Do you want to work for a progressive pharmaceutical company who are growing and have a clear and defined path for the future? We are currently recruiting for an experienced pharmaceutical QC Analyst on permanent contracts to join their team.
To perform all required Analytical testing for the support of incoming goods assessment, batch release, utilities, stability monitoring and non-routine requests in accordance with GLP, GMP and Regulatory Requirements
Use QC laboratory equipment (eg HPLC/GC/IR/Auto-titrations/wet chemistry) to ensure chemicals and bulk liquids conform to specification
Monitor the quality of components, raw materials, products and production processes by inspection, sampling and/or analysis.
Develop robust and repeatable new tests methods and modify existing test methods for both chemical raw materials and bulk liquids.
Perform and report analysis of customer complaint samples, raw material samples, utility samples and non-routine samples
Perform internal inspections within the QC Analytical Department to ensure ongoing compliance and implement improvements
TO keep all records up to date
What we need?
The role requires someone with excellent exposure to the pharmaceutical industry in the role as a QC Analyst with heavy use of HPLC (GC, KF…) and other analytical techniques. Other factors important to this role are -
Dealing with unplanned events and/ taking the lead in non-routine situations
A qualification to support your application (BSc, MSc, PhD...)
To get the ball rolling please press the apply now button on this page