Quality Control Analyst
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Quality Control Analyst
Denbigh
Our Client is looking for a Quality Control Analyst to join a team in Denbigh North Wales.
The role is Full Time Permanent
Mon - Fri 7am-3pm
Reporting to the QC Supervisor this fast pace and varied role will require laboratory testing on materials and documenting on procedures in a timely manner. Exceptional attention to detail and a drive for efficiency will be required to ensure compliance to all applicable regulatory standards, current company and cGMP procedures and practices are adhered to; consistence and accurate documentations are administered; supporting the wider compliance and quality teams and together strive towards our goal for continuous improvement and achieving the company’s business strategy, Vision, Mission and values.
Key Responsibilities:
- Conduct raw material, intermediate material testing, finished product, In-process, stability and water testing in accordance with Good Laboratory Practices principles (GLP) and SOPs adhering and delivering to test schedule assigned.
- Complete testing and timely documentation write-ups in accordance with Good Documentation Practices (GDP) and pass onto QC Supervisor/Designee for review.
- Notify QC Supervisor / Designee of any issues with methods, testing, instrumentation or materials that could impact on testing timelines.
- Notify QC Supervisor / Designee of any Out of Specification (OOS), Out of Trend (OOT) as soon as they occur.
- Author SOPs, protocols, change controls, reports in-line with GDP as required.
- Maintain Records to GDP in a timely manner, e.g. Laboratory Notebooks.
- Ensure workspace is hazard free and maintained in accordance with GLP.
- Ensure necessary equipment is within calibration and materials are available for testing.
- Ensure good adherence to test and laboratory operations scheduling as issued by the QC Supervisor.
- Champion QC Laboratory initiatives based on continuous improvement and 6S principles.
- Carry out ancillary QC tasks, e.g. housekeeping, stock checking as required by the QC Supervisor / Designee to ensure the QC laboratory operation runs seamlessly.
Skills/Qualifications:
- Degree level within a Scientific Discipline is desired
- 1 years’ experience in GMP environment within a pharmaceutical environment desired.
Apply with CV or call 0161 519 5505 and ask for Sharon
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