Andrea Redd Email & Phone Number
@fresenius-kabi.com
1 phone found area 888
LinkedIn matched
Who is Andrea Redd? Overview
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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.
Email format at Eli Lilly and Company
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AeroLeads found 1 current-domain work email signal for Andrea Redd. Compare company email patterns before reaching out.
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.
Andrea Redd's current company
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Andrea Redd work experience
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Associate Vice President, Global Regulatory Affairs, Drug Delivery & Combination Products
Current
Head Global Regulatory Affairs Pharma
Vice President Regulatory Affairs
Responsible for CMC, Labeling, and Publishing functions focused on new generic drug product development as well as lifecycle management.
Senior Director, Combination Products Regulatory Affairs
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.
Director, Regulatory Affairs Combination Products
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.
Associate Director, A&As Project Management, Regulatory Affairs
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.
Senior Program Manager
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.
Senior Regulatory Affairs Associate
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.
Regulatory Affairs Associate
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.
Sterility Assurance
Responsible for microbial validation of steam sterilization cycles for parenteral drug products.
Andrea Redd education
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University Of Illinois Urbana-Champaign
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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