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Working opportunity as QA/RA MANAGER in OREX PHARMA

OREX PHARMA, one of the leading manufacturers and exporters of the active pharmaceutical ingredients and intermediates. Our head office at thane and plant at dombivli. We are ISO / GMP certified company and we will get our who approval by april end. We are in process of expansion and launching new products

Post: QA/RA MANAGER


Opportunity for M.Pharm, B.Pharm, M.Sc at Central Drugs Standard Control Organization | Require Professional Consultants in Pharmacovigilance, Biopharmaceuticals, Clinical Trial, Cosmetics, Quality Management System, Medical Devices, Diagnostic Kit

The Central Drugs Standard Control Organization (HQ), FDA Bhawan, Kotla Road, Near Mata Sundari College, New Delhi -110002 requires Consultants, Technical Data Associates, Data Entry Operators and Office Assistants. These supporting staff will assist Senior Officers in matters related to Administrative & Technical works carried out in the office of CDSCO. Qualification, experience, job description, emoluments etc. for various posts are as under:-


Work as Regulatory Specialist I / II OTC GRA CMC in Novartis

A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes them one of the most rewarding employers in their field.


Require M.Pharm for Senior Executive/Manager-Regulatory Affairs - 2 posts

Formula HR consulting, Reputed pharmaceutical company

Post: Senior Executive/Manager-Regulatory Affairs- 2 No.'s



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.