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Karen Shiel
Life Science

+353 1 5079256
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Quality Manager

Reference:KS/HQ00001867 Location: Dublin
Qualification:DegreeExperience:4-5 Years
Job Type:PermanentSalary: Not Disclosed

Our client is an established organisation based in Dublin. They are currently seeking a Quality Manager who will be reporting to the Compliance Director. The Quality Manager is responsible for the management, direction and coordination of all quality and regulatory activities across the company. This includes providing the quality support to ensure that the required quality and regulatory standards are achieved. The Quality Manager is also responsible for actively promoting a culture of continuous quality improvement. This role provides leadership for Accreditation and inspections, safety assessments, educates others in the company on quality within the company.

• Lead the Quality functions & Quality Management Systems.
• Provide leadership and direction pertaining to quality across the company.
• Develop and maintain a collaborative working environment within the company by achieving quality standards and continuous improvement.
• Manage and develop the staff across departments through involvement, delegation, and regular reviews.
• Analyse customer complaints and modify processes/equipment/operator standards as necessary to eliminate defects.
• Responsible for ensuring adherence to all external and appropriate regulatory requirements (e.g. ISO, INAB).
• Be the contact person with all relevant Regulatory Bodies.
• Drive key changes and continuous improvement in site Quality Systems and Procedures.
• Be a key driver of GMP practices across the site.
• Manage quality metrics across the site and ensure adherence to company quality targets.
• Ensure the implementation of the Calibration Services Quality Management System is followed and continuous improvement addressed at all times.
• Manage internal quality audits.
• Maintain Quality Manuals.
• Training of staff pertaining to Quality Management System and adherence to National Accreditation Standards.

Educational Requirements:
• Bachelor’s Degree in an Engineering or Science Discipline.
• Ideally some post-graduation experience in Quality environment within Medical Devices/Pharmaceutical Industry.
• Excellent knowledge of an ISO 17025 environment.
• Experience in the preparation of Technical Documentation.
• Demonstrated ability to lead, direct and influence people.
• Excellent interpersonal and communication skills.
• Strong planning and organizational ability.
• Be self-motivated with a desire to drive the highest quality standards and build a quality orientated culture.

If you would like further Information you can contact the recruiter directly:

Karen Shiel | Tel: +353 (0) 1 5079256