14 часов назад
Associate Manufacturing Engineer (MedTech)
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Associate Manufacturing Engineer (MedTech): Developing and optimizing manufacturing processes for spinal implants from raw material through final cleaning and shipment with an accent on process documentation, validation, tooling, and inspection methods. Focus on reducing cycle time and waste, troubleshooting production issues, and implementing corrective actions in a regulated medical-device environment.
Location: West Carrollton, Ohio, United States
Company
develops medical technologies and spinal implants designed to improve surgical outcomes and quality of life for patients with musculoskeletal disorders.
What you will do
- Develop, implement, and maintain manufacturing methods, operation sequences, and processes for parts, components, sub-assemblies, and final assemblies.
- Support projects and coordinate cross-functional teams during the manufacturing launch of new and legacy products.
- Develop and optimize processes for spinal implants from raw material through final cleaning and shipment.
- Create manufacturing documentation, including pFMEAs, control plans, process flows, work instructions, and inspection plans.
- Improve machine and equipment efficiency through cycle-time reduction, waste elimination, tooling improvements, and changeover reduction.
- Perform process troubleshooting, equipment and process validation, non-conforming material review, root-cause analysis, and corrective and preventive actions.
Requirements
- Bachelor’s degree, typically in an engineering discipline; no previous professional experience is required.
- Ability to identify and report critical manufacturing process and control characteristics.
- Experience with print reading, GD&T, statistical process control, Lean Manufacturing, Six Sigma, and gage or fixture design.
- Ability to analyze production metrics and KPIs and support design-for-manufacturability reviews with CNC programmers, quality engineers, and development engineers.
- Experience in a 21 CFR 820 and/or ISO 13485 regulated environment.
- Ability to influence stakeholders, build consensus, and create organizational support.
Culture & Benefits
- Work is guided by innovation, customer focus, teamwork, and results-driven execution.
- Commitment to ethical business practices, regulatory compliance, inclusion, and a respectful work environment.
- Physical requirements include sitting, climbing or balancing, stooping, kneeling, crouching or crawling, and lifting up to 25 pounds occasionally.
- Specific close, distance, color, peripheral, and depth vision abilities are required.
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