Teva Pharmaceutical Industries Ltd. is an Israeli multinational pharmaceutical company with headquarters in Tel Aviv, Israel. It specializes primarily in generic drugs, but other business interests include active pharmaceutical ingredients and, to a lesser extent, proprietary pharmaceuticals
Job description
Regulatory Associates with experience range of 1-6 years in any of the markets/experience below
Qualification Requirements: Degree in science/life sciences/pharmacy or equivalent qualification(s)
Openings: 10
- EU (Post approval) – Experience in the Pharmaceutical Industry, ideally in Regulatory Affairs in EU Post Approvals
- US (Post Approval) – Experience in the Pharmaceutical Industry, ideally in Regulatory Affairs but R&D, Development or QA would also be considered
- Submissions Publishing- Regulatory Submission Publishing experience in EU, US & other market
- US Labeling- : Pharmaceutical industry experience, specifically in Regulatory Affairs with a focus on US Gx labeling
- RIMS- Experience of managing regulatory product registration data, ideally within a regulatory information management environment.
- RA Metrix & Compliance – Experience in the Pharmaceutical Industry with experience in data management,Basic Regulatory knowledge( US & EU) would be preferred as well as an understanding of regulatory data, Knowledge of Document Management Systems (DMS) and Learning management Systems (LMS)
Time and Venue
10th December , 10.00 AM – 4.00 PM
Venue: Teva Pharma D Wing, Tower 2, Sector – 40, Seawoods Grand Central,Seawoods (W), Navi Mumbai – 400706
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