QA/CSV Analyst -GxP, MyLabData, Windows 11, Empower - Hybrid

Summary: A global organization is seeking a QA/CSV Validation Analyst to support the implementation of My Lab Data, Windows 11, and Empower. This position is a hybrid role based in Greater London, with an initial contract duration of 6-12 months and potential for extensions. The ideal candidate will have extensive experience in CSV and equipment validation within regulated environments. Key responsibilities include ensuring data integrity and compliance with GxP standards.

Key Responsibilities:

• CSV and equipment validation expertise: Strong understanding of laboratory record keeping, data integrity, and software validation principles.
• Familiarity with electronic laboratory notebook systems, audit trail functionality, and validation of computerised systems (eg, Windows 11 environments).
• Quality experiences
• Analytical and critical thinking
• Collaboration and teamwork
• At least 3 years' experience in a laboratory, quality assurance, or data management role within a regulated environment (such as pharmaceuticals, biotechnology, or clinical research).
• Demonstrable experience with document review and approval processes, preferably in line with GxP and regulatory requirements.

Key Skills:

• CSV and equipment validation expertise
• Familiarity with electronic laboratory notebook systems
• Quality experiences
• Analytical and critical thinking
• Collaboration and teamwork
• At least 3 years' experience in a regulated environment
• Document review and approval processes experience

Salary (Rate): undetermined

City: Greater London

Country: UK

Working Arrangements: hybrid

IR35 Status: undetermined

Seniority Level: undetermined

Industry: Other

Detailed Description From Employer:

QA/CSV Analyst -GxP, MyLabData, Windows 11, Empower - Hybrid, Greater London

A large global organisation are looking for a QA/CSV Validation Analyst to assist on a Implementation of My Lab data, Windows 11 and Empower.

This will be an initial 6-12 months+ contract with the opportunity for multiple extensions.

The role will be worked on a hybrid basis, 2/3 days a week onsite in Greater London.

Key Responsibilities/Skills:

• CSV and equipment validation expertise: Strong understanding of laboratory record keeping, data integrity, and software validation principles.
• Familiarity with electronic laboratory notebook systems, audit trail functionality, and validation of computerised systems (eg, Windows 11 environments).
• Quality experiences
• Analytical and critical thinking
• Collaboration and teamwork
• At least 3 years' experience in a laboratory, quality assurance, or data management role within a regulated environment (such as pharmaceuticals, biotechnology, or clinical research).
• Demonstrable experience with document review and approval processes, preferably in line with GxP and regulatory requirements.

QA/CSV Analyst -GxP, MyLabData, Windows 11, Empower - Hybrid, Greater London