Government Affairs Representative supports the implementation of strategic plans and engagement objectives to develop and maintain productive relations with all levels of government authorities to achieve business goals. Liaises with government entities (federal, state, provincial, or local) that regulate or influence business activities. Being a Government Affairs Representative collaborates with industry groups and organizations with complementary objectives to achieve objectives. Monitors and analyses proposed legislation, emerging issues, and trends and prepare reports and informational documents to inform and support business leaders. Additionally, Government Affairs Representative requires a bachelor's degree in public policy, public administration, business or equivalent. Typically reports to a manager. The Government Affairs Representative work is generally independent and collaborative in nature. Contributes to moderately complex aspects of a project. To be a Government Affairs Representative typically requires 4 -7 years of related experience. (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
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