Quality Control Manager

Avery Dennison Corporation

Longford, Ireland
Not specified; not specified; healthcare allowance...
On-site
Formulate quality strategy for medical devices
Ensure compliance with cgmp and fda regulations
Drive improvements to quality systems
Avery Dennison Corporation is seeking a Quality Control Manager for their Longford, Ireland location. The role requires managing the quality function within the medical device sector, emphasizing compliance with regulatory standards and fostering a high-performance culture

Job Summary

  • You will manage the quality function by providing work direction for quality engineers and inspectors while interacting with engineering and manufacturing functions.
  • The role requires formulating a strategy to foster a high-performance culture suitable for a world-class medical device contract manufacturer.
  • Employees benefit from additional leave based on seniority up to 25 days after 10 years, flexible working arrangements, and free onsite parking.

Matching Summary

Match Score: 85

Avery Dennison Corporation is seeking a Quality Control Manager for their Longford, Ireland location. The role requires managing the quality function within the medical device sector, emphasizing compliance with regulatory standards and fostering a high-performance culture.

Salary

Not specified; Not specified; Healthcare allowance, Insurance & Pension, Service Awards, Gift Vouchers

Skills & Requirements

Must-have

  • Formulate quality strategy for medical devices
  • Ensure compliance with cGMP and FDA regulations
  • Drive improvements to quality systems
  • Review plant validation protocols and reports
  • Engage directly with customer quality representatives

Nice-to-have

  • Foster a culture of curiosity and courage
  • Build value with top 10 key accounts
  • Collaborative and dynamic work environment
  • Diverse teams and inclusive culture
  • Commitment to innovation in patient care

Key Requirements

  • Bachelor's degree in Engineering or scientific field
  • Minimum 4 years experience in medical device or pharmaceutical industry
  • At least 3 years experience in regulatory compliance and quality systems
  • At least 4 years experience managing a team
  • Thorough knowledge of ISO 13485 and 21CFR Part 820
  • Certified Quality Engineer (CQE) or Certified Quality Auditor (CQA)

Work Rights

Not specified

Tailored Resume

Cover Letter