Quality & Regulatory Specialist – Medical Devices

Steris plc.; Blyth; On-site; GBP 30,000 - 40,000; Full time

Job summary

A leading healthcare solutions provider located in Blyth, England, is seeking a Quality Specialist. The role includes assisting with the administration of quality functions to comply with ISO 9001, ISO 13485, and other regulatory standards. Responsibilities include managing customer complaints, facilitating investigations, and tracking quality data. This position offers an opportunity to make a difference in the medical and pharmaceutical industries while ensuring patient safety.

Responsibilities

• Assist in the administration of quality functions to assure adherence to regulatory standards.
• Complete document control transactions.
• Manage customer complaint investigations.
• Facilitate CAPA and NCR investigations.
• Review DHR's and support batch record release.
• Support site inspection activities.
• Support supplier quality assessments.
• Track and trend site quality data.
• Support targeted Lean activities.

Job description

A leading healthcare solutions provider located in Blyth, England, is seeking a Quality Specialist. The role includes assisting with the administration of quality functions to comply with ISO 9001, ISO 13485, and other regulatory standards. Responsibilities include managing customer complaints, facilitating investigations, and tracking quality data. This position offers an opportunity to make a difference in the medical and pharmaceutical industries while ensuring patient safety.