Quality Assurance Supervisor (spiddal Galway)

Integer

**
Bachelor's degree in engineering or related technical field
3 years of experience in quality management
Knowledge of iso 13485, iso 9001, fda regulations, and gmp
** Integer is seeking a Quality Assurance Supervisor in Spiddal, Galway, to lead a team of quality professionals in ensuring compliance with quality management systems and performance goals. The ideal candidate will have a technical background in quality engineering and demonstrate strong leadership, collaboration, and problem-solving skills. **

Job Summary

  • The primary purpose of this role is to be a functional leader within the quality organization, coordinating team deliverables to ensure manufacturing site quality requirements are met.
  • You will supervise, coach, and direct a team of quality professionals while promoting a diverse and inclusive work environment where team members feel supported.
  • Success in this role requires adherence to strict regulatory standards including EU MDR, ISO 13485, and FDA regulations while driving continuous improvement activities.

Matching Summary

Match Score: 75

** Integer is seeking a Quality Assurance Supervisor in Spiddal, Galway, to lead a team of quality professionals in ensuring compliance with quality management systems and performance goals. The ideal candidate will have a technical background in quality engineering and demonstrate strong leadership, collaboration, and problem-solving skills. **

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, and GMP
  • Experience with Quality Management Systems (QMS) and CAPA
  • Ability to lead teams and manage non-conforming material processes

Nice-to-have

  • Strong bias for action and problem-solving skills
  • Experience with risk-based approach to process control
  • Ability to work independently in a fast-paced environment
  • Commitment to fostering an inclusive and diverse work culture
  • Proficiency in data analysis for root cause identification

Key Requirements

  • Minimum bachelor's degree in engineering
  • 3 years minimum experience required
  • Specialized knowledge of medical device regulations
  • Auditing experience preferred

Work Rights

Not specified

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