Christopher Ignace
Senior Vice President, Quality, Scientific and Regulatory Affairs at Nusano | Mesa, Arizona, United States
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Christopher Ignace is a seasoned pharmaceutical professional with over 33 years of extensive experience, specializing in nuclear drugs and the development of both new and generic drug products. His career has been marked by a deep commitment to the pharmaceutical industry, where he has honed his expertise across various stages of the product life cycle, from initial formulation chemistry to quality control and regulatory compliance. Christopher's comprehensive understanding of GMP (Good Manufacturing Practices) and clinical operations has positioned him as a key player in ensuring that products not only meet but exceed industry standards.
Currently, Christopher is exploring senior leadership opportunities that will allow him to leverage his rich background in nuclear drug development. He is particularly drawn to roles that present strategic challenges, especially those involving new technologies that can transform patient care and enhance therapeutic outcomes. His belief in the power of team integration and effective planning is evident in his leadership style, where he emphasizes goal setting and risk management to drive project success.
Throughout his career, Christopher has successfully led key projects that have resulted in the approval of innovative drug therapies, demonstrating his ability to navigate complex regulatory landscapes and collaborate with cross-functional teams. His skills in pharmacology, formulation chemistry, and technical support have been instrumental in advancing product pipelines and ensuring compliance with quality standards. As he seeks to transition into a senior role in early 2024, Christopher is eager to contribute his expertise to organizations that prioritize innovation and excellence in the pharmaceutical sector.
Senior Vice President, Quality, Scientific and Regulatory Affairs at Nusano in May 2024 to Present
N/A at N/A in January 2024 to May 2024
Vice President, Scientific Affairs and Strategic Partner Management at Cardinal Health in January 2021 to December 2023
Vice President, Medical, Scientific and Regulatory Affairs at Cardinal Health in August 2017 to December 2020
Vice President, Technical Operations at Cardinal Health in February 2013 to July 2017
Senior Director, Regulatory Affairs at Cardinal Health in October 2010 to January 2013
Consultant, Pharmaceutical Industry at Self-employed in October 2009 to October 2010
Senior Director, Product Development at Abraxis BioScience in September 2008 to August 2009
Vice President, Product Development at Zila Pharmaceuticals in January 2005 to January 2008
Vice President, Clinical Operations at Zila Pharmaceuticals in January 2002 to January 2004
Director and General Manager at Zila Pharmaceuticals in January 1999 to January 2002
Manager, Product Development at Teva Pharmaceuticals in January 1996 to January 1999
Senior Scientist, Research and Development at Viatris in January 1995 to January 1996
Group Leader, Product Development at PhotoMedex in January 1992 to January 1995
Post-doctoral Fellow/Prior Research at University of Iowa in February 1991 to March 1992
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Senior Administration
Corporate Strategy
Product Specifications
Team Management
Supplier Quality
Regulatory Standards
Quality Control
Quality Assurance
Physicochemistry
Animal Models
Molecular & Cellular Biology
Pharmacology
Drug Design
Pharmacodynamic modeling
Analytical Chemistry
Clinical Trial Material Production
Analytical Method Validation
Formulation Chemistry
Manufacturing Scale-up
Business Strategy
Technical Operations
FDA GMP
Quality and Regulatory Compliance
Clinical Operations
Investigator Brochures
Manufacturing Operations Management
Business Intelligence (BI)
Business Partner Support
New Business Development
Global Compliance
Technical Support
Risk Management
CMC development
Regulatory Filings
Quality System Compliance
Department Management
Budgeting
FDA Regulatory (multiple approvals)
Product Development
Validations
Quality System
Medical Education
CRO Management
Regulatory Compliance
Clinical Development
Clinical Trials
Drug Development
FDA
Formulation
GMP
Leadership
Pharmaceutical Industry
Regulatory Affairs
Strategy
V
Medical Devices
Technology Transfer
CRO
Pharmaceutics
Validation
Biotechnology
U.S. Food and Drug Administration (FDA)
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Discover more about NusanoWhat is Christopher Ignace email address?
Email Christopher Ignace at [email protected] and [email protected]. This email is the most updated Christopher Ignace email found in 2026.
What is Christopher Ignace phone number?
Christopher Ignace phone number is +14806783117 and +16024546735.
How to contact Christopher Ignace?
To contact Christopher Ignace send an email to [email protected] or [email protected]. If you want to call Christopher Ignace try calling on +14806783117 and +16024546735. (updated on October 29, 2024)
What is Christopher Ignace net worth?
Christopher Ignace has an estimated net worth of $750,000 to $999,999
What company does Christopher Ignace work for?
Christopher Ignace works for Nusano
What is Christopher Ignace's role at Nusano?
Christopher Ignace is Senior Vice President, Quality, Scientific and Regulatory Affairs
What industry does Christopher Ignace work in?
Christopher Ignace works in the Hospitals And Health Care industry.
Christopher Ignace Email Addresses
Christopher Ignace Phone Numbers
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