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Experience in injectable plant IPQA, GLP- QA, Tech Transfer, Validation, Qualification, QMS. Preference will be given to the candidates having experience of working in sterile pharma plant. M.Pharm, B.Pharm, M.Sc

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. B.Pharm / M.Pharm. Supervising and Controlling Production areas like Isolator, Aseptic Filling, Vial Washing, Autoclave, Lyophilizer and Visual Inspection. Should have knowledge of QMS activities.

M.Pharma, MPT, MSc Nursing in Life Sciences or Equivalent. Or Graduate in Life Sciences BAMS, BHMS, Bsc Nursing, BPT or Equivalent from recognized University with three years of experience recognized University 

ICMR intends to engage following Non-Institutional Young Professional-II Technical/ Scientific position, purely on temporary contract basis to support Intramural Research for Institutional co-ordination and research grant management at ICMR Intramural Division of ICMR Hqrs; Post-graduates in Life Sciences/ Sociology/ MPH/ Statistics/ Social Work/ Pharmacy

Postgraduate, Graduate degree in Science Eg. B.Pharm, Life Science, B.Sc., Biotech, Zoology, Botany, etc. with Diploma in Clinical Research is mandatory. One year experience in clinical trial monitoring is desirable.

Lab experience for Analytical Method Development, regular and stability sample analysis. Handling of HPLC for Assay, Dissolution, Related substances tests for solid orals. Perform pre-formulation studies, R and D trials and support scale-up activities Conduct R and D trials for oral solid dosage forms tablets, capsules, etc. M.Pharm / MSc

Registration with State Pharmacy Council with duly allotted Registration Number is mandatory. Experience of working on computerized system desirable. Candidate should be prepared to work in shift duties, including night shift.

GLP, Raw Material -Packaging Material, In Process-Finished Product, Method Verification Protocol preparation & Document Section Knowledge required; Water sampling/testing, EM Observation, Culture Handling, Media Management, Having Digital exposure for LIMS/ MODA Software B.Sc/ M.Sc/ B.Pharm; Lead QC operations as Shift In-Charge. Review analytical data, Ensure compliance with LIMS, GLP, ALCOA ICH/FDA

Towards Discovery and Development of Novel Drugs and Pharmaceuticals. Experience in Natural Product Isolation and Characterization, Evident from Publication. Organic Synthesis, Natural Product Isolation, HPLC analysis.