Ingrid Markovic Email & Phone Number
@fda.gov
1 phone found area 301
LinkedIn matched
Who is Ingrid Markovic? Overview
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Ingrid Markovic is listed as Senior Science Advisor, Office of the Center Director, CBER/FDA at FDA, a company with 14770 employees, based in Silver Spring, Maryland, United States. AeroLeads shows a work email signal at fda.gov, phone signal with area code 301, and a matched LinkedIn profile for Ingrid Markovic.
Ingrid Markovic previously worked as ICH Q6 Regulatory Chair at Fda and Senior Science Advisor/CMC Lead at Fda. Ingrid Markovic holds Doctor Of Philosophy - Phd, Natural Products Chemistry from University Of Wisconsin-Madison.
Email format at FDA
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AeroLeads found 1 current-domain work email signal for Ingrid Markovic. Compare company email patterns before reaching out.
About Ingrid Markovic
Ingrid Markovic is a Senior Science Advisor, Office of the Center Director, CBER/FDA at FDA. She possess expertise in biotechnology, regulatory affairs, cmc, regulatory submissions, u.s. food and drug administration and 18 more skills. Colleagues describe her as "Ingrid is an exceptional leader who combines sharp analytical thinking with high emotional intelligence. She fosters collaboration even among loosely connected teams. Her contributions to regulatory and quality discussions are always invaluable and insightful. I highly recommend her." and "I have been working with Ingrid for several years. First as part of the ICH Q12 IWG and then as part of ICH M4Q EWG. We have also presented at different conferences on the same topic. I discovered in Ingrid a great person who is very knowledgable and a real team player! She has a very strong international reputation and leadership in promoting and bringing global regulatory harmonization. You can be sure that if Ingrid is involved in a project, it will be a success!! Looking forward… Show more"
Listed skills include Biotechnology, Regulatory Affairs, Cmc, Regulatory Submissions, and 19 others.
Ingrid Markovic's current company
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Ingrid Markovic work experience
A career timeline built from the work history available for this profile.
Senior Science Advisor/Cmc Lead
Current
Ich M4Q Fda Topic Lead
Senior Director, Head Of Us & Eu Regulatory Policy (Cmc)
Responsible for strategy and oversight of US & EU CMC regulatory advocacy, outreach, and benchmarking including establishing strategic relationships with internal and external stakeholders, working closely with Trade Associations and Pharmacopeias. Serving on strategic regulatory governance initiatives focusing on New Therapeutic Modalities & Advanced.
Ich Q3E Iwg Rapporteur
Champion, Cell & Gene Therapy Manufacturing Core Team
Member, Global Quality & Manufacturing Committee
Chair, Manufacturing Quality & Distribution Committee
Member, Ich Bio Delegation
Ich Q12 Fda Deputy Topic Lead
Advisor For Cmc To The Associate Director For Review Management, Cber, Office Of The Center Director
Provided leadership, strategic direction, and oversight for development, implementation, and integration of CMC regulatory policy and associated activities for complex biologics including Cell & Gene Therapy, Vaccine, and Biotechnology products CBER-wide. Co-developed strategic roadmap for CMC/Product Quality initiatives within the Center, including.
Expert Review Scientist, Cder, Office Of Biotechnology Products
Provided strategic direction and technical guidance for the development and implementation of E&L regulatory review policy within the Division and Office. Delivered authoritative advice on E&L to the Division and Office Management, external stakeholders in the Center, Agency, other Regulatory Authorities, and Industry. Conducted CMC review of Biological.
Cmc Reviewer For Therapeutic Proteins, Cder, Office Of Biotechnology Products
Conducted CMC review of Biological License Applications (BLAs), post-approval CMC submissions (PAS, CBE0/30, AR), INDs and pINDs, for innovator therapeutic protein products, including approval, CR or clinical hold recommendations. Conducted PAI and Biennial Establishment Inspections including recommendation pertinent to issuance of 483 observations..
Staff Fellow/Cmc Reviewer For Monoclonal Antibodies, Cber, Office Of Therapeutic Research & Review
Conducted CMC review of post-approval CMC submissions, INDs and pINDs, for monoclonal antibodies, including approval, CR or clinical hold recommendations. Conducted Biennial Establishment Inspections including recommendation pertinent to issuance of 483 observations. Conducted mission-relevant research to develop therapeutic treatment for HIV infection.
Postdoctoral Research Fellow
Performed independent research elucidating mechanism of influenza virus hemagglutinin (HA) and baculovirus glycoprotein 64 (gp64) conformational rearrangement to prevent viral infection. Provided leadership and tactical direction including conceptualizing and executing experiments and publishing study data.
Colleagues at FDA
Other employees you can reach at fda.gov. View company contacts for 14770 employees →
Chumin Zhao
Colleague at Fda
Silver Spring, Maryland, United States, United States
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DH
Dawn Hawkins
Colleague at Fda
Mount Rainier, Maryland, United States, United States
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PC
Patrick Cox
Colleague at Fda
Pillager, Minnesota, United States, United States
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YM
Yvette Montes
Colleague at Fda
El Paso, Texas, United States, United States
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KB
Katie Bray
Colleague at Fda
Stilwell, Kansas, United States, United States
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YW
Yiduo Wu
Colleague at Fda
Silver Spring, Maryland, United States, United States
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JC
John Coletta
Colleague at Fda
Winchester, Massachusetts, United States, United States
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MI
Mohamed I. Nounou
Colleague at Fda
Washington DC-Baltimore Area, United States
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RM
Rosina Motta
Colleague at Fda
Silver Spring, Maryland, United States, United States
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MJ
Mivoyel Jean Paul
Colleague at Fda
Jamaica, New York, United States, United States
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Ingrid Markovic education
Doctor Of Philosophy - Phd, Natural Products Chemistry
Post-Doc, Biophysics, Biochemisty
Frequently asked questions about Ingrid Markovic
Quick answers generated from the profile data available on this page.
What company does Ingrid Markovic work for?
Ingrid Markovic works for FDA.
What is Ingrid Markovic's role at FDA?
Ingrid Markovic is listed as Senior Science Advisor, Office of the Center Director, CBER/FDA at FDA.
What is Ingrid Markovic's email address?
AeroLeads has found 1 work email signal at @fda.gov for Ingrid Markovic at FDA.
What is Ingrid Markovic's phone number?
AeroLeads has found 1 phone signal(s) with area code 301 for Ingrid Markovic at FDA.
Where is Ingrid Markovic based?
Ingrid Markovic is based in Silver Spring, Maryland, United States while working with FDA.
What companies has Ingrid Markovic worked for?
Ingrid Markovic has worked for Fda, Genentech, Member Of The Roche Group, Phrma, Biotechnology Innovation Organization, and International Council For Harmonisation.
Who are Ingrid Markovic's colleagues at FDA?
Ingrid Markovic's colleagues at FDA include Chumin Zhao, Dawn Hawkins, Patrick Cox, Yvette Montes, and Katie Bray.
How can I contact Ingrid Markovic?
You can use AeroLeads to view verified contact signals for Ingrid Markovic at FDA, including work email, phone, and LinkedIn data when available.
What schools did Ingrid Markovic attend?
Ingrid Markovic holds Doctor Of Philosophy - Phd, Natural Products Chemistry from University Of Wisconsin-Madison.
What skills is Ingrid Markovic known for?
Ingrid Markovic is listed with skills including Biotechnology, Regulatory Affairs, Cmc, Regulatory Submissions, U.S. Food And Drug Administration, E&L, Biopharmaceuticals, and Policy.
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