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Analytical Specialist - Corporate QC Method Validation (m/f/d)


Your profile that will convince us:

  • University degree (MSc, Phd or equivalent) in chemistry/biosciences
  • Work experience in pharmaceutical industry especially in the field of method validation (GMP environment) is a plus
  • Willingness to travel due to business trips
  • Good knowledge in MS Word and MS Excel
  • Very good English communication skills (oral and written)
  • Social skills and presentation skills
  • Strong problem solving, organizational and time management skills
  • Ability to multitask and a high level of flexibility

Your new challenges which will inspire you:

  • Prepare validation documents and other GMP relevant documents with support of senior analytical specialists and team leaders
  • Develop and validate methods
  • Support troubleshooting in the QC laboratories
  • Sample administration and follow up of the validation related testing in the QC and R&D laboratories
  • Support of method transfer
  • Administrate documents required for submission and support within inspection tasks
  • Preparing statistical evaluation of data and reporting in Excel

» Job description

Octapharma Biopharmaceuticals GmbH
1100 Vienna [A]