QC Analyst

An opportunity has arisen for a Analyst to join our existing QC team within the Pharmaceutical Development and Support (PDS) department.

 

Key Responsibilities :

• Carry out the Quality Control of raw materials, bulk and finished products in accordance with relevant authorised documentation using HPLC, GC and wet chemical techniques.
• Perform swabbing and analysis of samples for cleaning verification of the pilot production facility.
• Take equal part in the overall running of the laboratory, including equipment maintenance, calibration of apparatus and other general duties such as solvent disposal.
• Perform manual and automated tests and assays in accordance with GMP to a high level of accuracy and precision and to operate associated analytical equipment.

 

You should ideally have the following attributes:

• A degree (or equivalent) in a chemistry-based discipline.
• A minimum of a years’ relevant experience in an analytical testing role, preferably in a GMP environment.
• Some experience in the techniques of HPLC and GC analysis.
• Excellent attention to detail and organisational skills and the ability to self-motivate under your own initiative.
• Collaborative skills to work closely with colleagues and managers.
• Use of software packages, such as Chromatography Data Handling, LIMS and Excel, for the collection, processing and reporting of data.