Suzanne Matlock
Director (Principal Scientist) at Merck | Philadelphia, Pennsylvania, United States
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Suzanne Matlock is a seasoned Regulatory Affairs professional with over 20 years of experience in the vaccine industry, currently serving as Director (Principal Scientist) at Merck. With a specialized focus on Vaccines Chemistry, Manufacturing, and Controls (CMC) for more than a decade, Suzanne has developed a deep expertise in navigating the intricate regulatory landscapes that govern vaccine development and post-approval processes. Her role involves managing a dedicated team of five to six direct reports, where she oversees the preparation of high-quality regulatory CMC documentation to support post-approval changes for four pediatric vaccines.
Suzanne's strategic oversight ensures that all regulatory milestones are met, as she meticulously assesses the probability of regulatory success while implementing robust risk mitigation measures. Her ability to represent regulatory CMC in cross-functional teams enhances collaboration across various departments, fostering an environment where scientific innovation aligns seamlessly with regulatory compliance.
Her extensive knowledge of global regulatory frameworks, particularly in complex markets like Japan, positions her as a key player in ensuring that Merck's pediatric vaccines meet the highest standards of safety and efficacy. Suzanne's skills in public speaking, leadership, and quality systems further amplify her impact, as she effectively communicates regulatory strategies and best practices to stakeholders at all levels. As a champion of Good Manufacturing Practices (GxP) and a proponent of rigorous cleaning validation and process simulation, Suzanne Matlock continues to drive excellence in vaccine regulatory affairs, contributing significantly to public health initiatives worldwide.
Director (Principal Scientist) at Merck in January 2021 to Present
Assoc. Dir., Regulatory Affairs - Vaccines (CMC) at Merck in November 2017 to January 2021
Sr. Specialist, Regulatory Affairs - Vaccines (CMC) at Merck in November 2012 to October 2017
Quality Control & Investigating Deviations at Merck in November 2008 to November 2012
Manufacturing Scheduler/Aseptic Process Simulation Coordinator at Merck in May 2004 to October 2008
Supervisor, Maintenance & Utilities at Merck in May 2000 to May 2004
Environmental Specialist at Merck in June 1998 to May 2000
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Written Communication
Multiple Projects Simultaneously
Microsoft Word
Regulatory Guidelines
Regulatory Documentation
Common Technical Document (CTD)
Document Management
Project Planning
Cross-functional Collaborations
Teamwork
GMP
Pharmaceutical Industry
Technical Writing
Public Speaking
Event Planning
Regulatory Affairs
Trackwise
Regulatory Requirements
CAPA
Vaccines
LIMS
21 CFR Part 11
Leadership
Sop
Quality Control
GxP
FDA
eCTD
Regulatory Submissions
Validation
Cleaning Validation
GLP
IND
Aseptic Processing
Environmental Monitoring
GCP
CMC
Beekeeping
Process Simulation
Quality System
Pharmaceutics
USP
Deviations
Quality Auditing
CMC Regulatory Affairs
UV
Deviation Management
Analytical Chemistry
FDA GMP
Change Control
Murals
Technical Illustration
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Discover more about MerckWhat is Suzanne Matlock email address?
Email Suzanne Matlock at [email protected] and [email protected]. This email is the most updated Suzanne Matlock email found in 2026.
How to contact Suzanne Matlock?
To contact Suzanne Matlock send an email to [email protected] or [email protected]. (updated on November 04, 2024)
What company does Suzanne Matlock work for?
Suzanne Matlock works for Merck
What is Suzanne Matlock's role at Merck?
Suzanne Matlock is Director (Principal Scientist)
What is Suzanne Matlock's Phone Number?
Suzanne Matlock's phone (215) ***-*261
What industry does Suzanne Matlock work in?
Suzanne Matlock works in the Pharmaceutical Manufacturing industry.
Suzanne Matlock Email Addresses
Suzanne Matlock Phone Numbers
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