Cell Therapy Specialist

001_1716203908
  • Hoofddorp, North Holland
  • Contract

Responsibilities include, but are not limited to:

  • Perform all tasks associated with the manufacture of clinical product following batch records and SOPs.
  • Work as part of a small team to execute GMP runs in close collaboration with Process Development and Quality.
  • Assist in the development of standard operating procedures, batch records, deviations and change controls.
  • Successfully troubleshoot processing and equipment issues.
  • Other duties as assigned.


Requirements:

  • MLO / MBO / Bachelor's degree preferred and/or advanced degree or 3 or more years of cGMP experience in a manufacturing pharmaceutical/biotechnology environment.
  • Cell culture processing experience.
  • Previous experience with cell therapy products is a plus.
  • Demonstrated knowledge of pharmaceutical manufacturing of biotechnology products, aseptic processing, cell culture products.
  • Strict adherence to SOPs and cGMP regulations, the ability to accurately complete documentation associated with clinical manufacturing.
  • Excellent aseptic/sterile techniques and prior experience with cell culture, cell culture equipment including Wave bioreactors.
  • Experience with handling and propagation of human primary cells, including T cells.
  • Excellent skill in Microsoft Word, Excel and data analysis.
  • Ability to think critically, and demonstrated troubleshooting and problem-solving skills.
  • Self-motivated and willing to accept temporary responsibilities outside of the initial job description
  • Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment.
  • Comfortable in a fast-paced small company environment with minimal direction and able to adjust workload based upon changing priorities.
  • Ability to work off-shift and extra hours as required.

Jack Wilson Senior Candidate Consultant II

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