Eric Cardwell Email & Phone Number
Director, Regulatory Information Management & Lifecycle Management @ AbbVie
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Eric Cardwell Location
- Chicago, IL, US
Eric Cardwell Work
- Director, Regulatory Information Management & Lifecycle Management @ (April 2019 - Present)
- Director, Combination Product Development @ (March 2017 - April 2019)
- Director Process Excellence Regulatory Affairs @ (June 2014 - March 2017)
- Director Quality Regulatory Affairs Presource @ (February 2012 - June 2014)
- Sr. Manager, Commercial Quality @ (November 2010 - February 2012)
- Quality Manager @ (May 2008 - November 2010)
- Program Manager CQE, CSSBB @ (March 2006 - May 2008)
- Continuous Improvement Manager @ (July 2002 - March 2006)
- Quality Analytical Technician @ (July 2000 - July 2002)
Eric Cardwell Education
- Roosevelt University
Master Of Business Administration (Business Administration)
2006-2010 - University of Illinois at Chicago
Bachelor Of Science (Biology, Spanish)
1996-2002
Eric Cardwell Skills
- Six Sigma
- ISO 13485
- Root Cause Analysis
- DMAIC
- Continuous Improvement
- CQE
- Quality System
- CAPA
- FDA
- Lean Manufacturing
- Quality Assurance
- V&V
- 21 CFR Part 11
- TQM
- ISO
- FMEA
- Manufacturing Operations Management
- Design Control
- 5S
- Kaizen
- Medical Devices
- ISO 14971
- Sop
- Manufacturing
- Validation
- GMP
- Program Management
- Quality Auditing
- Quality Management
- Minitab
- Change Control
- R&D
- Black Belt
- Manufacturing Operations
- Value Stream Mapping
- Cross-functional Team Leadership
- Operational Excellence
- Aseptic Processing
- Design for Manufacturing
- Product Launch
- Design of Experiments
- Supplier Quality
- Quality Control
- SPC
- GxP
- Regulatory Affairs
- Product Development
- FDA GMP
- Computer System Validation
- Iso 9000
- Accountability
- Coaching & Mentoring
- Combination Product
- Continuous Process Improvement
- Data Analysis
- Device Design Controls
- Employee Training
- External Audits
- Failure Mode and Effects Analysis (FMEA)
- Good Manufacturing Practice (GMP)
- IDMP
- Lean Six Sigma
- Manufacturing Process Improvement
- Metrics
- New Product Development
- Procedure Development
- Process Optimization (Manufacturing)
- Process Quality Improvement
- Product Launches
- Product Lifecycle Management
- Product Master Data
- Project Management
- Regulatory Affaris
- Regulatory Agencies
- Regulatory Compliance
- Regulatory Information Management
- Regulatory Requirements
- Risk Management
- Six Sigma Black Belt
- Six Sigma Green Belt
- Vendor Management
- Verification and Validation
- eCTD
- xEVMPD
Eric Cardwell Summary
- Eric Cardwell, based in Chicago, IL, US, is currently a Director, Regulatory Information Management & Lifecycle Management at AbbVie. Eric Cardwell brings experience from previous roles at AbbVie, Cardinal Health and Hospira. Eric Cardwell holds a 2006 - 2010 Master Of Business Administration in Business Administration @ Roosevelt University. With a robust skill set that includes Six Sigma, ISO 13485, Root Cause Analysis, DMAIC, Continuous Improvement and more. Eric Cardwell has 2 emails and 2 mobile phone numbers on RocketReach.
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