Regulatory QMS Specialist

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Regulatory QMS Specialist, Bourton-on-the-Water

Client: Cpl Life Sciences

Location: Bourton-on-the-Water, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Views: 4

Posted: 24.04.2025

Expiry Date: 08.06.2025

Job Description:

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. The role will be working across a wide product portfolio, including orthopaedic products.

Role responsibilities:

• Manage the supplier auditing program, including scheduling audits and assigning auditors.
• Perform supplier audits as required.
• Manage the internal audit program, including scheduling audits and assigning auditors.
• Perform internal audits as assigned.
• Manage the Quality Objectives procedure.
• Manage the NC/CAPA 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.

Qualifications 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.

This is a great opportunity to join a leading business that specializes in orthopaedic products. Please note that this is a hybrid position that will require 3 days on site per week.