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Form of work
SalaryQA 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.
What do you need to be considered?
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 ecellent written and verbal communication skills.
What to do next
Interested?
If you have a passion for quality and a desire to help advance drug development and you want to work in a support team environment, then this is the right opportunity for you!
Apply now to avoid disappointment as the company is looking to interview in the next 4 weeks.
