Daniel Loeven Email & Phone Number

Director, Global Regulatory Affairs and Quality Assurance for Research @ Population Council

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Daniel Loeven Location

New York, NY, US

Daniel Loeven Work

2011 -now Director, Global Regulatory Affairs and Quality Assurance for Research @
2017 -now Associate Director, Regulatory Affairs @
2011 -now Director, Regulatory Affairs and Quality Assurance @
2013 -2020 Senior Manager, Regulatory Affairs @
2011 -2013 Quality Assurance Manager @
2010 -2011 Quality Control Director @ Englewood Lab
2007 -2009 Acting Manager and Team Leader - QC Labs @
1996 -2007 Laboratory Supervisor and Team Leader @ Pfizer, Inc
1986 -1996 Stability Supervisor @ Glaxo-Wellcome
1992 -1996 Supervisor, Stability Laboratory @ Burroughs Wellcome

Daniel Loeven Education

Long Island University
Master’s Degree (Drug Regulatory Affairs)
1998-2000
SUNY Oneonta
BS (Chemistry)
1976-1980

Daniel Loeven Skills

Validation
HPLC
Pharmaceutical Industry
Change Control
Regulatory Affairs
Quality Assurance
Technology Transfer
UV/Vis
Dissolution
Cleaning Validation
Quality Control
GMP
Sop
IND
Regulatory Submissions
CAPA
FDA
GCP
Quality System
GLP
U.S. Food and Drug Administration (FDA)
Good Clinical Practice (GCP)
High-Performance Liquid Chromatography (HPLC)
Corrective and Preventive Action (CAPA)
Good Laboratory Practice (GLP)
Regulatory Filings
Training Videos
Project Management Training
Contractual Agreements
Instrumentation
Molecular Biology
Investigation
Arranging
Electronics
Stability
Strategic Planning
Method Transfers
Ctm
Purchasing
Concepts
Oracle RAC
FIX Protocol
CQE
Packaging
Snda
Academic
OOS
Dispositions
Honor
American
Training
Compliance Management
Analysis
Scheduling
Decommissioning
Internal Controls
Materials
Pharmaceutical Companies
Technical Investigations
Project Management
Documentum
NIR spectroscopy
FTIR
Measurements
Customer Satisfaction
System
Cross Training
NDA
u.s. Food and Drug Administration Fda
Chemistry
Ahead of Schedule
Quality Investigations
CQA
Auditing
Writing
Iso 9000
Reports
Pfizer
Laboratory
Statistical Software
Project Teams
Chemists
Brooklyn
Regulations
Pai
Google Groups
Troubleshooting
Pharmaceutics
Test Methodologies
Problem Analysis
Project Planning
Minitab
Product Transfer
Liaising
Surface Tension
Acting
Regulatory Compliance
Manufacturing Operations
Statistics
Batch Records
Coaching
Good Laboratory Practice Glp
Design
Microbiologists
Stability Testing
Guidelines
Cost Savings
EDRMS
Operations
Manufacturing
Management
Experimental Design
Spectra
Corrective and Preventive Action Capa
Introducing
Data Quality
Meetings
Shelf Life
Hosting
Method Development
Compliance
Rotation
Public Speaking
Gaps
Root Cause
Regulatory Requirements
Dissolution Testing
Leading by Example
New York
Technical Training
Libraries
Problem Solving
UV
Clinical Research
Method Transfer
Initiation
Process Validation
Contract Manufacturing
Internal Audit
Chiral
Supplemental
Technical Support
Testing
High Performance Liquid Chromatography Hplc
Net
Good Clinical Practice Gcp
High Performance Liquid Chromatography
u.s. Food and Drug Administration
Good Clinical Practice
Good Laboratory Practice
Corrective and Preventive Action

Daniel Loeven Summary

Daniel Loeven, based in New York, NY, US, is currently a Director, Global Regulatory Affairs and Quality Assurance for Research at Population Council. Daniel Loeven brings experience from previous roles at Population Council. Daniel Loeven holds a 1998 - 2000 Master’s Degree in Drug Regulatory Affairs @ Long Island University. With a robust skill set that includes Validation, HPLC, Pharmaceutical Industry, Change Control, Regulatory Affairs and more. Daniel Loeven has 3 emails and 1 mobile phone numbers on RocketReach.