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The Senior/Principal Quality Systems Specialist oversees various quality system aspects for medical devices, including conducting audits, compliance with ISO standards, client project management, and providing quality engineering support. They are responsible for gap analysis, developing implementation strategies, and assisting clients with FDA inspections and ISO audits. They play a vital role in enhancing quality systems and addressing client needs in the medical device field.

As a Senior Software Development Engineer, you will own team-level architecture, mentor junior engineers, and solve complex software challenges. You will design and implement high-quality code while ensuring collaboration among various teams and managing parallel work streams to deliver cohesive solutions.

The Program Manager III is responsible for enhancing program efficiency and service levels by monitoring performance and identifying improvement opportunities. This role involves managing multiple projects, leading cross-functional teams, developing operational strategies, ensuring compliance, and communicating effectively with stakeholders while utilizing project management tools.