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Clinical research courses

  • Merck Limited looking for Regulatory Toxicology Specialist

    Understanding the Global regulations like CLP, GHS etc. and creating compliant Safety Data Sheets by doing intensive data search and evaluating proper data.
  • Require Regulatory and Clinical Business Analyst at Infosys Limited
    As part of the Infosys consulting team, your primary role would be to actively aid the consulting team in different phases of the project including problem definition, effort estimation, diagnosis, solution generation and design and deployment
  • Walk in Drive for M.Pharm, B.Pharm, MSc in Production, QC, QA, Regulatory Affairs, F&D at Bharat Parenterals Ltd

    Bharat Parenterals Ltd. is a Gujarat based pharmaceutical company, established in 1992 by Mr. Ramesh Desai, who started the company with a vision of making world class affordable medicines and to take it to the forefront of contract manufacturing units in Gujarat.

    Walk In Interview

  • Recruitment for Professor, Assistant Professor at NIPER

    National Institute of Pharmaceutical Education and Research, Raebareli (NIPER-R) is “an Institute of National Importance” set up by an Act of Parliament under the aegis of the Department of Pharmaceuticals, Ministry of Chemicals & Fertilizers, Government of India, to impart higher education and undertake advanced research in the field of Pharmaceutical Sciences and Technology. 

  • Hiring for multiple positions at Apothecon Pharmaceutical - M.Pharm, MSc, BSc Apply
    Formulation Production Experience - Bottle Packing Section Oral solid manufacturing, Sterilization, Granulation, coating and documentation as per SOP.
  • Work as Regulatory Affairs Senior Manager at Genpact Limited
    Masters in Life Sciences. Participate, as needed, on global teams to complete assignments and tasks within a specific task force/project associated with labelling
  • Require M.Pharm, MSc Candidates in Regulatory Affairs at JAMP group
    M.Pharm / M.Sc; Candidates with exposure in the pharmaceutical industry with biologics, preferably in regulatory affairs for highly regulated markets.
  • AstraZeneca Hiring Regulatory Affairs Manager
    Regulatory Affairs Manager in the Regulatory Business Development Post Deal Management group is a regulatory specialist with project management capabilities responsible for both regulatory life cycle maintenance submissions and managing successful application transitions for products that are either divested or acquired.
  • Job for M.Pharm, MSc in Regulatory Affairs Department at Torrent Pharma
    Dossier submission and review of Module 1, 2 and 3. ANDA submission. DCP, MRP, National Filing for various EU countries. 
  • AstraZeneca looking for Regulatory Affairs Manager
    Accountable for regulatory transition activities to achieve relevant project turning points, as well as core business development operational activities including but not limited to running the green light process, preparation of documentation and risk, issue management.
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