Intern, R&D - Aurobindo Pharma USA, Inc.
Dayton, NJ 08810
About the Job
Aurobindo Pharma USA, Inc. is a generic pharmaceutical manufacturer and distributor and is a wholly owned subsidiary of Aurobindo Pharma Limited, a leading generic pharmaceutical company based in India. Headquartered in HITEC City, Hyderabad, India, founded in 1986 and becoming a public company in India in 1992.
Aurobindo Pharma USA, Inc. is committed to delivering a broad portfolio of quality, affordable generic pharmaceuticals to pharmacists and patients. Aurobindo Pharma USA, Inc. adds value through superior customer service in the distribution of a broad line of generic pharmaceuticals, leveraging vertical integration and efficient controlled processes. Aurobindo has business operations in more than 125 countries around the world. Aurobindo is a global pharmaceutical company with a broad portfolio of generic drugs that includes more than 180 product families and 450 individual product packages.
Aurobindo markets over 80% of the top 100 most prescribed products in the world. In past years, Aurobindo has received more ANDA approvals than any of our competitors. Aurobindo is now ranked 2nd among pharmaceutical companies based on Total Prescriptions Dispensed. (We are#27 in 2010)
Job Overview:This is an Intern, R&D role in generic pharmaceutical product development. This role is very hands-on. The ideal candidate should have some experience in development to large scale submission batch manufacture.
This is a temporary position.
Responsibilities:- Develop and file generic drug dosage forms (orals/liquids)
- Develop products using FBD, Compression and Encapsulation
- Complete projects from bench-top stage to large scale manufacture of submission batches
- Knowledge of pharmaceutics, pharmacokinetics and process scale-up
- Understanding of the ANDA (and preferably NDA) filing process in line with QbD elements in generic product development
- Ability to work and collaborate in a team environment
- Excellent spoken and written communication skills
- Must be currently enrolled in a Bachelor's or Master's degree program in Pharmaceutics or a related field
- Experience in formulation development and process development is preferred
- Experience in the generic drug industry with ANDA filing and/or working with DEA controlled drug substances and relevant regulations is a plus