Regulatory Affairs Jobs | Teva is Hiring in Navi Mumbai | Apply Now
Looking to start or grow your Life Science Jobs journey in global pharma? Teva Careers 2026 brings an excellent opportunity for aspiring professionals through Regulatory Affairs Jobs in Regulatory Publishing. This role is ideal for pharmacy and life science graduates who want hands-on exposure to global submissions, regulatory systems, and international agency standards.
Job Details
- Job Title: Regulatory Affairs Associate I
- Location: Navi Mumbai, India, 400706
- Job Id: 64525
About the Company
Teva Pharmaceuticals is one of the world’s leading manufacturers of generic medicines, serving millions of patients across nearly 60 countries. The company plays a vital role in improving access to affordable healthcare and produces several medicines listed on the WHO Essential Medicines List. With a strong global presence, Teva combines innovation, compliance, and scale to deliver quality healthcare solutions. Teva Careers offer exposure to international regulatory environments and structured professional growth. The organization is known for its inclusive culture and commitment to improving global health. Teva provides long-term opportunities for a meaningful Life Science Career.
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 the 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, and Lorenz Validator.
Education and Experience
- 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).
Skills
- Command over spoken and written English.
- Sensitivity to the cultural diversity of a global organization.
- Good understanding of regulatory IT systems.
These Regulatory Affairs Jobs at Teva Pharmaceuticals offer a strong foundation for professionals aiming to build a global Life Science Career. With exposure to international submissions, regulatory systems, and compliance-driven work, Teva Careers provide stability, learning, and long-term growth in the pharmaceutical industry.
