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Hyderabad

Pharma Courses
  • Jobs as Junior Scientific Officer and Senior Scientific Assistant in Central Drugs Testing Laboratory, CDSCO

    Filling up of one post of Senior Scientific Assistant Group B Gazetted, Non-Ministerial, in the Pay Level 7 Rs. 44900 - 142400 of pay matrix of 7th CPC in Central Drugs Testing Laboratory CDTL, Hyderabad, Central Drugs Standard Control Organisation, Directorate General of Health Services, Ministry of Health and Family Welfare on Deputation.
  • Recruitment for Pharmaceutical Sciences candidates at CCMB
    Masters, Integrated Masters Degree in Pharmaceutical Sciences or Natural or Agricultural OR bachelors degree in Engineering or Technology or Medicine from a recognized University or equivalent.
  • Vacancy for B.Pharm, MSc as JRF/Project Associate at University of Hyderabad
    To undertake proposed research involving data analysis, computational modeling and programming for the clinical data on diabetes. Experience in data analysis, computer programming and mathematical modeling is desirable.
  • Apply Online for Junior Research Fellow at NIAB
    Exploring how Theileria parasites repress host gene expression PARA- REPRESS. Post Graduate Degree in Natural Sciences with experience in research and development in industrial and academic institutions or Science and technology organizations. Candidate with experience in epigenomics, cancer biology, molecular biology, cell culture, and bioinformatics will be given preference. 
  • 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.
  • Work as Clinical Trial Support Manager at Sanofi
    Basic knowledge of clinical development, GCP & ICH guidelines, regulations by major regulatory bodies such as FDA, Food and Drug Administration and EMA, European Medicines Agency, and SOPs/ QDs. Review study team-developed documents as per SOP, such as study id card, protocol, amendments, WSI, eCRF Case Report Form and completion guidelines, Centralized Monitoring Plan, committee charters and or other operational documents as requested to provide operational input.
  • 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 Production, QA, QC, CQA at Hetero Drugs
    Hetero Drugs is an Indian pharmaceutical company and the worlds largest producer of anti-retroviral drugs. Heteros business includes APIs, generics, biosimilars, custom pharmaceutical services, and branded generics.
  • Walk in Drive for M.Pharm, B.Pharm in Production and Packing Department at Annora Pharma Pvt Ltd
    ANNORA Pharma is committed to provide medicines with highest quality, safety and efficacy that meets the needs of the customers with applicable statutory and regulatory requirements.
  • Require Regulatory Affairs Manager at Novartis
    Provides the labeling, artwork strategy, regulatory intelligence and knowledge which are required to develop, market, and maintain products. Provides strategic labeling input and support for global development projects and, or marketed products
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