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.
Key Duties And Responsibilities
- 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.
Role Requirements
- 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.
WHAT’S IN IT FOR YOU?
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.
Key Words
- Data Integrity
- GMP QC laboratory
- retrospective review
- HPLC / chromatography
- GDP documentation
- OOS investigations
- CAPA
- remediation
- pharmaceutical industry
Employer Information
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.