Analytical Development Coordinator

5 days ago


Oxford, Oxfordshire, United Kingdom Oxford BioMedica (UK) Limited Full time

We are seeking an experienced QC Compliance Officer II to join our team and contribute to our mission of delivering life-changing therapies to patients worldwide.

In this role, you will be responsible for ensuring timely reporting of analytical data, supporting outsourced QC testing, and providing oversight of GMP compliance.

About the Job:
  • Work closely with the ADQC Team to maintain high-quality standards and compliance with GMP regulations
  • Develop and implement effective processes for sample submission, shipment paperwork, and purchase requisitions
  • Manage and maintain controlled documents, including SOPs, QC testing documents, and sampling plans
  • Review and approve GMP documentation, ensuring adherence to regulatory requirements
  • Report results in QC Databases and manage Quality Records

A competitive salary package, including £55,000 - £70,000 per annum, is offered for this position.



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