Opportunity in France for a permanent Senior Quality Manager to head up the Quality function in a large manufacturing pharmaceutical site – are you looking for that next move in your career?
The person will ensure that the Quality Management System is implemented and maintained in conformity with ISO9001, ISO13485, 21CFR820 and all regulatory requirements (cf DOC9360/1) in order to ensure compliance during audits and inspections.
Ensure the quality of the products, through the controls, the work environment, the laboratory of analysis, the validations. Ensure continuous improvement and quality spirit in the company for customer satisfaction and Manage the “Quality Management System” process.
Ensure that the quality management system and processes are implemented and maintained in conformity with the standards ISO 9001, ISO 13485, 21CFR820 and the applicable regulatory requirements (DOC9360/1), while maintaining the certifications obtained (quality and regulatory).
Report on the operation and effectiveness of the quality management system to management in order to review it and serve as a basis for continuous improvement and overall encourage awareness of customer requirements and regulatory requirements within the company.
Build on relations with notified bodies and competent authorities (FDA, TGA) to organize, handle and follow-up all audits and inspections of the site.
For further Information on this role, please contact Michelle Murphy on 091-706711 for a confidential conversation or email firstname.lastname@example.org
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