Senior Validation Engineer

Syqe is a med-tech company developing technologies that enable the precise delivery of Cannabis and other therapeutic molecules by inhalation. Utilizing its breakthrough technology, Syqe aims to relieve the suffering of as many patients as possible in the fastest possible way.

We seek a qualified Senior Validation Engineer to join Syqes’ top-talented multidisciplinary Engineering team. The Senior Validation Engineer will validate and document all of Syqe's production tools and equipment and serve as the professional Focal Point for validation.

Responsibilities:

• Planning and executing validations for production equipment and test equipment in a medical product production line.
• Planning and executing validations for production equipment and test equipment in a pharmaceutical production line.
• Writing validation documents, such as IQ,OQ, PQ & PV, and others
• Project management for production line validation
• Reviewing machine documents, such as DQ, URS, FDS, FMEA, and user manuals.
• Perform validations (validation protocols, feasibility reports, validation reports, etc.)
  
  

• Experience of 7-8 years or more in writing validation in the production lines of Medical Device / Pharma companies (or the Food industry).
• Proven experience in writing IQ OQ PQ documents.
• Ability to manage validation projects.
• Good Technical understanding.
• Computer Skills - office (a must)
• Experience with MS-Project, writing documents (an advantage).
• Bachelor's degree in mechanical engineering/biomedical or another scientific degree (an advantage).
• The job includes traveling to our factory in Tiberias at least twice a week **