As a regulatory affairs specialist, you will play a pivotal role in ensuring the seamless launch of medical technologies worldwide. About the Role - The primary responsibility of this position is to oversee all regulatory filings for medical devices and equipment. Your Expertise - A Bachelor's degree in a relevant field such as life sciences or technical engineering is required. - Prior experience in the orthopedic or medical device industry is highly desirable. - A minimum of 3-5 years of experience in Regulatory Affairs, Engineering, Quality, or a related field is mandatory. Key Requirements - You must possess excellent communication and interpersonal skills to effectively collaborate with cross-functional teams. - A high level of attention to detail is crucial in maintaining registration databases and product registration records. - Strategic thinking and problem-solving skills are essential in developing regulatory strategies for new products. Benefits - This role offers the opportunity to work with a global leader in medical technology. - The ideal candidate will have the chance to contribute to the development of innovative solutions that enhance patient mobility. What We Offer - A dynamic and supportive work environment that fosters growth and professional development. - A competitive compensation package that reflects your value to the organization. - The possibility of traveling up to 10% of the time.