Aurobindo Pharma Recruitment: Regulatory Affairs Professionals roles
About Comapny
Founded in 1986 by Mr. P. V. Ramprasad Reddy, Mr. K. Nityananda Reddy and a small group of highly committed professionals, Aurobindo Pharma was born of a vision. The company commenced operations in 1988-89 with a single unit manufacturing Semi-Synthetic Penicillin (SSP) at Pondicherry.
Aurobindo Pharma became a public company in 1992 and listed its shares on the Indian stock exchanges in 1995. In addition to being the market leader in Semi-Synthetic Penicillins, it has a presence in key therapeutic segments such as neurosciences, cardiovascular, anti-retrovirals, anti-diabetics, gastroenterology and anti-biotics, among others.
Strengths and Leadership→
Large manufacturing facilities approved by leading regulatory bodies
Large diversified product portfolio
Large R&D facility in India for formulations and active ingredients
Aurobindo Pharma Limited is one of India’s leading pharmaceutical companies, recognized globally for its robust product p inortfolio and manufacturing capabilities
Requirement Details
Job Title : Regulatory Affairs (Formulations)
Experience :2-4yrs in US Regulatory Affairs
Work
Location :APRCI -Hyderabad, Telangana – 500090
Skills & Competencies :
Computer Knowledge/ eCTD software knowledge
Good knowledge in ICH & FDA guidelines
Experience Required
•Preparation, review & compilation of assigned ANDA/NDA [505 b(2)/projects for fling
•Knowledge of eCTD, Module 2 & 3
•Hands on experience in reviewing CMC documents of Solid & Liquid oral dosage forms
•Review of Pharmaceutical Development Reports (PDR), Manufacturing & analytical documents
Contact Details
Interested candidates can send their profiles to Hrret@aurobindo.com
More update for job join our
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