Matricelf is hiring – QA manager

Matricelf is a young biotech company in the field of regenerative medicine and cell therapy, developing an innovative technology for engineered autologous tissues and organs. We are looking for a sharp, self-directed and experienced QA manager.

The candidate will work closely with the R&D and operations teams.

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

What will you do?

  • Establish, implement and maintain company QMS
  • Lead and manage strategic cGMP QA operational activities associated with company’s development, manufacturing, regulatory and clinical affairs
  • Oversee and support the generation of cGMP related documents (SOPs, protocols, batch records, technical reports, etc.)
  • Serve as QA subject matter expert to support company’s overall activities to comply with regulatory requirements
  • Provide QA support for the establishment of in-house clean rooms for cGMP manufacturing towards clinical trials
  • Plan, conduct and follow-up of internal/external audits and trainings
  • Participate in the review and data verification of regulatory related documents
  • Drive continuous improvement utilizing quality tools to improve quality compliance

Employment type

  • Part time – 50-75%

Please send CV to tal@matricelf.com

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