Medical Device NPD Program Lead

Tap Growth ai; Palo Alto (CA); On-site; USD 140,000 - 200,000; Full time

Job summary

Tap Growth ai is seeking a Technical Program Manager to lead medical device new product development programs from concept through commercialization. You will coordinate technical teams across hardware, software, firmware, and regulatory to ensure on-time delivery and robust design controls.

The role requires 8+ years in program management within the medical device industry, with deep knowledge of FDA regulations, ISO 13485, ISO 14971, and IEC 62304, plus strong cross-functional leadership and

Qualifications

• Bachelor's degree in Engineering, Life Sciences, or related field.
• 8+ years total experience with 5+ years in medical devices.
• Experience in medical device NPD and program management.
• Knowledge of Design Controls, risk management, V&V, FDA regs, ISO 13485.
• Strong cross-functional leadership and stakeholder management.

Responsibilities

• Lead end-to-end medical device NPD programs from concept to commercialization.
• Develop integrated schedules, milestones, budgets, and resource plans.
• Coordinate cross-functional teams across hardware, software, QA, regulatory, manufacturing.
• Manage program governance, executive reporting, and stakeholder communications.
• Identify and mitigate technical, regulatory, operational, and schedule risks.
• Drive verification, validation, design transfer, and product launch activities.
• Manage vendors and external development partners.
• Facilitate design reviews and ensure adherence to Design Controls.
• Ensure compliance with FDA regulations and ISO 13485/14971, IEC 62304.

Skills

Technical PM

Medical device NPD

Stakeholder management

Cross-functional leadership

V&V

FDA regulations

ISO 13485

Design Controls

Project budgeting

Education

Bachelor’s degree in Engineering, Life Sciences, or related technical field

Tools

PMP certification

Job description

Tap Growth ai is seeking a Technical Program Manager to lead medical device new product development programs from concept through commercialization. You will coordinate technical teams across hardware, software, firmware, and regulatory to ensure on-time delivery and robust design controls.

The role requires 8+ years in program management within the medical device industry, with deep knowledge of FDA regulations, ISO 13485, ISO 14971, and IEC 62304, plus strong cross-functional leadership and