Maya Davis
Ex-FDA pharma GMP expert. Compliance and regulatory consultant. Scientist.
- Role
- Senior Vice President Regulatory Compliance at ELIQUENT Life Sciences
- Location
- Hartford, CT, US
- LinkedIn followers
- 500 followers
About Maya Davis
Maya is a 16 year veteran of FDA and works as a regulatory compliance consultant in medical products. Her background in FDA CGMP experience includes inspections, pre-approvals, compliance, mutual recognition, and quality surveillance. She is an expert at identifying and mitigating risks to help clients gain and maintain market authorization.
Experience
Senior Vice President Regulatory Compliance
Mar 2025 — Present · Washington, DC, US
Education
Yale University
Ph.D., Pharmacology
2005 — 2009
Amherst College
B.A., Neuroscience
1998 — 2002
Yale University
Master of Philosophy (M.Phil.), Pharmacology
2002 — 2003
Yale University
Master of Science (M.S.), Pharmacology
2003 — 2005
Skills
- Animal Models
- Science
- Biochemistry
- Quick Thinker
- Research
- Regulatory Requirements
- Process Transitioning
- Evidence Collection
- Problem Solving
- Creativity
- Organization
- Scientific Writing
- Quality Control
- Forecasting
- Statistics
- Multi Tasking
- Cgmp Practices
- Life Sciences
- Work Independently with Minimal Supervision
- Self-Driven
- Communication
- Analytical Reasoning
- Microsoft Office
- Pcr
- Process Improvement
- Molecular Biology
- Negotiation
- Time Management
- Quality Assurance
- Trend Analysis
- Public Speaking
- Cell Biology
- Data Analysis
- Pharmacology
- Cell Culture
- Neuroscience
- Western Blotting
- Management
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