Quality Assurance Lead – Batch Release & Compliance

Sanofi Group; Singapore; Hybrid; SGD 70,000 - 90,000; Full time

Job summary

Sanofi Group in Singapore seeks a QA Specialist to partner with GMP operations and validation teams to ensure quality and compliance across batch records, release and investigations. You will manage complex deviations, CAPA actions and risk assessments while supporting continuous improvement initiatives.

The role requires 3–5 years of pharma quality operations experience, a degree in engineering or science, and strong communication skills to interact with cross-functional teams.

Qualifications

• Engineering or science degree with 3–5 years in pharma quality operations.
• Experience in batch release, deviations and investigations preferred.
• Strong knowledge of GMP and regulatory requirements.
• Ability to analyze data, write reports and communicate clearly.

Responsibilities

• Review batch records and release documentation for compliance.
• Lead complex investigations and root cause analysis.
• Monitor CAPA actions and drive timely closure.
• Support internal/external audits and regulatory inspections.
• Participate in risk management and continuous improvement initiatives.

Skills

Quality operations

Batch release

Deviation handling

Investigation leadership

CAPA management

GMP compliance

Regulatory knowledge

Risk management

Audit support

Education

Engineering degree

Science degree

Job description

Sanofi Group in Singapore seeks a QA Specialist to partner with GMP operations and validation teams to ensure quality and compliance across batch records, release and investigations. You will manage complex deviations, CAPA actions and risk assessments while supporting continuous improvement initiatives.

The role requires 3–5 years of pharma quality operations experience, a degree in engineering or science, and strong communication skills to interact with cross-functional teams.