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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.
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