Skip to main content

5+

Join WhatsApp Channel 

Regulatory Affairs Courses
  • 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)

  • 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.
  • Hiring for CAR-T at Dr. Reddy's Laboratories - QA, QC, Microbiology, Manufacturing
    Contamination Control, Isolator handling, Environmental monitoring. Disinfectant studies, Rapid microbiology analysis.
  • 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.
  • 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
  • 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.
  • 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.
  • Intas Pharma Walk In Drive at Goa for M.Pharm, B.Pharm, M.Sc in Multiple Department
    M.Pharm, B.Pharm, M.Sc, B.Sc. Functional experience in Calibration, Instrumentation, QMS activities. relevant functional experience in OSD manufacturing and Packing operations / QMS activities. Through knowledge on cGMP norms & Laboratory safety
  • Inviting Quality Assurance BPCR and QMS Professionals at Gland Pharma
    B.Sc./ B. Pharmacy /M.Sc. M. Pharmacy; Preparation and review of Standard operating procedures Retrieval of BPCRs in case of batch cancellation, planning changes. Handling and Execution and investigation of QMS documents in change controls, deviations, and CAPA.
  • Walk in Drive for M.Pharm, B.Pharm, MSc in Quality Control and Quality Assurance at Mankind Pharma
    M.Sc. / B. Pharm / M. Pharm. Review of Electronic data on various QC instrument Like HPLC, GC, FTIR, UV-Visible Spectrophotometer, TOC analyzer etc. Details experience on Audit Trail review of All QC instruments. Hands on Experience on Various QC instrument calibration like HPLC, GC, FTIR, Polarimeter, UV-Visible Spectrophotometer, Dissolution etc. Experience on Handling of OOS, OOT, OOC, Laboratory Incident investigation, Deviation etc.
Subscribe to 5+