DRA

25 April 2013

Opening for B.Pharm/M.Pharm in Production, DRA, QC at Saudi Pharmaceutical | Require Formulator, Regulatory Affair Officer, QC Chemist

Saudi Pharmaceutical Industries first and only of its kind manufacturing veterinary and human drugs in Saudi Arabia.
Saudi Pharmaceutical Industries now manufactures high quality veterinary products and its eminence is compared with European standards. During this short period of time we have not only fulfilled the requirements of Saudi Arabia but also expanded our business to all GCC and number of African countries.

3 April 2013

Opening in Indian Drugs & Pharmaceuticals Limited - Govt. of India | Require Dy Manager QC, Sr Executive(Regulatory Affairs), Production Supervisor, Sr Chemist (Form. Development)

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 on e year which can be extended further on performance basis.

31 March 2013

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

24 February 2013

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.

12 February 2013

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

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3 February 2013

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.

23 January 2013

Work as Medical Writer in PPD Pharmaceuticals

20 January 2013

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.

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19 January 2013

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.

3 January 2013

Opportunity for Senior Manager-Regulatory Devices in Biocon