Regulatory Affairs Jobs | Teva is Hiring | Apply Now
Looking for high-growth Regulatory Affairs jobs in the pharmaceutical industry? A promising Teva Career opportunity is now open for life science professionals in Navi Mumbai. If you are searching for stable and globally recognized life science jobs in regulatory publishing and submission management, this role could be your gateway into international pharmaceutical compliance.
- Job Title: Regulatory Affairs Associate I – RA Publishing
- Location: Navi Mumbai, Maharashtra, India (400706)
- Job ID: 66406
About the Company
Teva Pharmaceuticals is a leading global biopharmaceutical company known for its strong generics portfolio and innovative medicines across neuroscience and immunology. With a presence worldwide, Teva focuses on delivering high-quality medicines while fostering a collaborative and inclusive workplace culture. This Teva Career opportunity allows professionals to contribute to global regulatory submissions across the EU, US, and Canada markets.
Key Responsibilities
- 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
- Master’s in Life Sciences.
- Total years of experience required for the role: 1-3 years (if any, preferred Regulatory Publishing experience in EU and US market).
Skills
- Command over spoken and written English.
- Sensitivity to the cultural diversity of a global organization.
- Good understanding of regulatory IT systems.
If you are actively seeking Regulatory Affairs jobs in a global pharmaceutical company, this Teva Career opportunity offers strong exposure to international regulatory publishing standards. Among competitive life science jobs, this position provides structured learning, compliance expertise, and career growth in global regulatory submission management.
