Manager, CSV Audit

JR United Kingdom; London; On-site; GBP 50,000 - 75,000; Full time

Job summary

A leading global company is seeking an experienced CSV Audit Manager for a 12-month contract in London. This role involves developing the Global CSV Audit Strategy and ensuring high-quality standards across various operational areas while collaborating with key stakeholders. The ideal candidate will have a solid background in quality assurance within the IT and pharmaceutical sectors, complemented by a scientific degree.

Benefits

Excellent salary

Bonus

Hybrid working

Qualifications

• Several years of experience in IT, pharmaceutical, or medical device industries.
• Experience in Quality Assurance for Manufacturing and Clinical Development.

Responsibilities

• Develop and execute the Global CSV Audit Strategy and Plan.
• Support the implementation and documentation of the Company’s Quality System.
• Manage global and local Standard Operating Procedures.

Skills

Quality Assurance

Pharmacovigilance

Computerised System Validation

Data Integrity

Project Management

Education

Degree in natural science

Job description

Social network you want to login/join with:

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 the Company’s 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 experience in the Information Technology (IT) industry, pharmaceutical industry, medical devices industry, Regulatory Authority, or relevant fields, preferably including Quality Assurance for Manufacturing, Pharmacovigilance, Clinical Development, and Computerised System Validation and Data Integrity.