Join CDP's US Healthcare & MedTech team to lead multi-phase programs (often >$1M) for life sciences , drug-delivery, and medical-device clients. You'll coordinate multidisciplinary teams across Raleigh and Cambridge (UK), manage complex stakeholder landscapes, and ensure delivery excellence under FDA design controls/QMSR (aligned to ISO 13485) and ISO 14971 risk management.
What you'll do- Lead early-stage project definition, including shaping technical approaches, defining scope, and aligning with client objectives
- Own end-to-end delivery for one or more device development programs -from concept through verification/validation to design transfer, balancing scope, schedule, budget, risks, and issues.
- Run program governance and phase gates; manage inter-project dependencies and shared resources across multiple workstreams.
- Develop structured project plans covering timelines, resourcing, risks, and dependencies across multidisciplinary teams
- Translate ambiguous client needs into clear Statements of Work, workstreams, and deliverables
- Build trusted client relationships (10-20% client-facing); run clear communications and status; present to executive stakeholders.
- Drive commercial health: author SOWs/proposals, manage MSAs and change orders, and support BD on account opportunities.
- Ensure regulatory alignment: FDA QMSR/ISO 13485 and ISO 14971 integration; maintain traceability from user needs to design inputs/outputs, V&V, and risk controls.
- Coordinate distributed teams in the US/UK and external partners/CMOs; assure hand-offs into pilot manufacture/transfer.
Work pattern & travelRaleigh-based hybrid (on-site 3 days/week) with collaboration across US and UK time zones; ~10-20% travel (domestic and to the UK).
Requirements- 8+ years leading medical-device development with responsibility for >$1M budgets and multi-phase delivery; success across late-stage D&V and design transfer.
- Strong client-facing leadership in consulting or OEM; adept with scope/change control, stakeholder management, and crisp executive reporting.
- Demonstrated command of FDA design controls under QMSR (ISO 13485-aligned) and ISO 14971 risk management; human factors/usability (IEC 62366) a plus.
- Experience leading distributed, cross-functional teams (HF, QA/RA, ME/EE, SW, manufacturing).
- Strong experience in scoping and structuring complex product development programs from early concept through to transfer
- Ability to break down ambiguous problems into clear workstreams, plans, and deliverables
- BS/MS in engineering or related field; PMP (or equivalent) helpful.
BenefitsWe're an employee-owned innovation partner with a growing US team in Raleigh, NC, part of the Research Triangle. We bring ideas to life-from insight to engineering to pilot manufacture-across consumer and healthcare.
