Unnee Ranjan, Senior Investigator III, Division of Human and Animal Drug Foreign Inspectorate at FDA

Unnee Ranjan

Senior Investigator III, Division of Human and Animal Drug Foreign Inspectorate at FDA | Parsippany, New Jersey, United States

Profile last verified June 2026
Law Enforcement Verified Profile Parsippany, New Jersey, United States Shenandoah University
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***@barrlabs.com

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Unnee Ranjan Socials
Unnee Ranjan Work Experience

Senior Investigator III, Division of Human and Animal Drug Foreign Inspectorate at FDA in March 2025 - Present

Team Lead - Office of Biotechnology Inspectorate (Team Biologics) OII at FDA in October 2023 - March 2025

Senior Investigator II - Team Biologics; ORA/Office of Biological Products Operations at FDA in May 2022 - September 2023

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Drug Specialist - ORA/Office of Pharmaceutical Quality Operations at FDA in August 2014 - April 2022

Senior Scientist, Process Engineering - R & D at Teva Pharmaceuticals in May 2013 - August 2014

Scientist II, Process Engineering - R & D at Teva Pharmaceuticals in May 2011 - April 2013

Scientist I, Process Technical Serivices at Barr Laboratories in August 2007 - April 2011

Formulation Scientist at Ascend Laboratories, LLC in February 2007 - July 2007

Formulation Scientist to Assistant Manager at Microlabs Ltd in September 2004 - October 2006

Formulation Scientist at Macleods pharmaceuticals Ltd. in May 2003 - September 2004

Unnee Ranjan Education

Shenandoah University, Doctor of Pharmacy (Pharm.D.)

Unnee Ranjan Skills
Conflict Resolution Readiness Assessments Risk Assessment Quality Management Quality Assurance Regulatory Compliance Auditing Analytical Skills Generic Programming Technology Transfer Drug Delivery Quality by Design Formulation Pharmaceutical Research Analytical Chemistry FDA UV Change Control Chromatography Pharmaceutics GMP Regulatory Affairs Cleaning Validation Validation Sop Regulatory Requirements Drug Development Pharmaceutical Industry HPLC GLP 21 CFR Part 11 UV/Vis GxP LIMS Design of Experiments ANDA Biopharmaceuticals Regulatory Submissions Process Simulation Computer System Validation Gas Chromatography Trackwise SOP TrackWise Standard Operating Procedure (SOP) Good Laboratory Practice (GLP) High-Performance Liquid Chromatography (HPLC) Corrective and Preventive Action (CAPA) U.S. Title 21 CFR Part 11 Regulation U.S. Food and Drug Administration (FDA)
About Unnee Ranjan’s Current Company
FDA

The Food and Drug Administration is an agency within the Department of Health and Human Services. The FDA is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices; and by ensuring the safety of our nation's food supply, cosmetics, and products that emit radiation. FDA also has responsibility for regulating the manufacturing, marketing, and distribution of tobacco products to protect the public health and to reduce tobacco use by minors. FDA is responsible for advancing the public health by helping to speed innovations that make medical products more effective, safer, and more affordable and by helping the public get the accurate, science-based information they need to use medical products and foods to maintain and improve their health. FDA also plays a significant role in the Nation's counterterrorism capability. FDA fulfills this responsibility by ensuring the security of the food supply and by fostering development of medical products to respond to deliberate and naturally emerging public health threats.

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Unnee Ranjan’s Colleagues
Tala Fakhouri

Tala Fakhouri

Bethesda, Maryland, United States

Associate Director for Data Science and AI Policy at FDA (Views My Own)

Associate Director for Policy Analysis at FDA
(October 2020 – Present)

Michael Dejos

Michael Dejos

Memphis, Tennessee, United States

Patient Safety and Healthcare Quality Leader | Continuous Improvement Professional | Pharmacy Executive

Assistant Professor at The University of Tennessee Health Science Center
(July 2020 – Present)

Ashley Boam

Ashley Boam

Silver Spring, Maryland, United States

Director at FDA

Director, Office of Policy for Pharmaceutical Quality, CDER at FDA
(January 2015 – Present)

Alonza Cruse

Alonza Cruse

Silver Spring, Maryland, United States

FDA - Office of Regulatory Affairs - Office of Medical Products & Tobacco Operations

Director, Office of Pharmaceutical Quality Operations at FDA
(October 2015 – Present)

Dave Benson

Dave Benson

Raleigh, North Carolina, United States

Acting Director, Enterprise Architecture, US FDA.

Sr. Technical Advisor at FDA
(April 2023 – Present)

Salim Roberts

Salim Roberts

Silver Spring, Maryland, United States

Strategic Acquisition Leader | FDA Director | JD | Other Transaction (OT) Expert | Pandemic & Biodefense Procurement | Advisor to Public Health & Government Innovation Initiatives

Director of Acquisition Services, FDA/CDRH at FDA
(February 2019 – Present)

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Frequently asked questions about Unnee Ranjan

What is Unnee Ranjan email address?

Email Unnee Ranjan at [email protected] and [email protected]. This email is the most updated Unnee Ranjan's email found in 2026.

How to contact Unnee Ranjan?

To contact Unnee Ranjan send an email to [email protected] or [email protected].

What company does Unnee Ranjan work for?

Unnee Ranjan works for FDA.

What is Unnee Ranjan's role at FDA?

Unnee Ranjan is Senior Investigator III, Division of Human and Animal Drug Foreign Inspectorate

What industry does Unnee Ranjan work in?

Unnee Ranjan works in the Law Enforcement industry.

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