Christopher Lussier

Christopher Lussier Email and Phone Number

Senior Director, Quality, Regulatory, and Clinical Research at Medacta USA, Inc. @ Medacta USA, Inc.
Christopher Lussier's Location
Memphis, Tennessee, United States, United States
Christopher Lussier's Contact Details

Christopher Lussier work email

Christopher Lussier personal email

n/a
About Christopher Lussier

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.

Christopher Lussier's Current Company Details
Medacta USA, Inc.

Medacta Usa, Inc.

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Senior Director, Quality, Regulatory, and Clinical Research at Medacta USA, Inc.
Christopher Lussier Work Experience Details
  • Medacta Usa, Inc.
    Senior Director, Quality, Regulatory, And Clinical Research
    Medacta Usa, Inc. Jan 2022 - Present
    Franklin, Tennessee, Us
    Lead the quality assurance and regulatory initiatives as well as support the clinical research activities for Medacta USA.
  • Medacta Usa, Inc.
    Senior Director, Quality And Regulatory
    Medacta Usa, Inc. Jan 2020 - Dec 2021
    Franklin, Tennessee, Us
    Led the quality assurance and regulatory initiatives for Medacta USA.
  • Medacta Usa, Inc.
    Director, Quality And Regulatory
    Medacta Usa, Inc. Jul 2016 - Dec 2019
    Franklin, Tennessee, Us
    Led the maintenance and continuous improvement of the Quality System for Medacta U.S.A.
  • Nuvasive
    Senior Manager, Quality Engineering
    Nuvasive Mar 2013 - Jul 2016
    San Diego, Ca, Us
    Led 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.
  • Nuvasive
    Manager, Quality Engineering
    Nuvasive Jun 2011 - Mar 2013
    San Diego, Ca, Us
    Managed 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.
  • Medtronic Spine & Biologics
    Senior Quality Engineer
    Medtronic Spine & Biologics Aug 2010 - Jun 2011
    Supported 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.
  • Sandvik Medical Solutions
    Program Manager, Spine
    Sandvik Medical Solutions Sep 2009 - Aug 2010
    Stockholm, Stockholm, Se
    Managed 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.
  • Sandvik Medical Solutions
    Principle Quality Engineer
    Sandvik Medical Solutions Sep 2008 - Sep 2009
    Stockholm, Stockholm, Se
    Managed 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.
  • Sandvik Medical Solutions
    Senior Quality Engineer
    Sandvik Medical Solutions Feb 2008 - Sep 2008
    Stockholm, Stockholm, Se
    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. Implemented the facility's in process inspection software / system and supported the initial development and implementation of the Sandvik Medical Solutions Quality System.
  • Medtronic Spine & Biologics
    Senior Manufacturing Quality Engineer
    Medtronic Spine & Biologics Dec 2006 - Feb 2008
    Supported 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.
  • Medtronic Spine & Biologics
    Design Quality Engineer
    Medtronic Spine & Biologics Nov 2004 - Dec 2006
    Supported 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.
  • Medtronic Spine & Biologics
    Product Compliance Engineer
    Medtronic Spine & Biologics Oct 2000 - Nov 2004
    Managed 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

Quality System Medical Devices Iso 13485 Design Control Validation Manufacturing Quality Management Dmaic Iso Continuous Improvement Six Sigma Cross Functional Team Leadership Quality Control Manufacturing Engineering Capa Quality Auditing Gd&t Process Improvement Root Cause Analysis Supplier Quality Design For Manufacturing Fmea Calibration Kaizen Value Stream Mapping Corrective And Preventive Action Iso 14971 Business Process Improvement Iso Standards Geometric Dimensioning And Tolerancing

Christopher Lussier Education Details

  • The University Of Memphis
    The University Of Memphis
    Mechanical Engineering
  • Union University
    Union University
    Mba

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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