QA Specialist II

Anter Consulting Pte. Ltd.; Singapore; On-site; SGD 54,000 - 67,000; Full time

Job summary

Anter Consulting Pte. Ltd. seeks a QA Specialist II to support Quality Operations at a biologics manufacturing facility in Singapore. This is a 6-month renewable contract, onsite Monday to Friday, 8:00 am–5:00 pm, with onboarding targeting 19 October 2026.

You will oversee day-to-day GMP activities, review materials and batch records, support deviations and CAPA follow-ups, and participate in audits to maintain inspection readiness.

Qualifications

• 2–3 years of GMP-regulated experience in pharma/biotech.
• Knowledge of biologics and cell culture bioprocessing.
• Experience with GMP document review and batch records.
• Awareness of data integrity and good documentation practices.

Responsibilities

• Review incoming materials and release documentation (COA, supplier docs, records).
• Review SOPs and batch records for accuracy and compliance.
• Support QC activities and data integrity checks.
• Assist with deviations, investigations and CAPA follow-up.

Skills

GMP experience

Biologics knowledge

Document review

CAPA follow-up

Cross-functional communication

Education

Life Sciences degree/diploma

Tools

Electronic batch records

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.