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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.

Prepare, review, and control product labels and Instructions for Use; manage translations, vendor proofs, and FDA UDI GUDID uploads; support labeling change controls, validations, regulatory submissions, and cross-functional labeling activities.

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.

The Toolmaker constructs and repairs tools, dies, jigs, and gauges using various equipment and adheres to quality and safety standards while collaborating with teams.

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.

As an Engineer II, you will perform general engineering tasks, ensure customer satisfaction, comply with quality standards, and support innovation in manufacturing.