Quality Supervisor

Integer

Base salary not specified; cash-based incentive pr...
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Bachelor's degree in engineering or related technical field
3 years of experience in manufacturing quality
Knowledge of iso 13485, iso 9001, and fda regulations
** Integer is seeking a Quality Supervisor to lead the quality organization within a manufacturing site, focusing on performance management and team development. The ideal candidate will have a background in engineering with knowledge of quality management systems and relevant regulations, driving process improvements and fostering a culture of quality. **

Job Summary

  • The primary purpose of this role is to be a functional leader within the quality organization, coordinating team deliverables to ensure quality requirements are met.
  • You will supervise, coach, and direct a team of quality professionals while promoting a diverse and inclusive work environment where mutual trust is shared.
  • The company offers a comprehensive benefits package including medical, dental, vision, disability, life insurance, and immediate eligibility for a 401(k) plan with company matching.

Matching Summary

Match Score: 75

** Integer is seeking a Quality Supervisor to lead the quality organization within a manufacturing site, focusing on performance management and team development. The ideal candidate will have a background in engineering with knowledge of quality management systems and relevant regulations, driving process improvements and fostering a culture of quality. **

Salary

Base salary not specified; Cash-based incentive program available; Comprehensive benefits including medical, dental, vision, 401(k) match, and 10 days holidays

Skills & Requirements

Must-have

  • Bachelor's degree in engineering or related technical field
  • 3 years of experience in manufacturing quality
  • Knowledge of ISO 13485, ISO 9001, and FDA regulations
  • Experience with CAPA and root cause analysis
  • Ability to lead and develop quality teams

Nice-to-have

  • Bias for action and decision making
  • Strong communication and interpersonal skills
  • Experience with EU MDR compliance
  • Positive can-do attitude in fast-paced environments
  • Cross-functional consensus building skills

Key Requirements

  • Minimum bachelor's degree in engineering or related technical field
  • Minimum 3 years of relevant experience
  • Specialized knowledge of quality system regulations (ISO 13485, FDA)
  • Auditing experience required
  • Technical aptitude for reviewing engineering change requests

Work Rights

Not specified

Tailored Resume

Cover Letter