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  • Hiring Lead Research Scientist at Stanford University

    Familiarity with institutional requirements for animal use and welfare in pharmacology experiments is essential. Additionally, you will effectively communicate the goals, protocols, and results, contribute to regulatory submissions, and foster cross-team collaboration to enhance IMA research innovation and decision-making processes.
  • Recruitment for M.Pharm, B.Pharm, MSc at Indian Pharmacopoeia Commission - Auditor, Technical Expert Post
    M.Pharm, M.Sc or in any equivalent field plus minimum of 2 years of experience in the design and development or manufacturing or research or testing or quality in medical device field.
  • DST-GDC I-NCUBATE Program
    The DST-GDC I-NCUBATE Program is a joint initiative of the Department of Science and Technology, Government of India, in partnership with the Gopalakrishnan-Deshpande Centre for Innovation and Entrepreneurship, IIT Madras, to identify and nurture the most promising deep-tech startups based on STEM research in Indian Universities and Labs.
  • Work as Head Formulation Development at Sandoz
    Plan, implement and evaluate experiments for establishing of composition, manufacturing procedures and packaging via support of def. evaluation experiments taking product stability, bioequivalence and possible production site into consideration.
  • Walk In Drive for M.Pharm, B.Pharm, M.Sc in Production, Stores Formulation at Macleods Pharmaceuticals
    2 TO 8 YEARS YEARS OF EXPERIENCE IN COMPRESSION, GRANULATION AND PACKING. EXPERIENCE IN RECEIPT & DISPENSING ACTIVITY, INWARD & OUTWARD ACTIVITY
  • Walk In Drive for M.Pharm, B.Pharm, M.Sc in QA, Packing, Beta Injection, QC, Production at Bharat Parenterals
    Must have Injectable Experience, and Knowledge of Aseptic Area, Autoclave, Filling, QMS, washing and sealing and Batch Manufacturing or fresher also apply. Must have Injectable Experience, and Knowledge of Aseptic Area, Autoclave, Filling, QMS, washing and sealing and Batch Manufacturing.
  • Sanofi looking for Quality Assurance Senior Specialist
    Verify the accuracy of transcribed data by cross-referencing with original sources and ensure an accurate presentation of data in the report. Ensure that all transcribed data complies with internal quality standards and external regulatory requirements.
  • Novo Nordisk Require Business Analyst - M.Pharm, B.Pharm, MSc Apply
    Conduct in-depth research and analysis of rare disease markets, including competitive landscape, market dynamics, and emerging trends. Develop and maintain a comprehensive understanding of the rare disease market, including key players, product portfolios, and future opportunities. Collaborate with cross-functional teams to gather and synthesise relevant data and insights to support strategic decision-making.
  • Regulatory Affairs Specialist Require at Medtronic
    Represent Regulatory Affairs as team member of product development projects from Concept through Commercialization. Review pre-clinical, and clinical protocols and associated reports to be used in submissions for assigned projects.
  • Applications are invited for post of Project Assistant at IISER
    Bachelors degree in any natural sciences. Experience with basic molecular biology and biochemical techniques, cell culture techniques, data analysis, and report writing. Ability and experience handling data
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