Skip to main content
  • Walk in interview for post of Clinical Trial Assistant in SCTIMST

    Sree Chitra Tirunal Institute for Medical Sciences & Technology (SCTIMST), Thiruvananthapuram is an Institute of National Importance  established by an Act  of the Indian Parliament  and  under the 2 administrative control of the Department of Science and Technology, Government of India.
    The Institute signifies the convergence of Medical Sciences and Technology and its mission is to enable the indigenous growth of biomedical technology, besides demonstrating high standards of patient care in medical specialties and evolving postgraduate training programs. It has a hospital for tertiary care of cardiovascular and neurological diseases, and research programmes in the areas of basic and applied medical sciences,  a Biomedical Technology Wing with facilities  and research programmes for developing medical  devices from a conceptual stage to commercialization, and The Achutha Menon Centre for Health Science Studies for training and research in public health.

    for a Project entitled “ATTEND-Family led rehabilitation after stroke in India” (P-5279)

    Post: Clinical Trial Assistant (TEMP)

  • Vacancies for B.Pharm, M.Pharm, M.Sc in Par Formulations in department of Regulatory Affairs, Production, QC, Technical services | Preference for Tamilnadu natives
    Vacancies for B.Pharm, M.Pharm, M.Sc in Par Formulations in department of Regulatory Affairs, Production, QC, Technical services | Preference for Tamilnadu natives

    Par Formulations Pvt. Ltd. a subsidiary of Par Pharmaceutical Companies Inc. (USA) is an USFDA approved facility located in Chennai facilitating Research & Development and engaged in manufacturing solid 6 semi solid dosage forms. Par Pharmaceutical Inc., is the 5th largest Generic Pharmaceutical Company in the US market and leader in Product Development and In-Licensing of generic pharmaceuticals with state of the art manufacturing facilities. In order to expand the operations of the Research & Development and Manufacturing unit in Chennai, we seek suitable candidates for the following positions:

    Post: General Manager / Dy. General Manager / Manager / Reviewer / Assistant Manager / Team Leader / Analyst / Supervisor / Technician

  • Vacancy for Clinical Data Analyst II in Parexel
    Vacancy for Clinical Data Analyst II in 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: Clinical Data Analyst II

  • Job for Document Management Associate/Assistant in Icon Clinical Research
    Job for Document Management Associate/Assistant in Icon Clinical Research

    ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialize in the strategic development, management and analysis of programs that support Clinical Development – from compound selection to Phase I - IV clinical studies
    ICON enjoys a strong reputation for quality and is focused on staff development. We make it our mission to attract the most diverse and creative minds into the business and we continually strive to provide opportunities for our people to excel, grow and build a great career. We understand that our greatest asset is the skills and talents of our people and they are truly what set us apart.

    Post: Document Management Associate/Assistant - 008035

  • Opening for Bachelors degree in Life Sciences as Safety Specialist in PPD Pharmaceuticals
    Opening for Bachelors degree in Life Sciences as Safety Specialist in PPD Pharmaceuticals

    PPD is a leading global contract research organization providing discovery, development and post-approval services as well as compound partnering programs. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 32 countries and more than 9,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a commitment to quality to help its clients and partners maximize returns on their R&D investments and accelerate the delivery of safe and effective therapeutics to patients

    Post: Safety Specialist (New Delhi)-114688

  • Join in Novartis as Manager Production | B.Pharm, M.Pharm can apply
    Join in Novartis as Manager Production | B.Pharm, M.Pharm can apply

    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.

    Post: Manager Production

  • Margdarshi Fellowships for Biomedical Research Fellowship Programme in India
    Margdarshi Fellowships for Biomedical Research Fellowship Programme in India

    The Wellcome Trust/DBT India Alliance(IA; India Alliance) was officially launched on 9 September 2008 and registered as a charitable trust in India. The organization is an equal partnership between the Wellcome Trust (UK) and the Department of Biotechnology (Government of India).

  • Required Manager - Environment, Health and Safety in United States Pharmacopeia
    Required Manager - Environment, Health and Safety in United States Pharmacopeia

    The United States Pharmacopeia (USP) is a non–governmental, official public standards–setting authority for prescription and over–the–counter medicines and other healthcare products manufactured or sold in the United States. USP also sets widely recognized standards for food ingredients and dietary supplements. USP sets standards for the quality, purity, strength, and consistency of these products–critical to the public health. USP's standards are recognized and used in more than 130 countries around the globe. These standards have helped to ensure public health throughout the world for close to 200 years.

    Post: Manager - Environment, Health and Safety

  • Vacancy for Executive-Regulatory Affairs in Leading Pharma Company- Aspiring Solution
    Vacancy for Executive-Regulatory Affairs in Leading Pharma Company- Aspiring Solution

    Leading pharma co. with huge range of products ranging from sterile preparation to oral solid dosage forms with international markets.

    Post: Executive-Regulatory Affairs (1 opening, Male Candidate Only)

    [adsense:336x280:8701650588]

  • Career for B.Pharm/B.Sc as Production Executive (Injactables)-Contact Manufacturing
    Career for B.Pharm/B.Sc as Production Executive (Injactables)-Contact Manufacturing

    Leading pharma co. with huge range of products ranging from sterile preparation to oral solid dosage forms with international markets.

    Post: Production Executive (INJECTABLES)-Contact Manufacturing (1 opening, Male Candidate Only)

    [adsense:336x280:8701650588]

Subscribe to B.Pharm