Editorial summary

The company is seeking a QA Specialist for a one-year contract within a pharmaceutical multinational corporation, based in Ubi. The role involves ensuring proper documentation practices, data integrity, and supporting regulatory inspections and site visits. Candidates should have relevant experience in quality assurance processes, with a focus on record management and change control. The position offers a salary of up to $4,000 per month and standard office hours from Monday to Friday.

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

Job description

[This job id 28893 first appeared in Job-Q.com on 31 Aug 2026]

Salary: up to $4000
Duration: 1 year

Working Days & Hours: Mon-Fri Office Hours

Location: Ubi

Job Description:

Responsible for timely archiving or records, checking for good documentation practices and data integrity.

Participate in the preparation of records and QA files in preparation for sponsor site visits and regulatory inspections. May participate in the support of client site visits.

Supports change management processes including monitoring of activities, action verification and its due date and working closely with other departments to ensure timely completion of actions.

Supports the quality system operations such as monitoring of investigation due dates, CAPAs, Internal audit completion, test protocol approvals and working with other department to ensure timely closure or extension.

Review quality records such as logbooks and manage its issuance.

Approve customer test reports and participate in reagent, equipment and facility release activities to support laboratory operations.

Assist in monitoring and verifying training and document management activities.

Performs all functions as tasked with high degree of accuracy and strict adherence to company’s quality requirements.

Maintains proper records and documentation of activities that are compliant with good documentation practices, continuous compliance ISO/IEC 17025, cGMP, PIC/S, Company global SOPs and data integrity principles for all activities.

Assists in quality system projects that involved system implementation for cGMP compliance

Job Requirements: Min Degree in Life Sciences or similar w min 2 yrs of relevant experience & QA 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

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