About Aurobindo Pharma

Aurobindo Pharma Limited is an Indian multinational pharmaceutical manufacturing company headquartered in HITEC City, Hyderabad, India. The company specializes in the production of generic pharmaceuticals and active pharmaceutical ingredients (APIs). Aurobindo Pharma is known for its extensive product portfolio and global presence, distributing its products to over 150 countries worldwide. Established in 1986, the company has grown significantly, driven by its commitment to quality, innovation, and affordability in healthcare. Aurobindo Pharma operates in key therapeutic segments such as antibiotics, antiretrovirals, cardiovascular, central nervous system, gastroenterology, and anti-allergics, among others.

Positions Open for Regulatory Affairs Experts

US Market – Post Approval

Experience: 3 to 6 Years
Qualification: M.Pharm (any specialization)
Key Skills: Handling Post-approval Activities, CB-0, CB-30, PASS, FDA Inspections

US Market – CMC

Experience: 3 to 10 Years
Qualification: M.Pharm (any specialization)
Key Skills: Filing ANDAs, Annual Submissions, Dossier Preparations

EU Market – Module 3

Experience: 3 to 10 Years
Qualification: M.Pharm (Pharmaceutics/Regulatory Affairs)
Key Skills: CMC, Initial Submissions, Dossier Preparations, Pre/Post Submissions, LCM

EU Market – Module 1

Experience: 3 to 10 Years
Qualification: M.Pharm (any specialization)
Key Skills: Administration, Preparation & Submission of Renewals, Response to Agency Queries, RSI & RFI

Job Location: APL Research Centre -1, Sy No. 313 & 314, Bachupally, Hyderabad

How to Apply: Send your applications to hrrc1@aurobindo.com

Application Deadline: 25th June 2024

For more articles, Kindly Click here.
For pharmaceutical jobs, follow us on LinkedIn

For more jobs, kindly visit our job section.

www.pharmaceuticalcarrier.com/Jobs

Regulatory Affairs Expert Required at Aurobindo Pharma- Apply before 25th June 2024