Christopher Clegg
New York, NY
currently: Please hire me!
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Work history
Associate Director QA/RA
How would you describe your time at DPC/Siemens?
With a staff of 14 administer Recall, Medical Device Reporting and required follow-ups with the FDA as well as communicate with European affiliates to assure adherence to GMP's and ISO Quality System standards while maintaining workflow through Receiving, In-Process and Final Inspection test points. Additionally perform internal, supplier and affiliate audits and review and approve corrective actions with Purchasing and Senior Management, as well as chair Material Review Board and authorize design, document and process changes. Also create departmental budget and monitor performance against budget as well as coordinate UL, ISO, FDA and customer audits and administer training of GMP, ISO and inspection. Other responsibilities include reviewing the Quality System, leading Continuous Improvement, serving as the Management Representative and monitoring quality indicators from the field and in-house, trending returns and assuring root-cause is identified. Additionally manage vendor program that includes an annual forum for zero-defect, cost of rejection trending, process controls and historical performance data, and identification of annual standards. Also lead Process/Quality System Measurement and Improvement Team.... 
QA Supervisor
How would you describe your time at Pfizer/Howmedica?
With a staff of 60 union employees lead development of 2nd shift Quality and Packaging functions to support company growth of 25% while maintaining work flow through a 48 CNC machine production facility and directing receiving, in-process and final inspection areas equipped with Coordinate Measuring Machines, Optical Comparators, Surface Plates and related tools. Other responsibilities included authorizing rework and process changes, while assuring staff was trained on inspection techniques and blueprint reading....
MLA
January 1986 to January 1990
How would you describe your time at MLA?
With a staff of 7 responsible for inspection of receiving and in-process as well as in-house machine shop, training of staff in GMP, ISO, and inspection techniques. Also established a source inspection program, Material Review Board and vendor audit program.
Quality Supervisor
How would you describe your time at Cavitron Ultrasonics?
With a staff of 5 union employees directed receiving inspection as well as Shipping/Receiving, Material Review Board and vendor audits.
Quality Supervisor
How would you describe your time at Union Carbide?
Started as Inspector, promoted to Group Leader then Supervisor.
Supervised the Receiving Inspection area and performed source inspection, vendor corrective actions and audits.
Education
General
How would you describe your time at Nyack High?
High School
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