Regulatory Affairs Specialist
hace 4 semanas
Zimmer Biomet is a global medical technology leader with a rich history of innovation and a commitment to improving the quality of life for people around the world. Our team members are part of a company that is shaping the future of healthcare and alleviating pain.
What to Expect
As a Regulatory Affairs Specialist, you will be responsible for ensuring that our medical devices comply with regulatory requirements and standards. You will work closely with cross-functional teams to develop and implement regulatory strategies, manage regulatory submissions, and maintain regulatory records.
Impact You Will Create
You will play a critical role in ensuring the quality and safety of our medical devices, which will have a direct impact on the lives of patients and healthcare professionals. Your expertise will help us to navigate complex regulatory landscapes and stay ahead of the competition.
What Sets You Apart
As a Regulatory Affairs Specialist, you will have the opportunity to work on a wide range of medical devices and technologies, from orthopedic implants to surgical instruments. You will be part of a team that is passionate about improving healthcare and making a difference in people's lives.
Your Experience
We are looking for a highly motivated and experienced Regulatory Affairs Specialist who has a strong background in medical device regulation and compliance. You will have a proven track record of success in managing regulatory submissions, developing regulatory strategies, and maintaining regulatory records.
Travel Expectations
This role may require occasional travel to attend industry conferences, meetings with regulatory agencies, and visits to our manufacturing facilities. However, most of your work will be done remotely, and you will have the flexibility to work from home or our office locations.
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