Quality Assurance Supervisor (spiddal Galway)

Integer

Galway, Ireland
**
Bachelor's degree in engineering or related technical field
3 years of experience in quality management
Knowledge of iso 13485, iso 9001, fda regulations
** Integer is seeking a Quality Assurance Supervisor in Galway, Ireland, to lead a team of quality professionals in a manufacturing setting. The role emphasizes performance management, quality compliance, and team development within a culture that values innovation, collaboration, and integrity. **

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.
  • Success in this role requires driving process improvements using a risk-based approach and ensuring compliance with FDA regulations and company policies.

Matching Summary

Match Score: 75

** Integer is seeking a Quality Assurance Supervisor in Galway, Ireland, to lead a team of quality professionals in a manufacturing setting. The role emphasizes performance management, quality compliance, and team development within a culture that values innovation, collaboration, and integrity. **

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, 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
  • Experience with root cause analysis methodologies
  • Ability to work in a fast-paced complex environment
  • Commitment to fostering inclusive work environments
  • Proficiency in data analysis practices

Key Requirements

  • Minimum bachelor's degree in engineering
  • 3+ years of relevant experience
  • Specialized knowledge of EU MDR and 21CFR820
  • Auditing experience required
  • Technical aptitude for manufacturing quality

Work Rights

Not specified

Tailored Resume

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