Role listed
Pharmaceutical Quality Consulting, Inc.
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Greg Kaster Email & Phone Number
Pharmaceutical Quality Consultant
at
Pharmaceutical Quality Consulting, Inc.
1 work email found
@abbott.com
LinkedIn matched
4 data sources
Profile completeness 100%
Current company
Pharmaceutical Quality Consulting, Inc.
Role
Pharmaceutical Quality Consultant
Location
Greater Chicago Area, United States, United States
Who is Greg Kaster? Overview
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Quick answer
Greg Kaster is listed as Pharmaceutical Quality Consultant at Pharmaceutical Quality Consulting, Inc., based in Greater Chicago Area, United States, United States. AeroLeads shows a work email signal at abbott.com and a matched LinkedIn profile for Greg Kaster.
Greg Kaster previously worked as Consultant at Pharmaceutical Quality Consulting, Inc. and Site R&D QA/ Corporate Quality Systems at Akorn, Inc. Greg Kaster holds Bachelor Of Arts, Chemistry from Northwestern University.
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{first}.{last}@abbott.com
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Profile bio
About Greg Kaster
Significant program management experience in pharmaceutical quality and laboratory system development, implementation, and maintenance. Successful leader of numerous cross functional teams to assess and implement global regulations and to address critical events.Drove assessment, audit preparation, and remediation teams and performed effectively in regulatory audit interface role.Implemented risk-based approaches aligned with corporate objectives and consistent with regulatory requirements. Completed Lean Six Sigma project and developed activity based cost tools to lead improvement programs and to optimize cost, quality, and customer service.Experienced as corporate correspondent with compendia globally to submit proposals and resolve technical issues related to monograph test methods and specifications. Recognized expertise in analytical reference standards and compendia compliance.Experience includes: • Pharmaceutical Quality System Policy, Process, and Procedure Development • Quality System Process Improvement Initiatives, Six Sigma Projects • Quality Laboratory Control• Stability Program Management• R&D Quality Assurance • Investigations • CAPA• Test Method Validation, Transfer, and Verification• Risk Management• Data Integrity• USP, Ph.Eur. Compendia Compliance • Analytical Reference Standard Characterization • Supplier QA • FDA, ISO, ICH, cGMP requirements • Compliance Assessment, Audit Preparation, Remediation and Regulatory Audit Interface • Equipment Qualification • Change Management • Training • Member, USP Chemical Medicines Monograph 1 Expert Committee (2015- current) • Chair, USP Joint- Reference Standard Subcommittee (2020- current)
Listed skills include Gmp, Pharmaceutical Industry, Quality Assurance, Fda, and 22 others.
Current workplace
Greg Kaster's current company
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Pharmaceutical Quality Consulting, Inc.
12 roles · 42 years
Greg Kaster work experience
A career timeline built from the work history available for this profile.
Consultant
Current
Pharmaceutical Quality Consulting, Inc.
Experienced pharmaceutical quality professional with a hands-on, collaborative problem-solving style and an ability to complete complex quality and compliance projects within timelines and budget, build relationships, and negotiate consensus among functional areas. Demonstrated leadership in numerous environments.
May 2019 - Present
Site R&D Qa/ Corporate Quality Systems
Developed, deployed, maintained, and provided quality oversight for the Akorn Quality System to assure alignment with applicable industry, compendia, and regulatory agency standards. Provided expertise in development, execution, review, and approval of verification and validation protocols for QA and R&D functions.
2016 - Apr 2019
Director, Quality Services, Established Pharmaceutical Division
Designed, developed, and maintained global quality systems and policies to ensure Established Pharmaceutical Division compliance as part of the Product Lifecycle Support organization. Led initiatives with cross-functional global scope. Deployed global, cost-effective, and risk-basedapproach aligned with corporate objectives and consistent with regulatory.
2013 - 2016
~3 yrs
Director, Qa Program Management, Global Pharmaceutical Operations
Served as the primary liaison between Supply Chain, Research & Development, Regulatory Affairs, Manufacturing Science & Technology (MS&T), Manufacturing Operations, and QA in support of QA Program Implementation. Insured Quality Programs were effectively implemented within the plants and provided efficient project execution that resulted in the achievement.
2009 - 2012
~3 yrs
Manager, Compendia Services & Reference Standards, Global Pharmaceutical Operations
Oversaw corporation's global reference standard program and division compendia compliance. Responsible for procurement, characterization, continued acceptability testing, and inventory of reference standard materials. Assured compliance with compendia requirements. Proposed and resolved test method, specification, and reference standard issues with.
2000 - 2009
~9 yrs
Program Manager
Led successful implementation of programs, which had significant Quality, Regulatory, and financial impact on the Specialty Products Division and its sister divisions.
1998 - 2000
~2 yrs
Manager, Laboratory Training Programs
Managed technical, exempt, and management training programs for QC production laboratories, analytical R&D, and QC services.
1995 - 1998
~3 yrs
Section Manager, Chemical Testing Laboratories
Oversaw five chemical testing laboratories (staff of over 50) in release of raw materials, in-process samples, and active pharmaceutical ingredients.
1992 - 1995
~3 yrs
Group Leader, Reference Standards Department
Supervised maintenance of reference standard inventory and dispensing to meet corporate needs. Evaluated characterization data. Maintained reference standard retest program. Managed department budget.
1990 - 1992
~2 yrs
Group Leader, Senior Scientist, Scientist, Associate Scientist
Fujisawa (Lyphomed)
Group Leader-- Managed stability group in shelf-life and stress testing of pharmaceutical finished products. Oversaw packaging group in release of packaging raw materials and utilized military standards. Senior Scientist-- Supervised stability group to write, revise, and approve SOPs and specifications. Performed batch record calculations. Provided.
1984 - 1990
~6 yrs
Research Assistant
University Of Illinois Medical Center
Developed HPLC methods to determine amine presence.
1984 - 1984
3 education records
Greg Kaster education
Bachelor Of Arts, Chemistry
Northwestern University
Master'S Degree, Chemistry
University Of Illinois Chicago
Master Of Business Administration
Lake Forest Graduate School Of Management
FAQ
Frequently asked questions about Greg Kaster
Quick answers generated from the profile data available on this page.
What company does Greg Kaster work for?
Greg Kaster works for Pharmaceutical Quality Consulting, Inc..
What is Greg Kaster's role at Pharmaceutical Quality Consulting, Inc.?
Greg Kaster is listed as Pharmaceutical Quality Consultant at Pharmaceutical Quality Consulting, Inc..
What is Greg Kaster's email address?
AeroLeads has found 1 work email signal at @abbott.com for Greg Kaster at Pharmaceutical Quality Consulting, Inc..
Where is Greg Kaster based?
Greg Kaster is based in Greater Chicago Area, United States, United States while working with Pharmaceutical Quality Consulting, Inc..
What companies has Greg Kaster worked for?
Greg Kaster has worked for Pharmaceutical Quality Consulting, Inc., Akorn, Inc, Abbott, Fujisawa (Lyphomed), and University Of Illinois Medical Center.
How can I contact Greg Kaster?
You can use AeroLeads to view verified contact signals for Greg Kaster at Pharmaceutical Quality Consulting, Inc., including work email, phone, and LinkedIn data when available.
What schools did Greg Kaster attend?
Greg Kaster holds Bachelor Of Arts, Chemistry from Northwestern University.
What skills is Greg Kaster known for?
Greg Kaster is listed with skills including Gmp, Pharmaceutical Industry, Quality Assurance, Fda, Quality System, Validation, Sop, and Regulatory Affairs.
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