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Clinical research courses

  • Life Sciences, Pharmacy Graduate Job at Teva

    Teva is a global pharmaceutical leader and the worlds 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.

    Post : Regulatory Affairs Associate III - 1436

  • Vacancy for Clinical Trial Associate, Clinical Research Associate at Zydus Lifesciences Limited

    Zydus Life sciences Limited for the first time in India came up with an all women division named EQUALSTWO. Enriched with 100% natural ingredients. EOUALSTWO offers quality skincare products made from the best of nature and science. Built on the foundation of balance the division aims to win the trust of mothers with a 100% natural and safe product range which is at par with international standards of skin care.

  • M.Pharm, M.Sc Career as Regulatory Affairs Lead Associate at Genpact Limited

    Genpact Limited, a global leader in business process and technology management services, leverages the power of smarter processes, smarter analytics and smarter technology to help its clients drive intelligence across the enterprise. Genpacts Smart Enterprise Processes (SEP) framework, its unique science of process combined with deep domain expertise in multiple industry verticals, leads to superior business outcomes.

    Post : Lead Associate - Regulatory Affairs-LIF007376

  • Job for M.Pharm, M.Sc in Regulatory Affairs department at Rusan Pharma Ltd

    Rusan Pharma Ltd. is a fully integrated global pharmaceutical company specializing in the treatment of Addiction and Pain Management.  We offer a complete range of products for de-addiction and pain management in countries across the globe including Europe, UK, Russia, CIS, South Africa, Mauritius, Nepal and Myanmar. We are one of the largest suppliers of life saving drugs to various organizations such as NACO, UNODC, UNOPS, Global Fund and Ministries of health in various emerging markets.

  • Walk in interview for B.Pharm, M.Sc in Production, Quality Control, Regulatory Affairs at SMS Pharmaceuticals Ltd

    SMS Pharmaceuticals Ltd. is a global player in API manufacturing having a strong research and manufacturing team supported by state of the art facilities. What started off as a single facility single product manufacturing company in 1990 grew to be a multi-location group having product list spreading across an array of therapeutic segments. SMS was given the export house status in the year 1997-98. SMS is currently a listed company having ever appreciating international and domestic customer base.

  • Job for Pharma Graduate at KAPL, Government of India Enterprise

    Karnataka Antibiotics and Pharmaceuticals Limited, KAPL Bengaluru is a Government of India Enterprise. Karnataka Antibiotics and Pharmaceuticals Limited is a Joint Sector Company of Government of India with shareholding from Government of Karnataka through Karnataka State Industrial Infrastructure Development Corporation KSIIDC. From a modest beginning in 1984, KAPL has grown exponentially in the areas of manufacturing and marketing of various life saving and essential drugs.

  • Require Regulatory Specialist at GSK Rx India

    GlaxoSmithKline Pharmaceuticals Ltd. (GSK Rx India) is one of the oldest pharmaceuticals company and employs over 5000 plus people. Globally, we are a £ 27.4 billion, leading, research-based healthcare and pharmaceutical company. In India, we are one of the market leaders. At GSK, our mission is to improve the quality of life by enabling people to do more, feel better and live longer. This mission drives us to make a real difference to the lives of millions of people with our commitment to effective healthcare solutions.

  • Career for M.Pharm or MSc to work in Ministry of Science and Technology, Govt of India | Salary upto Rs 90,000/- pm

    Translational Health Science and Technology Institute (THSTI) is an autonomous Institute of the Department of Biotechnology, Ministry of Science and Technology, Govt. of India. The institute is an integral part of the interdisciplinary NCR Biotech Science Cluster located at Faridabad, and is designed as a dynamic, interactive organization with the mission to conduct innovative translational research and to develop research collaborations across disciplines and professions to translate concepts into products to improve human health.

  • Job for M.Pharm, B.Pharm, M.Sc in Regulatory Affairs, F&D, Quality Control at Ind-Swift Laboratories Ltd

    Ind-Swift Laboratories Ltd is the fastest growing API Group. We are having 6+ API Manufacturing Facilities across the globe. We are dealing in regulated market having approvals like USFDA, MHRA, TGA, ANVISA, PMDA, EU GMP.

    Post: Officer/Sr. Officer - Regulatory Affairs, F&D, QC

  • Regulatory Affairs Consultant Require 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.

    Post : Regulatory Affairs Consultant

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