{ “@context”: “http://schema.org”, “@type”: “JobPosting”, “title”: “Quality Officer”, “description”: “
A growing Pharmaceutical company are looking to expand their Regulatory team with the addition of a Quality Officer. They are looking for an individual that is hard working and self-motivated to assist with all things quality.
Key Responsibilities
- Support the QA Manager with maintaining and improving the Quality Management System (QMS).
- Manage and progress Deviations, CAPAs, Change Controls and Complaints in a compliant and timely manner.
- Conduct batch review activities and support the batch release process, identifying and escalating any issues.
- Assist with internal audits, risk assessments, recalls and continuous improvement initiatives.
- Prepare and maintain documentation including SOPs, PQRs and KPI reports for management review.
- Support supplier/customer qualification and liaise with external partners to ensure QMS records are progressed to closure.
- Ensure compliance with GMP/GDP requirements and internal quality procedures.
Experience and Qualifications Required
- Minimum 3 years’ experience in a QA role within a pharmaceutical environment.
- Strong understanding of Quality Management Systems and GMP/GDP regulations.
- Experience managing Deviations, CAPAs, Complaints and Change Controls.
- Competent in document review, report writing and SOP creation.
- Skilled in root cause analysis and risk/impact assessments.
- Highly organised with strong attention to detail and the ability to prioritise effectively.
Personal Attributes
- Professional, proactive and solutions-focused.
- Passionate about quality, compliance and patient safety.
- Self-motivated, collaborative and confident in constructively challenging processes to drive improvement.
Company: X4 Life Sciences
Location:
Job Description:
A growing Pharmaceutical company are looking to expand their Regulatory team with the addition of a Quality Officer. They are looking for an individual that is hard working and self-motivated to assist with all things quality.
Key Responsibilities
- Support the QA Manager with maintaining and improving the Quality Management System (QMS).
- Manage and progress Deviations, CAPAs, Change Controls and Complaints in a compliant and timely manner.
- Conduct batch review activities and support the batch release process, identifying and escalating any issues.
- Assist with internal audits, risk assessments, recalls and continuous improvement initiatives.
- Prepare and maintain documentation including SOPs, PQRs and KPI reports for management review.
- Support supplier/customer qualification and liaise with external partners to ensure QMS records are progressed to closure.
- Ensure compliance with GMP/GDP requirements and internal quality procedures.
Experience and Qualifications Required
- Minimum 3 years’ experience in a QA role within a pharmaceutical environment.
- Strong understanding of Quality Management Systems and GMP/GDP regulations.
- Experience managing Deviations, CAPAs, Complaints and Change Controls.
- Competent in document review, report writing and SOP creation.
- Skilled in root cause analysis and risk/impact assessments.
- Highly organised with strong attention to detail and the ability to prioritise effectively.
Personal Attributes
- Professional, proactive and solutions-focused.
- Passionate about quality, compliance and patient safety.
- Self-motivated, collaborative and confident in constructively challenging processes to drive improvement.
#J-18808-Ljbffr…
Posted: May 20th, 2026