Flow Cytometry QC Coordinator

  • Location: Charleroi
  • Type: Perm
  • Job #14927

Flow Cytometry QC Coordinator

Charleroi – CDI

To lead its increasing number of development and manufacturing projects, our partner is looking for a highly motivated Flow Cytometry QC Coordinator.

What are your responsibilities?

The Flow Cytometry QC Coordinator main role is to support the Flow Cytometry QC Supervisor in his / her function to achieve goals of the platform and customers.

  • Support the Flow Cytometry QC supervisor in the team management
  • Support the Flow Cytometry QC supervisor by ensuring the requested delegated tasks 
  • Ensure the role of backup of the Flow Cytometry QC supervisor during his / her absence
  • Maintain effective, constructive and positive communication with all QC team members and other departments
  • Attend internal and/or external meetings with PL / client to present and discuss QC topics, results or issues when required
  • Be a reference person for questions regarding methods performed / equipment used in the platform
  • Share his/her expertise in analytical methods with other members of the QC team; participate in troubleshooting of experiment and equipment issues
  • Interpret analytical results and warn immediately the QC PL / Supervisor / Manager in case of unusual event/result/OOS
  • Initiate or review deviations, OOS, CHC linked to the Flow cytometry platform and lead necessary investigation. Implement CAPA
  • Double check filled forms or data generated by QC Experts / Specialists / Technicians, for testing which he / she is trained
  • Fill certificates of analysis and ensure that a product will only be released if its specifications are met
  • Participate to the drafting / review of instructions and forms in collaboration with MSAT / P&AD department
  • Ensure that all documents (forms, etc) and files (DWH, etc) are filled / double checked and CoA are generated in a timely manner according to release planning
  • Warn the QC Supervisor or QC Manager in case of problem
  • Takes part to internal and/or external audits, if necessary

Who are you?

  • Master degree or higher in biology, biomedical sciences, biochemistry, clinical chemistry or relevant experience in a similar position in the sector of biotechnology/pharma/cell therapy
  • Experience in people management 
  • Experience in Flow Cytometry is a strong asset
  • At least 2 years of experience in cGMP environment and/or quality control
  • Organization skills, multitasking, flexibility and autonomous
  • Efficient communication
  • Skills in use of FACS Celesta – FACS Verse – FACS MACSQuant Flow Cytometers are a plus
  • Results oriented; problem solving
  • Quality minded, rigorous and pro-active and continuous improvement driven
  • Fluent in French and in English (at least B1 level)
  • Computer skills: Microsoft office, Compliance Wire, Ms Teams, TrackWise are a plus

What can you expect?

Jefferson Wells offers you a permanent contract within a growing and dynamic biotech company. You will work in a human-sized working environment with convivial atmospheres and scientific challenges. You’re interested in this job? We kindly invite you to apply. Do you have any questions? You can contact Anaïs Malikian, [email protected]

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