QC Manager

I am partnered exclusively with an internationaladvanced pharmaceutical company that are growing key leadership andmanagement positions across UK sites.Thisspecific hire will take management and scheduling responsibilities forall site Quality Control (QC) activities with strong focus on methoddevelopment oversight and team leadership. A strong focus on the fullvalidation lifecycle from beginning to end is crucial in combinationwith solid regulatory understanding from an analytical chemistryperspective.Whilst this will not be hands on dayto day, given the size of the unit, you will need to be comfortablebeing in the laboratory and supporting the team, especially with outof specification challenges and development and validation activities.If you are looking for a varied position thatoffers you a chance to make a real impact on your own site and playthe key part in how the QC team delivers both now and for futuregrowth plans, please apply below or contact Mark Bux-Ryan for furtherinformation.Key experience:Experienced QC/Analytical Chemistry manager or supervisorwithin a pharmaceutical GMP environmentTechnical experiencewill include some of the following – HPLC, GC, Radio TLCExcellent understanding of pharmacopoeiaKnowledgeand experience of method validation activities from beginning to endQC, quality, control, chromatography,HPLC, GC, chemistry, analytical, method, validation, development, IQ,OQ, PQ, PQ, radiopharmaceutical, TLC, supervisor, leader, manager,group, lead
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