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  • Vacancy for Research Associate, Quality Assurance Executive, Regulatory Affairs Executive at Piramal Pharma Solutions

    Piramal Group is a global business conglomerate with interests in Pharma, Financial Services, Information Management, Glass Packaging and Real Estate. With offices in 30 countries and brand presence in over 100 markets, the Piramal Group has a global team of over 10,000 people from 21 diverse nationalities.  Since 1984, the Piramal Group has battled complex challenges to stay ahead of the curve. From one of the longest trade union strikes to fluctuating political stands, we have consistently attained organic and inorganic growth, thanks to strong global partnerships and strategic investments in core businesses.

  • Job for Manager in Regulatory Affairs at Baxter

    Baxter provides a broad portfolio of essential renal and hospital products, including home, acute and in-centre dialysis; sterile IV solutions; infusion systems and devices; parenteral nutrition; surgery products and anesthetics; and pharmacy automation, software and services. The company’s global footprint and the critical nature of its products and services play a key role in expanding access to healthcare in emerging and developed countries. Baxter’s employees worldwide are building upon the company’s rich heritage of medical breakthroughs to advance the next generation of healthcare innovations that enable patient care.

    Post : Manager Regulatory Affairs – Software

  • Job opening as Regulatory Affairs Professional at Siemens

    With a focus on electrification, automation and digitalization, Siemens India stands for engineering excellence, innovation, and reliability. As one of the world’s biggest producers of energy-efficient, resource-saving technologies, Siemens is a pioneer in infrastructure and energy solutions, automation and software for industry and is a leader in medical diagnosis. Siemens also provides business-to-business financial solutions, rail automation and wind power solutions.

    Post : Regulatory Affairs Professional

  • Job for Professor, Assistant Professor, Associate Professor at L. J. Institute of Pharmacy

    L. J. Institute of Pharmacy, commonly referred as LJIP, is a private management institute located in Ahmedabad, Gujarat, India. The institute is approved by All India Council for Technical Education (AICTE) and Pharmacy Council of India (PCI) and is the part of L.J. Group of Institutes managed by Lok Jagruti Kendra (LJK) Trust. The institute is affiliated to Gujarat Technological University (GTU).

  • Walk in interview for Regulatory Affairs professionals at Pfizer | M.Sc, M.Pharm, Ph.D

    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.

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  • Vacancy for M.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 Executive (EU market)

  • Job for M.Pharm in Global Regulatory Affairs at Apotex | Fresher apply

    Apotex is a proudly Canadian, global pharmaceutical company that produces high-quality, affordable medicines (both generic and innovative pharmaceuticals) for patients around the world. We are the 7th largest generic pharmaceutical company globally with more than 12,000 employees and estimated sales of approximately $3 billion. Our fully integrated operation is comprised of four lines of business: Global Generics; Apobiologix; Global Active Pharmaceutical Ingredients (API); and ApoPharma (Innovative Products).

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

  • Work as Regulatory Affairs Specialist at Abbott India Limited | B.Pharm, B.Sc

    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 : Regulatory Affairs Specialist

  • Job for M.Pharm, B.Pharm in Regulatory Affairs at SeQuent Scientific

    Alivira, a subsidiary of SeQuent Scientific, is a USD 150mn integrated global animal health company operating in the area of animal health with a strong presence across EU, Latin America, Turkey, Africa, India and CIS. Our operations are underpinned by comprehensive manufacturing capabilities, strict adherence to quality and compliance. We are headquartered in Mumbai with manufacturing facilities based in India, Turkey, Brazil and Spain with approvals from global regulatory bodies, including USFDA, EUGMP, WHO and TGA, among others.

    Post : Regulatory Affairs

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