Research & Development Engineer I (Medical Devices)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Location: Memphis, Tennessee, United States; onsite work at least four days per week. Domestic travel is less than 10%, typically 1–2 days per month. Candidates below Principal level must have unrestricted U.S. work authorization at hire and throughout employment; U.S. sponsorship is not available.
Salary: USD 74,400–111,600 per year, plus eligibility for the Incentive Plan.
Company
develops healthcare technologies, including spinal implants, instruments, and systems used to treat degenerative, deformity, and tumor/trauma conditions.
What you will do
- Develop mechanical concepts and designs for spinal implants, instruments, and systems from initial design through market release.
- Translate customer and clinical needs into stakeholder requirements, system requirements, design specifications, and product concepts.
- Evaluate interfaces, use cases, and design risks; investigate issues and implement design improvements.
- Design and conduct tests, experiments, numerical analyses, and evaluations to optimize product performance.
- Support verification and validation activities and incorporate feedback from customers, clinical users, suppliers, consultants, and cross-functional partners.
- Create engineering reports, presentations, drawings, and design documentation; build clinical-use knowledge through customer visits, pre-clinical in vivo labs, literature reviews, and training.
Requirements
- Bachelor’s degree in engineering or a technical discipline.
- Experience with mechanical design principles.
- Experience with engineering drawing standards, including Geometric Dimensioning and Tolerancing (GD&T) and tolerance stack analysis.
- For a bachelor’s degree earned outside the United States, the degree must satisfy 8 C.F.R. § 214.2(h)(4)(iii)(A).
Nice to have
- Bachelor’s degree in mechanical engineering or biomedical engineering with a mechanical design focus or experience.
- Experience with Creo, SolidWorks, or similar three-dimensional CAD software.
- Experience with systems engineering methodologies, including requirements development, analysis, allocation, traceability, verification, and validation.
- Knowledge of surgical instrumentation, spinal anatomy, clinical procedures, machining, or additive manufacturing/3D printing.
- Experience in an FDA-regulated medical device environment, including applicable ISO requirements, Quality System Regulations, and product lifecycle management systems such as Agile or Windchill.
Culture & Benefits
- Full-time regular employment with health, dental, vision, life, disability, retirement, paid time off, paid holidays, and employee assistance benefits.
- Additional benefits for regular employees working 20 or more hours per week include health savings and flexible spending accounts, dependent daycare spending, tuition assistance, and a global well-being program.
- Regular employees are eligible for incentive plans, a 401(k) plan with employer contribution and match, and an employee stock purchase plan.
- Reasonable accommodations are available for qualified individuals with disabilities.
Hiring process
- Applications should be submitted only through official channels.
- does not request payment or sensitive personal information during early recruitment stages.
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