Senior Process & Validation Specialist (NPI / TPM), 12-month, CBD

MANPOWER STAFFING SERVICES (SINGAPORE) PTE LTD

Singapore
Base: up to s$12k; bonus: 1-month bonus; benefits:...
Hybrid
Process development and design transfer
Iq oq pq validation protocols
Third-party manufacturer operations
The Senior Process & Validation Specialist position at MANPOWER STAFFING SERVICES (SINGAPORE) PTE LTD involves leading the transfer of new products and processes from R&D to production within a Third-Party Manufacturer (TPM) environment. The candidate will be responsible for ensuring compliant and validated manufacturing processes, project execution, and cross-functional collaboration in the medical device industry

Job Summary

  • The role serves as the onsite manufacturing lead responsible for transferring new products from R&D into production at a Third-Party Manufacturer.
  • Candidates must possess hands-on experience leading process validation activities including IQ, OQ, and PQ within a regulated medical device environment.
  • This is a 12-month contract position offering a salary up to S$12K plus a one-month bonus with immediate commencement.

Matching Summary

Match Score: 85

The Senior Process & Validation Specialist position at MANPOWER STAFFING SERVICES (SINGAPORE) PTE LTD involves leading the transfer of new products and processes from R&D to production within a Third-Party Manufacturer (TPM) environment. The candidate will be responsible for ensuring compliant and validated manufacturing processes, project execution, and cross-functional collaboration in the medical device industry.

Salary

Base: Up to S$12K; Bonus: 1-month bonus; Benefits: Not specified

Skills & Requirements

Must-have

  • Process development and design transfer
  • IQ OQ PQ validation protocols
  • Third-party manufacturer operations
  • ISO13485 and 21 CFR 820 compliance
  • SOP and work instruction documentation

Nice-to-have

  • Cross-functional team collaboration
  • Continuous improvement initiatives
  • Risk-based thinking and mitigation
  • Adaptability in ambiguous environments

Key Requirements

  • Bachelor's degree in Engineering or Science
  • 8+ years in medical device manufacturing
  • Experience with FAT/SAT activities
  • Knowledge of ISO 14971 risk management

Work Rights

Not specified

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