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Role Overview:
- Contribute to the development and lifecycle management of pharmaceutical labeling strategies.
- Ensure regulatory compliance and improve patient access to innovative treatments.
Key Responsibilities:
- Develop and maintain global labeling documents including CCDS, USPI, and regional labels.
- Manage post-approval labeling activities, safety variations, and regulatory submissions.
- Collaborate with cross-functional teams to ensure accurate, timely, and compliant product information.
Requirements:
- Bachelor's degree in Life Sciences, Pharmacy, Chemistry, or equivalent experience.
- 7-8 years of pharmaceutical regulatory affairs experience with labeling expertise.
- Proficiency in SPL and document management systems.
Benefits:
- Fully remote working arrangement based in India.
- Professional development and career growth opportunities.
- International collaboration across global markets.
Confidential
The hiring company is a pharmaceutical organization focused on developing and maintaining labeling strategies for innovative treatments. It offers a globally connected remote work environment that values precision, collaboration, and continuous professional development.