Programme Manager (CDMO Product Development)

RecruitPedia Pte Ltd; Singapore; On-site; SGD 120,000 - 170,000; Full time

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

Our client is a leading player in Manufacturing Industry. Due to business needs, they are now recruiting a CDMO Technical Program Manager to be part of their production Team for ongoing transformation projects. They are located in the North Area - easily accessible.

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.

Requirements

• Degree in Engineering or a related discipline.
• Minimum 8 years of product development experience in IVD consumables, medical devices, or biomedical precision assemblies.
• Minimum 3 years of technical leadership or project management experience within regulated MedTech product development.
• Experience with microfluidics, reagent integration, and tolerance analysis for complex assemblies.

• Experience with government grant initiatives, innovation or capability transformation programs, or specialized training in medical design, engineering, or quality systems will be an advantage.

We regret that only shortlisted candidates will be notified.