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2011 jobs found for Qc Qa Executive

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

  • 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 ...

  • Inspecting and checking the executed works to ensure the quality. 10. Maintaining Quality Manual and Quality Procedures Manual and ensure the awareness of all employees with regards to the criticality of quality and the adopted standards ...

  • "While going for an interview don't forget to mention you got this reference from Aasaanjobs"QA/QC Executive require at Nanded phata,pune Client (Ganesh Systems Placement )Education: be/btech/me/mtech - mechanical Exp: fresher onlySalary: No bar to right CandidateFor Registration & Interview Call

  • of managing and executing QA/QC audits &Quality Plan -Must be capable of developing and interpreting the QA/QC related procedures and guidelines and actively pursue all staff to adhere to the QA/QC standards. -Must be capable of training staff in QA/QC procedures -Must be able to develop reporting for QA/QC

  • related procedures and guidelines and actively pursue all staff to adhere to the QA/QC standards. -Must be capable of training staff in QA/QC procedures -Must be able to develop reporting for QA/QC statistics, and KPIs -Must be familiar with the different welding techniques and its quality requirements

  • One of the fastest growing pharmacutical company in India having approved USFDA &MHRA in Formulation/Oral Solid Dosage and Regulated Markets is in urgent need of the following candidates for immediate recruitment at their plat at PUNE 1. QC OFFICER/EXECUTIVE: Candidates should be M.Sc with 4 1CV Summary of Mr/Ms: Your Skype ID:___________Email ID__________ Contact Numbers 2.Attach a passport size ...

  • Experience in Q.C. chemical & instrument section analysis hands on experience in Hormone facility. Hands on Experience in Hormone facility. Exposure of 21CFR k , Quality Control Checkar & Analytical QA

  • Experience in Q.C. chemical & instrument section analysis hands on experience in Hormone facility. Hands on Experience in Hormone facility. Exposure of 21CFR k , Quality Control Checkar & Analytical QA

  • urgent require QC/QA manager for home textile export Company in Noida ...

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