Senior Program Manager – Medical Devices (consulting)

Cambridge Design Partnership

Raleigh, NC, US
On-site
8+ years leading medical device development
Manage budgets over $1m
Fda design controls and qmsr compliance
Join the US Healthcare & MedTech team to lead multi-phase programs often exceeding $1M for life sciences and medical device clients

Job Summary

  • Join the US Healthcare & MedTech team to lead multi-phase programs often exceeding $1M for life sciences and medical device clients.
  • You will ensure delivery excellence under FDA design controls, ISO 13485 quality management systems, and ISO 14971 risk management standards.
  • The role involves coordinating distributed teams across Raleigh and Cambridge while managing complex stakeholder landscapes and driving commercial health initiatives.

Matching Summary

Join the US Healthcare & MedTech team to lead multi-phase programs often exceeding $1M for life sciences and medical device clients.

Skills & Requirements

Must-have

  • 8+ years leading medical device development
  • Manage budgets over $1M
  • FDA design controls and QMSR compliance
  • ISO 14971 risk management experience
  • Cross-functional team leadership
  • Client-facing consulting experience

Nice-to-have

  • Human factors usability IEC 62366
  • PMP certification or equivalent
  • Experience with CMO coordination
  • Strong executive reporting skills

Key Requirements

  • BS/MS in engineering or related field
  • 8+ years of medical device development leadership
  • Responsibility for >$1M budgets
  • Success in late-stage D&V and design transfer

Work Rights

Not specified

Tailored Resume

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