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Clinical courses

 

Clinical research courses

  • Sun Pharma Walk in Drive for M.Pharm, B.Pharm, MSc in Production, QA, Micro | Only Experience candidates Apply

    Sterile manufacturing Suspension/emulsion /PFS / BFS as well as SKID operation. Should have experience in Aseptic process, complex manufacturing, Exposure to CIP/ SIP SKID, QMS.
  • Require Senior Research Scientist at o2h group
    Responsible for smoother operation of NMR instruments, shift planning and execution to achieve benchmark productivity month on month basis. Responsible for planning, prioritizing and executing work responsibilities in order to meet deadlines.
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    इंस्टिट्यूट ऑफ़ गुड मैन्युफैक्चरिंग प्रैक्टिसेज इंडिया
    Institute of Good Manufacturing Practices India

    Faculty of Clinical Research and Drug Safety (FCRDS)
    ए- 14/बी, कुतुब इंस्टिट्यूशनल एरिया, ओल्ड जे एन यु कैंपस के समीप, नई दिल्ली - 110067
                        A-14/B, A Block, Qutab Institutional Area, Near Old JNU Campus New Delhi-110067
                         E-mail: info@igmpi.ac.in, Phone: +91 11-26512850, +91 8448963304 (Mobile)
    Website: www.igmpi.ac.in

     

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    Post Graduate/Executive Diploma

    Clinical Research
    Medical Writing
    Pharmacovigilance
    Clinical Data Management (CDM)
    QA/QC (Clinical Research as Major)
    Pharmacology
    Clinical Engineering and Management

    CERTIFICATE

    Good Clinical Practice (GCP) Professional
    Clinical Research Associate
    Pharmacovigilance Associate (PV Associate)

    PROFESSIONAL CERTIFICATION

    Good Clinical Practice
    Drug Safety Aggregate Reporting
    MedDRA Coding
    Pharmacovigilance Audits & Inspections

     

    ENQUIRE NOW >>

    ✓ Programme duration: 12 months for Post Graduate Diploma and 3-6 months for Certificate programmes.

       ✓ Contact for Prospectus and last date on: +91 11-26512850 or info@igmpi.ac.in

       ✓ Placement Assistance

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  • Job for Degree in Professional Course at AIIMS, Salary Rs. 45,000 pm
    Post of Senior Research Fellow under BIRAC - BIG funded project entitled Minimally Invasive Nano-Enabled Targeted Technology for Sentinel Lymph Node (SLN) Detection in Head-Neck Cancer under Prof. Alok Thakar, BIG Grant Awardee
  • Zydus Life Sciences Walk in Drive for B.Pharm, M.Pharm in Production, QA, QC Department
    For all the positions, it is essential for candidates to have exposure in Injectable Sterile plant and regulatory requirements of documentation as per cGMP/GLP.
  • Interview for B.Pharm, MSc, BSc in Packing Department at IPCA Lab
    Having relevant experience to operation and maintenance of CAM/ IMA/Blister/ CVC/ Cartonator m/c.
  • Teva looking for Quality Specialist - B.Pharm Apply

    Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas.

  • Eurofins Scientific Hiring for Assistant Manager

    Eurofins Scientific is a group of international life sciences companies which provide a unique range of analytical testing services to clients across multiple industries. The Group believes it is the global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

  • Walk in Drive for M.Pharm, B.Pharm, M.Sc in Quality Control at Intas Pharma
    Having exposure related Environment Monitoring in formulation, water analysis, various Microbiological test like sterility, BET, MLT etc. Having exposure related to regulatory plant and basic know of GLP GMP .Ready to work in rotational shift.
  • Work as Regulatory Professional at Novo Nordisk - Ph.D, M.Pharm, MSc Apply
    You will be a member of a newly established virtual team - EU Submission Hub with colleagues in Denmark, Portugal, Poland and Bangalore focusing on clinical trial submissions in EU. EU Submission Hub is part of Submission Management department, who is responsible for electronic submissions to Health Authorities including New Drug Applications and Life Cycle submissions.
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