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QC Stability Unit head

Full Time
Rameda - 
6th of October, GizaPosted 2 years ago
33Applicants for1 open position
  • 15Viewed
  • 1In Consideration
  • 31Not Selected
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Job Details

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Job Description

 

 

  • Implemented the requirement ICH for establishing stability indicating method for the estimation of active ingredient in drug product.
  • Handled equipment installation and Qualification.
  • Handled OOS investigation for stability study.
  • Holding time stability .
  • Creating new method for old product  as recent pharmacopeia  and method & related comp to full file the registration  & export  .      
  • Conduct stability tests for drugs according to schedule . 
  • Holding stability study as per ICH and FDA for R&D  pilot scales . and commercial batch of three product as M.OH    requirement 
  • Prepare stability files for old product to new registration and for new product .
  • Ensures that all activities in his unit or section are done according the relevant cGMP and ISO standards (ISO 9001, ISO 14001/2004 , OHSAS 18001/2007).
  • Reports to Stability section head

    

Job Requirements

  • 5-7 Years’ experience 
  • PhD or M.Sc. in pharmaceutical sciences. Or relevant degree.
  • Analytical thinking, problem solving and communication skills.

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