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2005 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 ...

  • 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

  • "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

  • 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

  • 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

  • disciplines. 3. He should be well familiar with implementation, monitoring, control of Quality Process and functions during the project execution till mechanical completion and hand over to client . 4. Overall responsible for the quality assurance and control activities on the project should ensure

  • Knowledge of Solvent & Refinery Plant Responsible for overall QC/QA & R&D activities Looking Entire Quality Analysis of Raw Materials like Raw Oils, Chemicals & Packaging Materials Quality of Finished Products Maintenance of Analytical instrument

  • 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

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