Quality Assurance Specialist (Pharmaceuticals)

About the Role

Our client is seeking a meticulous Quality Assurance Specialist to join their manufacturing quality team in Liverpool . This role is essential for maintaining the highest standards of quality and compliance within our pharmaceutical manufacturing operations. You will be involved in auditing, documentation review, deviation management, and ensuring adherence to GMP and other regulatory requirements. This office-based position offers a hands-on approach to quality management within a state-of-the-art facility, ensuring product integrity and patient safety.

Key Responsibilities

• Perform internal audits of manufacturing processes, documentation, and quality systems.
• Review and approve batch records, validation documents, and quality-related reports.
• Investigate and manage deviations, CAPAs (Corrective and Preventive Actions), and change controls.
• Ensure compliance with cGMP, FDA, EMA, and MHRA regulations.
• Participate in external regulatory inspections and client audits.
• Contribute to the continuous improvement of the Quality Management System (QMS).

Requirements

• Bachelor's degree in a scientific or technical field (e.g., Chemistry, Pharmacy, Engineering).
• Minimum of 3 years of experience in Quality Assurance within the pharmaceutical industry.
• Thorough understanding of cGMP principles and regulatory expectations.
• Experience with Quality Management Systems (QMS), CAPA, and change control processes.
• Strong analytical and problem-solving abilities.
• Excellent documentation and communication skills.

Benefits

• Competitive starting salary with regular reviews.
• Comprehensive health, dental, and vision insurance package.
• Company-sponsored pension scheme.
• Generous annual leave entitlement.
• Training and development opportunities within the QA department.