Engineering Manager, Sustaining- Enabling Technologies

Posted 3 Days Ago
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Austin, TX, USA
In-Office
Senior level
Healthtech
The Role
Manages sustaining engineering and product development for medical devices, including project prioritization, resource allocation, mentoring engineers, prototyping, testing, design documentation, 3D CAD modeling, design history files, vendor coordination, and regulatory submissions. The role supports mechanical instrumentation, electronic hardware, and related software while collaborating with manufacturing, quality, marketing, purchasing, and regulatory teams.
Summary Generated by Built In
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.

Skills Required

  • Bachelor's degree in an engineering discipline
  • 8 or more years of professional experience, or 6 or more years with a master's degree
  • Experience in medical device product development
  • Familiarity with software development processes
  • Ability to apply mathematical operations for frequency distribution, test reliability, validity, and analysis
  • Ability to define problems, collect data, establish facts, and draw valid conclusions
  • Ability to interpret technical instructions in mathematical or diagram form and work with abstract and concrete variables
  • Experience with Microsoft Word, Excel, and Project
  • Experience with 3D CAD packages, preferably SolidWorks
  • Working knowledge of ISO 13485 and 21 CFR 820 requirements
  • Experience with enabling technologies such as preoperative planning, navigation, or robotics
  • Previous experience managing engineers
  • Experience developing orthopedic medical devices
  • Experience leading projects of moderate to large scope and complexity

Enovis Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Enovis and has not been reviewed or approved by Enovis.

  • Healthcare Strength — Healthcare coverage is positioned as comprehensive, with multiple medical, dental, and vision plan options plus HSA/FSA accounts. Income protection offerings are also described as robust, including life, AD&D, and short- and long-term disability coverage.
  • Retirement Support — Retirement benefits include access to a 401(k) plan with an employer match described as competitive. This adds to the overall total-rewards value even where cash compensation sentiment is uneven.
  • Leave & Time Off Breadth — Time-off provisions are described as ample, including vacation, sick leave, and holidays. Paid parental and family leave is also offered, with a stated maximum of six weeks for eligible employees after birth or adoption.

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The Company
HQ: Wilmington, DE
1,217 Employees
Year Founded: 2022

What We Do

We are a medical technology company focused on developing clinically differentiated solutions that generate measurably better patient outcomes and transform workflows. Powered by a culture of continuous improvement, extraordinary talent and innovation, we ‘create better together’ by partnering with healthcare professionals. Our extensive range of products, services and integrated technologies fuel active lifestyles.

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