Cameron Klug Email and Phone Number
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Experienced Quality Leader with competencies in Medical Device, Automotive, and Industrial Products. Data driven problem solver with a strong foundation in numerous manufacturing processes, CAPA/Six Sigma, and Lean methodology. Change agent with a passion for continuous improvement and operational excellence. Committed mentor who takes pride in helping team members develop and achieve their goals.
Nuvasive
View- Website:
- nuvasive.com
- Employees:
- 1
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Director Of QualityNuvasive Sep 2017 - PresentSan Diego, Ca, Us- Maintained and improved on QMS to ensure compliance with CFR820 and ISO13485 (BSI) - Management representative for 3rd party registrars and government agencies. - Quality planning and project planning for large scale projects including M&A and new facility start up.- Diligence for M&A targets. - Change management including PMA supplements and MDR tech files.- Validation Master Planning- Leadership of Corrective/Preventative Action program - Author and facilitate Management Review.- Implement and maintain risk management systems.- Coach, mentor, train, and evaluate a staff of ~60 direct and indirect reports - Develop Standard Operating Procedures and Work Instructions.- Project leadership with cross functional departments like Development, Regulatory, Marketing, Legal, and Clinical affairs.- Strategic planning and establishing quality team goals to align with business goals.- Design Transfer -
Vice President Of QualityTomz Corporation Apr 2024 - Oct 2024Berlin, Ct, Us -
Director Of Quality At Globus Medical (Fka: Nuvasive)Globus Medical Sep 2017 - Sep 2024Audubon, Pa, Us -
Quality ManagerAvalign Technologies Jul 2016 - Sep 2017Rosemont, Il, Us• Maintained and improved on QMS to ensure compliance with CFR820 & ISO13485 (BSI)• Manage Corrective/Preventative Action program (Customer/Internal/Suplier/Preventative)• Manage and maintain validation program.• Author and facilitate Management Review.• Implement and maintain risk management systems.• Coach, mentor, train, and evaluate a staff of 26. (Quality Engineers, Inspectors, Auditors, Technicians, Document and Record Control)• Develop Standard Operating Procedures and Work Instructions.• Review and approve engineering change requests.• Manage quality team goals to align with business goals.• Manage and perform internal and supplier audits.• Asist with design transfer activities. -
Plant Quality ManagerParker Hannifin Oct 2014 - Jul 2016Cleveland, Oh, Us• Maintained and improved on QMS to ensure compliance with ISO9001 registrar (DNV)• Author and facilitate Management Review• Manage Corrective/Preventative Action program (Customer/Internal/Suplier/Preventative) • Supplier Evaluation / Development • Train and facilitate quality culture and data driven problem solving. (PDCA-10 Step)• Implement process validation program• Track trend and facilitate visual management and problem solving for quality metrics.• Implement/Facilitate value added system for managing PFMEA’s• Interface with customers for and manage customer complaint system • Train and coach high performance teams, quality, and manufacturing personnel • Create Procedures, Work Instructions, & Standard work • Review and approve engineering change requests.• Manage quality team goals to align with business goals.• Review RFQs and give feedback to sales team.• Manage customer quality excellence programs.• Perform and manage internal and external audits. -
Quality Engineer/SupervisorSymmetry Medical May 2010 - Oct 2014Warsaw, In, Us• Initiate APQP and work with customers, manufacturing engineering and production to manage project launches and ensure successful device transfer • Author and present management reviews• Assist with supplier quality functions (scorecards, improvement plans, SCAR’s, APQP)• Act as team member management representative for audit functions. (BSI, FDA, Customer Audits)• Corporate Administrator for SPC and Qualtrend (Web based Quality Reporting Tool)• Track and trend quality metrics• Develop inspection methods for in-process inspection and first article inspection• Write control plans and (P)FMEA• Conduct statistical process studies • Measurement Systems Analyses • Change management (supplier and engineering change requests)• Champion and manage internal and external CAPA’s • Develop and/or Modify work instructions and/or SOP’s -
Multiple Positions (Program Manager, Supervisor, Lead Quality Tech)Ward Corporation Aug 1999 - Jan 2009• Oversaw and assisted in the completion of all PPAPs • Six Sigma Project • Set-up and trouble shot programming machining, permanent molding and sand casting.• Direct and prioritize daily goals for 2nd and 3rd shift supervisors, developed machine schedules Gage calibration and MSA. • CMM programming
Cameron Klug Skills
Cameron Klug Education Details
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Purdue UniversityIndustrial Engineering Technology -
Purdue University Fort WayneIndustrial Engineering Technology
Frequently Asked Questions about Cameron Klug
What company does Cameron Klug work for?
Cameron Klug works for Nuvasive
What is Cameron Klug's role at the current company?
Cameron Klug's current role is Vice President of Quality at TOMZ Corporation.
What is Cameron Klug's email address?
Cameron Klug's email address is ck****@****ech.com
What is Cameron Klug's direct phone number?
Cameron Klug's direct phone number is +126049*****
What schools did Cameron Klug attend?
Cameron Klug attended Purdue University, Purdue University Fort Wayne.
What skills is Cameron Klug known for?
Cameron Klug has skills like Spc, Lean Manufacturing, Fmea, Continuous Improvement, Manufacturing, Six Sigma, Value Stream Mapping, Capa, Root Cause Analysis, Medical Devices, Apqp, Iso 13485.
Who are Cameron Klug's colleagues?
Cameron Klug's colleagues are Erin Quinn, Dylan Azinger, Tabea Düsterhöft, Nina Hall, Benjamin Falls-Simison, David Baker, Bs, Cnim, Rpsgt, Jennifer Labrie.
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