Teva Pharmaceuticals inviting applications for multiple roles in Regulatory Affairs team
- Regulatory Associates with experience range of 1-6 years in any markets/experience below:
- Regulatory Associates with experience range of 8+ years in any markets/experience below:
Be a part of Teva Regulatory Affairs Team at Navi Mumbai. Inviting applications for multiple roles in Regulatory Affairs team.
Dear Candidate/Professional, suitable applicants are requested to fill in this form for registration purpose. Kindly respond to this form on or before 08th December 2022.
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.
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.
Regulatory Associates with experience range of 8+ years in any markets/experience below:
Qualification Requirements: Bachelor’s / Master’s degree in a scientific discipline, preferably in life sciences. B Pharmacy /M Pharma / MS in RA is a plus.
US Pre Approval – 8-10 years in the pharmaceutical industry with 6+ years in Regulatory Affairs (CMC)experience for new submissions in US market. Experience in complex generic, sterile products is added advantage.
Canada Pre Approval – 8-10 years in the pharmaceutical industry with 6+ years in Regulatory Affairs (CMC) experience for new submissions in Regulated market. Experience of having Canadian submission is added advantage.
USFDA Pre Approval– 8-10 years in pharmaceutical industry in RA with 6+ years in Regulatory Affairs (CMC). Experience of regulatory submissions & deficiency responses to USFDA is a distinct advantage.
Application Process : Interested & Eligible Candidates Share your Resume to [email protected] with the subject line as “Regulatory Affairs”. You may also apply on the QR code below:
