Manufacturing Specialist (Pharma/Biotech)

NUSANTARA PRIME CONSULTING PTE. LTD.

Singapore
Cgmp manufacturing operations experience
Regulatory inspection participation required
Capa and change management execution
The role involves performing technical investigations and implementing corrective actions within cGMP biologics production facilities

Job Summary

  • The role involves performing technical investigations and implementing corrective actions within cGMP biologics production facilities.
  • Candidates will collaborate cross-functionally to manage change plans, train new hires, and streamline work processes.
  • The position requires active participation in regulatory inspections and the authoring of GMP documents including electronic batch records.

Matching Summary

Match Score: 85

The role involves performing technical investigations and implementing corrective actions within cGMP biologics production facilities.

Skills & Requirements

Must-have

  • cGMP manufacturing operations experience
  • Regulatory inspection participation required
  • CAPA and change management execution
  • Electronic batch record authoring skills
  • Technical writing for investigations

Nice-to-have

  • Experience with Trackwise and SAP systems
  • Cross-functional team leadership ability
  • Agility to work under stress
  • Strong presentation and communication skills
  • Continuous improvement project drive

Key Requirements

  • BS degree or equivalent experience
  • 2 to 5 years relevant industry experience
  • Required experience with Regulatory inspections

Work Rights

Not specified

Tailored Resume

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