Validation Specialist

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We are working with a Croydon-based Medical Equipment Manufacturing organisation committed to innovation and excellence, seeking an experienced QA Validation Specialist.

This role is suitable for a Quality Assurance professional with a background in Medical Devices and Validation activities, looking for a new permanent position with ample progression opportunities.

The Role:

1. Perform validation activities and ensure compliance with EU GMP and regulatory requirements.
2. Manage and improve the Quality System, supporting improvement activities through CAPA.
3. Conduct Internal Audits and Quality Inspections on finished products.
4. Train employees in Quality Systems, Tools, and Objectives.
5. Conduct audits on manufacturers and suppliers.

About you:

• Have previous experience in medical device or pharmaceutical manufacturing.
• Possess practical experience in manufacturing technology and quality assurance.
• Understand Quality Management Systems for medical devices (EN ISO 13485, 21 CFR 820).
• Are experienced in validation/qualification and project management.

If you are interested and want to learn more, apply via the link or send me a message (emailprotected).

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