Job Title: Regulatory QMS Specialist
Job Type: Permanent, full-time position
Location: Bourton on the water, Gloucestershire, UK – Hybrid (3 days on site)
Remuneration: £35,000 – £40,000
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.
Responsible for managing the audit program, including internal auditing and supplier auditing. Supporting the Quality Management System, including Quality Objectives and NC/CAPA management.
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.
- Provide support during external audits, including collating pre-audit document requests.
- 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 who specialise in orthopaedic products. Please note this is a hybrid position that will require 3 days on site per week.
For more information, please reach out to lucy.kirkaldy@cpl.com
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