ROLE OVERVIEW
We are currently seeking a dedicated QA Officer to join a dynamic quality assurance team. This is an exciting opportunity for a quality assurance focused professional to contribute to maintaining and enhancing our client’s robust Quality Management System (QMS). Based at their site, you’ll play a key role in ensuring compliance, supporting internal and external audits, and driving continuous improvement initiatives.
This position offers a chance to work within a reputable organisation committed to high standards of quality and regulatory compliance. Join their team to help uphold excellence in health-related product development and manufacturing.
KEY DUTIES AND RESPONSIBILITIES
Your duties as the QA Officer will be varied however the key duties and responsibilities are as follows:
To develop, maintain, and improve the Quality Management System (QMS) to ensure ongoing compliance with industry standards and regulations.
Act as system administrator and primary contact for the electronic QMS (eQMS) platform, including user support and process management.
Support CSV projects
Deliver training on QMS processes and QA induction for new staff, facilitating understanding of change controls, deviations, and quality events.
As the QA Officer, you will organise and participate in internal audits, external audits, and inspections, ensuring readiness and compliance at all times.ROLE REQUIREMENTS
To be successful in your application to this exciting role as the QA Officer we are looking to identify the following on your profile and past history:
A Degree or higher level in a relevant scientific discipline (e.g., Pharmaceutical Chemistry, Quality Assurance, Quality Management).
Proven experience within a pharmaceutical or regulated laboratory environment, with a strong understanding of GxP standards, GMP, and quality management systems.
Familiarity with pharmaceutical computer systems and electronic quality management platforms. Must have experience of CSV and Gamp5.
Excellent analytical, organisational, and communication skills, with the ability to manage multiple projects effectively.WHAT’S IN IT FOR YOU?
Join our client’s team and enjoy a pivotal role in maintaining high standards of quality within a reputable organization. You will benefit from exposure to regulatory audits, ongoing professional development, and the opportunity to make a real impact in a dynamic environment committed to continuous improvement and excellence.
Key Words: QA / Quality Assurance / QMS / GxP / GMP / pharmaceutical / regulatory compliance / audit / training / continuous improvement / laboratory environment / electronic systems / internal audits / external inspections / process management
"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