Verification and Validation Engineer
Enovis · Texas
- Level
- Engineer
- Team
- Quality
- Degree
- Required
- Experience asked
- 5+ years
- Industry
- Medical devices
- Posted
- 10 days ago
The role in 30 seconds
An engineer-level quality role at Enovis (medical devices) in Texas. Partner closely with Software Engineering, Systems Engineering, Product Development, Quality, Regulatory Affairs, and Program Management teams to develop test strategies, execute verification and validation activities, document results, and support.
- They ask for
- 5+ years · degree required
- Tools it names
- ISO 13485, FDA / GMP, Validation (IQ/OQ/PQ), Robotics, Automation
Read from the posting. The full description is below.
At a glance
Pulled from the posting text. If it's not listed here, the posting didn't say.
How to get in at this plant
Five moves over a week or two. The first one takes ten minutes.
- 1
Pick 2–3 people on the Quality team at Enovis
We found 1 person at this company and state: 1 on the team. Engineers who joined in the last year or two reply the most. See them ↓
- 2
Send a short, curious note
One real question about their work. No favors yet. Each person gets a different note, written for this role.
Write to Tommy → (free) - 3
Turn a reply into a short call
Questions worth asking about this team:
- What does a normal week look like on your team?
- Which standards drive the work here: ISO 13485, IATF 16949, AS9100?
- How much of the job is customer complaints versus prevention?
- How did you land the job? What stood out in your interviews?
- 4
Apply with someone vouching for you
If the call went well, ask whether they’d pass your résumé to the hiring manager. Send your résumé link, apply that day, and let them know.
- 5
Bring proof to the interview
One page of before-and-after numbers from projects you led: scrap, OEE, cycle time, cost. Plant managers hire on results.
About the role
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 Enabling Tech 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/High Level Position Summary
- ◆We are seeking a detail-oriented and collaborative Verification & Validation (V&V) Engineer to support the verification and validation of software and system functionality for medical device products within Enovis' Enabling Technologies business. This role is responsible for ensuring software requirements, system designs, and user needs are thoroughly verified and validated through structured testing activities in compliance with medical device quality and regulatory standards.
- ◆The V&V Engineer II will partner closely with Software Engineering, Systems Engineering, Product Development, Quality, Regulatory Affairs, and Program Management teams to develop test strategies, execute verification and validation activities, document results, and support successful product releases. This position requires strong analytical thinking, technical problem-solving skills, and the ability to work effectively within an Agile software development environment.
- ◆The ideal candidate is a proactive team player with excellent technical writing and communication skills who is passionate about delivering high-quality, reliable medical device software.
Key Responsibilities
- ◆Develop, execute, and maintain verification and validation test plans, protocols, and reports for software and system-level requirements.
- ◆Review product requirements, software specifications, and design documentation to develop comprehensive test cases and validation strategies.
- ◆Perform hands-on software verification and validation testing for new product development and enhancements to existing products.
- ◆Document test results, identify defects, and work closely with development teams to investigate, troubleshoot, and verify software issues.
- ◆Review software documentation and participate in quality audits to ensure compliance with applicable medical device standards and company procedures.
- ◆Participate in Agile ceremonies, including daily stand-ups, sprint planning, backlog refinement, and retrospectives, providing updates on testing activities.
- ◆Track testing progress, maintain defect logs, and communicate project status, risks, and issues to engineering leadership.
- ◆Collaborate with cross-functional teams to ensure verification and validation activities support project timelines and product release objectives.
- ◆Assist with test planning, test automation initiatives, and continuous improvement of V&V processes and documentation.
- ◆Support regulatory submissions and quality system activities by providing verification and validation documentation as required.
Qualifications
- ✓Bachelor's degree in Biomedical Engineering, Software Engineering, Computer Science, or a related engineering discipline.
- ✓Minimum of 5 years of experience in software verification and validation, software quality assurance, or medical device development.
- ✓Experience in robotics
- ✓Experience working within regulated industries, preferably medical devices.
- ✓Knowledge of software development lifecycle (SDLC) and software verification and validation methodologies.
- ✓Experience creating test plans, test protocols, test cases, and verification reports.
- ✓Strong technical writing, analytical, and organizational skills.
- ✓Excellent written and verbal communication skills with the ability to work effectively on cross-functional teams.
Qualifications
- ✓Experience working in Agile software development environments.
- ✓Familiarity with FDA Quality System Regulation (21 CFR Part 820), IEC 62304, ISO 13485, and other applicable medical device standards.
- ✓Understanding of software architecture concepts and software design patterns.
- ✓Experience with defect tracking, test management, and
requirements
management tools.
- ✓Basic debugging skills, including reviewing application logs and troubleshooting software issues.
- ✓Understanding of musculoskeletal anatomy and orthopedic medical devices is preferred.
- ✓Experience supporting software validation for medical device products.
Show full description ↓Show less ↑
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 .
Job Title
Verification & Validation Engineer
Location
Austin, TX
Scope / Role Dimensions
- •Supports verification and validation activities across multiple software and system development projects.
- •Works collaboratively with Software Engineering, Systems Engineering, Quality, Regulatory Affairs, Product Development, and Program Management teams.
- •Responsible for executing verification and validation activities throughout the product development lifecycle.
- •Contributes to product quality, regulatory compliance, and successful product commercialization.
Core Competencies
- •Quality Focus: Maintains a high standard of accuracy and attention to detail throughout verification and validation activities.
- •Analytical Thinking: Identifies issues, evaluates risks, and develops