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  • Walk in Drive for D.Pharm, B.Pharm, M.Pharm in Production and Quality at Granules India
    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.
  • 10 January 2025
    Amneal Pharma Hiring Analytical Method Validation Analyst
    M.Pharm / M. Sc; Perform and review method validation of Assay, Dissolution, Related compound and Residual solvents etc. for new projects using instruments like HPLC,UV, IC ,GC,ICP MS and AAS etc. Preparation of method validation/verification protocol (API and finish product) like HPLC, GC, IC, and AAS etc.
  • 10 January 2025
    Require Analytical R&D Associate Scientist at Novartis
    Design, plan and perform scientific experiments for projects at different clinical phases of drug substance and drug product with minimal guidance. Well versed with regulatory guidelines, scientific literature, technology transfer and interpretation of the results to draw conclusions in reports.
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