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Regulatory affairs

  • 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

  • Opportunity for Ph.D in Pharmacology as Senior Research Officer at CDSA | Salary Rs.80,000 pm

    Clinical Development Services Agency (CDSA) is an extramural unit of Translational Health Science and Technology Institute (THSTI) and has been established as a not-for-profit society to provide cost affective, high quality preclinical and clinical product development support services to meet the country’s growing healthcare needs. It will tend enterprises; particularly SMEs involved in new technology innovation and facilitate translation of scientific know-how into viable products.

    Post : Senior Research Officer (Regulatory Affairs)

  • Walk in interview for Freshers B.Pharm or M.Pharm in Regulatory Affairs at Aurobindo Pharma Ltd | Hyderabad

    Aurobindo Pharma Ltd., is a Leading Pharmaceutical company having 23 plants worldwide with regulatory approvals from USFDA, UK MHRA etc. with a turnover of more than $2.5 billion dollars.

  • Require Senior Manager in Regulatory Affairs CMC at MSD

    MSD Manufacturing Division, is a team of dedicated, energetic individuals who are committed to being the most trusted supplier of pharmaceuticals and health products worldwide. Our facilities, along with our external contractors, suppliers, and partners, comprise an interdependent global manufacturing network that’s committed to delivering a compliant, reliable supply to customers and patients on time, every time, across the globe. MSD is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us.

    Post : Senior Manager - Regulatory Affairs CMC

  • Work as Director in Regulatory Affairs at Johnson & Johnson

    Johnson & Johnson was founded more than 120 years ago on a revolutionary idea: Doctors and nurses should use sterile sutures, dressings and bandages to treat peoples’ wounds.  Johnson & Johnson is ranked by Fortune Magazine as the 3rd most Admired Pharmaceutical Company in the world with an outstanding product range as well as an extensive research base with a number of life saving original research molecules.

    Post : Director - Regulatory Affairs

  • Require Regulatory Affairs Associate at Teva | B.Pharm, M.Pharm

    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.  We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation.

    Post : Regulatory Affairs Associate II

  • Job for Regulatory Affairs Manager Executive in MediPharma Konnect | M.Pharm, B.Pharm

    MediPharma Konnect (Earlier Nextus Solutions)  is one of the fastest growing and leading Advisory enterprise and Executive Search organization from last 10 years with experienced team of Professionals with Pharma and Healthcare industries.Clientele - Nestle, Abbott, Lupin, Dr Reddy's Lab, Boehringer, UCB, USV, Nutricia international, IPCA, Ajanta group, Unichem, Aristo,Troikaa, Dr Morepen ,Baxter, Otsuka,, FDC, Centaur, Corona remedies, Martin & Harris, Walter & Bushnell, Sifam Pharma,  Biotech visioncare, Sterling Hospital, CIMS Hospital, Aarna hospital, Asian Bariatrics, Nidhi hospital, Sachdeva eye, Ansh liver clinic  and many more Indian and Multinational companies..

    Post : Executive - Regulatory Affairs

  • Walk in interview in Regulatory Affairs Department at Caplin Point

    Caplin Point was established in 1990 to manufacture a range of ointments, creams and other external applications.  The Company was listed in 1994 following its Initial Public Offering (IPO) which was oversubscribed 117 times, the proceeds of which were deployed in setting up a manufacturing facility at Pondicherry. Thereafter, the Company expanded its product range and increased its production capacity.  The Company focused on the emerging markets of Latin America, Caribbean, Francophone and Southern Africa and is today one of the leading suppliers of Pharmaceuticals in these regions, with over 2800 product licenses across the globe.

    Post : Exe., Sr.Exe., AM & DM

  • Require Associate Director in Regulatory Affairs CMC at MSD

    MSD Manufacturing Division, is a team of dedicated, energetic individuals who are committed to being the most trusted supplier of pharmaceuticals and health products worldwide. Our facilities, along with our external contractors, suppliers, and partners, comprise an interdependent global manufacturing network that’s committed to delivering a compliant, reliable supply to customers and patients on time, every time, across the globe. MSD is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us.

    Post : Associate Director – Regulatory Affairs CMC

  • Job for Senior Manager in Regulatory Affairs CMC at MSD

    MSD is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products.   Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us.

    Post : Senior Manager - Regulatory Affairs CMC

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