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  • Job for M.Pharm B.Pharm, M.Sc in Regulatory affairs, QA, QC at Virchow Biotech

    THE VIRCHOW GROUP with an operational experience of over 4 decades has a global footprint in over 100 countries supporting about 3,500 employees with an annual turnover of over $600 million. The Virchow Group has a diversified business portfolio ranging from Biogenerics, Pharmaceuticals, Medical devices, and APIs. The group is the largest producer of Sulfamethoxazole and Ranitidine Hydrochloride in the world. Virchow Biotech Pvt.

  • Regulatory affairs Analyst require at Granules India | M.Pharm or M.Sc apply

    Granules India is a vertically integrated pharmaceutical company, headquartered in Hyderabad, India. We manufacture Active Pharmaceutical Ingredients APIs, Pharmaceutical Formulation Intermediates PFIs and Finished Dosages FDs, distributed to quality conscious customers in both regulated and semi-regulated markets.

    Post : Analyst - Regulatory affairs

  • Walk in interview for M.Pharm, M.Sc, B.Pharm in Regulatory Affairs, F&D, R&D at Alembic Pharma

    Legacy of Alembic Pharmaceuticals Limited (APL) dates back to over 100 years. Established in 1907 with an objective to develop and revolutionize the Pharmaceutical and Drug industry in the Indian subcontinent, Alembic Pharmaceuticals Limited today is one of the leading pharmaceutical companies in India.

  • Multiple Job openings at Sunlovis Pharmaceuticals | M.Pharm, B.Pharm, M.Sc apply

    Sunlovis Pharmaceuticals is a Fast Growing Pharmaceuticals Company with a Strong Focus on supply of good Quality yet Affordable Medicine in India and across the World and is a Trusted Name among the Healthcare Professionals.  Sunlovis Competitive Advantage Steps From the World Class Manufacturing Facilities. We have a sharp Focus on giving Value added Services to our customer cost effectively. We offer a Strong Product Portfolio Spanning in Beta-lactam Categories.

  • Require Regulatory Affairs Specialist at Tata Elxsi | M.Pharm, B.Pharm, Pharm.D apply

    Tata Elxsi works with leading medical device OEMs and technology companies for market research and human factor engineering, hardware and software engineering, verification & validation, regulatory standards & compliance requirements along with technologies such as artificial intelligence, cloud and IoT. Tata Elxsi’s Medical Device and Healthcare practice is ISO 13485 certified.

    Post : Regulatory Affairs Specialist - Tata Elxsi

  • Senior Manager Job In 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 : Senior Manager Regulatory Affairs - DCGI Filing

  • Walk in interview for M.Pharm, M.Sc, B.Pharm in QA, QC, Regulatory Affairs, RND, Manufacturing at Biocon Biologies

    Biocon is global biopharmaceutical company changing patients lives in over 120 countries by finding new and affordable ways to treat diabetes, cancer and autoimmune diseases.

    Qualification Required : MSc / M. Pharm / B. Pharm / B. Tech / M. Tech (Chemistry, Microbiology, Biochemistry & Biotechnology);
    Experience : 3-15 years | PhD (Biochemistry & Biotechnology); Experience : 0-3 years

  • Production, Regulatory Affairs, AR&D Jobs at Hetero Biopharma

    The leading edge of Hetero Group, Hetero Biopharma, is steadily establishing itself as a path breaking Biosimilar developer. As a strong R&D driven company offering some of the blockbuster Biosimilar Drugs, we at Hetero Biopharma are bringing about a paradigm shift in the way patients suffering from various chronic conditions are treated.

  • Walk in interview for M.Pharm, M.Sc, B.Pharm in Regulatory Affairs, RND, Manufacturing at Biocon Biologies

    Biocon is global biopharmaceutical company changing patients lives in over 120 countries by finding new and affordable ways to treat diabetes, cancer and autoimmune diseases.

  • M.Pharm, B.Pharm, MBA Jobs in Regulatory Affairs, Bussiness Development, Administration at Acme Generics Pvt. Ltd

    The Acme group began its journey in 2005 with a bold mission of becoming a leader in the contract manufacturing space and a preferred business partner for pharmaceutical companies looking for world class capabilities and scalable operations.  Guided by the founder's vision and purpose, the Acme group, over the years, has scaled new heights in the pharmaceutical value chain and today provides fully integrated contract manufacturing and development solutions to some of the top Indian and global pharmaceutical companies.

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