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Zimmer Biomet is a global medical technology leader with a rich history of innovation and commitment to improving patient outcomes. With a presence in nearly 100 countries, our products and technologies enhance patient mobility and quality of life.
Our MissionWe are dedicated to providing mobility and renewed life to people around the world. Our team is passionate about delivering exceptional products and services that meet the evolving needs of healthcare professionals and patients.
What You Can Expect- A dynamic and collaborative work environment that fosters growth and development
- A comprehensive benefits package that supports your physical and mental well-being
- Opportunities to work on cutting-edge projects and contribute to the development of new technologies
- A culture of recognition and performance awards that celebrates individual and team achievements
As a Regulatory Affairs Specialist at Zimmer Biomet, you will play a critical role in ensuring the compliance of our products with regulatory requirements. Your expertise will help us navigate complex regulatory landscapes and ensure that our products meet the highest standards of quality and safety.
What Sets Us ApartWe are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and has a strong sense of belonging. Our company culture is built on a foundation of trust, respect, and open communication.
Your ExperienceWe are seeking a highly motivated and experienced Regulatory Affairs Specialist to join our team. If you have a strong background in regulatory affairs and a passion for medical technology, we encourage you to apply.
Travel ExpectationsThis role may require occasional travel to support regulatory submissions and meetings with regulatory agencies.