Full-Time

Quality Assurance Engineer-Validation

Confirmed live in the last 24 hours

ENOVIS

ENOVIS

1,001-5,000 employees

Develops orthopedic and reconstructive medical devices

Healthcare

Junior, Mid

No H1B Sponsorship

Austin, TX, USA

Category
QA & Testing
Quality Assurance
Required Skills
Word/Pages/Docs
Excel/Numbers/Sheets

You match the following ENOVIS's candidate preferences

Employers are more likely to interview you if you match these preferences:

Degree
Experience
Requirements
  • A bachelor’s degree in engineering or other technical discipline degree is required
  • A minimum of 2 years of experience in quality engineering or related field with, with focus on, process validations, product development supports
  • Previous knowledge of FDA/GMP, CMDR, MDD and ISO 13485 quality standards
  • Experience with Quality related tools (D and P FMEA, QFD, SPC, Risk Analysis, DOE, and TQM)
  • Previous experience with Microsoft Word, or equivalent word processing software; Excel, or equivalent spreadsheet software, as well as statistical analysis and data base searches.
Responsibilities
  • Involvement in the Master Validation Plan (IQ, OQ, PQ) regarding validation and verification Processes
  • Participate in continuous improvement activities to enhance quality systems, such as 5S, Kaizen lean methods, etc.
  • Interface with Engineering and Operations to ensure transfer to Production of new products are in accordance with approved data.
  • Support the Quality Inspectors/Techs to ensure that products and processes comply with the relevant requirements of the quality management system (QMS).
  • Participate in audits, including Notified Body Audits, FDA inspections and other 3rd party audits as well as closingout audit findings, creating audit finding reports and determine proper corrective and preventive actions.
  • Analyze failure, corrective and preventive actions needed to respond to customer complaints/supplier failures.
  • Maintain company quality documentation, such as quality manuals, quality procedures, etc.
  • Maintain Nonconformance System and the COPQ Initiatives.
  • Facilitate and Manage Gage R&R, SPC and capability requirements
  • Participate on launch and current production engineering changes
  • Supports Incoming Inspection; help maintain files and backup supplies for inspection.
Desired Qualifications
  • Previous working knowledge of US and International quality system regulations.
  • Proven project management skills; able to complete technical projects with minimal supervision. Strong interpersonal communication and teamwork skill.
  • ASQ certification with active local membership is preferred.
  • Lean Six Sigma Green Belt or higher preferred.
  • Ability to understand and interpret drawings and data – GD&T knowledge to interpret mechanical part drawings, assembly drawings, block and flow diagrams, and BOMs
  • Agile and Oracle experience highly desired.
  • Experience in the Medical Device Industry and lean manufacturing is a plus.
  • Must have statistical aptitude and understand concepts of geometric dimensioning and tolerance and knowledge of problem solving techniques.
  • Personal computer skills are required, as well as excellent verbal and written communication skills.
  • Application and implementation of regulations such as GMP/QSR/ISO/MDD and Canadian Medical Devices a plus.

Enovis develops medical technology solutions aimed at improving patient outcomes and restoring mobility. The company operates in two main segments: Prevention & Recovery, which includes orthopedic solutions like bracing products and therapy systems for rehabilitation and sports medicine, and Reconstructive, which focuses on implant products for various joints and minimally invasive surgical tools. Enovis's products, including well-known brands like DonJoy and Aircast, are designed to address specific medical needs such as pain management and bone growth stimulation. What sets Enovis apart from competitors is its commitment to continuous improvement through the Enovis Growth Excellence (EGX) system, which enhances operations and customer satisfaction. The company's goal is to innovate in the medical technology field to create better outcomes for patients and healthcare providers globally.

Company Stage

IPO

Total Funding

N/A

Headquarters

Wilmington, Delaware

Founded

2022

Growth & Insights
Headcount

6 month growth

31%

1 year growth

31%

2 year growth

3%
Simplify Jobs

Simplify's Take

What believers are saying

  • Growing demand for minimally invasive surgical solutions boosts Enovis's market potential.
  • Integration of digital health technologies opens new avenues for product innovation.
  • LimaCorporate acquisition expands Enovis's market share in the European orthopedic sector.

What critics are saying

  • Increased competition from Stryker and Zimmer Biomet in the orthopedic market.
  • Potential supply chain complexities from integrating LimaCorporate operations.
  • Regulatory challenges in obtaining FDA approvals for new products.

What makes ENOVIS unique

  • Enovis offers a diverse portfolio of orthopedic and reconstructive solutions.
  • The company integrates advanced materials like vitamin E-doped polyethylene in implants.
  • Enovis's acquisition of LimaCorporate enhances its transatlantic business capabilities.

Help us improve and share your feedback! Did you find this helpful?

Benefits

Health Insurance

Dental Insurance

Vision Insurance

401(k) Retirement Plan

Paid Vacation

Paid Sick Leave

Paid Holidays

Legal Services