NPI Quality Engineer

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
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 Foot & Ankle Quality NPI 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:
NPI Quality Engineer
Reports To:
Sr. NPI Quality Manager
Location:
Houston, TX
Business Unit Description:
Foot & Ankle
Job Title/High-Level Position Summary:
Utilizing a comprehensive knowledge of engineering and problem-solving principles, this position is responsible for a variety of complex activities regarding the design, implementation, and maintenance of quality assurance procedures and work instructions to ensure external safety, quality, and compliance with complex Company standards and government regulations.
This position primarily supports New Product Development, Sustaining Product Development, and Complaint Investigations and serves as the QA representative on various PD initiatives.
Key Responsibilities:
Participating in design and manufacturing reviews
Generating DFMEAs/UFMEAs and participating in risk analysis discussions
Develop inspection strategy and methods to support the development and launch of new products.
Reviewing and approving design and development documentation
Serve as subject matter expert for design quality in ISO and FDA audits
Authoring procedures and work instructions that define and govern the quality system
Conduct internal audits of the quality system and other business functions
Evaluating nonconforming material and dispositioning based on cross-functional engineering review
Assuring compliance to internal and external specifications and standards (i.e. GMP, ISO, FDA, MDD)
Reviewing trends in device failures associated with customer complaints and nonconforming material
Leading and owning corrective and preventive actions and complaint investigations
Working on complex special projects as assigned
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.
Minimum Basic Qualifications:
Bachelor’s degree in Biomedical or Mechanical Engineering and 5+ years of experience (or equivalent combination of education and years of experience).
Background in Medical Device, Aeronautics, Automotive or other highly regulated industry required; preferred knowledge of ISO13485 quality standards.
Knowledge of technical writing quality and best practices.
Required basic knowledge of manufacturing processes: key focus into metrology, precision machining, grinding, product cleaning, and sterilization.
Individual should have knowledge of Microsoft Office Suite of software or equivalent.
Travel Requirements:
Up to 20%
Desired Characteristics:
Advanced knowledge of ISO 14971 and risk management principles
Experience with Class II/III Medical Devices
Preferred knowledge of the following: Solidworks, Solidworks ePDM, MiniTab, Netsuite, Agile PLM, CMM and/or automated inspection system programming.
Prefer CQE, Lean, or 6 Sigma Certification.
Detail oriented and analytical
Enovis values the contribution each employee brings to our organization. The pay range listed is what we reasonably and in good faith expect to compensate candidates who meet the specified qualifications and requirements for this role. Actual starting pay will depend on various factors, including but not limited to education and experience in the job and/or industry.
Base Pay Range: $86,520 - $94,760 - $104,174 (reflective of a full-time position)
Employees in this position are also eligible to earn an annual performance bonus.
“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:
Our Enovis Purpose, Values and Behaviors on Vimeo
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.

Skills
Agile, Technical Writing, Risk Management, SolidWorks, Patient Care, Documentation