#13276- Lead Specialist

Are you interested in working with the World’s leading AI-powered Quality Engineering Company? Ready to advance your career, team up with global thought leaders across industries and make a difference every day? Join us at Qualitest! Qualitest is seeking a Lead Specialist - for our team.

• Develop and execute comprehensive verification and validation protocols for medical devices, including software, hardware, and system components.
• Collaborate with cross-functional teams including R&D, Quality Assurance, Regulatory Affairs, and Manufacturing to ensure alignment with project requirements and regulatory standards.
• Conduct risk assessments and develop risk mitigation strategies throughout the product development lifecycle.
• Design and execute test cases to verify and validate system functionality, performance, and reliability.
• Analyze test results, identify issues, and work with the development team to implement corrective actions.
• Maintain thorough documentation of verification and validation activities in compliance with regulatory requirements.
• Stay updated on industry standards, regulations, and best practices related to medical device development and testing.
• Support regulatory submissions by providing documentation and evidence of verification and validation activities.
• Qualifications: B