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Main Purpose
To provide Medical Products manufacturing, packing operations and customers with a Quality Control analysis service so that process control, product quality, and current Good Manufacturing Practice (cGMP) requirements are satisfied.
This is a day role working Monday to Friday 8 am to 4 pm with flexibility required to move into a shift role in 6-12 months depending on business requirements.
Main Responsibilities
- To accurately analyze, validate and record results for samples from the medical products operation to ensure that production processes and final product quality is controlled within the agreed specification limits.
- To review and validate the analysis of other analysts in line with operating requirements.
- Prioritize work to ensure that business production, sales and customer support plans are achieved.
- Carry out investigation into any abnormal results and report to the Medical Quality Control Team Leader, production personnel, and/or the Quality Assurance department, as appropriate.
- Maintain the laboratory, processes and analysis equipment in line with full requirements of current Good Manufacturing Practice.
- Ensure all sample, analysis and testing work is carried out in full compliance with written procedures, cGMP and SHE standards.
Qualifications
Minimum: HNC/HND Chemistry.
Desirable: Degree in Chemistry or related subject.
Knowledge/ Experience Required
- Knowledge and experience of working to cGMP standards.
- Understanding of QC in the pharmaceutical industry.
- Experience of working in a QC laboratory preferably one working to cGMP standards.
- Full clean driving license.
