Quality Assurance Supervisor (spiddal Galway)

Integer

Not specified (assumed to be on-site given the manufacturing context)
Bachelor's degree in engineering or related technical field
3 years of experience in quality management
Knowledge of iso 13485, iso 9001, and fda regulations
Integer is seeking a Quality Assurance Supervisor to lead a quality team at their manufacturing site in Spiddal, Galway. The role requires a focus on performance management, adherence to quality standards, and fostering a collaborative and inclusive work culture

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 culture where every associate owns quality.
  • Success in this role requires adherence to strict regulatory standards including FDA regulations, ISO 13485, and Good Manufacturing Practices.

Matching Summary

Match Score: 85

Integer is seeking a Quality Assurance Supervisor to lead a quality team at their manufacturing site in Spiddal, Galway. The role requires a focus on performance management, adherence to quality standards, and fostering a collaborative and inclusive work culture.

Skills & Requirements

Must-have

  • Bachelor's degree in engineering or related technical field
  • 3 years of experience in quality management
  • Knowledge of ISO 13485, ISO 9001, and FDA regulations
  • Experience with Quality Management Systems (QMS)
  • Ability to lead teams and drive process improvements

Nice-to-have

  • Strong bias for action and decision making
  • Calm demeanor in high-energy manufacturing settings
  • Experience with EU MDR and Good Documentation Practices
  • Ability to foster inclusive and diverse work environments
  • Proficiency in data analysis and root cause investigation

Key Requirements

  • Minimum bachelor's degree in engineering
  • 3 years minimum experience required
  • Specialized knowledge of medical device regulations
  • Auditing experience required
  • Work authorization status not specified

Work Rights

Not specified

Tailored Resume

Cover Letter