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Regulatory affairs

 

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  • Vacancy for Research Associate, Scientist in Regulatory Affairs at Aurobindo Pharma

    Aurobindo Pharma Limited is an Indian multinational pharmaceutical manufacturing company headquartered in HITEC City, Hyderabad, India. The company manufactures generic pharmaceuticals and active pharmaceutical ingredients.

    Post : Research Associate / Scientist Position for Regulatory Affairs

  • Regulatory Affairs Jobs at Aurobindo Pharma

    Aurobindo Pharma Limited is an Indian multinational pharmaceutical manufacturing company headquartered in HITEC City, Hyderabad, India. The company manufactures generic pharmaceuticals and active pharmaceutical ingredients.

    Department : Regulatory Affairs (Oral Solids) - CMC

    Experience : 04 to 10 years

  • Walk in for M.Pharm, B.Pharm, MSc in Regulatory Affairs at Sun Pharma

    Sun Pharmaceutical Industries Ltd. (Sun Pharma) is the fourth largest specialty generic pharmaceutical company in the world with global revenues of over USD 5.1 billion. Supported by more than 40 manufacturing facilities, we provide high-quality, affordable medicines, trusted by healthcare professionals and patients, to more than 100 countries across the globe.

  • Interview for M.Pharm, MSc in Regulatory Affairs, ADL, F&D at Torrent Pharma

    Torrent Pharma, the flagship company of Torrent Group, is one leading pharma companies in the country. Torrent is all poised to spread wings across globe with strong technical capabilities and international accreditations.

    Regulatory Affairs Department
    Qualification : M.Pharm / M.Sc
    Experience : Asst Manager : 9 -12 yrs
    Executive : 2 - 8 yrs

  • AstraZeneca Hiring Director Regulatory Affairs

    AstraZeneca contributes meaningfully to the UK beyond the provision of our medicines and the benefits they provide to the health of the nation. We commissioned a report in 2009 to measure our significant investment to the UK economy, which includes investment in jobs and wealth creation. Oxera, an independent economic consultancy provided the analysis for this report.

  • Vacancy for M.Pharm, B.Pharm, M.Sc in API Regulatory Affairs at Zydus Lifesciences

    After a journey of growth spanning 27 years as Cadila Healthcare Ltd. and the Zydus Group, we have evolved and transformed ourselves in response to the changing times. Our legacy of over 70 years in healthcare and being dedicated to life in all its dimensions is reaffirmed in our new mission, vision and purpose. Unifying ourselves under the Zydus name, Cadila Healthcare Ltd., is renamed as Zydus Lifesciences Ltd.

    Inviting candidates for API Regulatory Affairs at Zydus API Park, Vadodara

  • Work as Regulatory Affairs Associate at Teva, M.Pharm, B.Pharm, MSc Apply

    Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas.

  • Work as CMC Regulatory Affairs Manager at MSD

    Merck & Co., Inc., Kenilworth, New Jersey, USA in the United States and Canada and MSD everywhere else. For more than a century, we have been inventing for life, bringing forward medicines and vaccines for many of the world's most challenging diseases. Today, our company continues to be at the forefront of research to deliver innovative health solutions and advance the prevention and treatment of diseases that threaten people and animals around the world.

  • Vacancy for M.Pharm, B.Pharm, M.Sc in Regulatory Affairs at Felix Generics Private Ltd

    A pharmaceutical generics business company. HPRA Approved (April 2021) facility for veterinary generic medicines. Parent entity based in Ireland.

    Post : Assistant Manager / Sr. Executive / Executive - Regulatory Affairs (R&D)

  • Require Regulatory Affairs Associate at Teva

    Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas.

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