CDMO Technical Program Manager - MedTech Manufacturing

RecruitPedia Pte Ltd

Singapore

On-site

SGD 120,000 - 170,000

Full time

14 days+

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Job summary

RecruitPedia Pte Ltd is recruiting a CDMO Technical Program Manager to drive complex product development programs in the medical industry. The role involves leading cross‑functional teams across engineering, quality, suppliers and manufacturing from concept through manufacturing scale‑up.

The ideal candidate has 8+ years in MedTech product development, with 3+ years in technical leadership or PM, and experience with regulated biomedical assemblies, microfluidics, and tolerance analysis.

Qualifications

  • Bachelor’s or higher in Engineering or related field.
  • 8+ years in product development within IVD/medical devices or biomedical precision assemblies.
  • 3+ years in technical leadership or project management within regulated MedTech development.

Responsibilities

  • Lead technical product development programs from concept to manufacturing.
  • Manage project schedules, milestones, budgets, and technical deliverables.
  • Review product designs, engineering documentation, and technical risks.
  • Support design verification, validation, and regulatory documentation.
  • Drive design for manufacturability (DFM) and manufacturing readiness.
  • Coordinate cross-functional teams across engineering, quality, suppliers, and manufacturing.
  • Support process validation, product transfer, and production scale-up.
  • Monitor project performance and resolve technical issues throughout development.

Skills

Technical leadership
Project management
MedTech experience
Microfluidics
Tolerance analysis

Education

Engineering degree

Job description

RecruitPedia Pte Ltd is recruiting a CDMO Technical Program Manager to drive complex product development programs in the medical industry. The role involves leading cross‑functional teams across engineering, quality, suppliers and manufacturing from concept through manufacturing scale‑up.

The ideal candidate has 8+ years in MedTech product development, with 3+ years in technical leadership or PM, and experience with regulated biomedical assemblies, microfluidics, and tolerance analysis.

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