Rose
Quality Program Manager at Eurofins | EAG Laboratories | United States
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Quality Program Manager at Eurofins | EAG Laboratories in September 2023 to Present
Quality Assurance Manager at Sentio BioSciences LLC in October 2021 to September 2023
Quality Assurance Management at Zydus Pharmaceuticals (USA) Inc. in August 2011 to October 2021
Quality Assurance Professional at KV Pharmaceutical in January 1998 to August 2011
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Webster University, Bachelor’s Degree
St. Louis Community College, Associate’s Degree
Faculty of Engineering Blaz Jurjev Trogiranin - Croatia, Major: Electrical & Mechanical Engineering
Faculty of Electrical Engineering, Mechanical Engineering and Naval Architecture, Split Croatia
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Quality Assurance Manager
Director of Quality Assurance - Quality Assurance Manager - Quality Lab Manager - Quality Specialist
ISO 17025:2017 Certified Lab Manager
ISO 17025 Lead Auditor (Exemplar Global Certified)
ISO 31000 Risk Management Guidelines
ISO 31000 Good Documentation Practice
ISO 31000 Failure Mode and Effects Analysis (FMEA).
VP Quality - Director of Quality - Quality Manager - Quality Engineer - Supplier Quality Engineer
ICH Quality Guidelines: | Q1A-Q1F Stability | Q2 Analytical Validation | Q3A - Q3E Impurities | Q4A - Q4B Pharmacopeias | Q5A - Q5E Quality of Biotechnological Products | Q6A-Q6B Specifications | Q7 GMP| Q8 Pharmaceutical Development | Q9 Quality Risk Management | Q10 Pharmaceutical Quality System | Q11 Development and Manufacture of Drug Substances | Q12 Lifecycle Management | Q13 Continuous Manufacturing of Drug Substances and Drug Products | Q14 Analytical Procedure Development |
Regulatory Compliance
Continuous Improvement
Specifications
Metod Validation
Technical Writing
Method Transfer
Method Verification
Analytical Techniques and Quality Guidelines for Laboratory
Medical Devices Stability Program
Labeling Expiration Dating System of Reagents and Solutions
Deviations Investigations
Data Integrity
Out of Specification Investigation Phase 1 and Phase 2
Change Management
Reference Standards Reference Material
Analytical Methods Development
ISO 14971 Risk Management
Laboratory Safety System
High-Performance Liquid Chromatography (HPLC)
Gas Chromatography
Installation Qualification (IQ)
Operational Qualification (OQ)
Performance Qualification (PQ)
Contract Laboratory Operations
Analytical Data Quality Manager Review and Approval
Laboratory Out of Service Procedure
ISO 13485
Medical Device R&D
Medical Device Quality Assurance
Medical Devices Laboratory Testing
Pharmaceutical Quality System
Good Manufacturing Practice (GMP)
Pharmaceutical Development”
Quality Risk Management
ICH Q1A(R2): Stability testing of new drug substances and products
ICH Q1B: Photostability testing of new drug substances and products
ICH Q1C: Stability testing for new dosage forms
ICH Q3A(R2): Impurities in new drug substances
ICH Q3B(R2): Impurities in new drug products
ICH Q3D(R2): Guideline for elemental impurities
ICH Q4B: Evaluation and recommendation of pharmacopeial texts for use in the ICH regions
ICH Q8: Pharmaceutical development
ICH Q9: Quality risk management
ICH Q10: Pharmaceutical quality system
ICH Q11: Development and manufacture of drug substances
ICH Q13: Guideline on continuous manufacturing of drug substances and drug products
ICH Q10 Development and Manufacture of Drug Substances
Strategic Leadership
Conflict Management
Intercultural Communication
Conflict Resolution
Intercultural Communication and Conflict Resolution
Resilient Leadership
GMP
FDA
Change Control
Quality Assurance
Pharmaceutical Industry
Validation
SOP
Technology Transfer
Quality Auditing
21 CFR Part 11
Corrective and Preventive Action (CAPA)
Standard Operating Procedure (SOP)
Data Analysis
Research and Development (R&D)
Quality System
Pharmaceutics
Regulatory Affairs
Good Laboratory Practice (GLP)
Medical Devices
Cleaning Validation
Biotechnology
Manufacturing
Verification and Validation (V&V)
Leadership
Cross-functional Team Leadership
Management
Laboratory Information Management System (LIMS)
GxP
Quality Control
Computer System Validation
Customer Relationship Management (CRM)
Quality Management
Process Simulation
Regulatory Submissions
Regulatory Requirements
Investigation
deviations
Quality Assurance Management
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Discover more about Eurofins | EAG LaboratoriesWhat is Rose email address?
Email Rose at [email protected] and [email protected]. This email is the most updated Rose's email found in 2026.
What is Rose phone number?
Rose phone number is 314-960-9687.
How to contact Rose?
To contact Rose send an email to [email protected] or [email protected]. If you want to call Rose try calling on 314-960-9687.
What company does Rose work for?
Rose works for Eurofins | EAG Laboratories
What is Rose's role at Eurofins | EAG Laboratories?
Rose is Quality Program Manager
Rose Email Addresses
Rose Phone Numbers
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