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Cindy Zhao Email & Phone Number

Sr. Manager, Global Quality Compliance Audit at Allergan
Location: Laguna Niguel, California, United States 12 work roles 2 schools
2 work emails found @allergan.com 2 phones found area 858 LinkedIn matched
✓ Verified August 2026 4 data sources Profile completeness 100%

Contact Signals · 2 work emails · 2 phones

Work email c****@allergan.com
Direct phone (858) ***-****
LinkedIn Profile matched
3 free lookups remaining · No credit card
Current company
Allergan
Role
Sr. Manager, Global Quality Compliance Audit
Location
Laguna Niguel, California, United States
Company size
10 employees

Who is Cindy Zhao? Overview

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Quick answer

Cindy Zhao is listed as Sr. Manager, Global Quality Compliance Audit at Allergan, a with 10 employees, based in Laguna Niguel, California, United States. AeroLeads shows a work email signal at allergan.com, phone signal with area code 858, and a matched LinkedIn profile for Cindy Zhao.

Cindy Zhao previously worked as Principal Auditor, Global Quality Compliance Audit / WWQA Audit at Allergan and Sr Manager at Abbvie. Cindy Zhao holds Master Of Science (M.S.), Chemistry from Portland State University.

Company email context

Email format at Allergan

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{first}.{last}@allergan.com
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AeroLeads found 2 current-domain work email signals for Cindy Zhao. Compare company email patterns before reaching out.

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Profile bio

About Cindy Zhao

ASQ Certified Quality Auditor (CQA) and Certified Biomedical Auditor (CBA). Hands-on experience of contract manufacturer qualification, pharmaceuticals and medical device supplier audit. Quality professional with extensive industrial experience related to supplier management and QC chemistry laboratory. Worked with commercial drug products as well as clinical study materials, including API, drug products and combination product.Participated in several IND, NDA and ANDA submissions and acquired a lot of experience on FDA’s pre-approval inspection (PAI), including documentation preparation for IND, NDA and ANDA filings and face-to-face discussion with FDA investigators during PAI. Extensive experience on coordinating and assisting timely review of analytical release data and disposition of drug products. Expertise in critical review and guidance for GMP documentations initiated by R&D to support R&D on cGMP compliance, including method validation and method transfer protocols and reports, deviation or OOS investigations. Very familiar with various USP test methods, HPLC and GC methods for incoming raw material inspection, in-process control, product release, and stability study. Valuable reviewer due to strong technical background. Demonstrated abilities to work in dynamic cross-functional team environment with other departments such as regulatory affairs, manufacturing and analytical laboratories.

Listed skills include Gmp, Fda, Pharmaceutical Industry, Quality System, and 22 others.

Current workplace

Cindy Zhao's current company

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Allergan
Allergan
Sr. Manager, Global Quality Compliance Audit
Allergan plc, Dublin, Coolock D17 E400, ie
Website
allergan.com
Employees
10
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12 roles

Cindy Zhao work experience

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

Sr. Manager, Global Quality Compliance Audit

Current
Allergan

Dublin, Coolock, Ie

Mar 2019 - Present

Principal Auditor, Global Quality Compliance Audit / Wwqa Audit

Allergan

Dublin, Coolock, Ie

Responsible for planning and executing the following types of audits: Allergan manufacturing and non-manufacturing sites, Allergan contract manufacturers, raw material manufacturers and re-packagers (API & Excipient), contract laboratories, packaging component manufacturers, labeling manufacturers, disinfectants and resin manufacturers, and service providers such as distribution centers, etc.Performed several international audits including suppliers located in China and Taiwan using local languages. Subject Matter Expert for auditing of QC laboratories using working knowledge in HPLC, GC, and various laboratory instrumentation, QC operations, LIMS, chromatography software such as EMPOWER, Out of Specification (OOS) investigations and a strong understanding of stability program.Revised WWQA standards for regulatory inspection. Assisted to host MOH inspections and ISO 13485 recertification audits.Created GMP and Regulatory Inspection related on-line training courses using Articular software and published in e-Learning Management System (Plateau)Participated in the development of a risk based supplier management program

Sr Manager

Abbvie

North Chicago, Illinois, Us

Qc Manager

Polypeptide Laboratories

Baar, Ch

Responsible for managing of all QC activities related to clinic material release and to be in compliance with regulatory requirements.

