Quality Administrator

Our client are a Pharmaceutical manufacturing organisation who are currently seeking a Quality Administrator to join their team based in Loughborough.

Responsibilities include:
- Documentation Control - Entering documents onto eMatrix system, distribution (paper and workspace), processing obsoletions, administration of accounts, routes, and issues.
- SOP/WI Review - Management and monitoring of the document review process.
- Product Quality Review (PQR) -Schedule communication, workspace maintenance, and recording of actions from meetings into SAP.
- External Audits - Provide support as required.
- eMatrix CMRs - Administration, support with issues, and closure of CMRs (verification).
- Change Review Board (CRB) - Provide meeting agenda and act as deputy when required.
- Train, coach and mentor new/other members of staff to ensure compliance and competence.
- Manage and support Green Belt/Lean Six Sigma projects as assigned.

Skills required:
- Experience working in a GMP, GLP or ISO accredited organisation.
- Knowledge of Continuous Improvement techniques including Lean Manufacturing/Six Sigma concepts, change control systems and root cause analysis.
- Computer literate including proficiency in MS Office programmes.

Full details available upon application.