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At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward.
As a general 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 versátil 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 ExpectResponsible for assisting the team with regulatory filings as necessary to market Zimmer Biomet products.
This position requires an intermediate understanding of medical devices and their use as well as an understanding of the regulatory submission process in different regions such as Asia Pacific,
Latin America and EMEA.How You'll Create ImpactPreparation, assembly, storage, tracking and retrieval of information pertinent to the regulatory processes, including the regulatory submissions process.
May author and publish electronic submissions for product registrations, renewals and registration changes.Maintains registration databases, product registration records, key performance indicators current, and communicates approved registrations.Executes registration processes in assigned countries, working closely with Business Unit Regulatory Teams to request information, business partners "distributors" to ensure registrations are submitted on time and kept current in compliance with applicable legislation.Provides regulatory direction to development project teams as a core team member; develops regulatory strategy for new products.Evaluate risk of proposed regulatory strategies; ma
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