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  • Career Opportunities at TCS Mumbai for M.Pharm, B.Pharm Candidates

    BACHELOR OF PHARMACY, BACHELOR OF SCIENCE ( B.Sc Degree ), MASTER OF PHARMACY; Validate clinical trial data to ensure consistency, integrity and accuracy based on project specific guidelines. Responsible & Accountable for the assigned study conduct activities, in clinical trials from TCS.
  • Roche Hiring Clinical Operations Manager
    Roche Hiring Clinical Operations Manager
    experience in Pharmaceutical / Biotech / Clinical Research industry with Clinical Operations. candidate for the Manager clinical operations role who can provide local strategic planning and operational delivery of clinical studies through all phases of study management preparation, study start-up, conduct, close-out, and manages local vendors
  • TCS Hiring Pharma graduates for Pharmacovigilance Executive Post
    TCS Hiring Pharma graduates for Pharmacovigilance Executive Post

    Helping Clients Create the Future TCS combines tech expertise and business intelligence to catalyze change and deliver results. Our mission is to help customers achieve their business objectives by providing innovative, best-in-class consulting, IT solutions and services and to make it a joy for all stakeholders to work with us.

    Post : Pharmacovigilance Executive

  • Applications are invited for post of Scientist at NIIH, Salary Rs. 69440 pm
    Applications are invited for post of Scientist at NIIH, Salary Rs. 69440 pm

    ICMR-National Institute of Immunohaematology was established in the year 1957 with an aim to conduct multidisciplinary research related to Immunohaematology offer diagnostic services and provide training to medical and non medical professionals in the field of haematology, Immunology, genetics and conduct awareness programmes on haematological disorders.

    Post : Scientist B (Non Medical)

  • Wipro is Hiring for Drug safety analyst - Literature specialist
    Wipro is Hiring for Drug safety analyst - Literature specialist

    At Wipro, the safety, health and well being of our employees is of paramount importance and over the past several weeks we have taken a series of preventive measures to protect our employees from the Coronavirus outbreak. Given the evolving situation, we have advised our employees to work from home wherever feasible and if their role allows them to do so. Wipro offices will remain open.

    Post : Drug safety analyst - Literature specialist

  • Job as Sr. Manager Project Management and Biopharmaceutics at Synergen Bio
    Job as Sr. Manager Project Management and Biopharmaceutics at Synergen Bio
    B.Pharm, M.Pharm, Msc; Lead the Bio- PK team to plan and execute BA BE studies for various regulatory markets. Manage the designing of PK studies for demonstrating bioequivalence for solid, liquid, topical and specialized dosage forms including parental.
  • Vacancy in Pharma QA, QC, Production at Centaur pharmaceuticals Pune and Goa Plant - only for experienced candidates
    Vacancy in Pharma QA, QC, Production at Centaur pharmaceuticals Pune and Goa Plant - only for experienced candidates
    M.Sc, M.Pharm; Experience must include analysis of Raw Material, In-Process, finished goods, Stability Testing and Stability sample handling Tablets / Capsules. Handling of HPLC, dissolution and other sophisticated instruments.
  • Pharmacist jobs at Tata Memorial Centre - walkin
    Pharmacist jobs at Tata Memorial Centre - walkin
    Diploma in Pharmacy and 3 months training in Pharmacy along with Registration with Central or State Pharmacy Council duly allotted Registration Number. One year experience in a hospital/ Dispensary is essential.
  • Opening as Senior Executive - Regulatory & Business Continuity - Branded at Sun Pharma
    Opening as Senior Executive - Regulatory & Business Continuity - Branded at Sun Pharma
    This position will support and manage the regulatory activities associated with the Chemistry, Manufacturing and Controls for New Drug Applications across globe. Regulatory activities focus on filing activities/query responses/post approval changes as suggested across globe.
  • Job as Regulatory Affairs Associate at Teva
    Job as Regulatory Affairs Associate at Teva
    This position provides medical and scientific expertise for regulatory submissions and implies in-depth expertise within medical science, with primary goal of authoring clinical and non-clinical expert reports and summaries supporting new submissions of Generics, Innovative and Medis organizations in international markets
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