Sustaining Manufacturing Engineer

About the role

At Enovis, we pay attention to the details. We embrace collaboration with our partners and patients, and take pride in the pursuit of scientific excellence — with the goal of transforming medical technology as we know it. As a key member of the Manufacturing Engineering Team, you will play an integral part in helping Enovis drive the medical technology industry forward through transforming patient care and creating better patient outcomes.

Responsibilities

• Develop, maintain, and improve process specifications, operating procedures, process controls, etc.
• Develop and maintain manufacturing engineering standards, labor standards, maintenance records, production routings, BOM standards, work instructions, etc.
• Provide production support to ensure manufacturing equipment and processes are operating safe and efficiently.
• Research and evaluate new and existing processes, operations, and support systems for adaptation and/or improvements needed to manufacture Enovis products.
• Provide Digital/CAD support for shop floor layout.
• Manage the installation, operational, and production qualification (IQ/OQ/PQ) of new and existing CNC/Robotic equipment.
• Conduct engineering studies in support of CNC/Robotic process validations.
• Write process/product specific protocols and validation reports.
• Implement cost reduction initiatives using Lean manufacturing principles in support of Enovis Growth eXcellence program (EGX).
• Develop process control solutions that are integrated into production or manufacturing process control systems e.g., vision systems, laser sensors, in-process/post process gage systems, data collection, etc.
• Conduct feasibility studies to ensure that implementation of recommended improvements would meet objectives with respect to safety, quality, market demands, competitive costs, and general financial criteria.
• Identify and implement corrective and preventative actions for scrap and rework.
• Provide engineering inputs in conjunction with the Quality group in support material disposition.

Requirements

• BS in Engineering, Science, or related field with 3+ years’ experience.
• 3-4 years verifiable experience in a CNC manufacturing environment.
• Relevant knowledge in med-device, or similar field of CNC manufacturing process development; QC Inspection; Process Monitoring (SPC).
• Excellent communication skills.
• Attention to Detail.

Qualifications

Desired characteristics include Six Sigma Green Belt, CNC Process Development, AutoCAD, SolidWorks, CAM System Experience (Multi-axis Milling and Turning), Strong Problem-Solving Skills, Strong GD&T Understanding, Agile PLM Experience, and Secondary Finishing Processes, Cellular Manufacturing.

Benefits

• Medical Insurance
• Dental Insurance
• Vision Insurance
• Spending and Savings Accounts
• 401(k) Plan
• Vacation, Sick Leave, and Holidays
• Income Protection Plans
• Discounted Insurance Rates
• Legal Services