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Manager, Quality Engineering

Job in Gainesville, Alachua County, Florida, 32601, USA
Listing for: Exactech
Full Time position
Listed on 2026-06-27
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, Quality Engineering
  • Engineering
    Regulatory Compliance Specialist, Quality Engineering
Job Description & How to Apply Below

Manager, Quality Engineering

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

  • 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 Advita Ortho

At Advita Ortho, everything we do is focused on innovation. Whether creating revolutionary ways to optimize the surgical experience, developing the latest in orthopedic implants and instruments, or using cutting-edge technology to improve efficacy and outcomes. These advancements transform the very experience of mobility and allow you to lead your patients to greater freedom. It's innovation in every step, every moment, every move.

Apply Now

Our Hiring Process

Stage 1:
Initial Interview

Stage 2:
Hiring Manager and Team Interview(s)

Stage 3:
Final Selection

Stage 4:
Offer

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