Regulatory Affairs Senior Specialist (Medical Device)

Develop and execute regulatory strategies for new and existing medical devices.Ensure compliance with local, regional, and international regulations.Prepare and submit regulatory documents.Maintain technical documentation and product registration databases.Support the team with regulatory approvals and documentation. At least 3-5 years of experience in regulatory affairs, preferably in the medical device industry.Bachelor’s degree in science. At least 3-5 years of experience in regulatory affairs, preferably in the medical device industry.Bachelor’s degree in science.