QA Specialist II

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.