Production QA Coordinator


We are looking for a self-motivated, driven, detail-oriented and highly organized person who is capable of working collaboratively with teams from various functions to be part of a new project at our company.

This is an entry-level, half-time position (50% FTE) with potential for increasing the working time. No experience is required, and training will be provided to the selected candidate.

The Production QA Coordinator will report to the Director of Quality Assurance and Regulatory Affairs.


  • Hands-on work doing inspections on incoming goods
  • Online documentation work
  • Ensuring good documentation practices during production
  • Review of production documentation
  • Ensuring that production is being performed according to work instructions and correct production process procedures

Required Qualifications

  • Bachelors Degree
  • Good attention to detail
  • English at Mother tongue level
  • Good spoken Hebrew
  • Quick learner
  • Excellent Microsoft Office skills
  • The ideal candidate will also be technically oriented

Priority will be given to candidates with

  • Experience working in a regulated environment
  • Experience in biotechnology or medical device industries
  • Quality management, or Software Quality Assurance experience

Accellix Mission

Personalized, cell-based therapy is emerging as a paradigm-shifting strategy in healthcare. To harness the potential of cutting-edge cellular engineering, stringent process controls must be put into place that monitor and measure critical parameters of the cell product at every step, from patient sample acquisition to drug product release. In essence, for Cell-therapy manufacturers, the process is the product.

Accellix offers a streamlined flow cytometry workflow solution that can be used as a central component of the stringent process controls implemented by our cell therapy customers.

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