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Ingrid Markovic Email & Phone Number

Senior Science Advisor, Office of the Center Director, CBER/FDA at FDA
Location: Silver Spring, Maryland, United States 15 work roles 2 schools
1 work email found @fda.gov 1 phone found area 301 LinkedIn matched
✓ Verified May 2026 4 data sources Profile completeness 100%

Contact Signals · 1 work email · 1 phone

Work email i****@fda.gov
Direct phone (301) ***-****
LinkedIn Profile matched
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Current company
FDA
Role
Senior Science Advisor, Office of the Center Director, CBER/FDA
Location
Silver Spring, Maryland, United States
Company size

Who is Ingrid Markovic? Overview

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Quick answer

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.

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Email format at FDA

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{first}.{last}@fda.gov
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Profile bio

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.

Current workplace

Ingrid Markovic's current company

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FDA
Fda
Senior Science Advisor, Office of the Center Director, CBER/FDA
silver spring, maryland, united states
Website
Employees
14770
AeroLeads page
15 roles · 29 years

Ingrid Markovic work experience

A career timeline built from the work history available for this profile.

Ich Q6 Regulatory Chair

Current
Fda
Apr 2024 - Present

Senior Science Advisor/Cmc Lead

Current
Fda

Silver Spring, Maryland, United States

Jul 2020 - Present

Ich M4Q Fda Topic Lead

Fda
Jul 2020 - Apr 2024

Senior Director, Head Of Us & Eu Regulatory Policy (Cmc)

Genentech, Member Of The Roche Group

Washington D.C. Metro Area

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.

Jun 2018 - Jul 2020

Ich Q3E Iwg Rapporteur

Feb 2020 - Jun 2020

Champion, Cell & Gene Therapy Manufacturing Core Team

Dec 2019 - Jun 2020

Member, Global Quality & Manufacturing Committee

Apr 2019 - Jun 2020

Ich Q12 Fda Deputy Topic Lead

International Council For Harmonisation
Nov 2014 - Jun 2018

Advisor For Cmc To The Associate Director For Review Management, Cber, Office Of The Center Director

Fda

Silver Spring, Maryland

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.

Jan 2013 - May 2018

Expert Review Scientist, Cder, Office Of Biotechnology Products

Fda

Bethesda, Maryland

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.

2008 - 2012 ~4 yrs

Cmc Reviewer For Therapeutic Proteins, Cder, Office Of Biotechnology Products

Fda

Bethesda, Maryland

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..

2004 - 2008 ~4 yrs

Staff Fellow/Cmc Reviewer For Monoclonal Antibodies, Cber, Office Of Therapeutic Research & Review

Fda

Bethesda, Maryland

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.

2001 - 2004 ~3 yrs

Postdoctoral Research Fellow

Bethesda, MD

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.

1997 - 2001 ~4 yrs
Team & coworkers

Colleagues at FDA

Other employees you can reach at fda.gov. View company contacts for 14770 employees →

2 education records

Ingrid Markovic education

Post-Doc, Biophysics, Biochemisty

National Institutes Of Health

Activities and Societies: Biophysical Society of America

FAQ

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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