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  • Evoke Hr, an Executive Search & HR Consultancy is a young emerging organization established by HR professionals with the objective of providing comprehensive staffing & Manpower solutions to the organizations. We believe in understanding the clients business, so as to pro actively align the HR

  • About Our Client Co. Our Client Co is leading & fastest Growing Pharma with Corporate office & RD Center in Mumbai & 4 Manufacturing Plants located across India. Position: Officer/Executive-Quality Control Location: Dahej, Bharuch Exp: 1 to 7 Yrs Qualification & Experience: MSC / M. Pharma, B ...

  • Evoke Hr, an Executive Search & HR Consultancy is a young emerging organization established by HR professionals with the objective of providing comprehensive staffing & Manpower solutions to the organizations. We believe in understanding the clients business, so as to pro actively align the HR

  • Handling instrument like HPLC/UV/Dissoltion Aparatus, Knowledge of current good laboratory practices,QMS system, Working standard & Refrence standard, Instrument management IQ/OQ/PQ Monitor the instrument for their trouble free working & calibration Candidate must have B.Sc/ M.sc ( Chemistry )having 2 to 3 years of Experience Reputed Industry ...

  • To be well versed working on analytical instrument such as HPLC, GC, UV, KF, IR etc. To carry out the calibration of instruments such as HPLC, UV, GC, etc. To have knowledge of QMS such as OOS / OOT and Deviation. To review the Documents related with OOS / OOT and Deviation. To have knowledge of cGMP,GDP & GMP policies. To have Audits exposure such USFDA, MHRA, NVISA,TGA etc. To do daily planning and allocate work to ...

  • To be well versed working on analytical instrument such as HPLC, GC, UV, KF, IR etc. To carry out the calibration of instruments such as HPLC, UV, GC, etc. To have knowledge of QMS such as OOS / OOT and Deviation. To review the Documents related with OOS / OOT and Deviation. To have knowledge of cGMP,GDP & GMP policies. To have Audits exposure such USFDA, MHRA, NVISA,TGA etc. To do daily planning and allocate work to ...

  • To be well versed working on analytical instrument such as HPLC, GC, UV, KF, IR etc. To carry out the calibration of instruments such as HPLC, UV, GC, etc. To have knowledge of QMS such as OOS / OOT and Deviation. To review the Documents related with OOS / OOT and Deviation. To have knowledge of cGMP,GDP & GMP policies. To have Audits exposure such USFDA, MHRA, NVISA,TGA etc. To do daily planning and allocate work to ...

  • To be well versed working on analytical instrument such as HPLC, GC, UV, KF, IR etc. To carry out the calibration of instruments such as HPLC, UV, GC, etc. To have knowledge of QMS such as OOS / OOT and Deviation. To review the Documents related with OOS / OOT and Deviation. To have knowledge of cGMP,GDP & GMP policies. To have Audits exposure such USFDA, MHRA, NVISA,TGA etc. To do daily planning and allocate work to ...

  • To be well versed working on analytical instrument such as HPLC, GC, UV, KF, IR etc. To carry out the calibration of instruments such as HPLC, UV, GC, etc. To have knowledge of QMS such as OOS / OOT and Deviation. To review the Documents related with OOS / OOT and Deviation. To have knowledge of cGMP,GDP & GMP policies. To have Audits exposure such USFDA, MHRA, NVISA,TGA etc. To do daily planning and allocate work to ...

  • To be well versed working on analytical instrument such as HPLC, GC, UV, KF, IR etc. To carry out the calibration of instruments such as HPLC, UV, GC, etc. To have knowledge of QMS such as OOS / OOT and Deviation. To review the Documents related with OOS / OOT and Deviation. To have knowledge of cGMP,GDP & GMP policies. To have Audits exposure such USFDA, MHRA, NVISA,TGA etc. To do daily planning and allocate work to ...

  • To be well versed working on analytical instrument such as HPLC, GC, UV, KF, IR etc. To carry out the calibration of instruments such as HPLC, UV, GC, etc. To have knowledge of QMS such as OOS / OOT and Deviation. To review the Documents related with OOS / OOT and Deviation. To have knowledge of cGMP,GDP & GMP policies. To have Audits exposure such USFDA, MHRA, NVISA,TGA etc. To do daily planning and allocate work to ...

  • To be well versed working on analytical instrument such as HPLC, GC, UV, KF, IR etc. To carry out the calibration of instruments such as HPLC, UV, GC, etc. To have knowledge of QMS such as OOS / OOT and Deviation. To review the Documents related with OOS / OOT and Deviation. To have knowledge of cGMP,GDP & GMP policies. To have Audits exposure such USFDA, MHRA, NVISA,TGA etc. To do daily planning and allocate work to ...

  • To be well versed working on analytical instrument such as HPLC, GC, UV, KF, IR etc. To carry out the calibration of instruments such as HPLC, UV, GC, etc. To have knowledge of QMS such as OOS / OOT and Deviation. To review the Documents related with OOS / OOT and Deviation. To have knowledge of cGMP,GDP & GMP policies. To have Audits exposure such USFDA, MHRA, NVISA,TGA etc. To do daily planning and allocate work to ...

  • Responsible for planning, organizing and managing the overall activities of receiving / outgoing /in process quality functions Preparation of QA reports ...

  • 1. Qualification - BSC / Msc Microbiology 2. Experience -1 to 4 years 3. Should have good communication skills 4. Good knowledge in Microbiology

  • Overall administration of QC department Ensure the QC procedures laid out in ISO are followed Organize / conduct training for development of QC executive and assistants Approve the issue of resins and additives for mixing after approving the Review and suggest changes to QC procedures based on latest development in technologies in market Review NC report register periodically to notice and perform ...

  • Overall administration of QC department Ensure the QC procedures laid out in ISO are followed Organize / conduct training for development of QC executive and assistants Approve the issue of resins and additives for mixing after approving the Review and suggest changes to QC procedures based on latest development in technologies in market Review NC report register periodically to notice and perform ...

  • QA- Analysis of finished Products (API) QC- In process & Finished goods Quality Check Production- Performing Process Development of API product.& Pilot Plant Completion of BMR's daily . INTRUMENT HANDLED: HPLC FTIR UV Spectrophotometer Karl Fischer Coulometer Karl Fisher autotitrator Polarimeter PH Meter Instrument For Melting Point Balance

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