Process Engineer, TechnologyLocation: Raynham, Massachusetts, USA
Department: Technology
The OpportunityAs 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 ForEssential Qualifications & Experience- Bachelor's degree in Mechanical Engineering, Electrical Engineering, Robotics Engineering, or a related discipline.
- 2-5 years' experience in Process Engineering, Manufacturing Engineering, or Process Development within a regulated industry.
- Experience implementing and optimising manufacturing processes.
- Understanding of process verification and validation activities.
- Knowledge of Lean Manufacturing and Six Sigma methodologies.
- Strong problem-solving and root cause analysis skills.
- Experience developing standard operating procedures and manufacturing documentation.
- Excellent communication and stakeholder management skills.
- Proficiency in Microsoft Office and engineering systems.
Desirable Experience- 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 software such as SolidWorks or Siemens NX.
- Knowledge of electrical components and assembly processes.
- Project management experience.
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, and product development while contributing to cutting-edge orthopaedic innovations.
We offer:
- Salary: $85,000 - $95,000 (depending on experience, education, and skills).
- Comprehensive benefits package.
- Career development and progression opportunities.
- Collaborative and innovative culture.
- The opportunity to work on products that make a real difference to patients worldwide.
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 orthopaedic technology at Corin.
