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  • Work as Medical Affairs Senior Team Lead at Cipla
    14 January 2025

    Work as Medical Affairs Senior Team Lead at Cipla

    Develop, strategize and plan business activities like portfolio selection, brand planning and launch, KOL management, compliance and other crucial activities in therapy and additional therapeutic areas. This is towards assimilation of scientific and medical know-how in aligning activities to meet the business goal of the concerned therapeutic areas, business unit. Understand on ground clinical practices by interacting with clinicians, to develop practical knowledge and utilize it to provide closer-to-market product solutions
  • 13 January 2025
    Job for M.Pharm in Analytical Development at Bioplus Life Sciences
    Analytical support for formulation development department in terms of analyzing in-process, finished products for drug release profiling, assay, content uniformity, blend uniformity, related substances, water content and other analysis
  • 13 January 2025
    Walk in Drive for D.Pharm, B.Pharm, M.Pharm in Production and Quality at Granules India

    Granules India is a vertically integrated, high-growth pharmaceutical company with 38 years of proven performance and increasing performance and increasing presence across the world. Headquartered in Hyderabad, India, Granules offers collaborative and strategic partnership to global pharmaceutical leaders by producing best quality API, PFI and FD through manufacturing excellence, process innovation and regulatory expertise.

    WALK-IN INTERVIEW Production & Quality (OSD Formulations)

  • 13 January 2025
    Require Principal Medical Writer at Merck - M.Pharm, B.Pharm, MSc Apply
    As a Principal Medical Writer you will play a pivotal role in leading the Medical Writing efforts for Marketed Products and Lifecycle Management, both globally and at regional, local levels. You will represent the department as a subject-matter expert on clinical study teams, leading document-related meetings and reviewing study-related documents.
  • 12 January 2025
    Walk In Drive for D.Pharm, B.Pharm, M.Pharm in Manufacturing, Packing, QA, QC, AMV at Ipca Laboratories
    B.Pharm/M.Pharm/D.Pharma; Having relevant experience to operate and maintenance of Compression Granulation, Coating m/c. Documentation QMS for Manufacturing Dept. experience in operation and supervision of CAM/ IMA/Blister/ CVC/ Cartonator/ Documentation QMS for Packing Dept.
  • 11 January 2025
    Hiring for CAR-T at Dr. Reddy's Laboratories - QA, QC, Microbiology, Manufacturing
    Contamination Control, Isolator handling, Environmental monitoring. Disinfectant studies, Rapid microbiology analysis.
  • 10 January 2025
    Opportunity for M.Pharm as Research Associate at Piramal Group
    The incumbent should be aware of the product development flow from the conceptualization to tech transfer. The incumbent is responsible for R&D trials batch making for various personal care, personal hygiene products like.
  • 10 January 2025
    Walk in Drive for M.Pharm, B.Pharm, MSc in QA, QC, Manufacturing, Filling at Torrent Pharma
    M.Sc / B.Pharm / M.Pharm. Material Dispensing, Ointment, Gel Manufacturing, Filling, Packing, Track and Trace, Labelling, Cartonator, QMS. IPQA, Document Cell, OOS, OOT, Process/ Cleaning Validation, Review of BMR & BPR, Training ,QMS Investigation, CAPA, SOPs etc.
  • 10 January 2025
    Require Regulatory Affairs Specialist at Medtronic - M.Pharm, B.Pharm Apply
    He, she participates in all activities relating to preparation, submission and follow up to obtain approvals, renewals for products and its variations and line extension indications and labeling approvals of medical devices of various business units of Medtronic. He, she will be responsible for providing technical support by interpreting federal and local regulations as they apply to products, processes, practices and procedures
  • 10 January 2025
    Walk in Drive for M.Pharm, B.Pharm, MSc in Production, QC at Biological E Limited
    Supervision of aseptic area activities, shift handling, aseptic area documentation, media fill activities, aseptic behaviour monitoring, and sterile operations. Handling area cleaning and sanitation activities, supervising steam sterilizer loads, filter integrity, disinfectant preparation and filtration activity, and related documents.
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