Aurobindo Pharma Ltd. is a reputed pharmaceutical company that delivers innovative solutions. Aurobindo Pharma is the market leader in Semi-Synthetic Penicillin, it has a presence in key therapeutic segments such as neurosciences, antiretrovirals, anti-diabetics cardiovascular, gastroenterology, and cephalosporins. Aurobindo has more than 300 products in various therapeutic segments.
Aurobindo Pharma has successfully launched a range of affordable products that are accessible across the world. Aurobindo Pharma has fifteen state-of-the-art formulation production units located in India, USA, Portugal & Brazil. Aurobindo facilities have received accreditation from the following regulatory bodies:
- US FDA (United States Food and Drug Administration)
- UK’s MHRA (United Kingdom’s Medicines and Health products Regulatory Agency)
- TGA Australia (Therapeutic Goods Administration)
- MCC South Africa (Medicines Control Council)
- ANVISA Brazil (National Health Surveillance Agency)
- Health Canada
- WHO (World Health Organization)
- GCC DR (Gulf Central Committee for Drug Registration)
Walk-In Interview at Unit-3, Bachupally For Production, Packing, QC
Aurobindo Pharma Walk-In Drive For training and Development Center
For Job, Applications Send Your Resume to [email protected]
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Aurobindo Pharma Key Formulation Facilities (8 in India, 1 each in US and Brazil)
Unit 3
- A multi-product oral dosage (OSD) form facility for non-cephalosporins and non-beta-lactams
Unit 4
- A dedicated manufacturing facility for generic sterile injectable (lyophilized and powder injections, prefilled syringes), ophthalmic and low volume parenteral.
Unit 7
- An ultra-modern unit based on the suite manufacturing concept delivering huge capacity.
- Manufactures non penicillins, non cephalosporins & ARVs
Unit 10
- Manufactures non penicillins & non cephalosporins products .
Unit 12
- A dedicated facility manufacturing oral and sterile beta-lactam formulations.
Unit 15
- An exclusive multi-product oral dosage form facility for supplying European markets.
- The unit has an installed annual capacity of 6 billion tablets and capsules.
Auronext
- Produces sterile penne formulations.
- Also manufactures sterile APIs.
Aurolife (Located in the US)
- USFDA approved cGMP compliant manufacturing facility located in New Jersey
- Manufactures non-penicillin and non-cephalosporin products
Brazil
- Manufacturing facility for SSPs, which caters to the requirements of Latin America
Aurobindo Pharma Regulatory History
Aurobindo Pharma has a very strong track record in the regulatory filings. Aurobindo has applied for 150 US DMFs and about 2000+ filings in other countries. Aurobindo has close to 500 patents in place.
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