Quality Systems Expert
3 days ago
About Quality Assurance in a GMP Environment
You will apply your quality systems expertise to the end-to-end manufacture of investigational therapeutic products in a Good Manufacturing Practice (GMP) setting.
Your responsibilities include reviewing environmental monitoring data; managing document control and change control; coordinating corrective and preventive actions (CAPA); supporting internal audits; supplier qualification and approvals; conducting trend analysis and reporting; and overseeing stock and supplier approvals.
As part of our team, you will work independently across multiple disciplines while strictly adhering to GMP procedures and maintaining accurate, audit-ready compliance documentation and records.
Requirements for Success- A minimum Diploma in Laboratory Skills or equivalent experience, ideally gained in a microbiology, clinical, biological, forensic, life science, medical laboratory, or pharmaceutical setting.
- Experience in quality control or quality assurance within cell therapy; medical laboratories; blood services; pathology; food manufacturing; pharmaceutical manufacturing; clinical trials facilities; or a similar setting.
- Excellent attention to detail and the ability to complete complex tasks precisely and consistently as defined in a Standard Operating Procedure (SOP).
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