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  • Teva looking for Quality Specialist
    30 April 2024

    Teva looking for Quality Specialist - B.Pharm Apply

    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.

  • 30 April 2024
    Eurofins Scientific Hiring for Assistant Manager

    Eurofins Scientific is a group of international life sciences companies which provide a unique range of analytical testing services to clients across multiple industries. The Group believes it is the global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

  • 30 April 2024
    Walk in Drive for M.Pharm, B.Pharm, M.Sc in Quality Control at Intas Pharma
    Having exposure related Environment Monitoring in formulation, water analysis, various Microbiological test like sterility, BET, MLT etc. Having exposure related to regulatory plant and basic know of GLP GMP .Ready to work in rotational shift.
  • 30 April 2024
    Work as Regulatory Professional at Novo Nordisk - Ph.D, M.Pharm, MSc Apply
    You will be a member of a newly established virtual team - EU Submission Hub with colleagues in Denmark, Portugal, Poland and Bangalore focusing on clinical trial submissions in EU. EU Submission Hub is part of Submission Management department, who is responsible for electronic submissions to Health Authorities including New Drug Applications and Life Cycle submissions.
  • 30 April 2024
    ICON plc looking for Medical Data Reviewer

    ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success.

  • 29 April 2024
    Job for M.Pharm, B.Pharm and MBA for Project Management department at Zydus Lifesciences
    Develop detailed project budgets, including cost estimates. Monitor project expenditures and ensure adherence to budgetary constraints. Develop project timelines and schedules, identifying critical milestones and dependencies. Also Monitor progress against timelines and implement adjustments as necessary to ensure on-time delivery
  • 29 April 2024
    Interview for M.Pharm, B.Pharm, MSc in Analytical R&D Department at Gland Pharma
    Analytical method development, stability samples analysis and impurities identification and characterization with hands on experience in HPLC, GC, LC-MS, GC-MS, ICP-MS and other analytical techniques. Preparation of analytical method development reports, validation protocols and reports in accordance with guidelines.
  • 29 April 2024
    Macleods Pharma Walk in Drive for M.Pharm, B.Pharm, MSc in QC, QA, Production | Only Experience candidates Apply
    Experience in into HVAC, Calibration,Utility Electrical, Documentation, Finished Goods, Raw Material, Stability, Dispensing & receipt of Raw Material & Packing Material
  • 29 April 2024
    Work as Quality Control Associate / Senior Associate at Stelis Biopharma
    Preparation of quality system related, Instrument operation related SOPs, Specification, STPs, GTPs, raw data sheet, certificate of analysis. Preparation, review, execution of method transfer and method validation protocols and reports etc.
  • 28 April 2024
    Job for M.Pharm, MSc as Medical Writing Associate at Teva
    M.Sc or M.Pharm. Coordinate with all concerned department to ensure timelines and compliance to regulatory or sponsor requirements for preparation, compilation and delivery of reports. Electronically generate, review study documents and submission of study reports in CTD/eCTD format as per regulatory requirements.
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