Cleanroom & R&D Practical Engineer \ Technician

Company Description

CorNeat Vision is an innovative medical device company based in Ra’anana, specializing in the development of implantable ophthalmic solutions.

We are seeking a highly responsible and hands-on Cleanroom & R&D Practical Engineer to own and manage all cleanroom-related activities while supporting the development and production of implantable medical devices.

Role Description

This role combines operational ownership of ISO-classified cleanroom environments, environmental control, equipment management, and experimental execution, with strict adherence to ISO 13485 and GMP standards, including:

• Own the daily operation and compliance of ISO-classified cleanrooms, ensuring adherence to gowning, hygiene, behavioral standards, and controlled work instructions.

• Monitor and maintain cleanroom environmental parameters (particle count, humidity, temperature, differential pressure) and ensure ongoing regulatory readiness.

• Manage maintenance, calibration, and qualification of cleanroom equipment in coordination with QA and external vendors.

• Execute and document batch activities and approved experimental protocols in compliance with GMP and ISO 13485 requirements.

• Maintain and control cleanroom documentation, including SOP implementation and controlled document updates.

• Manage cleanroom inventory and consumables to ensure uninterrupted operational readiness.

• Train and guide employees in cleanroom procedures, documentation discipline, and laboratory practices.

• Act as the internal focal point for cleanroom compliance and operational excellence.

Qualifications

• Certified Practical Engineer or B.Sc. in Engineering, Biotechnology, or related technical field.

• Minimum 1–3 years of hands-on experience in ISO-classified cleanrooms within a regulated medical device, biotech, or pharmaceutical environment.

• Solid understanding of GMP principles and ISO 13485 requirements.

• Proven experience in cleanroom environmental monitoring, equipment calibration, and audit readiness.

• Strong documentation discipline and experience working within controlled documentation systems.

• Experience supporting R&D activities and experimental protocol execution.

• High level of accountability, organizational skills, and ability to work independently.

• English proficiency – ability to read and understand technical documentation and write technical records.

Please send your CV to [email protected]