Matt ScotneyMatt has spent the last 18 years working within the biopharmaceutical industry.  He has held a number of Quality based roles within both the development and manufacture of recombinant proteins and monoclonal antibodies.

The initial part of his career was working in the GMP manufacturing arena within QA validation and in Batch release and API / biological intermediate medicinal product certification.  During this time he was also responsible ensuring the QPs employed by Lonza were sufficiently familiar with Biopharmaceutical product to carry out their duties.

Following this he spent 5 years heading a QA team which supported the Analytical and Process Development and QC, Engineering and Validation function of Lonza Biologics.  This role covered both GMP and non GMP development of processes and methods as well as the GMP testing of bulk product, final product and on-going stability studies.

Most recently he has moved to a new role and is now responsible for the quality management systems at Lonza Slough including the implementation of “a risk based approach to quality” and driving continuous improvement within the pharmaceutical quality system.

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