Chris Newman
About
Chris Newman is from Shillingford Hill, England, United Kingdom. Chris works in the following industries: "Research Services". Chris is currently Director Of Commercial Operations at Oxford Nanopore Technologies Ltd, located in Oxford, England, United Kingdom. In Chris's previous role as a Associate Director of Customer Services at Oxford Nanopore Technologies Ltd, Chris worked in Oxford, United Kingdom until Jan 2021. Prior to joining Oxford Nanopore Technologies Ltd, Chris was a Associate Director Business Operations at Oxford Nanopore Technologies Ltd and held the position of Associate Director Business Operations at Oxford, United Kingdom. Prior to that, Chris was a Associate Director Biologics Production at Oxford Nanopore Technologies Ltd, based in Oxford, United Kingdom from Oct 2015 to Jun 2018. Chris started working as Cell Team Leader at Nexeon Ltd in Abingdon in Jun 2014. From Apr 2013 to Jun 2014, Chris was Production Team Leader at Nexeon Ltd, based in Abingdon. Prior to that, Chris was a Production Manager at Aptuit from May 2010 to Apr 2013. Chris started working as Team Leader at Aptuit in Jun 2004.
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Chris Newman's current jobs
Chris Newman's past jobs
Enabling scalable business solutions and expanding into new markets.
Leading a team of scientists developing and testing silicon anode materials for lithium ion batteries. Evaluating external technology including due diligence and collaborating with development partners. Internal materials evaluation and performance benchmarking using a variety of cell formats (coin, pouch, cylindrical) and assisting material development teams with failure mode analysis.
Scale up and production of silicon anode materials. Project management of the design and construction of the manufacturing facility including integration of nouvelle technologies and hazardous materials containment. Plant startup and commissioning, ensuring H&S management system and documentation completion. Process development activities.
Production manager at a CRO company working on the scale up and manufacturing of pharmaceuticals for commercial supply and clinical trials. Technology transfer of new processes from development into production on a regular basis. Continuous improvement of operations using LSS methodologies. Expert in cleaning validation of potent compounds. MHRA and FDA audit experience including competition of remedial actions.
Leading a team producing pharmaceuticals for a CRO.
Testing milk/cream/butter at Europe's largest super dairy.