Senior Director, Quality, Regulatory, And Clinical Research
CurrentLead the quality assurance and regulatory initiatives as well as support the clinical research activities for Medacta USA.
Jan 2022 - Present
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Christopher Lussier Email & Phone Number
Senior Director, Quality, Regulatory, and Clinical Research at Medacta USA, Inc.
at
Medacta USA, Inc.
1 work email found
@nuvasive.com
5 phones found area 901, 312, and 858
LinkedIn matched
✓ Verified August 2026
4 data sources
Profile completeness 100%
Current company
Role
Senior Director, Quality, Regulatory, and Clinical Research at Medacta USA, Inc.
Location
Memphis, Tennessee, United States
Who is Christopher Lussier? Overview
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Quick answer
Christopher Lussier is listed as Senior Director, Quality, Regulatory, and Clinical Research at Medacta USA, Inc. at Medacta USA, Inc., based in Memphis, Tennessee, United States. AeroLeads shows a work email signal at nuvasive.com, phone signal with area code 901, 312, 858, and a matched LinkedIn profile for Christopher Lussier.
Christopher Lussier previously worked as Senior Director, Quality, Regulatory, and Clinical Research at Medacta Usa, Inc. and Senior Director, Quality and Regulatory at Medacta Usa, Inc.. Christopher Lussier holds Bsme, Mechanical Engineering from The University Of Memphis.
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Email format at Medacta USA, Inc.
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{first_initial}{last}@nuvasive.com
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Profile bio
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.
Listed skills include Quality System, Medical Devices, Iso 13485, Design Control, and 26 others.
Current workplace
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12 roles
Christopher Lussier work experience
A career timeline built from the work history available for this profile.
Senior Director, Quality And Regulatory
Led the quality assurance and regulatory initiatives for Medacta USA.
Jan 2020 - Dec 2021
Director, Quality And Regulatory
Led the maintenance and continuous improvement of the Quality System for Medacta U.S.A.
Jul 2016 - Dec 2019
Senior Manager, Quality Engineering
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.
Mar 2013 - Jul 2016
Manager, Quality Engineering
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.
Jun 2011 - Mar 2013
Senior Quality Engineer
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.
Aug 2010 - Jun 2011
Program Manager, Spine
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.
Sep 2009 - Aug 2010
Principle Quality Engineer
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.
Sep 2008 - Sep 2009
Senior Quality Engineer
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.
Feb 2008 - Sep 2008
Senior Manufacturing Quality Engineer
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.
Dec 2006 - Feb 2008
Design Quality Engineer
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.
Nov 2004 - Dec 2006
Product Compliance Engineer
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.
Oct 2000 - Nov 2004
2 education records
Christopher Lussier education
Bsme, Mechanical Engineering
The University Of Memphis
Mba
Union University
FAQ
Frequently asked questions about Christopher Lussier
Quick answers generated from the profile data available on this page.
What company does Christopher Lussier work for?
Christopher Lussier works for Medacta USA, Inc..
What is Christopher Lussier's role at Medacta USA, Inc.?
Christopher Lussier is listed as Senior Director, Quality, Regulatory, and Clinical Research at Medacta USA, Inc. at Medacta USA, Inc..
What is Christopher Lussier's email address?
AeroLeads has found 1 work email signal at @nuvasive.com for Christopher Lussier at Medacta USA, Inc..
What is Christopher Lussier's phone number?
AeroLeads has found 5 phone signal(s) with area code 901, 312, 858 for Christopher Lussier at Medacta USA, Inc..
Where is Christopher Lussier based?
Christopher Lussier is based in Memphis, Tennessee, United States while working with Medacta USA, Inc..
What companies has Christopher Lussier worked for?
Christopher Lussier has worked for Medacta Usa, Inc., Nuvasive, Medtronic Spine & Biologics, and Sandvik Medical Solutions.
How can I contact Christopher Lussier?
You can use AeroLeads to view verified contact signals for Christopher Lussier at Medacta USA, Inc., including work email, phone, and LinkedIn data when available.
What schools did Christopher Lussier attend?
Christopher Lussier holds Bsme, Mechanical Engineering from The University Of Memphis.
What skills is Christopher Lussier known for?
Christopher Lussier is listed with skills including Quality System, Medical Devices, Iso 13485, Design Control, Validation, Manufacturing, Quality Management, and Dmaic.
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