Biotech QA Executive: GMP, CAPA & Compliance Lead

No deviation; Singapore; On-site; SGD 40,000 - 60,000; Full time

Job summary

A dynamic engineering consultancy in Singapore is seeking a QA Executive to support quality assurance activities in a biomedical/biotech manufacturing environment. The role involves ensuring compliance with quality standards, managing deviations, and maintaining robust documentation. Ideal candidates will bring at least 2 years of QA experience, strong knowledge of QMS processes, and attention to detail. This position offers opportunities for professional development and a generous leave policy.

Benefits

Generous Leave Policy

Comprehensive Health & Wellness Coverage

Professional Development Opportunities

Inclusive Culture

Qualifications

• Minimum 2 years of QA experience in a biomedical or biotech manufacturing environment.
• Strong familiarity with QMS processes, including deviations, CAPA, and change control.
• Experience in quality review of batch records.
• Working knowledge of warehouse and inventory management from a QA perspective.
• Good understanding of GMP and quality compliance requirements.
• Ability to work independently and meet deadlines in a fast-paced environment.

Responsibilities

• Support day-to-day QA activities within a biomedical/biotech manufacturing setup.
• Review batch records and ensure compliance with GMP expectations.
• Manage QMS activities, including deviations and CAPA.
• Ensure proper documentation control and timely closure of quality records.
• Collaborate with cross-functional teams to meet quality standards.
• Participate in internal audits and assist in regulatory inspections.

Skills

QA experience

Familiarity with QMS processes

Batch record review

Warehouse and inventory management

GMP understanding

Strong communication skills

Attention to detail

Job description

A dynamic engineering consultancy in Singapore is seeking a QA Executive to support quality assurance activities in a biomedical/biotech manufacturing environment. The role involves ensuring compliance with quality standards, managing deviations, and maintaining robust documentation. Ideal candidates will bring at least 2 years of QA experience, strong knowledge of QMS processes, and attention to detail. This position offers opportunities for professional development and a generous leave policy.