Process Engineer

Corin • Raynham, MA

10d • Onsite

About The Position

Corin is seeking a Process Engineer, Technology to join its Global Operations team in Raynham, Massachusetts. The role develops, validates, and optimizes manufacturing processes supporting innovative medical technologies in a regulated medical device environment. The engineer works across teams to help ensure products are manufactured efficiently, safely, and to high quality standards, and supports technologies from development through production.

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 the 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