Marmon
Product Development Engineer 2 - Hand & Upper Extremity
United States · Work style not stated · Full time
Apply on the employer’s site ↗See how well you match this job
You apply directly with the employer. ROLIVA does not submit applications from this page and is not the employer.
About the role
Description from the employer’s posting. Check the employer’s page for the current version.
- EmployerMarmon
- LocationUnited States
- Work styleWork style not stated
- Employment typeFull time
- Employer posted
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 Product Development Engineer 2 supports the development of medical devices from concept to commercialization, including research, planning, concept development, specification generation, testing, validation, and communication with cross-functional teams, management, and customers.
Duties/Responsibilities
- Develop implant and instrument designs using CAD models, drawings, and GD&T based on clinical research and collaboration with cross-functional teams and clinical experts.
- Lead engineering deliverables for small projects or portions of larger projects within Product Development Teams (PDTs) from concept through product launch and sustaining transfer.
- Communicate technical concepts effectively with internal teams, vendors, sales teams, and healthcare professionals.
- Support design control and risk management activities including traceability matrices, design verification and validation, design reviews, and associated testing.
- Evaluate designs through engineering analysis and testing including mechanical testing, cadaver labs, FEA, root cause analysis, tolerance stack analysis, and statistical tools.
- Review CAD models and drawings for tolerancing and manufacturability and contribute to Best Known Methods (BKMs) and quality checks.
- Support engineering change management activities including drawing approvals and Engineering Change Orders within PLM systems (e.g., Windchill, SAP).
- Research intellectual property landscapes and contribute to generation of new intellectual property.
- Develop expertise in assigned technical specialty areas and apply anatomical knowledge to product development projects.
- Support literature research, competitive analysis, and occasional customer-facing events.
Show full description
Qualifications
- Bachelor’s degree in Mechanical Engineering, Bio-Mechanical Engineering, or equivalent with 2+ years’ experience preferred; or 8 years of medical device development experience.
- Ability to communicate clearly and effectively with teammates and managers.
- Ability to lead PDTs on small projects.
- Experience writing test protocols and reports and conducting testing with limited supervision.
- Applied knowledge of 3D/2D CAD modeling and drawings for implants or instruments.
- Knowledge of Level 1 & 2 GD&T principles.
- Basic FEA analysis knowledge to mitigate design risks.
- Experience managing ECOs through completion.
- Knowledge of root cause analysis techniques.
- Ability to review medical literature, summarize clinical data, and write reports.
- Ability to review patents and understand intellectual property considerations.
- Familiarity with design control processes in regulated environments.
- Understanding of anatomy and clinical indications for assigned projects.
- Ability to conduct literature searches and develop competitive product analyses.
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.
We are an equal opportunity employer, and all applicants will be considered for employment without attention to their membership in any protected class. If you require any reasonable accommodation to complete your application or any part of the recruiting process, please email your request to careers@marmon.com, and please be sure to include the title and the location of the position for which you are applying.
Check your resume against this job Free, no sign-up. Nothing you paste is stored.
Staying safe while you apply
- Never pay to apply, interview or accept an offer. ROLIVA never asks you for payment to apply to a job.
- Apply only through the official “Apply on the employer’s site” button, on the employer’s own site, and check that a recruiter’s email uses that employer’s own domain rather than a free email address.
- Be cautious of an offer made with no real interview, or pressure to decide quickly or share financial details early.
Does something look wrong with this listing? Use “Report broken link” in the role details, or read ROLIVA’s full job-safety guidance ↗.
Preparing for this role with ROLIVA
- Check the fit.
Compare the requirements with the experience you have confirmed, including gaps.
- Prepare honestly.
Build interview stories and application drafts from your own evidence.
- Keep track.
Save the role and record your own application status and follow-ups.
At a glance
- Employment typeFull time
- Employer posted
- Added to ROLIVA
- Last checked