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  • Require Clinical Trial Assistant at PRA Health Sciences

    At PRA Health Sciences, providing innovative solutions for our clients is what we do. Side-by-side with our clients, we strive to move drug discovery forward, helping them to develop life-saving and life-improving drugs. With our unique blend of expertise, we provide comprehensive clinical development services across all phases. From full service clinical development to the pioneering Embedded SolutionsTM model, PRA provides a broad spectrum of solutions that meet the demands of a diverse marketplace.

    Post : Clinical Trial Assistant

  • Work as Purchase - FDC at Syngene International
    Work as Purchase - FDC at Syngene International

    Syngene International is one of India’s premier contract research and manufacturing organizations in providing customized service. Our services encompasses all across discovery chain: early stage discovery, process development, cGMP manufacturing and formulation development both in the small molecule and novel biologics area. Based in Bangalore, Karnataka, the Company is situated in a 90 acre Special Economic Zone with over 100000 sq. mt of built up facilities.

    Post : Purchase - FDC

  • Vacancy for M.Pharm, M.Sc, B.Pharm as Regulatory Affairs Associate at PAREXEL
    Vacancy for M.Pharm, M.Sc, B.Pharm as Regulatory Affairs Associate at PAREXEL

    PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries. They have helped over 800 clients to develop and launch some of the most important drugs and devices of our time-helping people live better and healthier lives everywhere in the world. Headquartered near Boston, Massachusetts, PAREXEL operates in more than 50 countries around the world.

    Post : Regulatory Affairs Associate

  • Opportunity for Ph.D, M.Pharm, M.Sc as RWE Analyst at Novo Nordisk
    Opportunity for Ph.D, M.Pharm, M.Sc as RWE Analyst at Novo Nordisk

    Novo Nordisk is a global healthcare company with 89 years of innovation and leadership in diabetes care. The company also has leading positions within Haemophilia care, growth hormone therapy and hormone replacement therapy. Headquartered in Denmark, Novo Nordisk employs approximately 33,300 employees in 75 countries, and markets its products in more than 190 countries Novo Nordisk’s B shares are listed on NASDAQ OMX Copenhagen (Novo-B).

    Post : RWE Analyst

  • Job in Production, Raw Material Dispensing at PAR Formulations
    Job in Production, Raw Material Dispensing at PAR Formulations

    Par is a pharmaceutical company that develops, manufacturers and markets safe, innovative and cost-effective pharmaceuticals that help improve patient quality of life. Par Pharmaceutical offers a line of high-barrier-to- entry generic drugs. We offer a wide variety of interesting employment opportunities and are continually looking for key external talent to complement our existing workforce and enhance our organizational strength, adding the diversity required to continue along our successful path.

  • Work as Materials Regulatory Specialist at SMC Ltd
    Work as Materials Regulatory Specialist at SMC Ltd

    SMC’s exclusive focus in healthcare markets, combined with 30 years’ experience, provides expert knowledge for your finished device. As a contract manufacturer, we provide full service solutions for single use and single patient devices across a range of high volume to low volume needs. Globally located, all manufacturing sites are FDA registered.

    Post : Materials Regulatory Specialist

  • Sanofi looking for Production Manager
    Sanofi looking for Production Manager

    Sanofi is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.  With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe.

    Post : Production Manager

  • Walk in interview for M.Pharm, B.Pharm, M.Sc in Production, Stores, Quality Control, Quality Assurance, Packing at Aristo Pharma
    Walk in interview for M.Pharm, B.Pharm, M.Sc in Production, Stores, Quality Control, Quality Assurance, Packing at Aristo Pharma

    Aristo started its operations in 1971 with a manufacturing plant at Aurangabad, marketing operations in Mumbai with a field force of just 30 personnel. Since then Aristo has come a long way... From a turnover of US $ 8500 in 1971 to US $ 64 million in year 2000. The last few years have seen us blazing new trails and setting new standards in the pharmaceutical industry. The company has a formidable position in the industry. Sound infrastructure and well-qualified human force have helped Aristo to accomplish this achievement.

  • Job for M.Pharm, M.Sc, B.Pharm in Production, Quality Control, IPQA, QMS, Validations at Aurobindo Pharma
    Job for M.Pharm, M.Sc, B.Pharm in Production, Quality Control, IPQA, QMS, Validations at Aurobindo Pharma

    Aurobindo Pharma has identified international operations, catering to over 100 countries, as a major engine of growth and expanding global network of marketing and manufacturing operations across countries like China, Brazil, Japan, Netherlands, South Africa, Thailand, UK, USA, Russia, Netherlands and many more which will further expand its international reach.

  • Career for M.Pharm, B.Pharm as Senior Associate Regulatory Affairs at PAREXEL
    Career for M.Pharm, B.Pharm as Senior Associate Regulatory Affairs at PAREXEL

    PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries. They have helped over 800 clients to develop and launch some of the most important drugs and devices of our time-helping people live better and healthier lives everywhere in the world.

    Post : Senior Associate Regulatory Affairs

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