Technical Program Manager (Product Development) Medical Devices

recruitpedia pte. ltd.; Singapore; On-site; SGD 120,000 - 180,000; Full time

Job summary

Recruitpedia Pte. Ltd. is seeking a Technical Program Manager to join a multinational Contract Manufacturing team in Singapore.

The role focuses on leading end-to-end development for medical devices and consumables from concept to manufacturing, ensuring robust cross-functional collaboration and regulatory compliance. You will review designs, address technical challenges, and guide verification, validation, and manufacturing readiness while mentoring junior engineers and coordinating with

Qualifications

• Bachelor's degree in Mechanical Engineering, Biomedical Engineering, Mechatronics, Materials Engineering or related discipline.
• At least 8 years of product development experience in Medical Devices, IVD consumables, biomedical precision assemblies, or related regulated industry.
• Minimum 3 years of technical leadership or project management experience, with exposure to customer-facing projects.
• Experience in microfluidics, reagent integration, design controls (ISO 13485), and product verification & validation is advantageous.

Responsibilities

• Lead end-to-end product development programs for medical devices and consumables from concept to manufacturing.
• Drive cross-functional collaboration across Product Development, Process Engineering, Quality, and Manufacturing to ensure project success.
• Review product designs, resolve technical challenges, and support design verification, validation, and manufacturing readiness.
• Manage timelines, milestones, risks, budgets, and stakeholder communications to ensure on-time delivery.
• Support design transfer, process validation, and continuous improvement initiatives to enhance manufacturability and product quality.
• Work closely with customers, suppliers, and external stakeholders to support development activities and technical discussions.
• Ensure compliance with design control processes, ISO 13485, and applicable regulatory requirements.
• Mentor junior engineers while providing technical leadership across multiple development projects.

Skills

Leadership

Project management

Cross-functional collaboration

Mentoring

Customer-facing

Education

Bachelor's degree in engineering

Job description

Our client is a multinational company in the Contract Manufacturing industry. Due to their current expansion plan, they are looking for a Technical Program Manager to join their Engineer team, in hopes of developing the current high performing team. They are located in the North – easily accessible.

The Technical Program Manager's responsible:

• Lead end-to-end product development programs for innovative medical devices and consumables from concept to manufacturing.
• Drive cross-functional collaboration across Product Development, Process Engineering, Quality, and Manufacturing teams to ensure successful project execution.
• Review product designs, resolve technical challenges, and support design verification, validation, and manufacturing readiness.
• Manage project timelines, milestones, risks, budgets, and stakeholder communications to ensure on-time delivery.
• Support design transfer, process validation, and continuous improvement initiatives to enhance manufacturability and product quality.
• Work closely with customers, suppliers, and external stakeholders to support product development activities and technical discussions.
• Ensure compliance with design control processes, ISO 13485, and applicable regulatory requirements.
• Mentor junior engineers while providing technical leadership across multiple development projects.

Requirement

• Bachelor's Degree in Mechanical Engineering, Biomedical Engineering, Mechatronics, Materials Engineering, or a related discipline.
• At least 8 years of product development experience in Medical Devices, IVD consumables, biomedical precision assemblies, or a related regulated industry.
• Minimum 3 years of technical leadership or project management experience, with exposure to customer-facing projects.
• Experience in microfluidics, reagent integration, design controls (ISO 13485), and product verification & validation will be an advantage.