QA Auditor: CGMP Quality & CAPA Lead in Life Sciences

Lonza; Singapore; On-site; SGD 80,000 - 100,000; Full time

Job summary

A leading life sciences company in Singapore is seeking a Quality Assurance professional to ensure compliance in manufacturing processes. Responsibilities include reviewing documents, overseeing product status, and participating in quality investigations. The ideal candidate holds a degree in Science or Engineering and has experience in cGMP environments. This role offers an agile career and inclusive workplace.

Benefits

Agile career and dynamic working culture

Fully paid medical insurance

Daily company bus to site

Qualifications

• Experience in cGMP manufacturing environment, ideally in Cell and Gene Therapy.
• Hands-on experience with batch record review.
• Proven ability to lead investigations and change controls.

Responsibilities

• Review executed batch records and documentation for compliance.
• Compile lot genealogy and disposition packages.
• Provide QA oversight for product status and shipping documents.
• Support and approve deviation investigations.

Skills

Experience in Quality Assurance

Knowledge of cGMP

Communication skills

Stakeholder management

Batch record review

Deviation management

CAPA implementation

Education

Degree or Diploma in Science or Engineering

Job description

A leading life sciences company in Singapore is seeking a Quality Assurance professional to ensure compliance in manufacturing processes. Responsibilities include reviewing documents, overseeing product status, and participating in quality investigations. The ideal candidate holds a degree in Science or Engineering and has experience in cGMP environments. This role offers an agile career and inclusive workplace.