Teva Walk-In Drive for Regulatory Affairs Team at Navi Mumbai – 10th December 2022
Be a part of our Regulatory Affairs Team at Navi Mumbai!!!
Dear Candidate/Professional,
We’re inviting applications for multiple roles in our Regulatory Affairs team. Interested suitable applicants are requested to fill in this form for registration purpose. Kindly respond to this form on or before 8th December 2022. You may also email your CV to [email protected] with the subject line as “Regulatory Affairs”. You may also apply on the QR code below:
Regulatory Associates with experience range of 1-6 years in any markets/experience below:
Qualification Requirements:
Degree in science/life sciences/pharmacy or equivalent qualification(s).
EU (Post approval)
Experience in the Pharmaceutical industry, ideally in Regulatory Affairs in EU Post approvals.
US (Post Approval) –
Experience in Pharmaceutical industry, ideally in Regulatory Affairs but R&D, development or QA would also be considered. Submission 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)
10th December 2022 10 am to 4 pm
Venue-
10th Floor, D Wing, Tower 2, Sector-40, Seawoods Grand Central, Seawoods (W), Navi Mumbai-400706
