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  • Work as Centralized Study Associate at Covance

    Covance is one of the world’s largest and most comprehensive drug development services companies with more than 11,000 employees in 60 countries. Through its nonclinical, clinical and commercialization services, Covance has helped pharmaceutical and biotech companies develop one-third of all prescription medicines in the market today.

    Post : Centralized Study Associate II (Clin Ops)

  • Require Cliniacal Operations Manager at IQVIA
    Require Cliniacal Operations Manager at IQVIA

    Quintiles and IMS Health have come together to become IQVIA, The Human Data Science Company. Inspired by the industry we help, IQVIA commits to providing solutions that enable life sciences companies to innovate with confidence, maximize their opportunities and ultimately drive human health outcomes forward.

    Post : Manager, Clinical Operations

  • Job Principal Scientific Manager at GVK Biosciences PVT Ltd
    Job Principal Scientific Manager at GVK Biosciences PVT Ltd

    GVK BIO is a global Contract Research & Development Organization (CRDO) providing Drug Discovery and Development services to the biopharma industry. Established in 2001, GVK BIO for over 18 years has supported the Research and Development programs of innovator drug companies enabling them to bring their products to market quicker and cost- effectively.  We are a team of over 2100 highly qualified scientists, backed by well-defined and scalable processes, modern facilities and a strong customer-centric partnering approach. Our distinctiveness comes from our expertise in the breadth and depth of services that we provide in drug discovery and development. We recognize that our clients’ needs are diverse, and we have designed our services accordingly. GVK BIO’s capabilities include Integrated Drug Discovery, Chemistry, Biology, Large molecule R&D , Chemical Development, Formulation & Analytical development, Contract Manufacturing and Drug Repurposing.

    Post : Principal Scientific Manager - Hyd / Bangalore

  • Require Senior Manager in Regulatory Affairs CMC at MSD
    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
    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

  • Walk in interview for M.Pharm, M.Sc, B.Pharm in Quality Control at Strides Pharma Science Limited
    Walk in interview for M.Pharm, M.Sc, B.Pharm in Quality Control at Strides Pharma Science Limited

    Incorporated in 1990, Strides Pharma Science Limited is a global pharmaceutical company headquartered in Bangalore, India. The Company has two business verticals, viz., Regulated Markets and Emerging Markets.  Strides has a global manufacturing footprint with seven manufacturing facilities spread across three continents, including four US FDA approved facilities and two facilities for the emerging markets.  The Company has a dedicated R&D facility in India with global filing capabilities and a strong footprint across 100 countries.

    Post : Executive / Sr. Executive

  • Walk in interview for Trainee / Chemist in QC at Natco Pharma Limited
    Walk in interview for Trainee / Chemist in QC at Natco Pharma Limited

    Natco Pharma Limited was incorporated in Hyderabad in the year 1981 with an initial investment of INR 3.3 million. With a modest beginning of operations as a single unit with 20 employees, Natco today has five manufacturing facilities spread across India with dedicated modern research laboratories, capabilities in New Drug Development, etc.  Natco family currently consists of more than 3,200 employees, we are consistently ranked among fastest growing pharmaceutical companies in India. Natco is well recognized for its innovation in Pharmaceutical R&D.

    Post : Trainee / Chemist - QC

  • Walk in interview for Analytics at IQVIA
    Walk in interview for Analytics at IQVIA

    Quintiles and IMS Health have come together to become IQVIA, The Human Data Science Company. Inspired by the industry we help, IQVIA commits to providing solutions that enable life sciences companies to innovate with confidence, maximize their opportunities and ultimately drive human health outcomes forward.

    Post : Event Announcement - Analytics

  • Require Regulatory Specialist at GlaxoSmithKline Pharmaceuticals Ltd
    Require Regulatory Specialist at GlaxoSmithKline Pharmaceuticals Ltd

    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. 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.

    Post : Regulatory Specialist

  • Require Study Start Up Associate at ICON
    Require Study Start Up Associate at ICON

    ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialize in the strategic development, management and analysis of programs that support Clinical Development – from compound selection to Phase I - IV clinical studies ICON enjoys a strong reputation for quality and is focused on staff development.

    Post : Study Start Up Associate I

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