We are now recruiting an experienced QC Analyst to join our Raw Materials team.

What you will do

Responsible for the analysis process in accordance with Current Good Manufacturing Practice (cGMP) at our Romford site.

Day-to-day responsibilities

• Analysis of raw materials batches.
• Support the investment in facility expansion and new product launches across multiple dosage forms.
• Able to carry out associated laboratory tasks such as sampling, housekeeping, preparations of standardisation of reagents, the care of apparatus and the instrumentation.
• Ensure that Health and Safety and COSHH are adhered to throughout the laboratory.
• Perform relevant Quality Control responsibilities and ensure laboratory compliance requirements, testing protocols and safety standards are met.

About you

Our ideal candidate will have knowledge of cGMP and experience working in the pharmaceutical ...