GMP Batch Documentation Specialist

KERRY CONSULTING PTE. LTD.; Singapore; On-site; SGD 31,000 - 50,000; Full time

Job summary

KERRY CONSULTING PTE. LTD. is seeking a Batch Record Specialist for a 12-month contract in Singapore.

The role focuses on supporting manufacturing documentation within a regulated pharmaceutical environment and suits fresh graduates or candidates with limited industry experience who show strong attention to detail and an interest in GMP manufacturing. Responsibilities include reviewing and revising batch records, ensuring compliance, and coordinating document routing with Manufacturing and

Qualifications

• Diploma or degree in biotechnology, pharmaceutical science or related discipline.
• Fresh graduates are welcome to apply.
• Basic GMP knowledge and documentation practices preferred.

Responsibilities

• Review and revise Batch Manufacturing Records and related documents.
• Update documents based on approved process or equipment changes.
• Ensure records are clear, accurate and compliant with documentation standards.
• Perform formatting, proofreading and data-verification checks.
• Support routing of documents for review, approval and issuance.

Skills

Attention to detail

Communication

Collaboration

Education

Diploma or degree in Biotechnology, Pharmaceutical Science, Chemical Engineering, Biomedical Science, Life Sciences or related discipline

Tools

Microsoft Word

Microsoft Excel

Job description

KERRY CONSULTING PTE. LTD. is seeking a Batch Record Specialist for a 12-month contract in Singapore.

The role focuses on supporting manufacturing documentation within a regulated pharmaceutical environment and suits fresh graduates or candidates with limited industry experience who show strong attention to detail and an interest in GMP manufacturing. Responsibilities include reviewing and revising batch records, ensuring compliance, and coordinating document routing with Manufacturing and