Tagcor

Quality assurance Consultant

3+ years’ experience in Quality assurance including medical device design controls.
Knowledge of ISO 13485, and global quality assurance requirements for medical devices, including IEC 60601-1
Solid understanding of IEC 62304 Medical Software Development Process
Familiarity with Risk Management standards ISO 14971
Excellent analytical and decision-making skills, as well as strong written and verbal communication
Ability to speak effectively before groups of clients or employees.
Experience using a variety of software development methodologies (Waterfall, Phase Gate, Agile, SCRUM, Kanban, etc.) is a plus.
Experience in modern test automation is a plus.