Editorial summary

The company is seeking a QA Technical Specialist for a 6-month engagement (renewable) in a GMP-regulated biopharmaceutical manufacturing environment. The role involves leading end-to-end manufacturing deviation investigations as the deviation owner, driving RCA using structured methods (e.g., 5 Whys, Fishbone/Ishikawa), and developing and closing CAPA plans. Key requirements include strong experience in deviation investigations within biopharma, familiarity with RCA tools, and the ability to manage investigations from initiation to closure. Compensation is up to USD 7,000 per month, plus a completion bonus of USD 0.5 million, with work requirements on a Mon-Fri schedule in the Tuas area.

This summary is AI-generated and may contain inaccuracies. Please refer to the full job description below.

Job description

[This job https://singapore.job-q.com/jobs/detail/qa-technical-specialist-6-months-pharma-mnc-west-up-to-7k-hao-40771 first appeared in Job-Q.com on 30 Oct 2026]

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:

Ally Audrey Lok Xin Woon

Recruit Express Pte Ltd (Healthcare & Lifescience)

Company EA Licence number : 99C4599

Personnel EA License: R21102307

Scam prevention reminder: You should not make any pre-payment when applying for any job.

Illegal practices reminder: It is illegal for recruiter to collect payment (kickback) from the worker https://www.mom.gov.sg/-/media/mom/documents/publications/foreign-workers/what-are-kickbacks.pdf