This position is responsible for providing knowledge and expertise for compliance with the FDA Quality System Regulations ISO 13485 Quality System Standard MDD CMDR JPAL and other applicable regulations. This role will plan lead and participate in corrective and preventive actions improvement projects and objectives to implement and maintain a Global Quality Systems. Principal Duties and Responsibilities Functions as a regulatory compliance resource to the company. Provides guidance to facilitate the development of procedures and processes and to comply with applicable regulations and standards. Assists with new acquisition integration into the Zimmer Quality System. Leads directs or consults on projects...read moreApply NowCompany
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