3 дня назад
Manufacturing Engineer II (MedTech)
79 000 - 127 600$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Manufacturing Engineer II (MedTech): Controlling and optimizing medical device manufacturing processes in cardiovascular care with an accent on defect reduction, yield improvement, process qualification, and regulatory compliance. Focus on statistical process analysis, Lean and Six Sigma investigations, adhesive dispensing, tooling validation, and root-cause analysis using product teardowns and advanced imaging.
Location: Danvers, Massachusetts, United States of America
Salary: $79,000–$127,600 annually, plus eligibility for performance-based bonuses and long-term incentives.
Company
Johnson & Johnson MedTech develops cardiovascular solutions for heart recovery, electrophysiology, and stroke, including smarter and less invasive treatments.
What you will do
- Control and improve manufacturing processes to reduce defects, increase productivity, and improve product quality and yield.
- Use Lean, Six Sigma, statistical analysis, Minitab, process capability studies, Gage R&R, and design of experiments to identify and solve process issues.
- Qualify and optimize processes and tooling through IQ/OQ/PQ and develop manufacturing documentation, process flows, FMEAs, assembly procedures, and test procedures.
- Investigate non-conforming products and audit findings, perform root-cause analysis, and implement corrective action plans.
- Develop defect-tracking and operator-analysis data systems and conduct product teardowns, X-ray, and CT-scan analysis using advanced vision systems.
- Apply adhesive dispensing expertise, including knowledge of Loctite and Epo-tek materials, while collaborating with engineering peers and communicating business issues to management.
Requirements
- Bachelor’s degree in Mechanical Engineering, Industrial Engineering, or a related discipline.
- 3+ years of manufacturing experience, preferably in medical devices or a cleanroom environment.
- Knowledge of Lean, Six Sigma, continuous improvement, statistical analysis, and Minitab or an equivalent tool.
- Knowledge of FDA, QSR, and ISO regulations.
- Proficiency with Microsoft Office applications and compliance with applicable health, safety, environmental, and company regulations.
Nice to have
- Advanced degree.
- SAP experience.
- Experience with medical device manufacturing and cleanroom environments.
Culture & Benefits
- Inclusive work environment focused on individual dignity, diversity, and equal opportunity.
- Medical, dental, vision, life insurance, disability, business accident, and group legal insurance programs.
- Pension and 401(k) savings plans, subject to eligibility.
- Vacation, sick time, holiday pay, and work, personal, and family time benefits.
- Interview accommodations are available for applicants with disabilities.
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