Opportunity for a Quality Operations Manager production company based in South Dublin in a critical leadership role driving standards, productivity, quality and continuous improvement.
* Be a key member of the Quality Leadership Team and the site’s extended leadership team.
* Lead, inspire, and develop the Quality Engineering Team, promoting performance excellence through regular reviews and goal-setting.
* Partner with production teams to drive continuous improvement.
* Manage key quality system elements, including non-conformance processes, incident reporting, and customer complaint analysis.
* Oversee the activities of the Quality Control group.
* Lead key improvements in quality assurance and control systems.
* Build strong relationships with external customers.
* Ensure Regulatory compliance, maintain high-quality documentation, and audit preparation.
* Provide oversight and ensure GMP standards are consistently met in production and quality engineering activities.
Required:
* 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 proven track record of team development.
* Experience preparing technical documentation and managing CAPA systems.
* Familiarity with Statistical Process Control and Six Sigma methodologies (Greenbelt Certification is a bonus).
* Knowledge of FDA requirements and experience managing FDA audits.
* Experience with process validation, sterilization, and clean room environments is advantageous.
If interested in learning more please send an updated CV to aidan@synergyrecruitment.ie
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Manufacturing, Project Management, and Quality Assurance
Industries
Manufacturing
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