Validation Engineer III

As a Validation Engineer III, you will be responsible for leading and executing validation and verification activities for medical devices. This includes developing and implementing validation protocols, conducting risk assessments, and collaborating with cross-functional teams to ensure compliance with regulatory requirements. You will also be responsible for creating and maintaining documentation, including validation reports and technical files. Additionally, you will provide technical expertise and guidance to junior engineers and contribute to the development of new validation methodologies and tools.

Key Responsibilities

• Develop and execute validation protocols and plans for medical devices
• Conduct risk assessments and identify potential validation risks
• Collaborate with cross-functional teams to ensure compliance with regulatory requirements
• Create and maintain documentation, including validation reports and technical files
• Provide technical expertise and guidance to junior engineers
• Contribute to the development of new validation methodologies and tools

Requirements

• 5+ years of experience in validation engineering or a related field
• Strong knowledge of validation principles, regulations, and industry standards
• Experience with Agile development methodologies and SAP
• Strong analytical and problem-solving skills
• Excellent communication and collaboration skills