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B.Sc

 

Clinical courses

 

Clinical research courses

  • Walk in Drive for M.Pharm, B.Pharm, M.Sc in Production, QC, QA at Unichem Laboratories

    Familiar with cGMP guidelines and Quality Systems as per the international regulatory requirements. Experience in Oral Solid Dosage Manufacturing / CVC Packaging. Exposure to the latest manufacturing and packing techniques.
  • Deloitte Hiring pharma candidates as consultant for Risk Advisory team
    Quality guidelines mentioned by FDA, MHRA, and other regulatory bodies; GxP practices and GAMP5 guidelines. As a part of our Risk Advisory team you will build and nurture positive working relationships with teams and clients with the intention to exceed client expectations.
  • Job Openings for Ph.D, M.Pharm, MSc under different Projects at CDRI, 54 Openings
    Development of imine reductase based biocatalytic platoform for the synthesis of chiral amines building blocks for drug discovery and developmental applications
  • Job for B.Pharm, MSc, BSc in Production, QC Department at Hetero Drugs
    Granulation, Compression, Coating, IP, FP, Stability
  • Walk in Drive for M.Pharm, B.Pharm, M.Sc in Production, QC at Macleods Pharma
    Experience in Finished Products, Raw Material, Stability, Packing material and AMT, AMV
  • Walk in Drive for D.Pharm, B.Pharm, M.Pharm in Parenteral Department at Intas Pharma
    Complex Skid, NDDS, Aseptic, Manufacturing Clean Area, lyophilizer 
  • Work as Regulatory Affairs Senior Manager at ADVANZ PHARMA
    Helping the team with strategic planning for submissions, focussing on right classification of variation with an emphasis on urgency of change, nature of change, optimising submission cost, timelines for approval and any risk assessment needed.
  • Walk in Drive for B.Pharm, MSc, BSc in Production, QA, QC, Warehouse at Honour Lab

    Established in 2012, Honour Lab Limited is engaged in the manufacturing of Active Pharmaceutical Ingredients (APIs) & Intermediates. Honour Lab Limited has 5 state-of-the-art manufacturing facilities located in Hyderabad, Visakhapatnam and Pune which are approved by USFDA, TGA, MFDS, MOT, PMDA and PICS. Backed by a strong R&D with 100+ top notch scientists, the company excels at developing high-quality products which meet the demands of the rapidly growing global drug markets.

  • Teva looking for Quality Specialist
    Serve as a Subject Matter Expert on all In-Take Team complaint processes and scenarios and assists QAS employees to ensure compliance with Quality Assurance Services Standard Operating Procedures and Work Instructions
  • Walk in Drive for M.Pharm, B.Pharm, M.Sc in Pharmacovigilance at Tata Consultancy Services
    Ability to understand and analyses the complex data and performs the activities including accessing the case in Argus, code and enter data. Be fully competent to perform all steps within the case-handling processing.
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