Top Regulatory Affairs Executive oversees all regulatory matters and creates the overall strategy to ensure the organization complies with applicable regulations. Develops processes and systems to ensure that all necessary licensing, filings, certifications, and permits are processed and monitored. Being a Top Regulatory Affairs Executive establishes monitoring policies and procedures to ensure compliance with existing regulations. Anticipates new or changing regulations and coordinates with internal stakeholders to develop strategies to address changes in product, operations, or testing requirements. Additionally, Top Regulatory Affairs Executive investigates and addresses any reported issues of non-compliance. Requires a bachelor's degree. Typically reports to top management. The Top Regulatory Affairs Executive manages a business unit, division, or corporate function with major organizational impact. Establishes overall direction and strategic initiatives for the given major function or line of business. Has acquired the business acumen and leadership experience to become a top function or division head. (Copyright 2024 Salary.com)
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 recognized.
Requires a Bachelor’s degree in Regulatory Affairs, Engineering, or Life Sciences, or related field.
Requires 5 years of experience in the job offered or a related role.
Must have 3 years of experience in orthopaedic or medical device industry.
Must have 3 years of experience with FDA and EU regulations (including labeling regulations) and regulations outside of the US/EU.
Must have 2 years of experience working with medical products and advanced anatomic knowledge.
Must have 2 years of experience with Interpreting and applying FDA regulations to business practices and providing regulatory input, advice, and guidance to the organization and design teams.
Position permits remote work throughout the U.S. Position requires up to 15% domestic travel.
EOE/M/F/Vet/Disability
Clear All
0 Top Regulatory Affairs Executive jobs found in Elkhart, IN area