Matthew Cheetham

Experience

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  Clean Harbors

  Aug 2006 - now

  -Management of two employees working at a client site-Management of multiply waste streams: Hazardous, non-hazardous, wastewater, biological and lab packs -Radioactive Waste Management-Waste Water Tank and Cylinder management-Manifest management in shipping of non-hazardous, hazardous, and biological waste streams-Keeping training current for RCRA, DOT, Chemist courses, cGMP’s-Management if vendors at employee locations -24/7 365 Emergency spill response for vendor locations-Forklift certificated Show less

  • Household Hazardous Waste Tech III

    Aug 2006 - now

  • Lead InSite Chemist

    Sept 2013 - Oct 2014

  • InSite Chemist

    Jan 2010 - Sept 2013

  • InSite Technician

    Aug 2006 - Jan 2010
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  Genentech

  Nov 2014 - now

  Responsible for producing innovative biotherapeutic medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environment, and maintain areas in high state of inspection preparedness. Operates production equipment for cell culture or purification that may include culture growth, process monitoring, sampling, harvesting, purification, formulation, freeze thaw and transfer. Performs media/buffer solution preparation operations. Maintains records and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Responsible for being proficient in two or more functional areas and applies expert knowledge of mechanical, scientific principles, processes and biopharmaceutical processing equipment. Show less Responsible for producing innovative biotherapeutic medicine by interfacing with highly automatedproduction systems and controls in cGMP manufacturing environment, and maintain areas in highstate of inspection preparedness. Operates production equipment for cell culture or purificationthat may include culture growth, process monitoring, sampling, harvesting, purification,formulation, freeze thaw and transfer. Performs media/buffer solution preparation operations.Maintains records and clean room environment to comply with regulatory requirements utilizingcurrent Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP).Responsible for being proficient in two or more functional areas and applies expert knowledge ofmechanical, scientific principles, processes and biopharmaceutical processing equipment. Show less Responsible for performing duties in the Materials Management function (GMP receipt, quarantine andsampling, shipping to include raw materials and bulk drug substance, non-GMP receiving/delivery).Materials maybe of a hazardous/ controlled nature requiring regulatory endorsements prior to handling. Verifies quantity and conformance of materials; prepares records of materials shipped and boxes, and prepare parts and tooling for special shipment. This position can also involve Materials Management business requirements such as developing reports, preparing metrics and/or analyzing data, support site Change controls and Discrepancy management. Show less

  • Master Tech Bioprocess

    Apr 2020 - now

  • Lead Senior Bioprocess Technician

    Apr 2017 - Apr 2020

  • Pharmaceutical Materials Specialist

    Nov 2014 - Apr 2017