Jackie Ferro Email & Phone Number
VP of Regulatory Affairs, Codman Surgical Specialty @ Integra LifeSciences
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Jackie Ferro Location
- New York, NY, US
Jackie Ferro Work
- 2024 - now VP of Regulatory Affairs, Codman Surgical Specialty @
- 2015 - now Advisory Council Member @
- 2015 - now Advisory Council Member @
- 2022 - 2024 VP of Regulatory Affairs @
- 2020 - 2022 Global Vice President Regulatory and Quality Assurance @
- 2019 - 2020 Global Technology and Engineering Medical Device and Combination Products External Supply @
- 2017 - 2019 Vice President Regulatory Affairs and Quality Assurance @
- 2015 - 2017 Chief Compliance Officer @
- 2013 - 2015 Vice President Quality and Regulatory Assurance @
- 2012 - 2013 Director Quality and Management Representative @
- 2010 - 2011 Director Quality and Management Representative @
- 2007 - 2010 Director Quality Assurance @
- 2004 - 2007 Director, Quality Assurance and Validation Compliance @
- 2003 - 2004 Validation Manager @
- 1997 - 2003 Senior Project Manager @
- 1992 - 1997 Engineer @
Jackie Ferro Education
- New Jersey Institute of Technology
BS (Chemical Engineering)
1988 - 1992 - Roselle Catholic
High School Diploma
1985 - 1988
Jackie Ferro Skills
- 21 CFR
- Verification and Validation V&V
- u.s. Food and Drug Administration Fda
- Lead Quality Auditor
- Regulatory Requirements
- Manufacturing
- Standard Operating Procedure Sop
- ISO 14971
- Supplier Quality
- Software Documentation
- Cross Functional Team Leadership
- 21 CFR Part 11
- Cross Functional Team
- Fda Remediation
- Validation
- V&V
- Regulatory Affairs
- Aseptic Processing
- Director of Quality
- Quality Auditing
- ISO Standards
- Sop
- Customer Service
- Change Control
- Computer System
- ISO
- GxP
- Six Sigma
- GMP
- Strategic Planning
- Root Cause Analysis
- Corrective and Preventive Action Capa
- Quality Control
- R&d
- Research and Development R&d
- CAPA
- GLP
- DMAIC
- FDA
- Testing
- Quality Management
- Management
- Design Control
- Quality Assurance
- Pharmaceutical Industry
- Computer System Validation
- Good Laboratory Practice Glp
- Good Manufacturing Practice Gmp
- u.s. Food and Drug Administration
- Corrective and Preventive Action
- Verification and Validation
- Standard Operating Procedure
- Research and Development
- Good Manufacturing Practice
- Good Laboratory Practice
Jackie Ferro Summary
- Jackie Ferro, based in New York, NY, US, is currently a VP of Regulatory Affairs, Codman Surgical Specialty at Integra LifeSciences. Jackie Ferro brings experience from previous roles at GLG, AlphaSights, Kohler Ventures and Topcon Healthcare. Jackie Ferro holds a 1988 - 1992 BS in Chemical Engineering @ New Jersey Institute of Technology. With a robust skill set that includes 21 CFR, Verification and Validation V&V, u.s. Food and Drug Administration Fda, Lead Quality Auditor, Regulatory Requirements and more. Jackie Ferro has 5 emails and 3 mobile phone numbers on RocketReach.
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