Teva multiple opening for Regulatory Affairs department at Navi Mumbai



Teva multiple opening for Regulatory Affairs department at Navi Mumbai

HIRING ALERT!

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 Rekha.chavan@teva.co.in with the subject line as “Regulatory Affairs”. You may also respond to this form on or before 19th November 2022. You may also email your CV to 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.

• 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.Pharm/M.Pharm/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.

Link at The End 

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