Teva is one of the largest biopharmaceutical organization, committed to improving health and increasing access to quality health solutions
worldwide. Teva R&D is inviting Regulatory Affairs Professionals with experience in below skillsets.
📢 Walk-in Drive!!
Join us for our Recruitment drive on 21st February (Saturday)!!
We are looking for Regulatory Affairs professionals to join our GRA team at TEVA Pharmaceuticals!
Job Details:
- Qualification-Degree in science/Life sciences/pharmacy or equivalent qualification
- Work Location – Seawoods, Navi Mumbai
Open Positions:
- Regulatory Affairs Associate I/II/III – US post approvals (2-10 years of relevant US post approval experience)
Experience in Change control assessment for US market & post approval activities like annual report, СВЕ 0, СВЕ 30 and PAS - Regulatory Affairs Associate I – Global Requlatory Operations (2-4 years of experience)
Experience in regulatory data management in pharma domain, regulatory knowledge (US & EU) would be preferred - Regulatory Affairs Associate I/II– EU Market RA – Support Team (2-6 years of experience)
Experience in Regulatory Affairs knowledge of Blueprint reviews and approvals process, Veeva Vault systems, Office-365 applications. - Regulatory Affairs Associate I/II – EU post approvals (2-6 years of experience)
Experience in pharma industry ideally in Regulatory Affairs in EU post approvals
Register now using QR code to have career conversations with us.
Walk-In Drive Details:
- Date: Saturday 21st Feb 26
- Time: 10AM to 2PM
- Drive Venue:
Teva Pharmaceuticals, C-Wing, 8th floor, Time Square Building, Makwana Road, Taluka – Gamdevi, Marol, Andheri (East), Mumbai- 400059.
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