Chris Steinberg
Validation and Quality Compliance professional responsible for the direction, operation, and execution of projects and assignments for various... | Greater Philadelphia, Greater Philadelphia, United States
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Chris Steinberg’s Emails ch****@ke****.com
Chris Steinberg’s Phone Numbers No phone number available.
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Chris Steinberg’s Location Greater Philadelphia, Greater Philadelphia, United States
Chris Steinberg’s Expertise Validation and Quality Compliance professional responsible for the direction, operation, and execution of projects and assignments for various clients in various pharmaceutical environments including Bio-pharmaceutical and API manufacturing. I have an extensive background through out the pharmaceutical industry in Validation, Quality Compliance, Manufacturing Equipment, Systems Development & Support, cGMP Validation Program Development, Revalidation Programs, GAP analysis for GMP processes, Computer Systems Validation (CSV) I SDLC I GAMP 5 I ASTM E2500- 071, 21CFR part 11, FDA Regulations, CFR 210 and 211 and parts 600 and 820, ISO 19001 and 13485, authoring and quality review of documentation. Specialties: Utilities Qualifications Label Serialization Equipment Validation Facility Qualification Computer System Validation Automated Systems Validation Validation Quality Reviews Validation Master Plans Factory Acceptance Testing (FAT) Site Acceptance Testing (SAT) User and Functional Requirements Specifications (URS, FRS) Detailed Design Specifications (DDS) Commissioning Installation Qualifications Operational Qualifications Performance Qualifications Process Qualifications Summary Reports
Chris Steinberg’s Current Industry Kenvue
Chris
Steinberg’s Prior Industry
The College Of New Jersey
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The Validation
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Compli
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Integrated Project Services
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Techsource
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Quality Compliance Partners
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Rcm Technologies
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Pharmaceutical Validation Solutions
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Johnson And Johnson Consumer Healthcare
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Kenvue
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Work Experience
Kenvue
CSV Lead Kenvue Fort Washington Facility
Sun Jan 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Present
Johnson And Johnson Consumer Healthcare
Quality Assurance Validation Specialist IV
Tue Nov 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time) — Present
Integrated Project Services
Sr. Validation Consultant
Sat Aug 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Nov 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time)
Pharmaceutical Validation Solutions
Project Manager
Tue Jul 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Dec 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time)
Integrated Project Services
Sr. Consultant
Mon Oct 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Sep 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time)
Integrated Project Services
Sr. Consultant
Sun Apr 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Sep 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time)
Quality Compliance Partners
Automation Specialist
Thu Sep 01 2011 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Mar 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time)
Integrated Project Services
Sr. Validation and Automation Consultant
Fri Apr 01 2011 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Sep 01 2011 00:00:00 GMT+0000 (Coordinated Universal Time)
Rcm Technologies
Sr. Compliance and Quality Assurance Consultant
Mon Nov 01 2010 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Feb 01 2011 00:00:00 GMT+0000 (Coordinated Universal Time)
Quality Compliance Partners
Sr. Quality Compliance Consultant
Mon Jun 01 2009 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Jul 01 2010 00:00:00 GMT+0000 (Coordinated Universal Time)
Techsource
Sr. Validation Specialist
Mon Sep 01 2003 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Jan 01 2004 00:00:00 GMT+0000 (Coordinated Universal Time)
Integrated Project Services
Project Manager
Wed Jan 01 2003 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Sep 01 2008 00:00:00 GMT+0000 (Coordinated Universal Time)
Compli
Validation Specialist/Project Lead
Thu Nov 01 2001 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Jun 01 2003 00:00:00 GMT+0000 (Coordinated Universal Time)
The Validation
Validation Specialist III
Thu Jun 01 2000 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Nov 01 2001 00:00:00 GMT+0000 (Coordinated Universal Time)
The College Of New Jersey
Administrative Computer Coordinator
Thu Oct 01 1998 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Jun 01 2000 00:00:00 GMT+0000 (Coordinated Universal Time)Skills
Languages
Chris Steinberg Email Addresses
FAQ About Chris Steinberg
-
Chris Steinberg is located at
Greater Philadelphia, Greater Philadelphia, United States -
Chris Steinberg is a
Validation and Quality Compliance professional responsible for the direction, operation, and execution of projects and assignments for various clients in various pharmaceutical environments including Bio-pharmaceutical and API manufacturing. I have an extensive background through out the pharmaceutical industry in Validation, Quality Compliance, Manufacturing Equipment, Systems Development & Support, cGMP Validation Program Development, Revalidation Programs, GAP analysis for GMP processes, Computer Systems Validation (CSV) I SDLC I GAMP 5 I ASTM E2500- 071, 21CFR part 11, FDA Regulations, CFR 210 and 211 and parts 600 and 820, ISO 19001 and 13485, authoring and quality review of documentation. Specialties: Utilities Qualifications Label Serialization Equipment Validation Facility Qualification Computer System Validation Automated Systems Validation Validation Quality Reviews Validation Master Plans Factory Acceptance Testing (FAT) Site Acceptance Testing (SAT) User and Functional Requirements Specifications (URS, FRS) Detailed Design Specifications (DDS) Commissioning Installation Qualifications Operational Qualifications Performance Qualifications Process Qualifications Summary Reports Kenvue -
Chris Steinberg currently works in the
Kenvue -
Chris Steinberg specializes in
Validation and Quality Compliance professional responsible for the direction, operation, and execution of projects and assignments for various clients in various pharmaceutical environments including Bio-pharmaceutical and API manufacturing. I have an extensive background through out the pharmaceutical industry in Validation, Quality Compliance, Manufacturing Equipment, Systems Development & Support, cGMP Validation Program Development, Revalidation Programs, GAP analysis for GMP processes, Computer Systems Validation (CSV) I SDLC I GAMP 5 I ASTM E2500- 071, 21CFR part 11, FDA Regulations, CFR 210 and 211 and parts 600 and 820, ISO 19001 and 13485, authoring and quality review of documentation. Specialties: Utilities Qualifications Label Serialization Equipment Validation Facility Qualification Computer System Validation Automated Systems Validation Validation Quality Reviews Validation Master Plans Factory Acceptance Testing (FAT) Site Acceptance Testing (SAT) User and Functional Requirements Specifications (URS, FRS) Detailed Design Specifications (DDS) Commissioning Installation Qualifications Operational Qualifications Performance Qualifications Process Qualifications Summary Reports -
Chris Steinberg speaks the following languages:
No languages available. -
Chris Steinberg has prior experience in the following industries:
Integrated Project Services , Pharmaceutical Validation Solutions , Integrated Project Services , Integrated Project Services , Quality Compliance Partners , Integrated Project Services , Rcm Technologies , Quality Compliance Partners , Techsource , Integrated Project Services , Compli , The Validation , The College Of New Jersey -
Chris Steinberg has the following professional experience:
Kenvue , Johnson And Johnson Consumer Healthcare , Integrated Project Services , Pharmaceutical Validation Solutions , Integrated Project Services , Integrated Project Services , Quality Compliance Partners , Integrated Project Services , Rcm Technologies , Quality Compliance Partners , Techsource , Integrated Project Services , Compli , The Validation , The College Of New Jersey . -
You can view Chris Steinberg’s
LinkedIn profile at LinkedIn URL. -
Chris Steinberg’s work email addresses are
[email protected] . -
Chris Steinberg works at
Kenvue
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