Staff Product Development Engineer - Hand & Upper Extremity

Requirements

• Education/Experience: Bachelor's degree in Mechanical or Bio-Mechanical Engineering with 8+ years' experience preferred; or 14+ years in medical device development.
• Leadership: Ability to mentor/supervise engineers, mechanical drafters, and product designers; lead large, complex projects; communicate effectively with executives and cross-functional teams.
• Clinical & Market Insight: Effective at engaging with HCPs and surgeons, organizing cadaver labs, investigating new product opportunities, analyzing market/competition, and recommending ROI.
• Advanced Skills (Preferred): Independent patent analysis; writing technical product papers; proficiency in multiple technical specialty areas; ability to serve as independent reviewer for multiple projects.
• Following receipt of a conditional offer of employment, candidates will be required to complete additional job-related screening processes as permitted or required by applicable law .

Additional Information

Acumed LLC As a part of the global industrial organization Marmon Holdings-which is backed by Berkshire Hathaway- you'll be doing things that matter, leading at every level, and winning a better way. We're committed to making a positive impact on the world, providing you with diverse learning and working opportunities, and fostering a culture where everyone's empowered to be their best. Location: Hillsboro, Oregon Job Scope The Staff Product Development Engineer drives product development from concept to commercialization - including research, planning, concept creation, specifications, testing, validation, and communication with teams, management, and customers. Duties/Responsibilities Mentor and/or supervise engineers and designers across multiple projects. Collaborate with department leaders to shape corporate and technical strategy. Build and manage relationships with external design resources, KOLs, and surgeons. Define and oversee engineering scope and deliverables for complex projects. Develop and approve advanced testing protocols, methods, and Engineering Change Requests (ECRs). Act as internal reviewer/approver for Clinical Data Reports (CDRs). Guide business development and R&D with technical expertise and market insight. Participate in technical review boards and influence product direction. Partner with manufacturing on new technologies and processes. Ensure product designs and documentation meet FDA/ISO design control standards, including risk management, verification/validation, and proper use of CAD/PLM and ERP systems (e.g., GD&T, ECO/ECR, SAP). Organize and support cadaver labs with surgeons and design teams.

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