Senior Quality Engineering Leader - Medical Devices

CONMED Corporation

Largo (FL)

On-site

USD 120,000 - 160,000

Full time

7 days ago
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Benefits offered by this job

Competitive compensation
Excellent healthcare (medical, dental,
Vision and prescription coverage
401K with company match
Employee stock purchase plan
Tuition assistance

Job summary

CONMED Corporation seeks a Sr. Manager Quality Engineering to support the full product lifecycle from concept to commercialization, ensuring compliance with quality systems and regulatory requirements.

The role partners with cross-functional teams to embed quality in development and manufacturing, driving continuous improvement and patient safety. The position requires a BS in Engineering and 8+ years in medical devices, plus supervisory experience and travel up to 15%.

Qualifications

  • B.S. degree in Engineering and 8+ years medical device experience or equivalent.
  • Travel 0–15% (including international).
  • Minimum of 2 years supervisory experience.

Responsibilities

  • Foster a culture of quality prioritizing patient safety and regulatory compliance.
  • Provide direction to product development teams for quality deliverables.
  • Ensure design verification/validation protocols adequately address inputs and needs.
  • Review engineering designs/changes for quality, reliability, and manufacturability.
  • Direct investigations and corrective actions for quality issues.
  • Support internal audits and audit preparation activities.
  • Mentor employees and drive continuous improvement.

Skills

Quality engineering
Cross-functional collaboration
Regulatory compliance
Mentoring/leadership

Education

B.S. in Engineering (Electrical/Mechanical/Biomedical)

Tools

Statistical methods

Job description

CONMED Corporation seeks a Sr. Manager Quality Engineering to support the full product lifecycle from concept to commercialization, ensuring compliance with quality systems and regulatory requirements.

The role partners with cross-functional teams to embed quality in development and manufacturing, driving continuous improvement and patient safety. The position requires a BS in Engineering and 8+ years in medical devices, plus supervisory experience and travel up to 15%.

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