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The Sr. Associate Specialist in Regulatory Affairs is responsible for regulatory strategy and compliance for product submissions and renewals, coordinating with regulatory bodies, developing strategies, ensuring compliance, and supporting cross-functional teams.

Responsible for hunting, detecting and responding to digital security threats, collaborating with teams to secure applications, and promoting security standards and practices.

The Senior Manager of Strategic Sourcing will negotiate contracts, improve sourcing strategies, lead projects, and influence policy to enhance organizational efficiency.

The Radiology Account Manager drives sales for GE Healthcare's Imaging portfolio, manages strategic accounts, and fosters customer relationships in Czechia.

As a Clinical Applications Specialist, you'll provide training and support for the PET modality, enhancing customer experience and driving revenue through effective clinical education and strong customer relationships.

The role involves leading the Regulatory Affairs team, ensuring regulatory compliance, overseeing submissions, and engaging stakeholders while monitoring changes in regulations.

The Manufacturing Specialist is responsible for product assembly, quality control, maintenance, and improvement of manufacturing processes, collaborating with teams to enhance productivity and ensure compliance with safety and quality standards.

Lead projects in automation system design and development, enhance manufacturing productivity, and manage project teams while ensuring effective product introduction into production processes.

The Molecular Imaging Clinical Development Specialist maximizes clinical performance of GE MI scanners, leads workflow optimization projects, and provides expert clinical support to customers while traveling extensively within the designated territory.

The role oversees regulatory strategy for healthcare products, manages Regulatory Affairs teams, ensures compliance, and coordinates with global regulatory bodies. Requires expertise in medical device regulations and project management.