Global Regulatory Affairs Lead – Medical Devices

A leading health technology company is seeking a Senior Regulatory Affairs Specialist to support respiratory care products. The role requires extensive experience in regulatory processes within the medical devices industry, specifically in handling submissions and compliance with 21 CFR and EU MDR standards. A Bachelor's or Master's degree in relevant fields is required. The position entails collaborating with cross-functional teams and monitoring regulatory changes. This is an office role with competitive compensation and benefits. #J-18808-Ljbffr