Biologics QA Specialist II — GMP & Compliance (Onsite)

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

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.