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The Senior Engineer will apply engineering principles to various assignments, lead projects, develop new technologies, mentor teams, and ensure adherence to quality standards.

The Engineering Manager will oversee new product development, quality and regulatory compliance, and lead cross-functional teams while mentoring junior staff and improving manufacturing processes.

The Manufacturing Engineer III applies engineering principles to solve technical problems, ensuring quality and efficiency while collaborating with cross-functional teams to innovate and improve manufacturing processes.

The Account Manager drives revenue growth by managing relationships, identifying new business opportunities, and ensuring customer satisfaction in the medical device industry.

The Production Planner manages component and packaging production tasking to meet delivery dates, collaborating with multiple teams to improve operational efficiency.

Lead global inventory management strategy and execution across manufacturing sites: PFEP implementation, inventory system governance, BOM/master-data management, KPI reporting, SIOP alignment, site training/SME development, and supply chain continuous improvement with finance and senior leadership engagement.

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

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