At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised. **What You Can Expect** Maintain Document Control program to ensure compliance to domestic and international medical device regulations through supervision of Document Control and/or Records Management team members. **How You'll Create Impact** + Supervise Document Control and/or Records Management team member for maintaining, improving and overseeing all existing department processes and personnel + Ensures team members are well trained and have all necessary tools to execute their jobs and make the department successful + Organizes department priorities to ensure changes are processed timely and in the order which meets the demands of the business + Assists in internal and external audits to explain the process and facilitate the retrieval of documents to support the audit + Leads projects related to the improvement of department processes + Ensures Zimmer Biomet documentation including but not limited to DHRs, DHFs, DMR, work instructions, are handled appropriately. + Creates and manages department KPIs to measure performance of the department + Responsible for maintaining, improving and overseeing all existing department processes and personnel _This is not an exhaustive list of duties or functions and may not necessarily comprise all of the "essential functions" for purposes of the ADA._ **What Makes You Stand Out** + Knowledge of current Food and Drug Administration (FDA) laws, regulations and practices. + Ability to objectively deal with individuals using appropriate tact and diplomacy to establish and maintain a congenial relationship. + Proficiency in report writing. + Good word processing and data base skills. + Outstanding organizational skills. + High attention to detail. **Your Background** + High school diploma required, Bachelor’s degree a plus. + Minimum of 8 years combined industry (biomedical, medical device) and/or military experience; or 10 years of combined industry, military and/or related (general manufacturing, quality or logistics) experience. + A combination of education and experience will be considered. + 3 years supervisory or leadership experience required but 5+ years preferred; may include military leadership experience. **Travel Expectations** Up to 5% EOE/M/F/Vet/Disability