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The Senior Regulatory Affairs Specialist plans and oversees regulatory activities to obtain and maintain approvals in the US and internationally, ensuring compliance with FDA and ISO standards.

The Solutions Architect IV - Data Analytics will engage with stakeholders, define data architecture best practices, design data integration workflows, develop enterprise BI dashboards, and oversee cloud data warehouse optimizations.

The Sales Specialist is responsible for identifying new business opportunities, managing customer relations, and ensuring compliance with regulations while driving sales in the APAC market.

The Firmware Engineer is responsible for firmware design, development, testing, and maintenance of medical devices, collaborating across teams to ensure project success and innovation in device technology.

As a Quality Supervisor, you will lead a team of quality professionals, ensuring compliance with QMS and regulatory standards, drive process improvements, and support manufacturing operations while promoting a culture of quality and continuous improvement.

The IT Project Analyst is responsible for project financial management, resource tracking, PMO operations, compliance audits, and improving PMO tools and templates.

The Engineer II has responsibilities in applying engineering techniques, ensuring compliance with quality standards, and supporting manufacturing excellence innovation strategies in the medical device industry.

Responsible for leading technical accounting, supporting global audits, managing non-GAAP adjustments, and ensuring compliance with accounting standards. Requires collaboration with various departments and external experts.

This role focuses on quality engineering in medical devices, utilizing advanced tools to ensure product compliance and support continuous improvements.

Apply engineering principles to develop innovative solutions, ensure quality standards, lead projects, and mentor team members while maintaining compliance with regulations.