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Clinical research courses

  • Walk in Drive for M.Pharm, B.Pharm, MSc in QC, QA, AR&D Department at Hetero Drugs

    M.Pharm, B.Pharm, M.Sc, B.Sc; Hetero Drugs is an Indian pharmaceutical company and the world’s largest producer of anti-retroviral drugs.
  • Vacancy for M.Pharm, B.Pharm, M.Sc in ARD Department at Cronus Pharma
    B.Pharmacy, M.Pharmacy, MSc; Responsible for performing the analysis for process development/ development stability samples as per testing procedure and stability protocol. Responsible for performing the method validations/method verification as per the protocol by HPLC and GC
  • Walk in Drive for M.Pharm, B.Pharm, MSc in QA Department at Hetero Drugs
    B.Pharma, M.Pharma, M.Sc. Hetero Drugs is an Indian pharmaceutical company and the world’s largest producer of anti-retroviral drugs. Hetero’s business includes APIs, generics, biosimilars, custom pharmaceutical services, and branded generics.
  • Require Associate Content Editor at Clarivate
    Should hold a master’s degree in Pharma or Master’s in Pharmaceutical chemistry, Medicinal chemistry. Prepare abstract for patents in accordance with set rules defined in DWPI Abstracting policy document.
  • Walk in Drive for B.Pharm, MSc, MTech in Quality Control at Zydus Lifesciences
    B.Sc, B.Pharm, M.Sc. with 2 to 6 years of hands-on experience on HPLC, GC, Dissolution apparatus and UV –Visible Spectrometer. Should also have knowledge of weight analysis, stability studies, for Injectable dosage forms. Also require candidate with experience of Bio Assay QMS and analytical data Review.
  • Walk in for D.Pharm, B.Pharm, M.Pharm in Production, Packing, QA, QC at IPCA Laboratories

    For more than 60 years, Ipca has been a crucial healthcare partner in over 120 countries across the 6 continents. IPCA is a fully-integrated pharmaceutical company that manufactures over 350 formulations and 80 APIs for various therapeutic segments. Today, IPCA is one of the worlds largest manufacturers and suppliers of over a dozen APIs. These are produced from scratch at fully-automated manufacturing facilities, approved by the worlds most discerning drug regulatory authorities like UK-MHRA, EDQM-Europe, and WHO-Geneva, among others.

  • Aurobindo Pharma Hiring Regulatory Affairs Expert

    Aurobindo Pharma Limited is an Indian multinational pharmaceutical manufacturing company headquartered in HITEC City, Hyderabad, India. The company manufactures generic pharmaceuticals and active pharmaceutical ingredients.

    Positions open for Regulatory Affairs Expert

  • Require Purchase Executive at ACME Pharmaceuticals
    Review quality of purchased products. Enter order details into internal databases. Maintain updated records of purchased products, delivery information and invoices.
  • Torrent Pharma looking for Research Scientists - M.Pharm, MSc Apply
    M.Pharma, MSC with 3 to 8 years of relevant experience HPLC, GC method development for OSD having exposure to regulated, Semi Regulated & India markets including
  • Interview for B.Pharm, MSc in Quality Assurance, Production at Windlas Biotech
    MSc, BPharma, ITI, Diploma ; IPQA and well known for the aseptic behavior. Equipment Qualification like HVAC, RLAF, LAF, DPB, filling machine. Utilities Qualification- Nitrogen, Compressed Air. Computer System Validation.
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