Education<\/p>\n

Master of Pharmacy (M.Pharm) in Pharmacy<\/li>\n<\/ul>\n<\/div>\n
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Experience<\/p>\n
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  - 2 to 6 years<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n
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    The applicants should have experience in the following business area(s): Chemical Industries, Pharmaceutical\/Medicine Companies<\/li>\n
    Freshers are also encouraged to apply.<\/li>\n<\/ul>\n<\/div>\n<\/div>\n
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    Additional Requirements<\/p>\n
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    Age 24 to 30 years<\/li>\n<\/ul>\n<\/div>\n<\/div>\n<\/div>\n
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    Responsibilities & Context<\/p>\n
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    Develop robust formulations and processes for immediate release and modified\u00a0release\u00a0tablet and capsule dosage forms.<\/p>\n<\/li>\n<\/ul>\n
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    To operate & maintain FRO equipment\u00a0& instrument as per approved SOP.<\/p>\n<\/li>\n<\/ul>\n
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    To record & check all data in the laboratory notebook timely & accurately.\u00a0<\/p>\n<\/li>\n
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    To provide input\u00a0in relevant log book in a timely manner and in compliance with SOP.\u00a0\u00a0\u00a0 \u00a0<\/p>\n<\/li>\n
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    Work collaboratively with relevant\u00a0cross functional\u00a0teams on ANDA development and to resolve ingredient and product related technical issues for the timely delivery of product related activities.\u00a0<\/p>\n<\/li>\n
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    Execution of pre-exhibit and exhibit batches; technology transfer from R&D to TT team to meettimelines.\u00a0<\/p>\n<\/li>\n
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    Plan and contribute to project-related\u00a0scientific\/technical\u00a0\u00a0 \u00a0activities (e.g. interpret results, critical assessment of data, draw relevant conclusions and write reports).\u00a0\u00a0<\/p>\n<\/li>\n
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    Writing and approval of technical\/scientific reports\u00a0\u00a0 and author of technical documents including Product Development\u00a0Report, Quality overall Summary and other relevant documents for regulatory filing purpose.\u00a0\u00a0 \u00a0<\/p>\n<\/li>\n
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    Share current knowledge & R&D data to cross functional\u00a0 \u00a0department as needed.\u00a0<\/p>\n<\/li>\n
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    To perform any other formulation development related activities as and when assigned by superior.\u00a0<\/p>\n<\/li>\n
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    To update supervisor\/head\u00a0of R&D immediately whenever any deviation\/non-compliance is noticed.\u00a0 \u00a0<\/p>\n<\/li>\n
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    To prepare & update SOPs in compliance\u00a0with relevant\u00a0 \u00a0guidelines\u00a0of DGDA, WHO, USFDA, ICH and company`s\u00a0 \u00a0Quality\u00a0Module & Quality Manual.<\/p>\n<\/li>\n
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    To execute daily activities & behave in compliance with corporate code of conduct and HR rules and regulations.\u00a0<\/p>\n<\/li>\n
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    To maintain\u00a0confidentiality\u00a0as per confidentiality\u00a0policy of company.\u00a0\u00a0\u00a0\u00a0<\/p>\n<\/li>\n<\/ul>\n<\/div>\n<\/div>\n
    <\/div>\n
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    Skills & Expertise<\/h4>\n
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    Other Relevant Skills<\/span><\/p>\n