Job Description
We're seeking a dynamic QC Analyst to join our team and take their career to the next level!
As a QC Analyst, you will be responsible for performing routine and specialised testing of virology products and samples in compliance with Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP). You will perform laboratory development, validation and testing procedures in accordance with the relevant protocols, study plans and standard operating procedures (SOPs).
Key Responsibilities as a QC Analyst:
* Virology Testing: Perform routine virological assays, to assess the quality and potency of virological products.
* Sample Analysis: Analyse raw materials, in-process samples, and final products to ensure compliance with quality standards.
* Data Interpretation: Accurately record, analyse, and report test results, ensuring that all documentation is maintained according to GLP/GMP guidelines.
* Troubleshooting: Investigate deviations and out-of-specification results, performing root cause analysis and implementing corrective actions as needed.
* Equipment Maintenance: Ensure that laboratory equipment is properly calibrated, maintained, and validated for use in virological testing.
Qualifications
The ideal candidate will have experience in a laboratory environment, ideally within the pharmaceutical, biological science, or a similar sector.
You will also have:
* Bachelor’s degree in Microbiology, Virology, Molecular Biology, or a related field
* A proven ability to develop high technical competence
* Exceptional attention to detail
* Strong communication abilities
Join us and be a part of a team that values growth, quality, and excellence!
Additional Information
APPLY NOW for full consideration, you can be sure that your application will be treated confidentially and impartially, and you will always receive an update within 10 business days.