Quality Assurance Officer
Job in
Cardiff, Cardiff City Area, CF10, Wales, UK
Listed on 2026-10-09
Listing for:
Hyper Recruitment Solutions
Full Time
position Listed on 2026-10-09
Job specializations:
-
Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers, Data Analyst
Job Description & How to Apply Below
This role offers a unique chance to work within a dynamic environment, supporting the quality standards that underpin pharmaceutical manufacturing excellence. If you have a background in GMP environments and are seeking a role where your expertise makes a tangible impact, this could be the perfect opportunity for you.
KEY DUTIES AND RESPONSIBILITIES Your duties as the Quality Assurance Officer will be varied however the key duties and responsibilities are as follows:
• To maintain and continually improve the Quality Management System (QMS), ensuring compliance with industry standards and regulations.
• Reviewing and approving batch manufacturing documentation prior to batch release to ensure accuracy and compliance.
• Managing Deviations, CAPAs, Change Controls, Complaints, and OOS investigations to uphold quality standards.
• Supporting internal and supplier audits, as well as customer and regulatory audits, to facilitate continuous improvement and compliance.
• As the QA Officer, you will ensure all quality processes are followed diligently and foster a culture of quality awareness across teams.
ROLE REQUIREMENTS To be successful in your application to this exciting role as the Quality Assurance Officer we are looking to identify the following on your profile and past history:
• A Degree or higher level in a scientific discipline (e.g., Pharmaceutical Chemistry / Quality Assurance / Quality Management).
• Proven industry experience in GMP Quality Assurance within a pharmaceutical manufacturing environment.
• A working knowledge and practical experience with QMS, CAPAs, Deviations, and Change Controls.
WHAT’S IN IT FOR YOU?
Join a forward-thinking organisation that offers opportunity for growth and development, with the chance to genuinely influence quality practices within a respected sector. Enjoy a collaborative environment where your expertise is valued and your contributions recognised, all while working for a company committed to excellence and innovation.
Key Words:
Quality Assurance / GMP / Pharmaceutical / QMS / CAPA / Deviation Management / Batch Release / Regulatory Audits / Supplier Audits / Quality Systems / Continuous Improvement"Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career."
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