Process Engineer

Corin Group • Raynham, MA

14d • $85,000 - $95,000 • Onsite

About The Position

Corin is hiring a Process Engineer, Technology to join its Global Operations team in Raynham, Massachusetts. The role supports technology-driven manufacturing of orthopaedic medical products by developing, validating, and optimizing processes to help ensure efficient and safe production that meets quality standards and regulatory requirements. The engineer works with cross-functional teams to take new technologies from concept and development into production, and contributes to continuous improvement and operational excellence.

Requirements

• Bachelor's degree in Mechanical Engineering, Electrical Engineering, Robotics Engineering, or a related discipline.
• 2–5 years of experience in Process Engineering, Manufacturing Engineering, or Process Development within a regulated industry.
• Experience implementing and optimizing 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.

Nice To Haves

• 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.

Responsibilities

• Lead development, implementation, and optimization of manufacturing processes for technology-based products.
• Support transfer of products from development into full-scale manufacturing.
• Design, trial, validate, and launch new production processes.
• Drive process standardization, automation, and operational excellence initiatives.
• Manage product and process changes while ensuring patient safety, product quality, and regulatory compliance.
• Maintain Bills of Materials (BOMs) in systems such as Teamcenter and Sage.
• Perform process simulations, testing, and optimization 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 optimize manufacturing equipment and processes.
• Partner with New Product Introduction (NPI) teams on 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.

Benefits

• Comprehensive benefits package.
• Career development and progression opportunities.
• Collaborative and innovative culture.
• Opportunity to work on products that make a real difference to patients worldwide.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level