Regulatory Affairs Job at Teva for Life Sciences Grads in Navi Mumbai – Apply Now!
Are you a Life Sciences postgraduate ready to build your career in regulatory publishing? Teva Pharmaceuticals, a global leader in generic medicines, is hiring a Regulatory Affairs Associate I at its Navi Mumbai office. This role is ideal for professionals with 1–3 years of experience in regulatory publishing for EU and US markets. Join a purpose-driven team impacting 200 million lives daily.
About Teva Pharmaceuticals
Teva is the world’s leading manufacturer of generic medicines, impacting over 200 million lives daily. With operations in nearly 60 countries and a strong mission to improve healthcare access and affordability, Teva is home to innovation, diversity, and purpose. The company features products listed in the WHO Essential Medicines List and is driven by people dedicated to making a difference.
Job Details:
- Job Role: Regulatory Affairs Associate I
- Location: Navi Mumbai, India, 400706
- Job ID: 61912
- Reports To: Manager – Regulatory Submission Management
Job Overview
As a Regulatory Affairs Associate I, your role will focus on publishing and dispatching lifecycle management eCTD submissions for major global markets such as the EU, US, and Canada. You’ll work closely with Regulatory Affairs
teams and ensure timely, quality-controlled submissions aligned with agency standards.How will you spend your day
- 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 a working knowledge of internal and external publishing standards.
- Basic knowledge of ICH and eCTD related specifications/guidelines governing regulatory submissions (eCTD, NeeS, paper).
Your experience and qualifications
- Education: Master’s in Life Sciences
- Experience: 1–3 years of experience required for the role (preferably with regulatory publishing experience in the EU and US markets)
- Language: Strong command of spoken and written English
- Additional Skills: Sensitivity to the cultural diversity of a global organization, good understanding of regulatory IT systems
Keywords: Teva Pharmaceuticals, Regulatory Affairs Associate, Regulatory Affairs, Publishing, Regulatory Submissions, Life Sciences, Regulatory IT, Navi Mumbai
