Job Title: Regulatory QMS Specialist Job Type: Permanent, full-time position
Location: Bourton on the water, Gloucestershire, UK – Hybrid (3 days on site)
An exciting Regulatory QMS Specialist position working for a global leader in the provision of quality medical products. Supporting the Quality Management System, including Quality Objectives and NC/CAPA management.
Manage the Quality Objectives procedure.
Provide backup to the RA/QMS Administrator for document control and training activities on MasterControl.
Continuous improvement - To initiate, support and lead Continuous Improvement projects as required.
Experience of Quality Systems auditing is essential.
Experience within the Medical Devices industry is desirable.
Excellent working knowledge of Microsoft Office (Word, Excel, OneDrive.)
Excellent written and oral communication skills in English.
Please note this is a hybrid position that will require 3 days on site per week.