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Clinical courses

 

Clinical research courses

  • Novo Nordisk Require Medical Writing Specialist

    Communicate clinical data clearly and concisely, contributing to process improvements, knowledge sharing, and skill building. Mentor and train other medical writers as needed, while maintaining good relationships with stakeholders and colleagues.
  • EY Consulting Hiring Manager

    As a global leader in assurance, tax, transaction and advisory services, we hire and develop the most passionate people in their field to help build a better working world. This starts with a culture that believes in giving you the training, opportunities and creative freedom. At EY, we don't just focus on who you are now, but who you can become.

  • Job for B.Pharm, M.Pharm in Regulatory Affairs at JAMP group
    B.Pharm / M.Pharm; Preparation of responses to clarification requests received from Canadian authorities. Communicate with external suppliers for the preparation of packaging components and ensure technical feasibility.
  • Job for M.Pharm, B.Pharm in Production Manufacturing Department at Gracure Pharmaceutical
    B.Pharm / M.Pharm; Manager / Sr. Manager OSD Manufacturing, Team Leader OSD Manufacturing; Manager / Sr. Manager Liquid Syrup Manufacturing
  • Opportunity for M.Pharm, B.Pharm, MSc to Join Novo Nordisk as Regulatory Professional
    As Regulatory Professional II, the candidate will be responsible for making the timely submissions to the Health Authorities worldwide.
  • Regulatory Affairs Trainee Require at Apotex
    Perform all the labelling update activities and tracking in systems for record maintenance with respect to New Product Development NPD label creation and Product Life Cycle Management PLCM update for products in USA and Canada market
  • Cipla looking for RA Jr. Team Member
    Assist in submission of product documents to regulatory authorities in accordance with country specific regulatory requirements to ensure approvals and market launch in stipulated time and support in handling post-approval changes, maintenance, and updation of documents during the products life-cycle. Achieve timely submission of dossier/DMF and deficiency responses to regulatory authority by collation, and compiling documents in order to ensure approvals for launch in stipulated time
  • Job for M.Pharm, M.Tech, M.S Pharm as SRF at IIT-BHU
    Senior Research Fellow to work on CCRAS-sponsored Evaluation of Coded drug Ayush Rasayana B for treatment of high-altitude sickness using multi-dimensional drug discovery approach project.
  • Emcure looking for experienced professionals in QA department
    Should have detailed knowledge as well as experience of working for an injectable manufacturing process. Should have compendia and regulatory knowledge of aseptic processing and controls and Contamination control strategy program.
  • Vacancy for Principal, Professor, Associate Professor, Assistant Professor at Pratap University
    URGENTLY REQUIRED - Principal, Professor, Associate Professor, Assistant Professor at Pratap University, Jaipur
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