QA Specialist Trainee — Biotech Quality & Compliance

Roche; Singapore; On-site; SGD 60,000 - 90,000; Full time

Job summary

Roche Singapore is seeking a quality-focused professional to oversee QA for investigational and commercial products, ensuring compliance with global Roche PQS and local site requirements. The role includes batch record review, escalation of quality issues, and participation in cross-functional initiatives.

The ideal candidate has a Life Sciences or Engineering degree with 1–3 years of related experience and solid knowledge of cGMP and GDP. Shift flexibility and strong communication are essential.

Qualifications

• Degree in Life Sciences or Engineering discipline or equivalent.
• 1-3 years of related working experience for degree holders or equivalent holders with combination of education and relative work experience.
• Related working experience in a biotech or pharmaceutical operating environment is a plus.
• Good knowledge of cGMP and GDP relevant to the pharmaceutical industry.

Responsibilities

• Perform batch record, batch reports, logbook, cGMP documents and audit trail review to ensure quality of product, compliance to Roche requirements and on-time batch disposition per defined adherence to lead time.
• Provide guidance on categorization of unplanned events and GMP area, Utilities and equipment release.
• Review and approve discrepancies justification for resuming GMP processing.
• Execute Periodic Floor Walk and other assigned tasks while meeting timelines to achieve department objectives.
• Notify Senior Management of potential quality, regulatory and compliance issues.

Skills

QA oversight

GMP knowledge

cGMP

Batch review

Quality mgmt

Problem solving

Lean Production

Education

Life Sciences or Eng

Job description

Roche Singapore is seeking a quality-focused professional to oversee QA for investigational and commercial products, ensuring compliance with global Roche PQS and local site requirements. The role includes batch record review, escalation of quality issues, and participation in cross-functional initiatives.

The ideal candidate has a Life Sciences or Engineering degree with 1–3 years of related experience and solid knowledge of cGMP and GDP. Shift flexibility and strong communication are essential.