Data Integrity Consultant

Role Overview

We are currently looking for a Data Integrity Consultant to join a leading organisation in the pharmaceutical industry, based at their site. This is an exciting opportunity for a professional with proven experience in GMP QC laboratory environments to support critical retrospective Data Integrity reviews following a recent assessment. As a Data Integrity Consultant, you will play a key role in ensuring the accuracy and compliance of laboratory data, helping to maintain the highest standards of GMP and data integrity across the organisation.

• Review historical laboratory records and data as part of retrospective Data Integrity assessments.
• Support review of unexplained trial injections, especially related to HPLC / chromatography data.
• Assess completeness, accuracy, and compliance of laboratory records, focusing on GDP documentation issues.
• Support retrospective review of OOS investigations to confirm appropriate investigation, root cause, impact assessment, and closure.
• Ensure documentation is accurate, compliant, and aligns with regulatory standards.

• A Degree or higher level in a scientific discipline.
• Proven industry experience in GMP QC laboratory environments.
• A working knowledge and practical experience with Data Integrity, ALCOA+ / ALCOA++, and laboratory documentation review.

This role offers an excellent opportunity to contribute to high standards within the pharmaceutical industry, in a reputable organisation committed to compliance and quality. You will gain valuable experience in Data Integrity and GMP practices, with the chance to influence critical quality processes.

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements.