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.
What You'll Do
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 Research and Development 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.
Business Unit Description: Driven by Enovis’ desire to create innovative products that help improve quality of life and restore movement to those suffering from degenerative arthritis, Enovis Surgical provides orthopedic surgeons with modern, patient-focused solutions for total joint arthroplasty. 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: Participates in all aspects of projects from proposal to final design/release by working cross-functionally across a product team consisting of product development engineers, marketing product managers, manufacturing engineers, regulatory and QA engineers in the design and development of surgical instruments and implants medical devices used in Total Shoulder Arthroplasty. Manages and develops lower level engineers and co-ops.
Key Responsibilities:
Develop and manage lower level engineering personnel.
Participates as an active member of the New Product Development Team:
Identifies and incorporates surgeon design requirements and product characteristics
Confers with cross-function teams (by way of example and not exclusion, Manufacturing Engineering, Purchasing and Regulatory); accepts and completes tasks as assigned
Creates product designs and documentation used to substantiate those devices (i.e. risk assessments, verification / validation activities, design review documentation, etc.)
Uses 3-D Modeling to develop concepts and mechanism design (Solidworks)
Compiles Design Dossiers or Design History Files
Assuring compliance to FDA and ISO regulations and internal procedures
Establishing and maintaining project schedule and budget
Reviewing designs for feasibility, accuracy and technical soundness
Defining and implementing testing requirements associated with projects
Participate in the evaluation of new concepts presented to Enovis Surgical by surgeons or other Enovis Surgical employees.
Collaborate / lead other engineering personnel in formulating project plans, designs, cost estimates, and specifications.
Assures proper preparation of documentation as required per project plans including user needs, surgeon feedback / IP, engineering drawings, test plans, manufacturing instructions, design verification and validation, engineering change notices, artwork and other supporting engineering documents.
Working with manufacturing, supply chain and quality assurance, reviews and monitors quality and process improvements for new product development.
Participates in surgeon symposia, focus groups and surgeon consultant meetings
Assists product development engineers and the Engineering Manager or Director of Shoulder Product Development with New Product Development projects
Attends cadaver labs for learning purposes.
Works with both the marketing team and customers to develop conceptual designs, typically in the form of SLA models or metal prototypes of the product and present those designs back to the customers for evaluation
Maintains all documentation necessary for a Design History File (DHF), including Design Input Documents, Design Validation Plans/Reports, Test Protocols/Reports, and Design Input/Output Matrix
Develops project plans using appropriate planning software and periodically report on the progress of the project to upper management
Develops detail engineering drawings, CAD modeling and release through design change system; understands GD&T and can apply it in tolerance stacking activities
Works through internal prototype shop or contract through external vendors on developing prototypes.
Maintain basic knowledge of competitive technologies, in addition to medical, clinical, technical and biomedical developments in the field.
Maintain communications with customers and suppliers.
Relies on instructions and pre-established guidelines to perform the functions of the job
60% of time is spent in a resource capacity. 40% of responsibilities are in leadership activities.
Minimum Basic Qualifications:
A minimum of 6 years of design / development experience
BS in Mechanical Engineering, Biomedical Engineering, or equivalent
Experience with 3D CAD packages
Ability to present information and respond to questions from groups of managers, clients, and customers
Ability to apply advanced mathematical concepts and operations such as exponents, logarithms, quadratic equations, and permutations, as well as frequency distribution, determination of test reliability and validity, statistical analysis
Ability to work in varying environments including but not limited to a Cadaver Lab, Mechanical Testing Lab, office setting etc.
To perform this job successfully, an individual should have knowledge of Word Processing software; spreadsheet software; internet software; contact / change management systems
Travel Requirements:
Less than 15%
Desired Characteristics:
Engineering co-op or internships are strongly desirable
A minimum of 2 years of people management or mentorship is strongly desirable
Experience working in a regulated industry preferred
Experience in medical devices and/or orthopedics preferred
Experience with 3D CAD packages (SolidWorks, NX preferred)
Currently, Enovis does not provide sponsorship for employment visas (e.g., H-1B) and will not offer such sponsorship in the future. Applicants must already have full-time work authorization in the United States, both now and in the future, without requiring sponsorship.
“Creating better together”. It’s the Enovis purpose, and it’s what drives us and empowers us every day on a global scale. We know that the power to create better – for our customers, our team members, and our shareholders – begins with having the best team, pursuing common goals, operating at the highest levels, and delivering extraordinary outcomes.
What does creating better together mean to us at Enovis? Discover the “why” behind our purpose, values and behaviors:
We offer a comprehensive benefits package that includes:
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
Join us in creating better together.
EQUAL EMPLOYMENT OPPORTUNITY Enovis provides equal employment opportunities based on merit, experience, and other work-related criteria without regard to race, color, ethnicity, religion, national origin, sex, age, pregnancy, disability, veteran status, or any other status protected by applicable law. We also strive to provide reasonable accommodation to employees’ beliefs and practices that do not conflict with Enovis policies and applicable law. We value the unique contributions that every employee brings to their role with Enovis.
