Über
The Opportunity We're supporting a UK manufacturer of cannabis‑based medicines that has recently brought a new, state‑of‑the‑art growing, processing and lab facility online in the Southwest. The organisation runs a sustainability‑led operation that's carbon‑negative by design and is scaling to meet growing patient demand.
What you'll be doing
Own core elements of the GMP QMS – write, update and review SOPs/records; ensure Good Documentation Practice; track SOP review cycles and training; and maintain complete, compliant records.
Manage quality events – identify and raise deviations, lead root cause analysis, define and implement CAPAs, oversee change control and complete post‑implementation reviews, track metrics and report into the business.
Drive inspection readiness – plan and run self‑inspections, conduct independent audits and risk assessments, and keep current with relevant regulatory requirements.
Supplier & customer oversight – support approvals and liaise with external supplier QA where needed.
Controlled drugs compliance – assist with Home Office licensing requirements as needed.
Broader quality support – help maintain the GACP QMS alongside GMP activities.
About you
A relevant scientific or technical degree (or equivalent experience).
Experience in a quality focused position within a GMP production environment.
Experience of GMP QMS.
Comfortable working in a dynamic, change‑driven setting.
Knowledge of GACP would be advantageous but training and support will be provided.
Please note - to be considered for this position you will need to pass an enhanced DBS Check.
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Sprachkenntnisse
- English
Hinweis für Nutzer
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