
Real job — pulled straight from Advita’s careers page · Verified September 10, 2026 · No reposts.
Job description
Advita is hiring a Manager, Quality Engineering — a full-time, based in Gainesville, FL role. Apply directly on Advita's careers page below.
Director, Quality Engineering
Department: Quality
Employment Type: Full Time
Location: Gainesville, Florida, Gainesville, FL
Key Responsibilities
Organizational Leadership: Lead, develop, and scale the Quality Engineering function; set clear objectives, build leadership capability, allocate resources, and ensure team priorities align with enterprise and operational goals.
CAPA & Quality System Effectiveness: Direct systemic root cause analysis, corrective and preventive action strategy, and cross-functional remediation efforts to eliminate recurring quality issues and strengthen QMS effectiveness.
Complaints, Nonconformance & Risk Escalation: Oversee complaint, nonconformance, containment, disposition, and escalation processes; ensure timely resolution, appropriate risk-based decision-making, and alignment with regulatory and business expectations.
Quality Metrics & Governance: Define, monitor, and communicate Quality Engineering performance metrics, trends, and risk indicators; support Management Review, Quality Governance, and leadership decision-making.
Audit & Inspection Leadership: Serve as a senior Quality Engineering leader during internal audits, external audits, notified body assessments, and regulatory inspections; represent the function with credibility and sound judgment.
Cross-Functional Influence: Partner with Operations, R&D, Regulatory Affairs, Clinical, Supply Chain, and executive stakeholders to resolve complex issues, improve quality outcomes, and align quality priorities with business needs.
Skills Knowledge and Expertise
- Bachelor’s Degree in Science from an accredited institution required; Master’s Degree preferred
Experience:
- Minimum of 12 years of progressive quality, engineering, manufacturing, or regulatory experience, preferably in orthopedic or other medical device environment
- Demonstrated ability to establish, lead, and improve Quality System processes, including governance mechanisms that measure effectiveness and drive sustained compliance.
- Minimum of 8 years of leadership experience in Quality Engineering, Quality Assurance, or a related medical device function, including experience leading managers, technical teams, or cross-functional quality initiatives.
- Advanced knowledge of inspection strategy, specification development, statistical techniques, gage R&R, GD&T applications, process validation, and risk-based quality decision-making.
- Significant experience representing Quality Engineering during FDA inspections, notified body audits, customer audits, and senior-level quality governance forums.
- Executive-level verbal, written, presentation, and leadership communication skills, with the ability to influence decisions and communicate risk clearly across all levels of the organization.
- Strong business acumen and ability to partner effectively with Operations, R&D, Regulatory Affairs, Clinical, Supply Chain, Commercial, and executive leadership to align quality priorities with business objectives.
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Frequently asked questions
What skills are required for Manager, Quality Engineering at Advita?
The required skills for Manager, Quality Engineering at Advita include: Auditing.
What is the seniority level for Manager, Quality Engineering at Advita?
Manager, Quality Engineering at Advita is a Manager level position.
How do I apply for Manager, Quality Engineering at Advita?
You can view the full description and apply for Manager, Quality Engineering at Advita on EchoJobs: https://echojobs.io/job/advita-manager-quality-engineering-quality-wcgn3.