At a Glance
- Tasks: Join our Quality Control team to validate and analyse methods in a regulated GMP environment.
- Company: Leading global healthcare and life sciences manufacturer based in Liverpool.
- Benefits: Competitive pay rate, hands-on experience, and opportunity to work on impactful projects.
- Other info: 12-month contract with potential for career growth in a dynamic field.
- Why this job: Make a difference by closing critical validation gaps and ensuring data integrity.
- Qualifications: Proven industry experience in a regulated environment and strong analytical validation skills.
The predicted salary is between 29700 - 36300 £ per year.
Contract Length: 12-Months
Location: Liverpool, full time on site
Pay rate: Negotiable
Our client, a leading global healthcare and life sciences manufacturer, is seeking an experienced and proactive Validation Analyst to join their Quality Control team on an initial 12-month contract. This is a newly created, project-driven role established to tackle and close out critical validation and analytical gaps ahead of target deadlines in early 2027. You will take ownership of method validation packages, historical data reviews, and robustness studies across instrument and wet chemistry workflows within a strictly regulated GMP environment.
Key Responsibilities
- Analytical Method Validation: Execute end-to-end QC chemistry (and microbial, where applicable) method validation in compliance with ICH Q2(R2), USP, and Ph. Eur. guidelines across both instrumentation and traditional wet chemistry techniques.
- Gap Remediation & Robustness: Address and close out identified technical gaps, including assessing method robustness and completing analytical remediation protocols.
- Historical Data Review: Conduct thorough historical QC method performance reviews and data validation assessments to bring analytical packages up to modern compliance standards (addressing multi-year data validation backlogs).
- System & Instrument Review: Support QC analytical instrument and data system validation reviews, ensuring data integrity and audit readiness.
- Technical Reporting: Compile, analyze, and present complex analytical validation data into clear, regulatory-compliant reports and validation summaries.
Requirements & Qualifications
- Essential Experience:
- Proven Industry Experience: Prior industrial laboratory experience in a regulated GMP environment (Pharmaceutical, Biopharma, Fine Chemicals, or Medical Devices/Healthcare). This role requires hands-on experience and is not suitable for recent graduates.
- Analytical Validation Expertise: Demonstrated track record with analytical method validation, verification, and transfer protocols against ICH/pharmacopoeial standards.
- Laboratory Competencies: Strong working background in HPLC analysis and troubleshooting. Hands-on proficiency with wet chemistry techniques and standard laboratory instrumentation (e.g., UV-Vis, pH, conductivity, titrations).
- Data Management: Strong numerical analysis and data interpretation skills; intermediate-to-advanced proficiency in Microsoft Excel and the broader MS Office suite.
- Systems: Adaptable to learning proprietary in-house Laboratory Information Management Systems (LIMS) and quality management platforms.
Randstad Business Support is acting as an Employment Business in relation to this vacancy.
Validation Analyst in Liverpool employer: Randstad Delivery (GBS) Careers
As a Product Investigation Engineer in Witney, you will be part of a dynamic team dedicated to enhancing the quality and safety of medical devices. Our company fosters a collaborative work culture that prioritises employee growth through continuous training and development opportunities, ensuring you can advance your career while making a meaningful impact on healthcare. With competitive pay and a commitment to regulatory excellence, we offer a rewarding environment where your contributions are valued and recognised.
Contact Details:
Randstad Delivery (GBS) Careers Recruitment Team
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