Regulatory Affairs Labeling Specialist (Fully Remote)

Manage regulatory labeling activities for medicinal products across multiple procedures. Ensure accurate and compliant product information through collaboration with internal and client teams. Responsibilities: Conduct regulatory impact assessments and maintain product information documentation. Prepare and submit variations, notifications, and renewals to Health Authorities. Coordinate labeling updates, translations, and post-approval activities in Veeva RIMS. Requirements: Bachelor's degree in Life Sciences, Pharmacy, Chemistry, or related field. At least 6 years of experience in regulatory affairs or labeling. Strong knowledge of regulatory procedures, Veeva RIMS, and TrackWise. Work remotely from India with international team exposure. Access continuous learning and career growth opportunities. Contribute to meaningful patient-focused regulatory compliance. Jobgether A global clinical research organization dedicated to improving patient outcomes through regulatory affairs and medicinal product compliance. It fosters a collaborative, patient-focused culture with opportunities for professional development. #J-18808-Ljbffr