Nov 2011 - Dec 2011

Sr. Manager, Quality System - Qc

Arena Pharmaceuticals

San Diego, Ca, Us

Responsible for review and approval analytical data for in-coming raw material inspection, in-process control and release of starting materials, intermediates, APIs and final drug products manufactured in house for early phase clinical studyResponsible for review and approval analytical test methods, method validation and method transfer protocols and reports Responsible for QC laboratory operations to ensure cGMP compliance

Aug 2011 - Sep 2011

Sr. Research Associate - Preclinical Science Of Pharm R&D

Diversa Co.
Nov 2004 - Apr 2005

Quality Analyst - Qa/Qc

Diversa Co.
Mar 2002 - Nov 2004
Team & coworkers

Colleagues at Allergan

Other employees you can reach at allergan.com. View company contacts for 10 employees →

刘 刘巧莲 刘巧莲 Colleague at AllerganJiulongpo District, Chongqing, China View → RB Rashid Bodla Rashid Bodla Colleague at AllerganPakistan View → NM Niya M. Niya M. Colleague at AllerganUnited States View → WP Wesley Poth Wesley Poth Colleague at AllerganWoodway, Texas, United States View → CO Criostoir Ohaolain Criostoir Ohaolain Colleague at AllerganCounty Mayo, Ireland View → EO Elizabeth Outlaw Elizabeth Outlaw Colleague at AllerganRaleigh-Durham-Chapel Hill Area, United States View → MT Mike Timmons Mike Timmons Colleague at AllerganLynnfield, Massachusetts, United States View → VW Vaibhav Waman Vaibhav Waman Colleague at AllerganMumbai, Maharashtra, India View → GB Gregg Bailey Gregg Bailey Colleague at AllerganAurora, Colorado, United States View → DS Dan Smart Dan Smart Colleague at AllerganHendersonville, Tennessee, United States View →
2 education records

Cindy Zhao education

Master Of Science (M.S.), Chemistry

Portland State University

Bachelor Of Science (B.S.), Chemisry

Peking University
FAQ

Frequently asked questions about Cindy Zhao

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

What company does Cindy Zhao work for?

Cindy Zhao works for Allergan.

What is Cindy Zhao's role at Allergan?

Cindy Zhao is listed as Sr. Manager, Global Quality Compliance Audit at Allergan.

What is Cindy Zhao's email address?

AeroLeads has found 2 work email signals at @allergan.com for Cindy Zhao at Allergan.

What is Cindy Zhao's phone number?

AeroLeads has found 2 phone signal(s) with area code 858 for Cindy Zhao at Allergan.

Where is Cindy Zhao based?

Cindy Zhao is based in Laguna Niguel, California, United States while working with Allergan.

What companies has Cindy Zhao worked for?

Cindy Zhao has worked for Allergan, Abbvie, Polypeptide Laboratories, Arena Pharmaceuticals, and Diversa Co..

Who are Cindy Zhao's colleagues at Allergan?

Cindy Zhao's colleagues at Allergan include 刘巧莲, Rashid Bodla, Niya M., Wesley Poth, and Criostoir Ohaolain.

How can I contact Cindy Zhao?

You can use AeroLeads to view verified contact signals for Cindy Zhao at Allergan, including work email, phone, and LinkedIn data when available.

What schools did Cindy Zhao attend?

Cindy Zhao holds Master Of Science (M.S.), Chemistry from Portland State University.

What skills is Cindy Zhao known for?

Cindy Zhao is listed with skills including Gmp, Fda, Pharmaceutical Industry, Quality System, Hplc, Quality Assurance, Validation, and Quality Control.

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