Enovis
Who We Are
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.
Visit
www.enovis.com
to learn more.
What You’ll Do As a key member of the Quality Department, you will play an integral part in helping Enovis drive the medical technology industry forward through transforming patient care and creating better patient outcomes. You will support and manage quality processes including Field Actions, CAPAs, SCARs and NCMRs, ensuring full compliance with internal procedures and regulatory standards. You will maintain and report critical quality metrics that reflect the overall health of plant operations and production/quality controls. These metrics are regularly shared with senior leadership and cross‑functional teams to drive performance, accountability and compliance across the organization. You will collaborate with cross‑functional teams to gather data and ensure timely resolution of quality issues and identify trends, recurring issues, and opportunities for process improvement.
Job Title & Details
Job Title:
Quality Specialist
Reports To:
Associate Manager, QMS
Location:
Austin, TX
Business Unit Description:
Quality Department
Key Responsibilities
Support the initiation, investigation, and closure of quality records.
Corrective and Preventive Actions (CAPA).
Supplier Corrective Action Requests (SCAR).
Non‑Conformance Reports (NCMR).
Trends in Quality Metrics and Key Performance Indicators (KPIs).
Maintain accurate and timely documentation within the Quality Management System (QMS).
Collaborate with cross‑functional teams to gather data and ensure timely resolution of quality issues.
Monitor and report the status of open quality records.
Assist in root cause analysis and effectiveness verification for CAPAs and SCARs.
Ensure compliance with company policies, procedures, and applicable regulations (FDA, ISO 13485, etc).
Participate in internal audits and support external audits as needed.
Identify trends, recurring issues, and opportunities for process improvement.
Minimum Basic Qualifications
Bachelor’s degree in Engineering, Life Sciences, or a related field.
0-2 years of experience in a Quality or Regulatory environment.
Familiarity with CAPA, SCAR, NCMR, and Quality KPI processes is preferred.
Strong attention to detail, organization, and analytical skills.
Excellent written and verbal communication abilities.
Ability to work independently and collaboratively in a cross‑functional team environment.
Proficiency in Microsoft Excel; experience with OBIEE and Agile PLM is preferred.
Travel Requirements
0-25%
Benefits
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.
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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Visit
www.enovis.com
to learn more.
What You’ll Do As a key member of the Quality Department, you will play an integral part in helping Enovis drive the medical technology industry forward through transforming patient care and creating better patient outcomes. You will support and manage quality processes including Field Actions, CAPAs, SCARs and NCMRs, ensuring full compliance with internal procedures and regulatory standards. You will maintain and report critical quality metrics that reflect the overall health of plant operations and production/quality controls. These metrics are regularly shared with senior leadership and cross‑functional teams to drive performance, accountability and compliance across the organization. You will collaborate with cross‑functional teams to gather data and ensure timely resolution of quality issues and identify trends, recurring issues, and opportunities for process improvement.
Job Title & Details
Job Title:
Quality Specialist
Reports To:
Associate Manager, QMS
Location:
Austin, TX
Business Unit Description:
Quality Department
Key Responsibilities
Support the initiation, investigation, and closure of quality records.
Corrective and Preventive Actions (CAPA).
Supplier Corrective Action Requests (SCAR).
Non‑Conformance Reports (NCMR).
Trends in Quality Metrics and Key Performance Indicators (KPIs).
Maintain accurate and timely documentation within the Quality Management System (QMS).
Collaborate with cross‑functional teams to gather data and ensure timely resolution of quality issues.
Monitor and report the status of open quality records.
Assist in root cause analysis and effectiveness verification for CAPAs and SCARs.
Ensure compliance with company policies, procedures, and applicable regulations (FDA, ISO 13485, etc).
Participate in internal audits and support external audits as needed.
Identify trends, recurring issues, and opportunities for process improvement.
Minimum Basic Qualifications
Bachelor’s degree in Engineering, Life Sciences, or a related field.
0-2 years of experience in a Quality or Regulatory environment.
Familiarity with CAPA, SCAR, NCMR, and Quality KPI processes is preferred.
Strong attention to detail, organization, and analytical skills.
Excellent written and verbal communication abilities.
Ability to work independently and collaboratively in a cross‑functional team environment.
Proficiency in Microsoft Excel; experience with OBIEE and Agile PLM is preferred.
Travel Requirements
0-25%
Benefits
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.
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.
#J-18808-Ljbffr