{ “@context”: “http://schema.org”, “@type”: “JobPosting”, “title”: “Quality Officer”, “description”: “
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
- 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
- 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
- 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.
We are unable to provide VISA sponsorship for this position.
#J-18808-Ljbffr”, “datePosted”: “2026-05-20”, “hiringOrganization”: { “@type”: “Organization”, “name”: “Nexus Life Sciences”, “sameAs”: “https://uk.whatjobs.com/pub_api__cpl__436769664__4861?utm_campaign=publisher&utm_medium=api&utm_source=4861&geoID=33161” }, “jobLocation”: { “@type”: “Place”, “address”: { “@type”: “PostalAddress”, “addressLocality”: “Wirral” } } }Company: Nexus Life Sciences
Location: Wirral
Job Description:
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
- 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
- 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
- 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.
We are unable to provide VISA sponsorship for this position.
#J-18808-Ljbffr…
Posted: May 20th, 2026