Wed. Feb 21st, 2024

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

Vacancy Details

  • Department: Regulatory Affairs (Oral Solids) – CMC
  • Experience: 04 to 10 Years
  • Specification: Must have a good exposure with US & Europe Market
  • Work Locon: Hyderabad, Telangana-500090

For US Market:

  • Preparation, review and compilation of assigned ANDA/NDA [505 b(2)]/projects for filing and knowledge of eCTD, Module 2 and 3. Hands on experience in reviewing CMC documents of Solid and Liquid Oral Dosage forms.

For Europe Market:

  • Competent with Europe filing wrt. Module 2&3. well versed with EU – Regulatory guidance and processes. Post Approval Variations and Compilations.

Date: 03rd December 2023 (Sunday)
Time: 9.00 AM to 2.00 PM
Venue
: APL Research Center – 1 Bachupally, Coco Cola Road.

Interested candidates can send their profiles to SravanKumar.Bhimuni@aurobindo.com& Ext. No.: 1345 for any further queries

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By Sivamin

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