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  • Opportunity for B.Pharm as Chemist Quality Control at Lonza

    Lonza is one of the world’s leading and most-trusted suppliers to the pharmaceutical, biotech and specialty ingredients markets. We harness science and technology to create products that support safer and healthier living and that enhance the overall quality of life.

    Post : Chemist Quality Control

  • Require Associate, Senior Associate Scientist at Colgate-Palmolive

    Colgate-Palmolive is a leading global consumer products company, tightly focused on Oral Care, Personal Care, Home Care and Pet Nutrition. Colgate sells its products in over 200 countries and territories around the world under such internationally recognized brand names as Colgate, Palmolive, elmex, Tom’s of Maine, Sorriso, Speed Stick, Lady Speed Stick, Softsoap, Irish Spring, Protex, Sanex, Elta MD, PCA Skin, Ajax, Axion, Fabuloso, Soupline and Suavitel, as well as Hill’s Science Diet and Hill’s Prescription Diet.

    Post : Associate / Sr. Associate Scientist [Product Development - Personal Care / Home Care]

  • Require Project Manager 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 : Project Manager - Reimbursed Business

  • Walk in interview in Production, Quality Control at Biological E. Limited

    Established during the ‘Swadeshi Movement’ of India, Biological E. Limited (BE) started during a time when the nation sought access to critical healthcare products. Founded and led by Dr. DVK Raju, Biological E. Limited commenced its operations in 1953 as a biological products company manufacturing liver extracts and anti-coagulants. With an objective of transitioning from treating diseases to preventing them, Biological E. Limited launched its Biotechnology Division (now Vaccines and Biologics Division) and commenced large-scale production of DPT vaccines as early as 1962.

  • Work as Junior Regulatory Affairs Associate at PAREXEL | M.Pharm, B.Pharm

    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.

    Post :  Junior Regulatory Affairs Associate

  • Opportunity for B.Pharm as Quality Specialist at Teva Pharmaceuticals

    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 Specialist III - 6019

  • Job for M.Pharm, M.Sc Assistant Manager in Regulatory Affairs at GSK Rx India

    GlaxoSmithKline Pharmaceuticals Ltd. (GSK Rx India) is one of the oldest pharmaceuticals company and employs over 5000+ people. Globally, we are a £ 27.4 billion, leading, research-based healthcare and pharmaceutical company. In India, we are one of the market leaders.

    Post : Assistant Manager – Regulatory Affairs

  • Work as Lead Clinical Trials & Regulatory Intelligence at MakroCare

    MakroCare Expert Strategic Development and Commercialization Global Partner for Pharmaceutical, Biotechnology and Medical Device industries. Our Experience, Programs and Processes bring a New Dimension to Development Strategy, Regulatory/Risk Planning & Management, Clinical Research, Medical/Scientific Support and Emerging Region Expansion.

    Post :  Lead Clinical Trials & Regulatory Intelligence

  • U.S. Pharmacopeial Convention looking for Scientist

    The U.S. Pharmacopeial Convention (USP) is a scientific non-profit organization that sets standards for the identity, strength, quality, and purity of medicines, food ingredients, and dietary supplements manufactured, distributed and consumed worldwide. USP’s drug standards are enforceable in the United States by the Food and Drug Administration, and these standards are used in more than 140 countries.

    Post : Scientist III

  • Vacancy for Regulatory Affair Executive at Oracity Life Sciences

    Oracity Life Sciences was focusing on solid oral dosage forms (Tablets / capsules) with immediate as well as modified release technology. We will be catering Granules for immediate release, modified release tablets, different range of pellets formulation ready to encapsulate, MUPS ready to compress along with finished dose formulation of tablets and capsules. We have designed the facility / systems to meet all regulatory standards (like WHO, MHRA, USFDA etc…) and will be catering to domestic, ROW and highly regulated market.

    Post : Regulatory Affair Executive - 03 posts

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