Who are we?

Matricelf is a young biotech company in the field of cell therapy and regenerative medicine, developing an innovative technology for engineered autologous tissues and organs. We are looking for a talented, highly motivated team player to join our RD team.

The candidate will join the RD team in the development of implant for treating spinal cord injuries, from early design up to prototype production, including physical, biochemical and biomechanical characterization and in vitro & in vivo studies. The position includes experiments planning, day to day laboratory work, execution and results analysis.

Product Development Engineer

Ness Ziona

What will you bring?

  • M.Sc. or PhD in biology, biotechnology/biomedical engineering or an engineer with experience in biotechnology/pharma industries
  • RD experience in a biotech company – advantage
  • Experience in handling human samples and cell culture, preferably stem cells
  • Highly skilled in variety of lab techniques (ELISA, FACS analysis, imaging and various biochemical assays)
  • Experience in development of scaffolds / matrices-based medical products – advantage
  • Understanding in quality assurance, ISO and GMP practices and documentation – advantage
  • Excellent English speaking and writing skills
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Stem Cells/Developmental Biologist

Ness Ziona

What will you bring?

  • M.Sc. or PhD in biology, biotechnology/biomedical
  • Experience in biotechnology/pharma industries – advantage
  • Deep knowledge in developmental biology and stem cells – must
  • Background in neurobiology – advantage
  • Experience in iPSCs reprogramming, maintenance and differentiation – advantage
  • Experience in tissue / cell culture – must
  • Highly skilled in variety of lab techniques (FACS, PCR, imaging and various biochemical assays)
  • Familiarity with quality assurance, ISO and GMP practices and documentation – advantage
  • Excellent communication and interpersonal skills
  • Excellent English speaking and writing skills
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QA manager

Ness Ziona

What will you bring?

  • B.Sc. in biology, chemistry, biotechnology/biomedical engineering
  • 10+ years of experience in the biotech industry
  • +8 years of experience as quality assurance manager
  • 4+ years of experience in cell therapy cGMP manufacturing
  • Practical knowledge of cGMP principles with respect to FDA and EMA regulations
  • Experience in QMS establishment and management
  • Working knowledge of risk management
  • Ability to work independently and with various work groups
  • Excellent communication and interpersonal skills
  • Excellent English speaking and writing skills
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