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  • Require Clinical Data Review Consultant at Accenture

    Accenture is a global management consulting, technology services and outsourcing company, with approximately 275,000 people serving clients in more than 120 countries. Combining unparalleled experience, comprehensive capabilities across all industries and business functions, and extensive research on the world’s most successful companies, Accenture collaborates with clients to help them become high-performance businesses and governments. The company generated net revenues of US$28.6 billion for the fiscal year ended Aug. 31, 2013.

    Post : CDM - Clinical Data Management

  • Job for B.Pharm, B.Sc as Technical Associate in Regulatory Affairs at Genpact

    Genpact is a global professional services firm that makes business transformation real. We drive digital-led innovation and digitally-enabled intelligent operations for our clients, guided by our experience running thousands of processes primarily for Global Fortune 500 companies. We think with design, dream in digital, and solve problems with data and analytics. Combining our expertise in end-to-end operations and our AI-based platform, Genpact Cora, we focus on the details – all 90,000+ of us. From New York to New Delhi and more than 30 countries in between, we connect every dot, reimagine every process, and reinvent companies’ ways of working.

    Post : Technical Associate - Regulatory Affairs

  • Job openings for Ph.D or M.Pharm, M.Sc in Research project at NCCS | Emoluments upto Rs. 1,50,000/-

    The National Centre for Cell Science (NCCS) is an autonomous institution of Department of Biotechnology, Ministry of Science & Technology, Government of India, with a mandate of basic research, teaching & training, and as a national repository for cell lines/hybridomas etc. The center is located in the midst of academically enriched environment of University of Pune Campus, Pune.

  • Vacancy for M.Pharm, B.Pharm, M.Sc as Regulatory Affairs Associate at Teva Pharmaceutical

    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.

    Post : Regulatory Affairs Associate I

  • Career for M.Pharm, M.Sc as Senior Research Fellow at NIRRH

    National Institute for Research in Reproductive Health (NIRRH), formerly known as Institute for Research in Reproduction is a premier research institute of the Indian Council of Medical Research (ICMR). It is situated in the vicinity of a number of hospitals and research institutes in central Mumbai. Since its inception in 1970, it has been making vigorous efforts to improve the reproductive health of people through research, education and health care services.

    Post : Sr. Research Follow (SRF)

  • Work as Associate / Assistant Manager - Regulatory Affairs at Abbott India Limited

    Abbott India Limited is a subsidiary of Abbott Laboratories, USA, a global, iversified health care company devoted to the discovery, development, manufacture and marketing of pharmaceutical, diagnostic, nutritional and hospital products. The company now employs approximately 70,000 people and markets its products in 130 countries worldwide.

    Post : Associate / Assistant Manager - Regulatory Affairs

  • Work as Quality Senior Specialist at Teva Pharmaceutical

    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.

    Post : Quality Sr Specialist

  • Job as CRA/ Sr.CRA/ Medical Writer/ Data Management at MediClin CR - contract research organization

    MediClin is a leading contract research organization (CRO) which is having corporate office in Mumbai providing comprehensive, integrated drug development and product lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, and government organizations.

    Post: CRA/ Sr.CRA/ Medical Writer/ Data Management

     

  • Career as Safety Officer at Pfizer - B.Pharm with min. 6 years of experience can only apply

    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.

  • Job Openings for Ph.D or M.Pharm, M.Sc as Domain Analyst at IISER

    Indian Institute of Science Education and Research Pune is a premier autonomous Institution established by the Ministry of Human Resource Development, Government of India, for the promotion of high-quality science education and research in the country.

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