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Lori Johnson Email & Phone Number

Quality Assurance Senior Manager of Product Disposition at Alkermes at Alkermes
Location: Cincinnati Metropolitan Area, United States 5 work roles 2 schools
1 work email found @alkermes.com LinkedIn matched
✓ Verified August 2026 4 data sources Profile completeness 100%

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Work email l****@alkermes.com
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Current company
Role
Quality Assurance Senior Manager of Product Disposition at Alkermes
Location
Cincinnati Metropolitan Area, United States
Company size

Who is Lori Johnson? Overview

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Quick answer

Lori Johnson is listed as Quality Assurance Senior Manager of Product Disposition at Alkermes at Alkermes, a with 2241 employees, based in Cincinnati Metropolitan Area, United States. AeroLeads shows a work email signal at alkermes.com and a matched LinkedIn profile for Lori Johnson.

Lori Johnson previously worked as Quality Assurance Senior Manager- Product Disposition at Alkermes and Quality Assurance, Product Release at Alkermes. Lori Johnson holds Bachelor Of Arts (B.A.), English Literature/ Secondary Education And Teaching from Northern Kentucky University.

Company email context

Email format at Alkermes

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{first}.{last}@alkermes.com
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AeroLeads found 1 current-domain work email signal for Lori Johnson. Compare company email patterns before reaching out.

Profile bio

About Lori Johnson

Lori Johnson is a Quality Assurance Senior Manager of Product Disposition at Alkermes at Alkermes. She possess expertise in pharmaceutical industry, teamwork, continuous improvement, gmp, microsoft office and 12 more skills. She is proficient in English.

Listed skills include Pharmaceutical Industry, Teamwork, Continuous Improvement, Gmp, and 13 others.

Current workplace

Lori Johnson's current company

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Alkermes
Alkermes
Quality Assurance Senior Manager of Product Disposition at Alkermes
dublin, dublin, ireland
Website
Employees
2241
AeroLeads page
5 roles

Lori Johnson work experience

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

Quality Assurance Senior Manager- Product Disposition

Current
Mar 2024 - Present

Quality Assurance, Product Release

Current

-Release of finished product commercial batches (batch record review, certificate of analysis generation, deviation review, etc).-Release of Clinical batches to be used in clinical studies.-Release of Bulk batches and raw materials.-SAP QM problem solving and implementation-Quality systems project work (SAP, Trackwise, LIMS, eBR, etc)-Continuous Improvement Project work-SOP Revisions-Specification and SOP review-SAP Training

Oct 2005 - Present

Senior Quality Assurance Specialist- Product Release

Current

-Responsible for the Quality release of raw materials and finished product at the Wilmington facility. -Work in a team environment within the Quality Release group, where I am a mentor and leader as a senior associate. -Primary trainer for all aspects of the Quality Release activities. -Represent the Quality group in various continuous improvement/operational excellence projects.-Collaborate with other sites internationally on various projects and problem solving regarding release of materials.-Make decisions utilizing internal procedures and regulatory guidelines for releasing raw materials, finished product and general troubleshooting on a daily basis. -Contribute during regulatory agency audits as a troubleshooter/subject matter expert. -Responsible for reviewing and approving SOP’s, change controls, deviations and validation protocols.

Nov 2013 - Present

Manufacturing Compliance Specialist

-Write and revise batch records and SOP's for commercial manufacturing Bulk lines.-Write and revise batch records and SOP's for start up manufacturing lines.-Ensure that manufacturing lines are ready for audits from various agencies such as the FDA and MHRA.-Represent manufacturing in cross departmental continuous improvement projects.-Revise batch records and SOP's to be operator centered and easy to follow.-Perform manufacturing duties when needed on Vivitrol and Polymer lines.-Perform various audit activities when applicable agencies are at the facility.-Perform internal audits of other departments.

Oct 2005 - Nov 2013

Quality Assurance Product Disposition Manager

Current
Mar 2021 - Present
Team & coworkers

Colleagues at Alkermes

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2 education records

Lori Johnson education

Bachelor Of Arts (B.A.), English Literature/ Secondary Education And Teaching

Bachelor of Arts Degree in English Literature, with a Concentration in Education.

FAQ

Frequently asked questions about Lori Johnson

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

What company does Lori Johnson work for?

Lori Johnson works for Alkermes.

What is Lori Johnson's role at Alkermes?

Lori Johnson is listed as Quality Assurance Senior Manager of Product Disposition at Alkermes at Alkermes.

What is Lori Johnson's email address?

AeroLeads has found 1 work email signal at @alkermes.com for Lori Johnson at Alkermes.

Where is Lori Johnson based?

Lori Johnson is based in Cincinnati Metropolitan Area, United States while working with Alkermes.

What companies has Lori Johnson worked for?

Lori Johnson has worked for Alkermes and Alkermes Inc.

Who are Lori Johnson's colleagues at Alkermes?

Lori Johnson's colleagues at Alkermes include Trenton Smart, Chamnann Ok, Clare Sheridan, Emily Della Monica, and Alex Lazar.

How can I contact Lori Johnson?

You can use AeroLeads to view verified contact signals for Lori Johnson at Alkermes, including work email, phone, and LinkedIn data when available.

What schools did Lori Johnson attend?

Lori Johnson holds Bachelor Of Arts (B.A.), English Literature/ Secondary Education And Teaching from Northern Kentucky University.

What skills is Lori Johnson known for?

Lori Johnson is listed with skills including Pharmaceutical Industry, Teamwork, Continuous Improvement, Gmp, Microsoft Office, Microsoft Excel, Customer Service, and Microsoft Word.

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