cGMP Manufacturing Documentation Specialist (Contract)

Recruit Express Pte Ltd

Singapore

On-site

SGD 56,000 - 67,000

Part time

2 days ago
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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 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.

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