Senior Manager, Global Quality Management

Parkside Office Professional

Posted 22 days ago, valid for 21 days

Windsor, Berkshire SL4 4AY, England

£60,000 - £72,000 per annum

Full Time

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Senior Manager, Global Quality Management
GxP related CSV audits and inspections
Pharma Background

My client a well know pharma company is seeking an experienced Senior Manager, Global Quality Management to join their Global Quality Management team.Based in Berkshire my client offers a generous package including a competitive salary, car allowance and bonus. You must have worked within the pharmaceutical industry with experience in GxP related CSV audits and inspections RoleThe main task is to manage and perform audits with focus on Computer System Validation (CSV) audits.Additional tasks are to support the continuous improvement of the Quality System, the inspection management, the regulatory intelligence activities, the SOP and WP management, and the project liaison activitiesWorking in close collaboration with the Head of Global Quality Management of GCP, CSV & GVP, Senior Director Global Quality Management and the CSV Audit Lead: Key Accountabilities

Support the development, implementation, continuous improvement and documentation of Companies’ Quality System
Support inspections
Support the audit process
Support Regulatory Intelligence
Support the management of the global, regional and local Standard Operating Procedures (SOPs) and Working Practices (WPs)
Support the validated state of computerised systems
Provide advice and act as project liaison

Skills & Experience

Degree in natural science or equivalent business experience
Several years of Information Technology (IT) industry/pharmaceutical industry/medical devices industry/Regulatory Authority or otherwise relevant experience, preferably including Quality Assurance for Manufacturing, Pharmacovigilance and Clinical Development and Computerised System Validation and Data Integrity
Expert knowledge/experience in relevant regulations and guidance documents, e.g., in the area of Computerised System Validation, Data Integrity, Manufacturing, Pharmacovigilance, Clinical Development, Medical Device, IMP management, Regulatory Affairs and Pharmacovigilance
Experience as a Lead Auditor on internal audits and external vendor audits.
Experienced in GxP related CSV audits and inspections
Knowledge and understanding of computerised systems in the GxP environment, experience in software validation and/or development
Understanding of computer hardware and network/infrastructure requirements

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