Quality Officer
CV-LibraryCH25, Birkenhead, Metropolitan Borough of WirralpermanentPosted: 13 April 2026
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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
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