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50 jobs found for Claris Lifesciences

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  • Manpower Handling & line shift supervision. Must have experience in injectable production/ manufacturing & regulated plant. To do on line operation checking and ensure online entries in Batch Manufacturing Record (BMR), log books & related documents as per Standard Operating Procedure (SOP) To supervise manufacturing activities i.e. sterilization, mixing, filling in allocated shifts and ensure process adherence as ...

  • To maintaining the safety and security of the principal To prepare for the protection of the principal & covering from likely threats and risks To maintain security and confidentiality of the plan and information regarding the principal To understand the itinerary details of the principal, and to advise on the nature & type of close protection detail To maintain situational awareness, and to monitor ...

  • 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 create business plan and strategy for the new business, and pass on & discuss all the information, plans, and strategy with the concerned persons at HQ, maintaining high confidentiality To identify the products for international markets, and to provide market estimation of those products To be responsible for global business development, new customer identification, and creation of NPD strategies for ...

  • To create business plan and strategy for the new business, and pass on & discuss all the information, plans, and strategy with the concerned persons at HQ, maintaining high confidentiality To identify the products for international markets, and to provide market estimation of those products To be responsible for global business development, new customer identification, and creation of NPD strategies for ...

  • Line clearance at various stages like Dispensing, Mixing Filling, Sterilization and Packing activity. Verify all activity during Issue and Return of all Raw Materials & Primary Packing Materials & Secondary Packing Materials. Verify all activity during Dispensing of Raw Materials like API & Recipients and Primary Packing Materials like Rubber Stopper and Flip off Seal. Verify all activity during ...

  • Line clearance at various stages like Dispensing, Mixing Filling, Sterilization and Packing activity. Verify all activity during Issue and Return of all Raw Materials & Primary Packing Materials & Secondary Packing Materials. Verify all activity during Dispensing of Raw Materials like API & Recipients and Primary Packing Materials like Rubber Stopper and Flip off Seal. Verify all activity during ...

  • Line clearance at various stages like Dispensing, Mixing Filling, Sterilization and Packing activity. Verify all activity during Issue and Return of all Raw Materials & Primary Packing Materials & Secondary Packing Materials. Verify all activity during Dispensing of Raw Materials like API & Recipients and Primary Packing Materials like Rubber Stopper and Flip off Seal. Verify all activity during ...

  • Line clearance at various stages like Dispensing, Mixing Filling, Sterilization and Packing activity. Verify all activity during Issue and Return of all Raw Materials & Primary Packing Materials & Secondary Packing Materials. Verify all activity during Dispensing of Raw Materials like API & Recipients and Primary Packing Materials like Rubber Stopper and Flip off Seal. Verify all activity during ...

  • Line clearance at various stages like Dispensing, Mixing Filling, Sterilization and Packing activity. Verify all activity during Issue and Return of all Raw Materials & Primary Packing Materials & Secondary Packing Materials. Verify all activity during Dispensing of Raw Materials like API & Recipients and Primary Packing Materials like Rubber Stopper and Flip off Seal. Verify all activity during ...

  • Information to be conveyed over phone to the concerned person and co-ordination of the same. To enhance the image of the company by treating and making visitors comfortable. To maintain discipline and decorum at the reception area. To update the welcome-board as per instruction. To maintain Visitor register on daily basis. To operate the telephone lines and keeping all the lines status updated. To greet ...

  • 15 20 years of experience in Pharmaceutical Industry with at least 8 years of experience in injectable or parenteral manufacturing operations, exporting to regulated markets. Should have faced audits from USFDA and other regulatory bodies. Functional Expertise : Should have knowledge and experience of Terminal, Lyophilized, Aseptic sterilization for Injectable products. Should have good understanding of ...

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