What are the responsibilities and job description for the Manufacturing Engineer-Medical Device position at Trelleborg Brand?
Join Our Team at Trelleborg Medical Solutions!
Imagine working for one of the world’s leading contract medical device manufacturers, nestled just 30 miles from California’s stunning Central Coast. At Trelleborg Medical Solutions, we are not just a premier manufacturer of life-saving medical components; we are a forward-thinking company committed to excellence and innovation. Our journey in lean manufacturing has been ongoing for years, and we are on the path to becoming a showcase of excellence in the medical industry.
Seize this rare opportunity to be part of a healthcare and medical business with over 100 years of history, all while enjoying the benefits of living in one of California’s most desirable locations!
Why Join Us?
As a valued Trelleborg team member, you will enjoy:
- Greater opportunity for impact
- Competitive compensation
- Outstanding benefits package: Health, Dental, Vision, STD, LTD, Life, 401k
- Generous paid time off
- Bonus potential
Position: Manufacturing Engineer
In this role, you will adhere to Good Manufacturing Practices (GMP) and principles to provide engineering support and develop robust manufacturing processes. Your primary responsibility will be to engineer new, modified, and existing manufacturing operations within a clean-room environment.
Essential Functions:
- Analyzes new product specifications and translates these into manufacturing processes to establish production rates, achieve expected quality levels and establish the reliability of the finished product.
- Responsible for the completion of the design and development of optimal, cost-effective, and reliable manufacturing processes.
- Use demonstrated strengths in multiple aspects of medical component and device design and manufacturing capabilities to plan and accomplish goals.
- Develops process parameters, procedures, and related documentation
- Conducts data analysis and collaboration with Operations and Quality Engineering.
- Identifies Operational Qualification (OQ) process parameters and Performance Qualification (PQ) settings.
- Develops and documents standard operating procedures (SOP) and product-specific operating procedures (PSOP).
- Performs DOEs, and participates in the development of control plans, Process Maps, and PFMEA documentation.
- Organizes internal cross-functional teams and corresponding outside vendors needed to meet project needs. Procures equipment as needed.
- Uses standard problem-solving tools, e.g., 8D, 5 Whys, Fishbone.
Education and Experience:
- 4-year degree in Engineering or a related discipline
$85,000-$115,000
Salary : $85,000 - $115,000
