Process Engineer
- Compensation
- $85K–$95K
- Location
- Raynham, MA, US
- Work setup
- Not specified
- Seniority
- Not specified
- Employment
- Not specified
- Experience
- 2+ years
- Category
- Industrial engineering
- Posted
Skills
Nice to have
- Medical device industry experience. Knowledge of ISO 13485 Quality Management Systems. Familiarity with FDA 21 CFR Part 820 and Good Manufacturing Practice (GMP) requirements. Experience with CAD soft
- Why Join Corin? At Corin, you'll have the opportunity to work on technologies that directly improve patients' quality of life. You'll collaborate with talented teams across engineering, manufacturing,
- Salary: $85,000 - $95,000 (depending on experience, education, and skills). Comprehensive benefits package. Career development and progression opportunities. Collaborative and innovative culture. The
- Ready to Apply? If you're passionate about manufacturing innovation, process improvement, and advancing medical technology, we'd love to hear from you. Apply today and help us build the future of orth
Full description
Process Engineer, Technology
Location: Raynham, Massachusetts, USADepartment: Technology
Help Shape the Future of Orthopaedic Technology
At Corin, we're passionate about improving patient outcomes through innovative orthopaedic solutions. As we continue to expand our technology-driven manufacturing capabilities, we're looking for a Process Engineer, Technology to join our Global Operations team in Raynham, MA.
This is an exciting opportunity for an engineer who enjoys bringing new technologies from concept to production, driving continuous improvement, and making a real impact within a highly regulated medical device environment.
The Opportunity
As a Process Engineer, Technology, you will play a key role in developing, validating, and optimising manufacturing processes that support the production of innovative medical technologies. Working closely with cross-functional teams, you'll help ensure products are manufactured efficiently, safely, and to the highest quality standards.
What You'll Be Doing
Lead the development, implementation, and optimisation of manufacturing processes for technology-based products.
Support the transfer of products from development into full-scale manufacturing.
Design, trial, validate, and launch new production processes.
Drive process standardisation, automation, and operational excellence initiatives.
Manage product and process changes while ensuring patient safety, product quality, and regulatory compliance.
Maintain Bills of Materials (BOMs) within systems such as Teamcenter and Sage.
Perform process simulations, testing, and optimisation activities.
Lead Process Verification and Validation (PV/PQ) activities for new manufacturing technologies.
Apply root cause analysis, Lean, and Six Sigma methodologies to improve performance.
Conduct process risk assessments and PFMEA activities.
Lead continuous improvement projects focused on efficiency, quality, and CAPA resolution.
Collaborate with suppliers and service providers to optimise manufacturing equipment and processes.
Partner with New Product Introduction (NPI) teams to support Design for Manufacture (DFM) initiatives.
Create and maintain manufacturing documentation, technical records, and work instructions.
Ensure compliance with ISO 13485, FDA 21 CFR Part 820, and GMP requirements.
What We're Looking For
Essential Qualifications & Experience
Bachelor's degree in Mechanical Engineering, Electrical Engineering, Robotics Engineering, or a related discipline.