• 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.

Requirements

Job Requirements: Min Degree in Life Sciences or similar w min 5 yrs of relevant experience & QA ops in pharmaceutical industry

What we offer

Salary: up to $7000 + 0.5m completion bonus Duration: 6 months renewable

How to apply

Interested candidates, please submit your resume to: allylok@recruitexpress.com.sg

allylok@recruitexpress.com.sg

Other

Working Days & Hours: Mon-Fri Office Hours

Location: Tuas (islandwide company pickup)

Personnel EA License: R21102307