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M.Sc

 

Clinical courses

 

Clinical research courses

  • 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.
  • MSc Pharma Recruitment at Regional Centre for Biotechnology
    MSc Pharmacy, Pharmacology. Engineering of Long-lasting Breast Hydrogel Implants for Cancer Immunochemotherapy
  • Applications are invited for post of JRF at Indian Institute of Integrative Medicine
    A multi-OMICS Approach to Decipher the Stress Signaling Network in Rhodiola imbricate Edgew. Post Graduate Degree in Basic Sciences or Graduate/ Post Graduate Degree in Professional Courses
  • Work as Research Intern at National Institute of Immunology
    The research intern will perform cloning, and over expression of proteins along with bioinformatic analysis. The preference will be given to candidates who have background knowledge in at least two of the following areas: Molecular Biology, Protein biochemistry, Structural Biology, and Bioinformatics
  • 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.
  • Opportunity for Ph.D or M.Pharm, MSc, MTech as Team Lead at Dr. Reddys Laboratories
    To develop approaches for Downstream processes, designing and managing multiple process development projects; to take up new technology initiatives within the downstream development group. To draft primary documents for functional deliverables.
  • Work as PV RA MW Coordinator at Thermo Fisher Scientific
    Provides critical support and coordination in the review of safety and regulatory publishing documents, ensuring timely and accurate processing upon receipt. Plays a key role in maintaining document quality by tracking safety and regulatory publishing data, ensuring seamless uploading into internal and/or external electronic trial master files.
  • Vacancy for M.Pharm, B.Pharm, MSc in QA Department at Gufic Biosciences Ltd
    Candidate must have an injectable background. Candidate must have knowledge of Software like Lab Solution, Chromeleon & Spectrum. Candidate must have knowledge of Instruments like UV, HPLC, FUR, GC, LPC, TOC, Polari meter, Refractometer.
  • Require Regulatory Professional at Novo Nordisk
    As Regulatory Professional II, the candidate will be responsible for making the timely submissions to the Health Authorities worldwide. The candidate is expected to establish and maintain the CMC part of the core regulatory file. 
  • Opportunity for M.Pharm or MSc, MTech to work in DST sponsored project at JNCASR
    Candidates with laboratory experience in human cell culture, animal handling and prior knowledge of developing therapeutics for different infectious and non-communicable diseases will be preferred 
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