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11 jobs found for Reliance Lifescience Laboratory

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  • of cGMP,GDP & GMP policies. To have Audits exposure such USFDA, MHRA, NVISA,TGA etc. To do daily planning and allocate work to subordinates. To review and prepare SOP. To ensure Good Laboratories Practices are followed in the lab. To review and provide training to ensure good working environment ...

  • of cGMP,GDP & GMP policies. To have Audits exposure such USFDA, MHRA, NVISA,TGA etc. To do daily planning and allocate work to subordinates. To review and prepare SOP. To ensure Good Laboratories Practices are followed in the lab. To review and provide training to ensure good working environment ...

  • of cGMP,GDP & GMP policies. To have Audits exposure such USFDA, MHRA, NVISA,TGA etc. To do daily planning and allocate work to subordinates. To review and prepare SOP. To ensure Good Laboratories Practices are followed in the lab. To review and provide training to ensure good working environment ...

  • of cGMP,GDP & GMP policies. To have Audits exposure such USFDA, MHRA, NVISA,TGA etc. To do daily planning and allocate work to subordinates. To review and prepare SOP. To ensure Good Laboratories Practices are followed in the lab. To review and provide training to ensure good working environment ...

  • of cGMP,GDP & GMP policies. To have Audits exposure such USFDA, MHRA, NVISA,TGA etc. To do daily planning and allocate work to subordinates. To review and prepare SOP. To ensure Good Laboratories Practices are followed in the lab. To review and provide training to ensure good working environment ...

  • of cGMP,GDP & GMP policies. To have Audits exposure such USFDA, MHRA, NVISA,TGA etc. To do daily planning and allocate work to subordinates. To review and prepare SOP. To ensure Good Laboratories Practices are followed in the lab. To review and provide training to ensure good working environment ...

  • of cGMP,GDP & GMP policies. To have Audits exposure such USFDA, MHRA, NVISA,TGA etc. To do daily planning and allocate work to subordinates. To review and prepare SOP. To ensure Good Laboratories Practices are followed in the lab. To review and provide training to ensure good working environment ...

  • of cGMP,GDP & GMP policies. To have Audits exposure such USFDA, MHRA, NVISA,TGA etc. To do daily planning and allocate work to subordinates. To review and prepare SOP. To ensure Good Laboratories Practices are followed in the lab. To review and provide training to ensure good working environment ...

  • of cGMP,GDP & GMP policies. To have Audits exposure such USFDA, MHRA, NVISA,TGA etc. To do daily planning and allocate work to subordinates. To review and prepare SOP. To ensure Good Laboratories Practices are followed in the lab. To review and provide training to ensure good working environment ...

  • To conduct independent literature investigation to define an appropriate basis for analysis To conduct method development activities as directed in a timely and efficient manner To document development activities, draft specifications and procedures as appropriate To use various laboratory 2 - 7 years of experience in F&D/ R&D department in Pharmaceutical industry, preferably in injectable ...

  • 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 subordinates. To review and prepare SOP. To ensure Good Laboratories Practices

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