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Responsible for production planning, managing operators, ensuring quality and productivity in manufacturing medical devices, and leading continuous improvement efforts.

Develops and sustains manufacturing processes for medical device production, conducts root-cause analysis, time and cost studies, implements process improvements, supports product transfers and NPI, ensures quality/regulatory compliance, and collaborates with operations, R&D, suppliers, and customers.

Manage journal entries and reconciliations (leases, debt, prepaids), administer BlackLine, perform intercompany reconciliations and eliminations, support audits and new accounting standard implementation, maintain GL and financial system tie-outs (Adaptive to EPICOR), assist junior staff, and drive process improvements.

The Operations Associate I will operate production equipment, meet quality goals, complete documentation, and ensure compliance with regulations while working in rotating shifts.

Supervise the Quality Control team, oversee inspection activities, ensure product compliance with standards, and drive continuous improvement initiatives.

The Engineering Manager will lead a team in developing metrology systems for medical devices, overseeing new product development and laboratory quality management.

The Senior Staff Process Development Engineer oversees manufacturing line design, capacity analysis, and process validation while leading cross-site initiatives and mentoring junior engineers.

The Operations Associate III will perform routine tasks in medical device assembly, operate machines, and ensure compliance with safety and production standards.

Responsible for process development from prototype to manufacturing, analyzing data to resolve issues, and ensuring regulatory compliance while supervising technicians.

The PD Quality Engineer Senior Staff oversees quality standards, diagnostics, risk management, and regulatory compliance in medical device product development.