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QC Analyst - Pharmaceuticals in Hertfordshire


Achieves competency in Analytical Chemistry laboratory methods and procedures.
Performs routine and non-routine testing activities of Raw Materials, intermediates, bulk and finished packaged samples in compliance with authorised test procedures using HPLC, GC, IR, UV, Wet chemical techniques.
Trains other QC analysts in laboratory methods and procedures when required.
Writes and reviews laboratory SOPs and WIs as directed.
Ensures QC activities are carried out in compliance with cGMP and company quality standards.
Is an active member of the QC group and provides assistance with other group activities as required and communicates relevant issues to the QC Manager, anticipates and plans for future requirements in the area.
Deals with non-conformances/ deviations in an accurate and timely manner.


As a successful candidate you will need to have previous experience within a QC laboratory, a strong knowledge of HPLC and GC including method development (desired) analysis and an understanding of Good Manufacturing Practices.

A minimum of 1 years experience in an analytical laboratory testing environment preferably within the pharmaceutical industry.






£20,000 to £25,000
£18k - £22k

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