Regulatory Affairs Associate I – Teva Pharmaceuticals | Pharma Graduates
- Regulatory Affairs Associate I – Teva Pharmaceuticals | Pharma Graduates | Bangalore Location | 1+ Year Experience
- Regulatory Affairs Associate I – Join Teva’s Global Labeling Team
- Your experience and qualifications
- Reports To
- Apply Online
Regulatory Affairs Associate I – Teva Pharmaceuticals | Pharma Graduates | Bangalore Location | 1+ Year Experience
Apply for Regulatory Affairs Associate I at Teva Pharmaceuticals in Bangalore. Open to Pharma graduates with 1+ year of regulatory affairs or editorial experience.
Regulatory Affairs Associate I – Join Teva’s Global Labeling Team
Teva Pharmaceuticals, a global leader in generic and specialty medicines, is hiring a Regulatory Affairs Associate I for its Bangalore location. This opportunity is ideal for pharmaceutical and medical science graduates with basic knowledge or hands-on experience in regulatory affairs, European pharmaceutical law, or editorial roles.
- Publish and dispatch major and complex routine/lifecycle management eCTD submission projects for EU, US and Canada.
- Exposure in handling post approval submissions publishing and transmitting quality submissions to agency.
- Perform document level publishing activities, troubleshoot document issues and perform quality control checks for submission ready documents as per the agency guidance.
- Collaborate with scientific personnel for planning, preparation and publishing
- Maintain working knowledge of internal and external publishing standards.
- Basic knowledge of ICH and eCTD related specification/guidelines governing regulatory submissions (eCTD, NeeS, paper)
- Must be aware of technical systems like Global Insight, Veeva Vault, ISI Toolbox, Adobe Acrobat, Lorenz Validator
Your experience and qualifications
- B. Pharm/M. Pharm/ Master of Life Sciences.
- Total years of experience required for the role: 1-3 years (if any, preferred Regulatory Publishing experience in EU and US market)
- Command over spoken and written English
- Sensitivity to the cultural diversity of a global organization
- Good understanding of regulatory IT systems
Reports To
Manager – Regulatory Submission Management
Apply Online
If you are passionate about global healthcare compliance and have the necessary background in Pharma or Life Sciences, this could be your next step forward.
apply online: Click to Apply
To apply for this job please visit careers.teva.
