QC scientist

  • Ness Ziona
  • Full-time

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about this position

Duties

  • Perform QC testing on In-process samples and final Drug products.
  • Documentation of the test procedures performed according to cGMP standards and assess data to make sure product specifications are met.
  • Analytical/Microbiological method validation, including writing and execution of method qualification protocols and reports under cGMP requirements.
  • Responsible for stability studies including design, protocols, execution and reports.
  • Investigation of out of specification results.

Requirements

  • BSc degree in Life Sciences, Biotechnology engineering or equivalent.
  • Advanced knowledge and experience in QC microbiological departments in pharmaceutical industry - an advantage.
  • Experience in working under cGMP requirements
  • Ability to assess and prioritize multiple tasks, projects and demands.
  • Good communication skills and leadership and excellent interpersonal relationships
  • Excellent organizational skills


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