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The Senior Manager, Quality Assurance leads the implementation and maintenance of the quality management system, ensuring compliance with regulatory requirements and overseeing quality assurance operations. This role involves providing technical leadership, managing quality functions, and establishing departmental budgets while maintaining high standards of quality in a medical device manufacturing environment.

The Operator 2 is responsible for performing manufacturing processes, coordinating materials flow, ensuring compliance with cGMP regulations, and maintaining quality standards in production. Duties include operating equipment, supporting production schedules, performing in-process testing, and documenting production parameters. This role involves teamwork and adherence to safety and quality protocols within a dynamic manufacturing environment.

As a Systems Engineer I, you will be responsible for enhancing product quality and managing engineering solutions within the R&D systems lifecycle, while ensuring project constraints are met. Key tasks include refining requirements, defining system interfaces, conducting feasibility studies, and participating in system integration activities.