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Technical Program Manager (Product Development) Medical Devices

recruitpedia pte. ltd.Singapore
Full-timeMid Level
$1k - $2k
per year
👁️ 4 views📝 0 applicationsPosted 8/3/2026Expires 9/5/2026

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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. #J-18808-Ljbffr

Required Skills

Cross-functional CollaborationLeadershipMedical DevicesProject ManagementStakeholder Management

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