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Clinical courses

  • Advance DoE Workshop 2024

    For pharma and biopharma companies, building quality into your products from an early stage is a key factor in regulatory approval and market success. Thus, the FDA mentions “Design of Experiments” (DoE) as an essential tool for achieving both regulatory compliance and faster time to market. To help you build quality into your process as outlined by ICH Q8, Q9, and Q10, Eminence Business Media is planning a two-day robust training program on “Advance DoE Workshop 2024” on May 9th – 10th.

  • Nitrosamine Advanced Workshop 2024

    Nitrosamine Advanced Workshop 2024
    May 9th – 10th, 2024 | Radisson Blu Mumbai International Airport

    About the Event :
    Presence of Nitrosamines, which are probable human carcinogens, has been an evolving challenge facing the pharmaceutical industry. Regulators became first aware of this impurity in mid – 2018, when NDMA was found in blood pressure medicine known as sartans. Ever since, the pharmaceutical industry has been working hard to mitigate the formation of Nitrosamines Impurities.

  • Work as Operation Quality Lead at GSK

    GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years. 

    Post : Operation Quality Lead (Value Stream)

  • Abbott looking for Therapy Business Manager

    Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals, and branded generic medicines. Our 109,000 colleagues serve people in more than 160 countries.

    Post : Therapy Business Manager -Neurolife

  • Opportunity for B.Pharm, M.Pharm as Protocol Writer at Synergen

    Synergen Bio Private Limited is a DCGI(CDSCO) approved new age CRO with all necessary infrastructure to cater to the Pharmaceutical and Biotech industry, established by a group of enthusiastic professionalswith a vision to set-up a premium Clinical Research Organization known for its Quality, Knowledge and Expertise. Synergen Bio understands the importance of quality clinical research services and our significantly experienced team strives to provide the same to our sponsors at significant cost advantages.

    Post : Protocol Writer

  • Job for M.Pharm, MSc as Formulation ADL Analyst at Cipla

    Cipla, as an organisation has been built brick-by-brick on the foundation of care. Caring For Life has always been and continues to remain, our guiding purpose. Driven by the same purpose, we have extended our presence to 80+ countries providing over 1,500 products across various therapeutic categories in 50+ dosage forms. To make healthcare more affordable globally, we are deepening our presence in the key markets of India, South Africa, the U.S. among other economies of the emerging world.

  • Apotex Inc Hiring Regulatory Affairs Executive - M.Pharm, B.Pharm, MSc Apply

    Apotex Inc. is a proudly Canadian, global pharmaceutical company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 8,000 people worldwide in manufacturing, R&D, and commercial operations.  Apotex Inc. exports to more than 100 countries and territories and operates in more than 45 countries, with a significant presence in Canada, the US, Mexico, and India.

  • Applications are invited for the Post of Project Assistant at Agharkar Research Institute

    MACS - Agharkar Research Institute  (ARI)  an  autonomous  Institute  of  the  Department  of Science and Technology (DST), Government of India is committed to the promotion of science and technology with emphasis on high standards of research and development activities for the benefit  of  humankind  and  the  nation.  The  current  research  activities  encompass  biological sciences   and   focus   on   six   thematic&

  • Teva looking for Formulation Researcher, Analytical Researcher, Quality Analyst

    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. 

    Teva Global Business Services (GBS) is inviting talent to fuel its ambitious growth plans for the year.

  • Hiring for Regulatory Affairs at FDC India

    FDC is a people-oriented organization, dedicated to innovate, manufacture and market high-quality healthcare products that enhance the quality of human life all over the globe, and in turn, increase shareholders value.

    Post : Executive / Senior Executive

    Regulatory Affairs (US/EU) - Executive/ Senior Executive
    No of post : 01
    Experience : 4 to 8 years
    Job Description : Preparation of New Applications, Query responses, Post approval changes for EU & US market

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