At a Glance
- Tasks: Support Quality Assurance operations in a GMP-regulated environment and manage quality documentation.
- Company: Leading pharmaceutical organisation focused on quality and compliance.
- Benefits: Opportunity to build your career in a collaborative team with growth potential.
- Other info: Join a dynamic team committed to quality and compliance.
- Why this job: Make a real impact in pharmaceutical quality assurance and support continuous improvement initiatives.
- Qualifications: Experience in GMP environments and strong organisational skills are preferred.
The predicted salary is between 30000 - 40000 £ per year.
CY Partners are recruiting for a Pharmaceutical QA Officer to join a leading pharmaceutical organisation. This is an exciting opportunity for a quality-focused professional to support Quality Assurance operations within a GMP-regulated manufacturing environment.
The Role
As a Pharmaceutical QA Officer, you will support the Quality team by managing controlled documentation, maintaining quality records, and assisting with key Quality Management System (QMS) activities. You'll play an important role in ensuring GMP compliance, supporting audits and inspections, and contributing to continuous improvement initiatives.
Key Responsibilities
- Prepare, maintain and control GMP documentation, including SOPs, reports and quality records.
- Manage document version control and electronic QMS systems.
- Retrieve documentation to support audits, inspections and quality reviews.
- Collate and report quality data, including deviations, CAPAs and change controls.
- Support QA projects through the maintenance of trackers, action logs and project documentation.
- Assist with document reviews, training records and other routine QMS activities.
About You
You’ll ideally have:
- Experience working within a GMP-regulated pharmaceutical, biotechnology or life sciences environment.
- Experience using electronic QMS or document management systems such as Veeva, TrackWise or VQMS.
- Excellent attention to detail with strong organisational and administrative skills.
- Good working knowledge of Microsoft Office, particularly Excel and Word.
Experience supporting deviations, CAPAs, change controls or audit activities would be advantageous.
If you’re looking to build your career in Pharmaceutical Quality Assurance and want to join a collaborative team committed to quality and compliance, we’d love to hear from you.
CY Partners is acting as an Employment Agency in relation to this vacancy.
Quality Assurance Specialist in Essex employer: CY Partners
CY Partners is an exceptional employer for those seeking a fulfilling career in Pharmaceutical Quality Assurance. With a strong commitment to quality and compliance, the company fosters a collaborative work culture that encourages professional growth and development. Located in a GMP-regulated environment, employees benefit from hands-on experience with cutting-edge quality management systems and the opportunity to contribute to meaningful projects that enhance patient safety and product integrity.
