Director Of Quality Operations

HydraFacial

Base: $140,000 - $170,000; bonus: annual bonus inc...
Onsite
10+ years regulated industry experience
5+ years quality leadership in manufacturing
Iso 13485 and 21 cfr part 820 expertise
HydraFacial is seeking a Director of Quality Operations who will lead initiatives to enhance manufacturing and product quality within a regulated environment, particularly in medical devices and cosmetics. The ideal candidate will possess extensive experience in quality leadership, compliance, and continuous improvement methodologies

Job Summary

  • This role serves as the strategic quality leader responsible for driving excellence in manufacturing quality and product realization across global medical device and cosmetic initiatives.
  • The successful candidate will partner with executive leadership to align quality priorities with growth while ensuring robust compliance with ISO 13485 and 21 CFR Part 820.
  • HydraFacial offers a competitive total rewards package including base pay between $140,000 and $170,000 plus bonus, comprehensive benefits, and opportunities for professional growth.

Matching Summary

Match Score: 85

HydraFacial is seeking a Director of Quality Operations who will lead initiatives to enhance manufacturing and product quality within a regulated environment, particularly in medical devices and cosmetics. The ideal candidate will possess extensive experience in quality leadership, compliance, and continuous improvement methodologies.

Salary

Base: $140,000 - $170,000; Bonus: Annual bonus included; Benefits: Medical, dental, vision, 401(k) match, PTO, and more

Skills & Requirements

Must-have

  • 10+ years regulated industry experience
  • 5+ years quality leadership in manufacturing
  • ISO 13485 and 21 CFR Part 820 expertise
  • Supplier quality management and development
  • Lean Six Sigma continuous improvement
  • CAPA and root cause analysis methodologies
  • Cross-functional team leadership

Nice-to-have

  • Experience scaling quality systems in high-growth
  • Familiarity with ISO 14971 risk management
  • Knowledge of FDA OTC monographs
  • Cosmetic GMP regulatory frameworks
  • MDSAP or MDR working knowledge
  • Proven ability to build high-performing teams
  • Strong executive presence and communication

Key Requirements

  • 10+ years experience in regulated industries (medical devices preferred)
  • 5+ years in quality leadership role within manufacturing
  • Deep expertise in ISO 13485 and 21 CFR Part 820
  • Demonstrated success with Lean Six Sigma methodologies
  • Proven ability to lead cross-functional teams

Work Rights

Not specified

Tailored Resume

Cover Letter