Regulatory Affairs Specialist

Role Overview: As a Regulatory Affairs Specialist at Philips, you will be recognized as a key talent in International Regulatory filings and procedures. You will play a crucial role in the Centralization of Regulatory Operations to ensure regulatory compliance in markets where Philips products are commercialized. Your expertise will be invaluable as you contribute as a key regulatory point person. Additionally, you will be an impactful member of the Regulatory Affairs (RA) team, trusted by management to handle multiple projects independently. Your responsibilities will include assisting in the establishment of a center of excellence for RA operations to centralize regulatory functions for improved compliance, efficiency, and global market readiness. With your function spanning multiple geographies, effective prioritization, team meetings, and meeting project deadlines will be essential. Key Responsibilities: - Bring 6+ years of experience in international regulatory affairs to the table - Showcase expertise in Regulatory Affairs, Dossier Preparation, and experience in Class I, II - Possess a Bachelor's Degree in any Engineering field, preferably in Biomedical Engineering - Exhibit strong interpersonal skills and effective communication abilities Qualifications Required: - Hold a Bachelor's Degree in any Engineering, preferably in Biomedical Engineering - Have a minimum of 6 years of experience in Regulatory Affairs, Quality Compliance, Product Development in Medical Devices Industry or equivalent About the Company: Philips is a health technology company dedicated to providing quality healthcare to all individuals. Their mission is to ensure that everyone has access to the healthcare they deserve. If you are passionate about making a difference in the healthcare industry, Philips offers you the opportunity to contribute significantly to improving the lives of others.,