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  • Job for QC Analysis(10 posts) at Titan Laboratories

    Titan Laboratories Pvt. Ltd. is one of the leading TGA and EU–GMP APPROVED MANUFACTURER in the field of Sustained Release and Modified Release Pellets, Directly Compressible Granules and Finished Formulations.

    Post : QC Analysis

  • Titan Laboratories looking for Sr. Executive / Executive - Quality Control - 05 posts
    Titan Laboratories looking for Sr. Executive / Executive - Quality Control - 05 posts

    Titan Laboratories Pvt. Ltd. is one of the leading TGA and EU–GMP APPROVED MANUFACTURER in the field of Sustained Release and Modified Release Pellets, Directly Compressible Granules and Finished Formulations.

    Post: Sr. Executive / Executive - Quality Control

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  • Job for Assistant Managing Editor in Pharmaceutical Sciences at Cactus
    Job for Assistant Managing Editor in Pharmaceutical Sciences at Cactus

    Cactus Communications a company dedicated to the pursuit of good English. We provide editing, educational, transcription, and training services to individual and institutional clients worldwide. All our businesses are linked together by one common factor—great written English. Since our establishment in April 2002, we have carved a niche for ourselves as a company providing language solutions of the highest quality.

    Post : Assistant Managing Editor, Pharmaceutical Sciences

  • Opening for Executive- R&D in Johnson & Johnson
    Opening for Executive- R&D in Johnson & Johnson

    Caring for the world, one person at a time... inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world.

    Post: Executive- R&D

  • Work for Medical Writer II in Parexel
    Work for Medical Writer 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: Medical Writer II

  • Job for M.Pharm, M.Sc as Content Developer at Himalayas
    Job for M.Pharm, M.Sc as Content Developer at Himalayas

    Working in Himalayas means to learn and grow continuously.Opportunities to work on the finest ever products in the herbal space, competitive salaries and excellent benefits. We offer challenging assignments, a world class working environment, professional management and ample prospects to train and learn along with exceptional rewards.

    Post : Content Developer

  • Vacancy for M.Pharm, M.Sc in Regulatory Affairs at Pfizer | walk in - Only experienced candidates
    Vacancy for M.Pharm, M.Sc in Regulatory Affairs at Pfizer | walk in - Only experienced candidates

    Founded in 1849, Pfizer is the world's premier biopharmaceutical company taking new approaches to better health. We discover, develop, manufacture and deliver quality, safe and effective prescription medicines to treat and help prevent disease for both people and animals. We also partner with healthcare providers, governments and local communities around the world to expand access to our medicines and to provide better quality health care and health system support. At Pfizer, colleagues in more than 90 countries work every day to help people stay happier and healthier longer and to reduce the human and economic burden of disease worldwide.

    Post: Regulatory Affairs - CMC Roles

  • Opening in Parexel as Senior Associate
    Opening in Parexel as Senior Associate

    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.

  • Walk in interview for Executive / Officer / Manager / Deputy Manager in Manufacturing, Packing, CQA at Zydus Cadila
    Walk in interview for Executive / Officer / Manager / Deputy Manager in Manufacturing, Packing, CQA at Zydus Cadila

    Zydus Cadila is an innovative global pharmaceutical company that discovers, develops, manufactures and markets a broad range of healthcare products. The group"s operations range from API to formulations, animal health products and cosmeceuticals. Headquartered in the city of Ahmedabad in India, the group has global operations in four continents spread across USA, Europe, Japan, Brazil, South Africa and 25 other emerging markets.
    In its mission to create healthier communities globally, Zydus Cadila delivers wide ranging healthcare solutions and value to its customers. With over 13,000 employees worldwide, a world-class research and development centre dedicated to discovery research and eight state-of-the-art manufacturing plants, the group is dedicated to improving people"s lives.

    Post: Executive / Officer / Manager / Deputy Manager

  • CLINICA -2017 : Recent trends and approaches in Clinical research, Clinical trial and Medical writing
    CLINICA -2017 : Recent trends and approaches in Clinical research, Clinical trial and Medical writing

    Clinica 2017 will explore various disciplines involved in the clinical research, conduct of clinical trials. It will educate health care researchers about study design, operation, organizing, research computing, regulatory aspects and reporting of clinical trials.

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