Job Advertisement: Quality Officer

Overview

We are seeking a dedicated and detail-oriented Quality Officer to join our quality team at a leading pharmaceutical manufacturing organisation. This is a great opportunity for a QC analyst / QA officer to start / progress their career as a Quality Officer to contribute to the delivery of pharmaceutical products that meet both customer and regulatory requirements.

Responsibilities

As a Quality Officer, your key responsibilities will include:

• Preparing quality documentation to support site operations, including works orders, specifications, bills of materials, and batch documentation.
• Performing environmental monitoring of the facility in accordance with schedules and procedures.
• Producing and maintaining administrative quality reports and documents.
• Managing document administration for the Quality team, including issuing, retaining, and archiving documents, and maintaining records within the electronic Quality Management System (eQMS).
• Providing quality support across key business areas.
• Assisting with deviation investigations, corrective and preventive actions (CAPAs), change controls, and liaising with customers and suppliers on issues, investigations, and projects.
• Participating in inspection readiness activities and the internal audit program.
• Taking opportunities to develop within the QA Operations team and deputising as appropriate.

Qualifications

The ideal candidate will possess:

• A strong understanding of quality principles and practices, preferably within a pharmaceutical or manufacturing environment.
• Excellent organisational and documentation skills.
• The ability to work collaboratively across teams and communicate effectively with internal and external stakeholders.
• A proactive approach to problem-solving and a commitment to continuous improvement.
• Familiarity with eQMS systems and regulatory requirements is desirable.

Day-to-Day

Your day-to-day activities will involve:

• Preparing and reviewing quality documentation to ensure compliance with regulatory standards.
• Conducting routine testing and environmental monitoring to maintain product and facility quality.
• Collaborating with cross-functional teams to address quality-related issues and support operational excellence.
• Managing and maintaining accurate records within the eQMS.
• Participating in audits and readiness activities to uphold the organisation’s high standards.

Benefits

• Competitive salary up to £30,000.
• Opportunity to work in a dynamic and innovative pharmaceutical manufacturing environment.
• Professional development and growth opportunities within the Quality Assurance team.
• A supportive and collaborative workplace culture.

Note: We are unable to provide VISA sponsorship for this position.