Manufacturing Engineer – Yavne Site
Scinai Biopharma Services, CDMO · Yavné
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
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Published 1 month ago
Expires 4 days from now
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Scinai Biopharma Services, CDMO
Yavné
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