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Opening for M.Pharm as Manager - Regulatory Affairs @ VINS Bioproducts

VINS Bioproducts Limited entered the arena of biologicals and bio-pharmaceuticals at the turn of the century with a view to produce life saving drugs for rural areas. Early on, the company focused on finding remedies for diseases that are endemic in India, the tropics and other less developed nations. True to its initial objective, the company commenced work to develop AntiSnake Venom Serum (ASVS), which was launched in early 2000. VINS' ASVS, is a life saving product much needed in rural areas where people engaged in agriculture activities are regularly exposed to snake bites.

I am interested in pursuing my MS in regulatory affairs. Hence, i wish to know the future prospects of the course and career opportunities in India as well as abroad

Food & Drug Administration is main regulatory body which regulates and implements rules to pharma industries. It has many branches and sub branches in different parts of the world. There are various regulatory bodies such as TGA for Australia, HPB for Canada, USFDA for USA, FIDMD for Germany, CDSCO for India and many more.

Opportunity for M.Pharm/B.Pharm to work as Team Member - Regulatory Affairs (Plant) in Mylan

Mylan is one of the world’s leading generics and specialty pharmaceutical companies, providing products to customers in more than 150 countries and territories. The company maintains one of the industry’s broadest and highest quality product portfolios, which is regularly bolstered by an innovative and robust product pipeline. With a workforce of more than 16,000, Mylan has attained leading positions in key international markets through its wide array of dosage forms and delivery systems, significant manufacturing capacity, global commercial scale and a committed focus on quality and customer service.

Multiple vacancies in Production, Regulatory Affairs, QC, QA at Indian Drugs & Pharmaceuticals Limited | 6 Posts

M/s. Indian Drugs & Pharmaceuticals Limited (I.D.P.L.) is a Central Public Sector Undertaking wholly owned by the Govt. of India engaged in manufacture of pharmaceuticals. A Unit of I.D.P.L. situated at Rishikesh requires to engage trained and experienced professionals in following fields on a fixed term contract basis initially for a period of one year which can be extended further on performance basis.

Work as Manager - Regulatory Affairs in Pfizer India

Founded in 1849, Pfizer is the world's premier biopharmaceutical company taking new approaches to better health. We discover, develop, manufacture and deliver quality, safe and effective prescription medicines to treat and help prevent disease for both people and animals. We also partner with healthcare providers, governments and local communities around the world to expand access to our medicines and to provide better quality health care and health system support. At Pfizer, colleagues in more than 90 countries work every day to help people stay happier and healthier longer and to reduce the human and economic burden of disease worldwide.

HBL invites Deputy Manager - Formulation, Production, QA, QC, Regulatory Affairs, Animal House

HLL Biotech Limited (HBL) is a 100% subsidiary of HLL Lifecare Limited, a Mini Ratna Schedule B Central Public Sector Enterprise under the Ministry of Health & Family Welfare. HBL is setting up a vaccine complex at Chengalpett, Chennai for manufacturing of Bacterial and Viral Vaccines & developing a strong R&D base for vaccine technologies within the country.