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Advances patient lives through innovative orthopedic solutions and integrated surgical technologies

Manager, Quality Engineering

Posted: 6 months ago
Job Location
Remote Work Policy

In office

Visa Sponsorship

Not Available

RelocationAllowed
Skills
GD&T
gage R&R
Statistical Techniques
Inspection Specification Development

About the job

Manager, Quality Engineering

Department: Quality

Employment Type: Full Time

Location: Gainesville, FL

Reporting To: Director, Quality Management Systems

Description

The Manager, Quality Engineering, provides leadership to the Quality Engineering team by inspiring individuals and teams while creating an environment of organizational excellence to deliver results.

Key Responsibilities

  • Quality & Regulatory Compliance: Ensure alignment with FDA, ISO 13485, MDSAP, EU MDR, and internal QMS; maintain audit readiness and certification compliance.
  • Quality Engineering Leadership: Lead and develop the Quality Engineering team; align goals, performance, and resources to business objectives.
  • Product Realization (Design & Manufacturing): Oversee design controls, risk management, verification/validation, and process validation; ensure compliance with GD&T, inspection, and statistical requirements.
  • CAPA & Investigations: Drive root cause analysis, corrective/preventive actions, and cross-functional resolution of quality issues.
  • Complaints & Nonconformance: Lead investigation, containment, disposition, and timely resolution of complaints and nonconforming product; escalate risks as needed.
  • Data & Reporting: Track, analyze, and report quality metrics; support Management Review and Quality Governance.
  • Audit Support: Serve as SME during internal and external audits/inspections.

Skills Knowledge and Expertise

Education:

  • Bachelor’s Degree in Science from an accredited institution required; Master’s Degree preferred

Experience:

  • Minimum of 7 years experience, preferably in orthopedic or other medical device field.
  • Working understanding and leadership capability to ensure Quality System requirements are implemented and measured for effectiveness.
  • Minimum of 0-5 years prior QA Engineering management experience in a Medical Device Company.
  • Experience in inspection specification development, statistical techniques, gage R&R, and G,D&T applications
  • Prior audit experience with FDA and notified bodies.

Functional/Technical Knowledge, Skills and Abilities Required:

  • Excellent verbal, written communication and leadership skills.
  • Ability to work with all organizational functions.

About the company

Advita Sarl company logo
Advances patient lives through innovative orthopedic solutions and integrated surgical technologies201-500 Employees
Company Location
Grenoble
Company Size
201-500
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