Job description

Who We Are 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 . What You ll Do Job Description: At Enovis™ we sweat the little things. We embrace collaboration with our partners and patients, and we glory in the grind 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. As a key member of the Enabling Technologies 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. Job Title: Engineering Manager, Sustaining- Enabling Technologies Reports To: Director, R&D Product Development Location: Austin, TX Business Unit Description: Enabling Technologies Job Title/High Level Position Summary: The Manager, Base Business directs the sustaining engineering activities for the Enabling Technologies business unit. In addition to managing product development resources, the Manager individually contributes to development efforts. This includes but is not limited to creating prototypes, testing, and documenting test results; scheduling, coordinating, and managing multiple projects; and communicating with vendors to ensure proper design transfer. The Manager will be responsible for products including mechanical surgical instrumentation, electronic hardware, and software used by electronic hardware. Key Responsibilities: Manage project prioritization and resource allocation Mentor direct reports by providing technical guidance, coaching, performance management, and professional development opportunities Participate in product development including concept, generation, decision matrices, prototype, manufacture, and associated metrics Provide expert product leadership for the development projects assigned; this includes an unrelenting attention to minimizing project delays and resource overages Creates product designs and documentation used to substantiate those devices (i.e. risk assessments, verification/validation activities, design review documentation, etc.) Develops detailed engineering drawings using 3-D Modeling to document designs and design changes (SolidWorks) Confers with cross-functional team to identify tasks and requirements (Product Development, Manufacturing Engineers, Quality Engineers, Marketing, Purchasing and Regulatory Affairs) 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. Assist in the regulatory submission process(FDA 510k, EU MDR, TGA, PMDA) by providing official information for regulatory review Minimum Basic Qualifications: Bachelor s degree in an engineering discipline 8 years of professional experience (6 years with a Masters degree)in a regulated industry Experience in medical device product development Experience with enabling technology (pre operative planning, navigation, robotics) preferred. Familiarity with software development processes Prior experience applying mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis. Prior experience defining problems, collecting data, establishing facts, and drawing valid conclusions. Prior experience interpreting an extensive variety of technical instructions in mathematical or diagram form and dealing with several abstract and concrete variables. Must be experienced in MS Word, Excel and Project. Experience with 3D CAD packages (SolidWorks preferred)   Working knowledge and requirements of ISO 13485 and 21CFR820. Travel Requirements: <5% of travel required Desired Characteristics: Previous experience managing engineers Previous experience developing orthopedic medical devices(either implant development or enabling technology used with orthopedic implants) Previous experience leading projects of moderate to large scope and complexity Work Environment: While performing the duties of this job, the employee is exposed to the manufacturing environment. While performing the duties of this job, the employee is exposed to the office environment. Employee is expected to work in varying environments, including office setting, mechanical testing lab, and cadaver lab. The noise level in the work environment is usually moderate. Physical Demands: While performing the duties of this job, the employee is regularly required to sit, talk and hear. The employee frequently is required to sit and use hands to operate computer keyboard, and telephone. The employee is frequently required to stand, walk, and reach with hands and arms. This position works in a typical office/manufacturing/warehouse environment. The employee must occasionally lift and/or move up to 30 pounds.  Perform job duties for 8 or more hours a day. “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. Watch this short video and discover what creating better together means to us at Enovis:   Our Enovis Purpose, Values and Behaviors on Vimeo We offer a comprehensive benefits package which 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 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.

Requirements

Must-haves

What You ll Do
At Enovis™ we sweat the little things. We embrace collaboration with our partners and patients, and we glory in the grind 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.
As a key member of the Enabling Technologies 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.
Engineering Manager, Sustaining- Enabling Technologies
Director, R&D Product Development
Enabling Technologies
Manage project prioritization and resource allocation
Mentor direct reports by providing technical guidance, coaching, performance management, and professional development opportunities
Participate in product development including concept, generation, decision matrices, prototype, manufacture, and associated metrics
Provide expert product leadership for the development projects assigned; this includes an unrelenting attention to minimizing project delays and resource overages
Creates product designs and documentation used to substantiate those devices (i.e. risk assessments, verification/validation activities, design review documentation, etc.)
Develops detailed engineering drawings using 3-D Modeling to document designs and design changes (SolidWorks)
Confers with cross-functional team to identify tasks and requirements (Product Development, Manufacturing Engineers, Quality Engineers, Marketing, Purchasing and Regulatory Affairs)
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.
Assist in the regulatory submission process(FDA 510k, EU MDR, TGA, PMDA) by providing official information for regulatory review
Bachelor s degree in an engineering discipline
8 years of professional experience (6 years with a Masters degree)in a regulated industry
Experience in medical device product development
Familiarity with software development processes
Prior experience applying mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis.
Prior experience defining problems, collecting data, establishing facts, and drawing valid conclusions.

Nice-to-haves

Experience with enabling technology (pre operative planning, navigation, robotics) preferred.
Experience with 3D CAD packages (SolidWorks preferred)

Application prep

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Platform: workday
Effort: long

Benefits

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Dental

Vision

401(K)

Professional Development