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The Manager of Quality Systems oversees multiple Global Quality Systems functions including Non-Conforming Events, Corrective and Preventive Actions, Training, Document Control, Management Controls, Quality Planning, Quality Systems Metrics, and Trends. They collaborate with all levels of the organization to achieve quality objectives and ensure compliance with domestic and international regulations and standards. This role requires effective leadership, communication, and problem-solving skills in a regulated environment.

Technical Implementation Specialist at Haemonetics responsible for provisioning software environments for customers, completing installations, custom report building, data conversions, and troubleshooting. Requires strong technical skills in various tools/languages and 5+ years of experience in technical roles. Remote role with self-starting responsibilities and customer interaction.

Sr System Requirements Engineer responsible for owning and managing requirements for New Product Innovation at Haemonetics. Tasks include maintaining consistent practices, troubleshooting DOORS errors, developing and running scripts, and creating technical documentation.

Lead the development and execution of automated test procedures for medical technology products, mentor junior engineers, design and maintain automated test scripts, and ensure accurate and repeatable test results.

The Global Senior Product Manager role at Haemonetics involves strategic and tactical management of the Structural Heart portfolio, including product strategy development, lifecycle management, cross-functional leadership, market analysis, product launch, financial management, and regulatory compliance.

The Senior Project Manager is responsible for planning, executing, and managing large projects within budget and deadlines. They analyze project risks, create work plans, manage project scope, and ensure compliance with quality and regulatory standards. The role involves leading cross-functional teams, mitigating conflicts, and sharing project learnings. The ideal candidate has at least 5 years of experience in project management, particularly in medical device development under FDA and ISO regulations.