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The Senior Electrical Design Engineer will design schematics, develop PCB layouts, conduct electrical tests, and collaborate across teams in R&D, ensuring compliance and quality in medical devices.

As a Staff Validation Engineer, you will lead validation projects, mentor teams, and implement quality improvement initiatives in a hybrid work environment.

As a Staff Validation Engineer, you will guide validation teams, develop procedures, ensure compliance, and lead process improvements using methodologies such as Lean and Six Sigma.

As a Regulatory Affairs Intern, you will support regulatory compliance by gathering data, assisting with documentation, and contributing to process improvements while gaining valuable industry experience.

The Clinical Specialist provides clinical product support during surgeries, trains staff, reports on complaints, helps in sales, and builds relationships with surgeons.

The Senior Test Engineer will conduct performance and lifecycle testing for medical devices, coordinate testing with teams, and develop test protocols and systems. Responsibilities include equipment selection, protocol development, and maintaining good laboratory practices.

The Associate Sales Representative will engage with customers to build relationships, promote products, support existing accounts, and work closely with experienced colleagues in the Craniomaxillofacial division.

Lead and manage internal audit projects, strengthen internal controls, conduct testing, and coach junior staff while driving improvements in risk management.

The Quality Engineer will collaborate with suppliers, manage PPAP activities, lead problem-solving efforts, and promote continuous improvement practices.

The Foot & Ankle Sales Associate will support Sales Representatives, educate medical staff on Stryker products, manage inventory, and develop customer relationships, while attending surgeries and training in sales. Travel required up to 25%.