Our client, a fast growing organisation operating in the London area, are currently recruiting a Quality consultant in the biotech space.
This is an excellent opportunity to join a growing, international team and contribute to a strong culture of quality and continuous improvement.
Key Responsibilities:
* Maintain and manage controlled documents, ensuring accurate issuance, revision, and archiving of SOPs in line with document control requirements.
* Support the leadership of the QA team, including QA specialists, auditors, and document control personnel.
* Contribute to internal audits and inspection-readiness efforts by preparing, organizing, and providing QA documentation and records.
* Work closely with Production, QC, and other departments to monitor quality actions, resolve issues, and drive continuous improvement initiatives.
How to apply
If you are interested in this opportunity, please send your CV and a short cover letter highlighting your relevant experience. Applications will be handled in confidence and reviewed on a rolling basis.