QC Analyst

Cpl Life Sciences; United Kingdom; On-site; GBP 80,000 - 100,000; Full time

Job summary

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.

Qualifications

• Experience in Quality Control batch testing.
• Knowledge of cGMP and regulatory standards.
• Good Manufacturing and Laboratory Practices understanding.

Responsibilities

• Conduct testing of Quality Control batches in compliance with cGMP.
• Ensure accurate data recording and audit readiness.
• Collaborate across QC areas for broader laboratory goals.

Skills

Attention to detail

Data recording

Laboratory practices

Job description

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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 Policy

Overview

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 Policy

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