Pharmaceutical QA Officer
Location: Essex
Contract: 6-12 months
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.