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Manufacturing Engineer – Yavne Site

Scinai Biopharma Services, CDMO · Yavné

Mid 🇬🇧 English
cGMP technology transfer scale-up process validation risk assessment change control

Job description

About the role

Scinai BioServices is seeking a Manufacturing Engineer to join its Yavne CDMO facility. You will bridge R&D and production, ensuring that new chemistry‑based products move smoothly from development to GMP manufacturing.

Key responsibilities

  • Lead technology transfer from R&D and pilot‑scale to commercial manufacturing.
  • Support scale‑up activities and transition prototypes to manufacturable processes.
  • Author, review, and maintain Master Batch Records, manufacturing procedures, and other GMP documentation.
  • Develop and optimise processes to improve product quality, efficiency and reproducibility.
  • Provide day‑to‑day technical support, troubleshoot process issues, and assist with investigations of deviations, OOS results and CAPA.
  • Participate in process qualification, validation, risk assessments, change control and continuous‑improvement initiatives.
  • Report project status and manufacturing activities to the Manufacturing Manager.

Required profile

  • B.Sc. in Chemical Engineering, Biotechnology, Industrial Engineering, Pharmaceutical Engineering, Chemistry or a related discipline (practical engineering degree also acceptable).
  • 2‑3 years of experience in a regulated environment such as pharmaceutical, chemical, medical device or biotechnology manufacturing.

Required skills

  • cGMP compliance
  • Technology transfer
  • Scale‑up and process optimisation
  • Process validation and qualification
  • Manufacturing documentation (Master Batch Records, SOPs)
  • Risk assessment and change control

Questions fréquentes

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Published 1 month ago

Expires 4 days from now

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Scinai Biopharma Services, CDMO

Yavné