Manager, CSV Audit

Parkside Recruitment; Slough; On-site; GBP 55,000 - 75,000; Full time

Job summary

A leading recruitment agency is seeking an experienced CSV Audit Manager for a global team on a 12-month contract. The position involves developing and executing audit strategies while collaborating with quality management teams. Ideal candidates will possess a degree in natural science and several years in relevant industries, including strong competencies in Quality Assurance and Computerised System Validation.

Qualifications

• Several years of relevant experience in IT/pharmaceutical industry.
• Qualification as an auditor is preferred.

Responsibilities

• Develop and execute the Global CSV Audit Strategy.
• Support the management of global, regional, and local Standard Operating Procedures and Working Practices.
• Ensure continuous improvement of the Companies’ Quality System.

Skills

Quality Assurance

Computerised System Validation

Data Integrity

Pharmacovigilance

Education

Degree in natural science or equivalent business experience

Job description

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Base pay range

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My client is seeking an experienced CSV Audit Manager to join their global team on a 12 month contract.

Excellent salary and benefits including bonus and hybrid working/

The main task is the development and execution of the Global CSV Audit Strategy and Global CSV Audit Plan in close collaboration with the CSV Audit Lead and the Head of Global Quality Management. This includes defining risk standards and methodologies, audit methodology and best practices to ensure consistency of approach.

Key Responsibilities

• Support the development, implementation, continuous improvement and documentation of Companies’ Quality System
• Support inspections
• Support the audit process
• 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

• 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
• Qualification as an auditor

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Job function

  Quality Assurance

• Industries

  Biotechnology Research and Pharmaceutical Manufacturing

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