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Role Overview:
- 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.
Benefits:
- 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.