Quality Supervisor

Integer

Base: not specified; bonus/equity: cash-based ince...
Bachelor's degree in engineering or related technical field
3 years of experience in quality management
Knowledge of iso 13485 and fda regulations
The primary purpose of this role is to be a functional leader within the quality organization, coordinating team deliverables and providing daily direction to quality professionals

Job Summary

  • The primary purpose of this role is to be a functional leader within the quality organization, coordinating team deliverables and providing daily direction to quality professionals.
  • You will ensure adherence to the Quality Management System, support corrective and preventive actions investigations, and contribute to the successful attainment of quality KPIs.
  • Our total rewards program includes base salary, a cash-based incentive program, comprehensive benefits with immediate eligibility, and a 401(k) plan with company matching contributions.

Matching Summary

The primary purpose of this role is to be a functional leader within the quality organization, coordinating team deliverables and providing daily direction to quality professionals.

Salary

Base: Not specified; Bonus/Equity: Cash-based incentive program supporting pay-for-performance; Benefits: Medical, dental, vision, disability, life insurance, adoption benefits, parental leave, 401(k) with match

Skills & Requirements

Must-have

  • Bachelor's degree in engineering or related technical field
  • 3 years of experience in quality management
  • Knowledge of ISO 13485 and FDA regulations
  • Experience with Quality Management Systems (QMS)
  • Ability to lead and develop quality teams

Nice-to-have

  • Strong bias for action and decision making
  • Calm demeanor in high energy environments
  • Experience with EU MDR and 21CFR820
  • Proficiency in root cause analysis techniques
  • Commitment to inclusive work environment

Key Requirements

  • Minimum bachelor's degree in engineering
  • 3 years minimum experience required
  • Specialized knowledge of ISO 13485 and FDA regulations
  • Auditing experience required
  • Technical aptitude in manufacturing quality

Work Rights

Not specified

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