Analytical Specialist (m/f)

  • University degree (PhD, MSc or equivalent) in chemistry / biosciences
  • Work experience in pharmaceutical industry in the field of method validation (GMP environment) is a plus
  • Support of method development in collaboration with the product specialists at R&D
  • Issue of risk assessments and planning the setup of method validations
  • Follow up and support of the validation related testing in the QC laboratories or external contractors
  • Preparing statistical evaluation of data and reporting in Excel
  • Support of method transfer and implementation of the methods at the receiving laboratory
  • Presenting test methods during internal and external audits
  • Issue of responses for authority requests

» Job description

Octapharma Pharmazeutika Produktionsges.m.b.H.
1100 Vienna [A]

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