Quality Manager
3 weeks ago
Quality Manager
Our client is an innovative and progressive global company and is sourcing for a Quality Manager to join their team in Greater Dublin. This organisation has a manufacturing presence in over 40 countries around the world, with over 30 million people reliant on their products that serve to improve their lives.
The Quality Manager role is open to those who enjoy delivering a critical leadership role and have experience in providing the highest standards of quality, continuous improvement, and compliance. You will have the opportunity to work with a collaborative and skilled workforce alongside an encouraging leadership team within an organisation that is committed to empowerment, development, and career growth.
Responsibilities will include:
- Be a key member of the Quality Leadership Team and the site's extended leadership team.
- Lead, inspire, and develop the Quality Engineering Team, fostering collaboration, delegation, and performance excellence.
- Partner with production teams to drive continuous improvement initiatives.
- Manage key quality system elements.
- Oversee the activities of the Quality Control group, ensuring seamless integration and high performance.
- Lead key improvements in quality assurance and control systems, championing innovation and operational excellence.
- Build strong relationships with external customers, ensuring their needs and expectations are met.
- Ensure timely and compliant completion of CAPAs, maintain high-quality documentation, and prepare for audits with confidence.
- Provide oversight and ensure GMP standards are consistently met in production and quality engineering activities.
Education and Experience:
- A third-level qualification in Engineering or a Science discipline is required.
- 5+ years in an ISO 9001/2000 or ISO 13485 environment, ideally in Medical Devices or the Pharmaceutical industry.
- At least 3 years of supervisory experience with a track record of team development.
- Experience preparing technical documentation and managing CAPA systems.
- Familiarity with Statistical Process Control and Six Sigma.
- Knowledge of FDA requirements and experience managing FDA audits.
- Experience with process validation, sterilization, and clean room environments is advantageous.
This role offers a competitive salary & benefits package. For further details, please apply directly below or contact Darrach Teague.
Skills:
Quality Management, Continuous Improvement, Compliance
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