7 дней назад
Reliability Engineer II (Medical Devices)
84 800 - 127 200$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Reliability Engineer II (Medical Devices): Analyzing post-market product performance and supporting reliability, risk management, verification, and validation for implantable cardiac devices with an accent on product quality, patient safety, and regulated medical-device engineering. Focus on investigating quality issues, evaluating design and process risks, interpreting system requirements, and using statistical techniques to improve product reliability.
Location: Mounds View, Minnesota, United States; hybrid model with a minimum of 4 days per week on-site
Salary: $84,800–$127,200 USD annually, plus eligibility for a short-term incentive plan.
Company
develops healthcare technologies, including implantable cardiac devices, to improve patient health and extend life.
What you will do
- Analyze product performance data and support post-market surveillance for pacemakers, defibrillators, and leads.
- Support reliability engineering, debugging, and recommendations for design or process changes.
- Assist with risk analyses covering product quality and patient safety.
- Prepare risk assessments, technical reports, and documentation of analysis results.
- Support requirements traceability, testability, verification, and validation of device systems.
- Investigate quality issues with cross-functional partners and support corrective actions.
Requirements
- Bachelor’s degree in Engineering, Science, or a related technical discipline.
- At least 2 years of experience in engineering, science, or a related technical field, or an advanced degree with no prior work experience.
- Unrestricted U.S. work authorization is required at hire and throughout employment; sponsorship is not available for this role.
- Experience or knowledge in reliability engineering, risk management, root cause investigation, or regulated product development.
- Ability to analyze data using statistical techniques and reliability tools.
- For degrees earned outside the United States, the degree must satisfy the applicable requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A).
Nice to have
- Understanding of cardiac rhythm management products and their clinical use.
- Clinical experience using cardiac rhythm management products.
- Experience with 21 CFR 820, ISO 13485, and ISO 14971.
- Experience evaluating and debugging electrical designs, including RF performance.
- Experience with Class III medical-device design, verification, and validation.
Culture & Benefits
- Purpose-driven work focused on healthcare technology and patient outcomes.
- Health, dental, and vision insurance, plus health and dependent-care spending accounts.
- Life insurance, disability coverage, paid time off, and paid holidays.
- 401(k) plan with employer contribution and match, employee stock purchase plan, and incentive plans.
- Tuition assistance or reimbursement and employee assistance resources.
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