Quality Officer Release & Stability

You will join the Analytical Development Department and ensure that documents such as assay run sheets are compliant. Are you looking for a job as documentalist in the pharmaceutical industry? Apply now!

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Wat ga je doen

As Quality Officer Release & Stability you are responsible for release and stability testing as well as the corresponding reporting of Janssen's virus and antibody products for use in clinical trials and the analytical support of the pilot plant activities. Furthermore you:

  • Review documents such as assay run sheets (ARS) and laboratory notebooks in order to meet predefined data delivery timelines with expected quality
  • Actively participate in setting up documents and or updating documents to ensure compliance
  • Initiate and participate in continuous improvement projects that progresses the department in quality, EHS and efficiency
  • Setting up and or keeping track of KPIs within the release and stability department
  • Ensure on time initiation and closure of deviation

Wat vragen wij

For the position as Quality Officer Release & Stability you have a bachelor degree or higher and have more than 2 years cGMP experience in the Pharmaceutical industry. Furthermore you have:

  • Good communication skills in Dutch and English, written and spoken
  • Affinity or experience with biological and or analytical assays
  • Affinity or experience with document related tasks
  • A can-do attitude and you are highly motivated

Wat hebben we te bieden

  • Secondment via CheckMark Labrecruitment
  • Salary indication ranging from €2.700,- to €3900,- gross per month based on a full-time position
  • Position for 40 hours/week
  • Dayshift

Waar ga je aan de slag

A large pharmaceutical company dedicated to bringing life-saving innovation to global health.

Wil je meer weten?

Jurjen Wilschut
088 00 21 122
Sebastiaan Loriaux
088 00 21 126
Vacaturenummer: 6764

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