Teams at Advanced Medical Solutions Group plc

Maintains regulatory technical documentation, product approvals, submissions, quality-system changes, post-market surveillance, vigilance reporting, recalls, labeling, and audit readiness for medical devices worldwide. Interprets medical device regulations, supports risk management and product lifecycle processes, liaises with regulatory authorities and customers, and collaborates with clinical, quality, engineering, operations, and commercial teams.

Supports quality and regulatory compliance for medical device manufacturing. Responsibilities include managing nonconformances and corrective actions, conducting audits, developing risk assessments and quality documentation, supporting product development and validation, monitoring suppliers, analyzing process data, delivering GMP training, and driving continuous improvement. The role also supports regulatory inspections, customer quality issues, change control, and medical device quality management system activities.

Manage end-to-end supply chain operations, including production planning, capacity and manpower forecasting, material sourcing, supplier negotiations, logistics, inventory accuracy, warehouse operations, ERP optimization, and root-cause corrective actions. Lead and develop the supply chain team, improve OTIF performance, manage operational risks, support sustainability objectives, and implement process and technology improvements.