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Principal Consultant – Quality/Scientific
We are working with a Croydon based Medical Equipment Manufacturing organisation committed to innovation and excellence in their search for an experienced QA Validation Specialist.
This role would suit a Quality Assurance professional with a background in Medical Devices and Validation activities looking for a new permanent position with plenty of progression opportunities.
The Role:
* Validation activities and ensuring compliance with EU GMP and regulatory requirements.
* Management and improvement of the Quality System including supporting improvement activities through CAPA
* Conducting Internal Audits and Quality Inspections on finished products
* Training of employees in Quality Systems, Tools and Objectives
* Conducting Audits on manufacturers and suppliers
About you:
* Has previous experience in medical device or pharmaceutical manufacturing.
* Possesses practical experience in manufacturing technology and quality assurance.
* Understands Quality Management Systems for medical devices (EN ISO 13485, 21 CFR 820).
* Experienced in validation/qualification and project work/project management.
If you are interested and want to learn more, apply with the link or send me a message jamie.keith@cpl.com
Seniority level
* Seniority level
Associate
Employment type
* Employment type
Full-time
Job function
* Job function
Quality Assurance
* Industries
Medical Equipment Manufacturing
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