Job Description

We are seeking a QA Specialist II to support Quality Operations at a biologics manufacturing facility in Singapore. This is a 6-month renewable contract, working onsite Monday to Friday, 8:00 am-5:00 pm. Target onboarding is 19 October 2026.

The role provides day-to-day quality oversight of manufacturing activities to ensure compliance with GMP, approved SOPs and site quality standards.

Responsibilities:

Review incoming materials for release, including Certificates of Analysis, supplier documents, and receipt and inspection records.
Review SOPs, work instructions, executed batch records and other GMP documents for accuracy, completeness and compliance.
Support QC activities and check associated records for data integrity.
Participate in discussions of deviations and quality events, including impact assessments, investigations and CAPA follow-up.
Work with Manufacturing, QC, Warehouse and Engineering to resolve quality issues and maintain inspection readiness.
Support audits, regulatory inspections and continuous improvement activities as required.

Requirements

At least 2-3 years of relevant experience in a GMP-regulated environment pharmaceutical or biopharmaceutical experience is preferred.
Working knowledge of biologics and cell culture bioprocessing, with some Quality Operations or on-the-floor QA experience.
Experience with GMP document and SOP review, incoming material release, deviation management and batch record review. Electronic batch record experience is an advantage.
Understanding of data integrity principles and good documentation practices.
Diploma or degree in Life Sciences, Biotechnology, Chemistry, Pharmaceutical Science or a related discipline. A degree is not required.
Strong attention to detail and communication skills, with the ability to work across teams and contribute quickly in a manufacturing environment.