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Manage quality engineering, oversee regulatory compliance, and guide a team to achieve quality assurance goals in the medical device industry.

The IT Support Specialist I provides technical support to end users, troubleshooting equipment and ensuring connectivity, while maintaining records and assisting with user onboarding/offboarding.

The Customer Solutions Specialist II manages customer relations, processes orders, prepares quotations, handles complaints, and ensures compliance with company regulations.

The Quality Assurance Engineer conducts process validation, leads quality improvement projects, handles documentation, and ensures compliance in the manufacturing of medical devices.

Responsible for production planning and inventory control, prioritizing operations to enhance performance and minimize delays in manufacturing.

The Planner is responsible for coordinating materials planning and scheduling activities for medical device production, ensuring compliance and efficiency, and collaborating with customers and teams.

The Senior Value Stream Manager leads daily operations across production shifts, ensuring efficient and cost-effective performance while driving continuous improvement and team development.

The Operations Associate III will perform routine tasks in medical device assembly, operate machines, and ensure compliance with safety and production standards.

Responsible for maintaining quality standards, inspecting products, conducting audits, and ensuring compliance with regulations in a medical device setting.

The Mechanical Design Engineer II is responsible for process development, fixture design, and improving manufacturing efficiency in the medical device sector.