2 дня назад
Sr Mechanical Design Engineer (Medical Devices)
106 400 - 159 600$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Sr Mechanical Design Engineer (Medical Devices): Designing, developing, verifying, and validating mechanical and electromechanical medical device products and systems with an accent on advanced mechanical engineering, design controls, and regulatory requirements. Focus on solving complex product and manufacturing challenges, performing DFMEA, DFMA, tolerance, and structural analyses, and providing technical leadership across engineering, quality, manufacturing, and supplier teams.
Location: Onsite in Lafayette, Colorado, United States; regular in-person collaboration is required. Travel of up to 10% may be required.
Salary: $106,400–$159,600 per year, plus eligibility for the Incentive Plan.
Company
develops healthcare technologies for neurological, spinal, cranial, biologics, and navigation-enabled procedures.
What you will do
- Design, develop, verify, and validate mechanical and electromechanical medical devices, components, assemblies, and systems.
- Apply advanced mechanical engineering methods to solve product, manufacturing, and system-level technical challenges.
- Evaluate materials, mechanisms, instruments, controls, plastics, metals, and electromechanical assemblies.
- Perform tolerance analysis, DFMA, DFMEA, structural analysis, and finite element analysis as applicable.
- Prepare and review engineering drawings, specifications, technical documentation, and GD&T practices.
- Represent Mechanical Engineering in cross-functional projects, provide technical recommendations, mentor engineers, and support suppliers, risk management, and verification and validation activities.
Requirements
- Bachelor’s degree in STEM, preferably Mechanical Engineering, with 4+ years of relevant experience, or an advanced STEM degree with 2+ years of relevant experience.
- Experience designing mechanical components and assemblies with 3D modeling and engineering drawing tools.
- Working knowledge of GD&T, tolerance analysis, risk analysis, design controls, and design verification and validation.
- Experience independently solving complex technical problems and developing engineering recommendations.
- Experience collaborating with engineering, quality, manufacturing, and supplier teams in a regulated product development environment.
- Unrestricted U.S. work authorization is required at hire and throughout employment; sponsorship is not available for this below-Principal role.
Nice to have
- Medical device industry experience and knowledge of FDA QSR, ISO 13485, ISO 14971, IEC 60601, IEC 62304, and international regulatory requirements.
- Experience with SolidWorks or Creo.
- Experience with complex mechanical and electromechanical products, DFMEA, DFMA, tolerance stack-up analysis, or ANSYS.
- Six Sigma certification, technical project leadership, supplier activity leadership, or engineering mentorship experience.
Culture & Benefits
- Purpose-driven work focused on improving patient outcomes and advancing healthcare technology.
- Health, dental, and vision insurance, plus health and dependent-care spending accounts for eligible regular employees.
- 401(k) with employer contribution and match, paid time off, paid holidays, short-term and long-term disability coverage, and life insurance.
- Tuition assistance or reimbursement, incentive plans, employee stock purchase plan, employee assistance program, and a global well-being program.
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