QA SPECIALIST (GLP/GCP) - GROWING CRO IN NORTH YORKSHIRE

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QA Specialist required for a rapidly expanding Contract Research Organisation based in the North Yorkshire area

Company: Part of a multinational Contract Research Organisation, but has a family feel and caring culture; helping to advance drug development.

Hours of work: 37.5 hours per week - Monday to Friday - Flexible start times. 

Why join? 

• Opportunity to work in a modern GLP/GCP environment.
• Lots of variety and learning opportunities.
• Career progression. 
• 25 + 8 days holiday (increases with service duration).
• Pension, Healthcare and Bonus schemes

Location:  North Yorkshire

Duration: Permanent

Salary: £30-38k dependent on skills and experience.

You  will be involved in:

• Reviewing study plans/phases in line with compliance to GLP and GCP standards. 
• Producing reports from QA audits, data and inspections.
• Advising management on any deviations and regulatory deficiencies.
• Scheduling and helping perform audits as required.
• Conducting facility inspections to ensure compliance.

You will need:

• Experience of working in a  GLP/GCP compliant facility within a QA capacity.  
• Science based qualification ideally to degree level.
• Working knowledge of quality audits and systems (CAPA, NCR, OOS) along with wider regulatory requirements within clinical research.
• Knowledge/experience of bioanalysis would be a distinct advantage.
• Excellent attention to detail, along with written and verbal communication skills.