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Andrea Redd Email & Phone Number

Associate Vice President, Global Regulatory Affairs, Drug Delivery and Combination Products at Eli Lilly and Company
Location: Greater Chicago Area, United States, United States 11 work roles 1 school
1 work email found @fresenius-kabi.com 1 phone found area 888 LinkedIn matched
✓ Verified May 2026 4 data sources Profile completeness 100%

Contact Signals · 1 work email · 1 phone

Work email a****@fresenius-kabi.com
Direct phone (888) ***-****
LinkedIn Profile matched
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Current company
Role
Associate Vice President, Global Regulatory Affairs, Drug Delivery and Combination Products
Location
Greater Chicago Area, United States, United States

Who is Andrea Redd? Overview

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Quick answer

Andrea Redd is listed as Associate Vice President, Global Regulatory Affairs, Drug Delivery and Combination Products at Eli Lilly and Company, based in Greater Chicago Area, United States, United States. AeroLeads shows a work email signal at fresenius-kabi.com, phone signal with area code 888, and a matched LinkedIn profile for Andrea Redd.

Andrea Redd previously worked as Associate Vice President, Global Regulatory Affairs, Drug Delivery & Combination Products at Eli Lilly And Company and Head Global Regulatory Affairs Pharma at Baxter International Inc.. Andrea Redd holds B.S., Microbiology from University Of Illinois Urbana-Champaign.

Company email context

Email format at Eli Lilly and Company

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{first}.{last}@fresenius-kabi.com
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AeroLeads found 1 current-domain work email signal for Andrea Redd. Compare company email patterns before reaching out.

Profile bio

About Andrea Redd

Over 22 years of experience in pharmaceutical industry in R&D, regulatory, and quality control organizations. Results-oriented, highly motivated individual with strong skills in program management, global regulatory affairs, and analytical systems. Leadership and skills profile includes: Project Management CMC Regulatory ManagementBusiness Alliance ManagementCombination Product ExperienceDirect interaction with global regulatory agencies to negotiate and establish regulatory strategies for submission of both on-market product changes as well as new drug product applicationsManagement of global outsourcing programs, including Due Diligence and Contract Negotiation Team Leadership & FacilitationCFR, ISO, GMP, GDP knowledgeManufacturing & Quality OperationsThorough understanding of global regulatory guidances

Listed skills include Pharmaceutical Industry, Validation, Regulatory Affairs, Gmp, and 21 others.

Current workplace

Andrea Redd's current company

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Eli Lilly and Company
Eli Lilly And Company
Associate Vice President, Global Regulatory Affairs, Drug Delivery and Combination Products
Chicago, IL, US
AeroLeads page
11 roles · 25 years

Andrea Redd work experience

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

Associate Vice President, Global Regulatory Affairs, Drug Delivery And Combination Products

Eli Lilly And Company

Chicago, IL, US

Associate Vice President, Global Regulatory Affairs, Drug Delivery & Combination Products

Current

Indianapolis, Indiana, US

Jan 2023 - Present

Vice President Regulatory Affairs

Lake Zurich, Illinois, US

Responsible for CMC, Labeling, and Publishing functions focused on new generic drug product development as well as lifecycle management.

Aug 2020 - Jun 2021

Senior Director, Combination Products Regulatory Affairs

Lake Zurich, Illinois, US

Responsible for a team of 40+ employees including CMC specialists, regulatory labeling and regulatory operations. Product portfolio focused on small molecule injectable products in differentiated delivery systems. Experience in new product development as well as post approval lifecycle management including the expansion of existing manufacturing facilities.

Aug 2018 - Aug 2020

Director, Regulatory Affairs Combination Products

Lake Zurich, Illinois, US

CMC Regulatory Affairs director for generic injectable product portfolio. Manages team of 16 managers and CMC specialists responsible for the entire life-cycle of the product, including feasibility through post-approval changes and annual reports. Specialize in differentiated packaging systems and combination products including pre-filled syringes and.

Mar 2014 - Aug 2018

Associate Director, A&As Project Management, Regulatory Affairs

North Chicago, Illinois, US

Associate Director of Project Management within Area and Affiliate Strategy in global regulatory affairs. Led the global team responsible for the processing of all legalized documentation required for submission of global dossiers. Documents included CPPs, GMPs, MLs, etc. Instituted stream-lined process for requesting and coordination of legalized.

Feb 2013 - Feb 2014

Senior Program Manager

Lake Forest, IL, US

Managed cross-functional teams responsible for the development of new global generic injectable pipeline products. Simultaneously led the development of 11 new generic injectable molecules at various stages of the product development process, ranging from pre-concept through launch with core teams consisting of 15 – 20 members. Responsible for the.

Jan 2008 - Jan 2013

Senior Regulatory Affairs Associate

Lake Forest, IL, US

Primary regulatory point of contact for Hospira’s One2One organization, which was focused on the contractual development and manufacture of molecules for Third Party Customers. Served as regulatory CMC point person to Third Party Customers for the submission of new drug product applications in the global regulatory environment. Clients consisted of.

Sep 2006 - Dec 2008

Regulatory Affairs Associate

Lake Forest, IL, US

Responsible for all post-approval container closure system commodity changes and the implementation into commercial product lines. Submitted multiple supplemental applications and stability bracketing proposals to the appropriate regulatory agencies in support of material changes to existing primary and secondary packaging components. Coordinated all.

Sep 2004 - Sep 2006

Sterility Assurance

Deerfield, Illinois, US

Responsible for microbial validation of steam sterilization cycles for parenteral drug products.

2001 - 2004 ~3 yrs
1 education record

Andrea Redd education

  • University Of Illinois Urbana-Champaign
    University Of Illinois Urbana-Champaign
    Microbiology
FAQ

Frequently asked questions about Andrea Redd

Quick answers generated from the profile data available on this page.

What company does Andrea Redd work for?

Andrea Redd works for Eli Lilly and Company.

What is Andrea Redd's role at Eli Lilly and Company?

Andrea Redd is listed as Associate Vice President, Global Regulatory Affairs, Drug Delivery and Combination Products at Eli Lilly and Company.

What is Andrea Redd's email address?

AeroLeads has found 1 work email signal at @fresenius-kabi.com for Andrea Redd at Eli Lilly and Company.

What is Andrea Redd's phone number?

AeroLeads has found 1 phone signal(s) with area code 888 for Andrea Redd at Eli Lilly and Company.

Where is Andrea Redd based?

Andrea Redd is based in Greater Chicago Area, United States, United States while working with Eli Lilly and Company.

What companies has Andrea Redd worked for?

Andrea Redd has worked for Eli Lilly And Company, Baxter International Inc., Fresenius Kabi Usa, Abbvie, and Hospira.

How can I contact Andrea Redd?

You can use AeroLeads to view verified contact signals for Andrea Redd at Eli Lilly and Company, including work email, phone, and LinkedIn data when available.

What schools did Andrea Redd attend?

Andrea Redd holds B.S., Microbiology from University Of Illinois Urbana-Champaign.

What skills is Andrea Redd known for?

Andrea Redd is listed with skills including Pharmaceutical Industry, Validation, Regulatory Affairs, Gmp, Fda, Cross Functional Team Leadership, Capa, and Change Control.

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