We’re seeking a highly experienced Validation Engineer to lead and manage all validation activities within our company.
You’ll be responsible for ensuring processes, systems, and equipment meet our validation requirements and comply with regulations.

Responsibilities:

• Manage and coordinate validation projects across all departments.
• Prepare, execute, and finalize validation protocols and reports.
• Collaborate with cross-functional teams to establish validation strategies and objectives.
• Provide training and support on validation processes as needed.
• Ensure all departments comply with relevant quality standards and regulations (GMP, ISO13485, FDA etc.).
• Maintain up-to-date knowledge of EU and US validation regulations.
• Monitor validation project progress and keep teams on track.
• Lead reviews of validation practices, identify improvement opportunities, and implement them.

Qualifications:

• 5-7 years of validation experience in a medical device company.
• Bachelor’s degree in Engineering (Biomedical/Biotechnology preferred).
• Experience with data analysis (preferred).
• Strong background in reviewing qualification documentation.
• Excellent technical and engineering knowledge.
• Strong written and verbal communication skills in Hebrew and English.
• Team player with excellent collaboration skills.