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Design, implement, and improve manufacturing processes for medical device production. Integrate automation, enforce quality control, analyze production data, estimate costs, and train production staff while collaborating across design, procurement, and QA.

The Regulatory Affairs Specialist supports global regulatory submissions and compliance, ensuring medical devices meet regulatory requirements throughout their lifecycle. Responsibilities include preparing filings, maintaining regulatory documents, collaborating with cross-functional teams, and supporting market approval processes.

The Regulatory Affairs Manager develops and implements regulatory strategies for product registrations, ensures compliance with regulations, and handles regulatory submissions and documentation for medical devices.

Lead the technical implementation of QAD ERP, driving projects to go-live, overseeing manufacturing modules, and providing technical direction while managing stakeholders and integration teams.

The Director of Supply Chain oversees supply chain strategy, procurement, inventory management, logistics, and supplier relations, ensuring operational efficiency and alignment with organizational goals.