Teva Pharmaceuticals, a global leader in the pharmaceutical industry and the world’s largest producer of generic medicines, is inviting experienced professionals for an exciting Regulatory Affairs (US Post Approval) opportunity.
If you’re a passionate Regulatory Affairs professional with a strong background in US post-approval processes, this is your chance to join a team that drives global compliance and quality.
Recruitment Drive Details
Date: Saturday, 11th October 2025
Time: 10:00 AM – 2:00 PM
Venue: Teva Pharmaceuticals, Seawoods Grand Central, E Wing, Tower II, R-1, Sec 40, Navi Mumbai – 400706.
Open Position:
Regulatory Affairs Associate II / III – US Post Approvals
Experience Required: 4–10 years of relevant experience in Regulatory Affairs (US post-approval activities)
Key Skills & Responsibilities
M. Pharm candidates with solid experience in US post-approval submissions
Strong knowledge in Change Control Assessment for the US market
Hands-on experience with post-approval activities such as:
Annual Reports
CBE-0, CBE-30
PAS (Prior Approval Supplements)
Note: Only candidates with experience in US post-approval regulatory activities will be considered.
Why Join Teva?
At Teva, you’ll be part of a globally recognized pharmaceutical organization known for innovation, regulatory excellence, and career growth opportunities. The company has been Great Place To Work® Certified (India, 2024–2025) — a testament to its employee-first culture and professional development environment.
📩 How to Register
To participate in the recruitment drive, register yourself by clicking the link below or scanning the QR code in the post:
🔗 https://lnkd.in/gemDv3MC
OR https://lnkd.in/gemDv3MC
Make an Impact, Make it Yours.
Join Teva Pharmaceuticals and contribute to improving global health through regulatory excellence and innovation.
