Quality Assurance Specialist
Posted 6 days ago
- Leighton Buzzard, Bedfordshire
- Permanent
- £35,000 to £40,000 /Yr
- Sponsored
- Expires In 22 days
Quality Assurance Specialist
Leighton Buzzard, Bedfordshire
£35,000 - £40,000
We are seeking a Quality Assurance Specialist to join a leading pharmaceutica logistics company. This role focuses on supporting the implementation and maintenance of the Quality Management System (QMS) in line with ISO 9001 and ISO 13485 standards, and ensuring compliance with EU GDP guidelines.
Key Responsibilities:
* Maintaining and enhancing the QMS to meet regulatory, ISO, and client requirements.
* Supporting audits (regulatory, ISO, client, supplier) and managing CAPA plans.
* Driving a culture of quality excellence across the business.
* Conducting supplier audits, internal inspections, and management reviews.
Key Requirements:
* Proven experience in a GMDP or similar regulated environment.
* Strong knowledge of GDP, GMP, ISO 9001, and ISO 13485 standards.
* Excellent organizational, communication, and stakeholder management skills.
* A positive attitude toward promoting quality across all departments.
* Proficiency in MS Office applications (Word, Excel, PowerPoint, Teams).
If you have the skillset required and looking for your next career move, please apply for immediate consideration
Leighton Buzzard, Bedfordshire
£35,000 - £40,000
We are seeking a Quality Assurance Specialist to join a leading pharmaceutica logistics company. This role focuses on supporting the implementation and maintenance of the Quality Management System (QMS) in line with ISO 9001 and ISO 13485 standards, and ensuring compliance with EU GDP guidelines.
Key Responsibilities:
* Maintaining and enhancing the QMS to meet regulatory, ISO, and client requirements.
* Supporting audits (regulatory, ISO, client, supplier) and managing CAPA plans.
* Driving a culture of quality excellence across the business.
* Conducting supplier audits, internal inspections, and management reviews.
Key Requirements:
* Proven experience in a GMDP or similar regulated environment.
* Strong knowledge of GDP, GMP, ISO 9001, and ISO 13485 standards.
* Excellent organizational, communication, and stakeholder management skills.
* A positive attitude toward promoting quality across all departments.
* Proficiency in MS Office applications (Word, Excel, PowerPoint, Teams).
If you have the skillset required and looking for your next career move, please apply for immediate consideration