Christopher Lussier Email and Phone Number
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I have been dedicated to fulfilling customer needs in various project implementations. My focus has always been to identify and understand my internal and external customers to ensure that my personal goals are realized and are aligned with the direction of the organization I support.
Medacta Usa, Inc.
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Senior Director, Quality, Regulatory, And Clinical ResearchMedacta Usa, Inc. Jan 2022 - PresentFranklin, Tennessee, UsLead the quality assurance and regulatory initiatives as well as support the clinical research activities for Medacta USA. -
Senior Director, Quality And RegulatoryMedacta Usa, Inc. Jan 2020 - Dec 2021Franklin, Tennessee, UsLed the quality assurance and regulatory initiatives for Medacta USA. -
Director, Quality And RegulatoryMedacta Usa, Inc. Jul 2016 - Dec 2019Franklin, Tennessee, UsLed the maintenance and continuous improvement of the Quality System for Medacta U.S.A. -
Senior Manager, Quality EngineeringNuvasive Mar 2013 - Jul 2016San Diego, Ca, UsLed the Quality Control, Quality Engineering, and Instrument Servicing teams at the Memphis Distribution Center; which supports daily operational needs such as receiving inspection of medical devices, design transfer as part of the product development process, global temperature monitoring, calibration, instrument refurbishment, and continuous improvement of the operations group. Additionally, supporting the coordination and compliance of the Global Safety Program. -
Manager, Quality EngineeringNuvasive Jun 2011 - Mar 2013San Diego, Ca, UsManaged the Quality Control and Quality Engineering teams at the Memphis Distribution Center, which supports daily operational needs such as receiving inspection of medical devices, design transfer as part of the product development process, and continuous improvement of the operations group. -
Senior Quality EngineerMedtronic Spine & Biologics Aug 2010 - Jun 2011Supported the Product Development Process by developing inspection criteria for medical devices. Participate in print reviews. Support Product CAPA's to: contain affected product, identify root causes, and develop / implement appropriate corrective and preventive actions. Continuously improve the documented quality system. -
Program Manager, SpineSandvik Medical Solutions Sep 2009 - Aug 2010Stockholm, Stockholm, SeManaged 1 Quality Engineer and 1 Manufacturing Engineer to support the spine portion of the business. Supported the QC group to ensure product verification / documentation requirements were in line with the established customer requirements. Quoted Spinal Instrument and Implants to support the needs of the customer. Monitored the production of new product to ensure quality / engineering issues are identified and communicated / resolved with support from the customer as needed. Coordinated / supported the contract review process to ensure customer requirements were identified and implemented throughout the facility. Supported the implementation of Advanced Quality Planning throughout the facility. Supported CAPA’s as necessary to ensure known root causes of product nonconformities are reduced. Monitored in process capabilities of implant and instrument groups and determined if any training or update to Advanced Quality Planning documentation was necessary. Served as the Engineering customer interface to various OEM’s. -
Principle Quality EngineerSandvik Medical Solutions Sep 2008 - Sep 2009Stockholm, Stockholm, SeManaged 2 Quality Engineers, 1 Quality Specialist, and 2 Quality Engineering interns. Participated in contract reviews to ensure customer requirements were realized and implemented. Implemented Advanced Quality Planning throughout the facility to mitigate risk and minimize product nonconformances. Developed inspection criteria and coordinate necessary MSA activities. Completed software validations as needed. Served as the Quality Engineering customer interface to various OEM's. -
Senior Quality EngineerSandvik Medical Solutions Feb 2008 - Sep 2008Stockholm, Stockholm, SeParticipated in contract reviews to ensure customer requirements were realized and implemented. Implemented Advanced Quality Planning throughout the facility to mitigate risk and minimize product nonconformances. Developed inspection criteria and coordinate necessary MSA activities. Completed software validations as needed. Served as the Quality Engineering customer interface to various OEM's. Implemented the facility's in process inspection software / system and supported the initial development and implementation of the Sandvik Medical Solutions Quality System. -
Senior Manufacturing Quality EngineerMedtronic Spine & Biologics Dec 2006 - Feb 2008Supported the Product Development Process by developing inspection criteria for purchased and in-house manufactured devices. Participated in print reviews. Supported Product CAPA's to: contain affected product, identify root causes, and development / implement appropriate corrective and preventive actions. Continuously improved the documented quality system. -
Design Quality EngineerMedtronic Spine & Biologics Nov 2004 - Dec 2006Supported the Product Development Process by ensuring design history files were compliant to FDA QSR / ISO 13485 requirements. Participated in Internal Audits to ensure compliance to FDA QSR and ISO 13485. Coordinated Product CAPA's to: contain affected product, identify root causes, and development / implement appropriate corrective and preventive actions. Continuously improved the documented quality system. -
Product Compliance EngineerMedtronic Spine & Biologics Oct 2000 - Nov 2004Managed the Metrology Lab which was utilized for analysis of returned devices as well as measurement of customs and specials devices. Performed source inspections to assist with the verification of launch product. Managed the investigation of potential product quality issues (internal and external). Continuously improved the documented quality system.
Christopher Lussier Skills
Christopher Lussier Education Details
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The University Of MemphisMechanical Engineering -
Union UniversityMba
Frequently Asked Questions about Christopher Lussier
What company does Christopher Lussier work for?
Christopher Lussier works for Medacta Usa, Inc.
What is Christopher Lussier's role at the current company?
Christopher Lussier's current role is Senior Director, Quality, Regulatory, and Clinical Research at Medacta USA, Inc..
What is Christopher Lussier's email address?
Christopher Lussier's email address is cl****@****ive.com
What is Christopher Lussier's direct phone number?
Christopher Lussier's direct phone number is +190153*****
What schools did Christopher Lussier attend?
Christopher Lussier attended The University Of Memphis, Union University.
What skills is Christopher Lussier known for?
Christopher Lussier has skills like Quality System, Medical Devices, Iso 13485, Design Control, Validation, Manufacturing, Quality Management, Dmaic, Iso, Continuous Improvement, Six Sigma, Cross Functional Team Leadership.
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