What are the responsibilities and job description for the Quality Assurance Engineer II position at Enovis?
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.
Enovis History
In April of 2022, Colfax, which includes orthopedic leader DJO, separated from ESAB Corporation and rebranded to Enovis. In recognition of our successful history of growth and innovation, the distinctive "O" in our new Enovis logo was deliberately carried over from our Colfax logo as it represents continuous improvement - a cornerstone of our business's success that will continue at Enovis. Enovis is poised to become one of the world's leading medical technology companies.
What You'll Do
Summary:
Must possess the knowledge, skills and abilities or be able to explain and demonstrate that they can perform the essential functions of the job, with or without reasonable accommodations, using some other combination of skills and abilities.
Must be able to communicate in English clearly and fluently, in both written and verbal skills
EOE AA M/F/VET/Disability Statement
All qualified applicants will receive consideration for employment and will not be discriminated against on the basis of race, religion, color, national origin, sex, protected veteran status, disability, or any other basis protected by federal, state or local laws.
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.
Enovis History
In April of 2022, Colfax, which includes orthopedic leader DJO, separated from ESAB Corporation and rebranded to Enovis. In recognition of our successful history of growth and innovation, the distinctive "O" in our new Enovis logo was deliberately carried over from our Colfax logo as it represents continuous improvement - a cornerstone of our business's success that will continue at Enovis. Enovis is poised to become one of the world's leading medical technology companies.
What You'll Do
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 Product Development, serves as the QA representative on design initiatives, and supports Quality System activities (i.e., CAPAs, Complaints, Audits, Nonconformances, DHR reviews).
- Participating in design reviews
- Generating DFMEAs/UFMEAs and participating in risk analysis discussions
- Reviewing and approving design and development documentation
- Serve as subject matter expert for design quality and quality assurance in ISO and FDA audits
- Authoring procedures and work instructions that define and govern the quality system
- Initiating, developing, and recommending updates or changes to quality standards and procedures.
- Conduct internal audits of the quality system and other business functions
- Assuring compliance to internal and external specifications and standards (i.e., GMP, ISO, FDA, MDD)
- Evaluating nonconforming material and dispositioning based on cross-functional review
- Evaluating and investigating customer complaint investigations
- Reviewing trends in device failures associated with customer complaints and nonconforming material
- Leading and owning corrective and preventive actions
- Assisting with document control, change control, calibration, metrics, supplier management, DHR reviews, and training aspects of the QMS
- Supporting validation planning and testing on computer-assisted surgery systems
- Working on complex special projects as assigned
- Bachelor's in Biomedical or Engineering or Science and 2 years of experience (preferred). Equivalent experience may be considered in lieu of a degree for exceptional candidates
- Background in Medical Device or other highly regulated industry required; preferred knowledge of ISO 13485 quality standards.
- Knowledge of technical writing quality and best practices.
- Required basic knowledge of design and manufacturing processes: preferably with electro-mechanical assemblies and components
- Individual should have knowledge of Microsoft Office Suite of software or equivalent.
- Preferred knowledge of electronic QMS software.
Must possess the knowledge, skills and abilities or be able to explain and demonstrate that they can perform the essential functions of the job, with or without reasonable accommodations, using some other combination of skills and abilities.
- Accurate and professional communication
- Accurate and professional written communication (email, text and formal letter)
- Position is office based (Austin, TX)
- Must be able to lift 50 lbs.
- Must be able to bend, twist and lift overhead.
- Must possess professional ethics and demeanor
- Must demonstrate excellent customer service.
- Computer skills (Excel, Word, Power Point).
Must be able to communicate in English clearly and fluently, in both written and verbal skills
EOE AA M/F/VET/Disability Statement
All qualified applicants will receive consideration for employment and will not be discriminated against on the basis of race, religion, color, national origin, sex, protected veteran status, disability, or any other basis protected by federal, state or local laws.
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