Validation Engineer

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

The Validation Engineer will be responsible for validating all of the production tools and equipment at the company, documenting them, and serving as the professional focal point for validation.

Job 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.)

Position Requirements:

• Experience of 5 years or more in writing validation in the production lines of Medical Device / Pharma companies (or 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