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  • Recruitment for M.Pharm, M.Sc to work in CNNS at Clinical Development Services Agency - Govt. Job | Emoluments Up to Rs. 75,000 pm

    Department of Biotechnology (DBT), Ministry of Science & Technology, Government of India launched CDSA on 28 September 2009 as an extramural unit of Translational Health Science & Technology Institute (THSTI). It was created to facilitate development of affordable healthcare products for public health diseases. Registered as a not-for profit research organization, it aims to develop an eco-system for training and learning and work with public sector institutions, and small and medium enterprises (SME) to translate innovative technologies into medical products for public good.

    CDSA invites applications for following positions, for the Project ‘‘Concurrent Monitoring of Comprehensive National Nutrition Survey (CNNS)’’, from high performing professionals with a desire to serve public health needs of the country

    Post : Zonal Program Manager

  • Job for Product Manager in Baxter

    Baxter International Inc. develops, manufactures and markets products that save and sustain the lives of people with hemophilia, immune disorders, infectious diseases, kidney disease, trauma, and other chronic and acute medical conditions. As a global, diversified healthcare company, Baxter applies a unique combination of expertise in medical devices, pharmaceuticals and biotechnology to create products that advance patient care worldwide. Baxter had 2012 sales of $14.2 billion and has approximately 50,800 employees.

    Post: Product Manager

  • Working Opportunity for M.Pharm, M.Sc, MBA as Site Operations Manager at Medtronic

    Together, we can change healthcare worldwide.  At Medtronic, we push the limits of what technology can do to help alleviate pain, restore health and extend life.  We challenge ourselves and each other to make tomorrow better than yesterday.  It is what makes this an exciting and rewarding place to be.

    Post : Site Operations Manager

  • National Brain Research Centre (NBRC) invites Junior Research Fellow for RNA related research work

    NATIONAL BRAIN RESEARCH CENTRE (NBRC) invites application for the position of “Junior Research Fellow (Project)” in DBT funded project entitled “CRISPRI system: A toolbox to investigate novel regulatory mechanisms of synapse formation by long non-coing RNAs”.

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  • Job for Senior Manager in Analytical Development at Sentiss Pharma

    Over the years Sentiss Pharma (erstwhile known Promed group) has positioned itself as the No 3 Ophthalmic Company* in Russia and has expanded its foothold in the US and European markets.
    Our key competitive advantage lies in having the R&D center together with the world class manufacturing facility that has enabled us to provide end-to-end solutions from product development to marketing. Our manufacturing facility at Nalagarh (India) is EU GMP certified and TGA (Australia) approved.

  • Opportunity for Senior Research Scientist in Product Development at Sentiss Pharma

    Established in the early 90's, this organization has emerged as an integrated pharmaceutical company offering products to the global market. Headquartered at Delhi NCR, India and plant in North India, the Company develops, manufactures and markets a wide range of quality products in diverse area of treatment.Over the years, the organization has positioned itself as a significant player in the Russian and CIS markets and has expanded its foothold in the US, Europe, India and other markets. The key competitive advantage lies in having the Research & Development centre together with the world class manufacturing facility that has enabled it to provide end-to-end solutions from product development to marketing. The manufacturing facilities are approved by many regulatory bodies including EUGMP and WHOGMP thereby allowing the company to reach International markets.

    Post : Senior Research Scientist - Product Development

  • Career in Regulatory Affairs as Manager at RB

    RB is the world's leading consumer health and hygiene company. Every day, across 60 countries, we work with the best people to challenge conventional thinking and strive to find even better ways to give people innovative solutions for healthier lives and happier homes. We trust people in what they do and we give full accountability and autonomy to make things happen. That’s how we generate the game-changing ideas that built 19 iconic Powerbrands around the world, such as Mucinex, Lysol, MegaRed, Finish and Airwick.

    Post : Manager Regulatory Affairs

  • Career Opportunity in Production, QA, Marketing at Indian Drugs and Pharmaceuticals Limited (IDPL) | Government of India Job

    Indian Drugs and Pharmaceuticals Limited (IDPL) is a Central Public Sector Undertaking wholly owned by the Government of India engaged in manufacture of pharmaceuticals with plants at Rishikesh, Gurgaon & Hyderabad and two Subsidiary Units at Chennai and Muzaffarpur. IDPL was established with main objective of creating self-sufficiency in respect of essential life saving medicines, to free the country from dependence on imports and to provide medicines to the millions at affordable prices and not to make millions from the medicines. IDPL was basically conceived and established as a part of Healthcare Infrastructure and has played a pioneering infra-structural role in the growth of Indian Drug Industry base. Recently, the Company has entered in the field of OTC as well as Surgical Products.

  • Job for M.Pharm to work in Regulatory Affairs at Sentiss Pharma

    Established in the early 90's, this organization has emerged as an integrated pharmaceutical company offering products to the global market. Headquartered at Delhi NCR, India and plant in North India, the Company develops, manufactures and markets a wide range of quality products in diverse area of treatment.Over the years, the organization has positioned itself as a significant player in the Russian and CIS markets and has expanded its foothold in the US, Europe, India and other markets. The key competitive advantage lies in having the Research & Development centre together with the world class manufacturing facility that has enabled it to provide end-to-end solutions from product development to marketing. The manufacturing facilities are approved by many regulatory bodies including EUGMP and WHOGMP thereby allowing the company to reach International markets.

    Post : Senior Executive/Asstt. Manager- Regulatory Affairs

  • Career for Clinical Research Associate in iKMC Study at Clinical Development Services Agency | M.Pharm, M.Sc

    Clinical Development Services Agency (CDSA) is an extramural unit of Translational Health Science and Technology Institute (THSTI) and has been established as a not-for-profit society to provide cost affective, high quality preclinical and clinical product development support services to meet the country’s growing healthcare needs. It will tend enterprises; particularly SMEs involved in new technology innovation and facilitate translation of scientific know-how into viable products.

    Post : Clinical Research Associate (iKMC Study), 01 Position

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