The Manufacturing Process Engineer will report directly into the Engineering Manager and be responsible for:
- Continuously evaluate and enhance manufacturing processes to improve efficiency, quality, and overall performance.
- Collaborate with cross-functional teams to ensure seamless integration of new products into the manufacturing process.
- Identify and resolve issues related to manufacturing processes, equipment, and materials promptly.
- Implement and maintain rigorous quality control measures to meet regulatory standards and ensure the production of high-quality medical devices.
- Work closely with R&D, Quality Assurance, and other departments to foster a collaborative and innovative work environment.
Apply today for immediate consideration!
MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.
- Bachelors Degree in Biomedical Engineering or a related field
- 3-5 years of experience in medical device manufacturing
- Knowledge of regulatory requirements (ISO 13485)
- Proficiency in CAD software (e.g., SolidWorks, AutoCAD)
- Sound analytical and problem-solving skills
- Experience with FEA analysis tools is a plus
- Strong communication skills and ability to work in cross-collaborative teams
- Experience transitioning products from prototype to production
My client is a global leader in providing innovative applications of optical technology. This company focuses on innovation, precision and efficiency within their manufacturing processes to drive success within the industry.
- Competitive compensation
- Comprehensive benefits plan
- Career growth opportunities
- Access to high level management
- 401K match
- Excellent work life balance