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A leading company in life sciences is seeking a QC Analyst for a 3-6 month contract in Hull. The successful candidate will conduct testing of Quality Control batches in compliance with cGMP and ensure accuracy in data recording, all while supporting regulatory inspections and continuous improvement initiatives.
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– Conduct testing of Quality Control batches in compliance with cGMP and regulatory standards.
– Prioritize and manage individual workload to meet customer and stakeholder needs.
– Ensure accurate data recording, audit readiness, and adherence to Good Manufacturing and Laboratory Practices.
– Maintain safe working practices, laboratory housekeeping, and equipment calibration/qualification.
– Support Regulatory Authority inspections and QC line management when required.
– Contribute to continuous improvement initiatives and performance monitoring.
– Handle basic laboratory equipment tasks, including SOP writing and maintenance.
– Ensure completion and compliance with training and personal development plans.
– Collaborate across QC areas to align individual activities with broader laboratory goals.
Apply
Full name Email address Cover Message (optional) Upload CV Choose File Upload your CV and any other relevant file. Contact via SMS (optional) I would like to be contacted via SMS Privacy Policy I have read and agree to the Clinical Professionals Group Privacy PolicyOverview
QC Analyst
Hull
£12.96 per hour
3-6 month contract
Key Responsibilities:
– Conduct testing of Quality Control batches in compliance with cGMP and regulatory standards.
– Prioritize and manage individual workload to meet customer and stakeholder needs.
– Ensure accurate data recording, audit readiness, and adherence to Good Manufacturing and Laboratory Practices.
– Maintain safe working practices, laboratory housekeeping, and equipment calibration/qualification.
– Support Regulatory Authority inspections and QC line management when required.
– Contribute to continuous improvement initiatives and performance monitoring.
– Handle basic laboratory equipment tasks, including SOP writing and maintenance.
– Ensure completion and compliance with training and personal development plans.
– Collaborate across QC areas to align individual activities with broader laboratory goals.
Apply
Full name Email address Cover Message (optional) Upload CV Choose File Upload your CV and any other relevant file. Contact via SMS (optional) I would like to be contacted via SMS Privacy Policy I have read and agree to the Clinical Professionals Group Privacy PolicyFind our privacy policy here