? Manufacturing Documentation Specialist | Science MNC #HHLT

Recruit Express Pte Ltd; Singapore; On-site; SGD 56,000 - 67,000; Part time

Job summary

Recruit Express Pte Ltd is seeking a Manufacturing Documentation Specialist for a Science MNC. The role is based in Joo Koon, Singapore, on a 1-year contract, with duties including batch documentation, data integrity, and quality system support.

The ideal candidate will hold a Diploma in Science/Engineering/Pharmaceutical/Biotechnology and have strong cGMP documentation and batch record review experience, plus familiarity with CAPA and technology transfer projects.

Qualifications

• Min. diploma in Science, Engineering, Pharmaceutical, Biotechnology or related discipline.
• Strong cGMP manufacturing documentation and batch record review experience.
• Experience in CAPA, investigations, change control and quality systems preferred.
• Technology transfer / project coordination experience advantageous.

Responsibilities

• Prepare, review and close batch manufacturing records.
• Ensure documentation accuracy, data integrity and cGMP compliance.
• Support batch disposition and release activities.
• Update SOPs, Work Instructions and controlled documents.
• Support investigations, CAPA, change control and quality systems.
• Coordinate technology transfer projects across Manufacturing, QA, Engineering, Validation, MSAT and Supply Chain.
• Track project timelines, risks, milestones and deliverables.

Skills

cGMP documentation

Batch record review

CAPA investigations

Technology transfer

Project coordination

Education

Diploma in Science/Engineering/Pharmaceutical/Biotechnology

Job description

Recruit Express will never request for your Singpass details in our recruitment process. Please contact us at 6732 6006 or email to [e-mail] if you are unsure if it is a scam.

? Manufacturing Documentation Specialist | Science MNC #HHLT

? Joo Koon
? Mon–Fri, 8am–5:15pm
? Up to $5,500/month
? 1-Year Contract

? Responsibilities

• Prepare, review and close batch manufacturing records
• Ensure documentation accuracy, data integrity and cGMP compliance
• Support batch disposition and release activities
• Update SOPs, Work Instructions and controlled documents
• Support investigations, CAPA, change control and quality systems
• Coordinate technology transfer projects across Manufacturing, QA, Engineering, Validation, MSAT and Supply Chain
• Track project timelines, risks, milestones and deliverables

? Requirements

• Min. diploma in Science, Engineering, Pharmaceutical, Biotechnology or related discipline
• Strong cGMP manufacturing documentation and batch record review experience
• Experience in CAPA, investigations, change control and quality systems preferred
• Technology transfer / project coordination experience advantageous