Qualifications

• 2+ years of experience in medical device design verification or a related field.
• Proficiency in the V-model and requirements traceability matrix.
• Experience in formal protocol writing.

Responsibilities

• Participate in requirements engineering, including creation and review.
• Develop and execute formal test protocols aligned with relevant standards.
• Capably perform statistical sample size calculations and analyze compliance data.
• Design innovative test methods and fixtures for verification.
• Document test reports, maintain defect logs, and investigate anomalies.
• Troubleshoot and resolve testing issues effectively.

Benefits

• Commitment to diversity and inclusion in the workplace, fostering a supportive environment.
• Opportunities for internal rotation and international mobility to advance your career.
• Clear career progression paths with rapid company growth since 2021.
• Flexible, casual culture with various employee events and recreational amenities.
• Access to QualityAI Tech academy providing extensive training and mentorship programs.
• Bonuses available through Client Referral and Employee Referral Programs.