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1253 jobs found for Qc Qa Executive

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  • 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 ...

  • To be well versed working on analytical instrument such as HPLC, GC, UV, KF, IR etc. Looking for RM/PM/IPPI/FP Section. Candidate should be from Pharmaceuticals Company. To carry out the calibration of instruments such as HPLC, UV, GC,TOC, 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 ...

  • 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 ...

  • Reporting Structure : Project Manager (Indirect) and Sr. QA/QC Projects Manager(Direct) Supervisory Responsibilities: 1. QA/QC on job sites 2. QC Engineers 3. Document Controller Responsibilities: 1. Supervise and implement operation of QA/QC procedures on site including Vendors

  • issues and coordinating with Client and Consultants. Prepare the Ranagement review report, Quality assurance plan and other quality related manual for the project. Ensure that QA team performs the quality audit/surveillance audits. Responsibility to maintain a quality audit program and to carry out

  • issues and coordinating with Client and Consultants. Prepare the Ranagement review report, Quality assurance plan and other quality related manual for the project. Ensure that QA team performs the quality audit/surveillance audits. Responsibility to maintain a quality audit program and to carry out

  • issues and coordinating with Client and Consultants. Prepare the Ranagement review report, Quality assurance plan and other quality related manual for the project. Ensure that QA team performs the quality audit/surveillance audits. Responsibility to maintain a quality audit program and to carry out

  • issues and coordinating with Client and Consultants. Prepare the Ranagement review report, Quality assurance plan and other quality related manual for the project. Ensure that QA team performs the quality audit/surveillance audits. Responsibility to maintain a quality audit program and to carry out

  • issues and coordinating with Client and Consultants. Prepare the Ranagement review report, Quality assurance plan and other quality related manual for the project. Ensure that QA team performs the quality audit/surveillance audits. Responsibility to maintain a quality audit program and to carry out

  • issues and coordinating with Client and Consultants. Prepare the Ranagement review report, Quality assurance plan and other quality related manual for the project. Ensure that QA team performs the quality audit/surveillance audits. Responsibility to maintain a quality audit program and to carry out

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