ABOUT ENOVIS™
Enovis Corporation (NYSE: ENOV) is an innovation-driven medical technology growth company dedicated to developing clinically differentiated solutions that generate measurably better patient outcomes and transform workflows. Powered by a culture of continuous improvement, global talent and innovation, the Company's extensive range of products, services and integrated technologies fuels active lifestyles in orthopedics and beyond. For more information about Enovis, please visit www.enovis.com .
Responsibilities
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.
Because that's how we change the lives of patients for the better. And that's how we create better together. Why work at Enovis? See for yourself .
As a key member of the NPI Manufacturing Engineering group you will play an integral part in helping Enovis drive the medical technology industry forward through transforming patient care and creating better patient outcomes.
Job Title:
Manager, Process Engineering
Reports To:
Director, NPI Engineering
Location:
Austin, Texas
Business Unit Description:
Enovis Surgical offers surgeons and their patients a full range of primary and revision implants for hip, knee, shoulder, and elbow reconstructive joint surgeries, in addition to the tools and digital health technology needed in today's changing healthcare environment.
Job Title/High-Level Position Summary
Lead a team of NPI Manufacturing Engineers and technicians responsible for launching new products.
Serves as a cross functional team member as primary process and manufacturing expert on new product introduction on cross functional teams.
Guides teams to assess process capabilities, prioritizes process improvement opportunities, and innovates and implements process improvements on new development projects.
Applies technical knowledge to innovate, design, and develop processes, procedures, tooling and/or automation.
Executes the functional deliverables associated with the CAPA, Project Management, and Quality Systems.
Guides team to plans, organizes, and conducts all aspects of manufacturing technical reviews.
Ensures proper documentation is completed to meet quality systems requirements. (e.g., BOM's, Routers, FMEA's, etc.)
Writes and reviews validation protocols and reports applicable to new processes.
Oversees development builds associated with the project using technical work requests.
Provides Design for Manufacturability (DFM) input to the engineering print package.
Responsible for conveying the process and manufacturing limits and capabilities to the development team.
Contributes ideas to or generates Intellectual Property submissions.
May train manufacturing personnel when required as part of a validation.
Participate in lean reviews, and Kaizen events.
Coach Engineers and Technicians.
Minimum Basic Qualifications:
This position requires bachelor's degree in science or BSME, or related Engineering Degree
Minimum of 10 years experience in process/manufacturing engineering role.
Minimum of 3 years experience managing an engineering team
Experience with Measurement Systems (CMM's, Vision Inspection and Profilometers).
Experience with GD&T
Experience with data analysis (Minitab) preferred
Desired Characteristics:
Experience in Medical Device Manufacturing.
Previous experience in the areas of Design for Manufacturing (DFM), Lean Manufacturing, and Process Control Concepts, Design of Experiments (DOE), Process Validation and product/process Failure Mode and Effects Analysis (FMEA).
Use of Problem Solving and Process Improvement Methodologies