Sergio Richard Wolff Ms Cqa
Experienced analytical chemist, chemical engineer and quality executive with over 20 years of cGMP experience in pharmaceuticals, biotech,... | North Haven, Connecticut, United States
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Sergio Richard Wolff Ms Cqa’s Emails sw****@in****.com
Sergio Richard Wolff Ms Cqa’s Phone Numbers No phone number available.
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Sergio Richard Wolff Ms Cqa’s Location North Haven, Connecticut, United States
Sergio Richard Wolff Ms Cqa’s Expertise Experienced analytical chemist, chemical engineer and quality executive with over 20 years of cGMP experience in pharmaceuticals, biotech, nutritionals, medical devices and compounding pharmacy. Specialties: Executive site quality management including QC, QA , stability, investigations, CAPA, change control, specifications, raw material/supply chain management. Quality Systems design, implementation and validation for cGMP manufacturing. Analytical research, development and validation. Internal and external auditing, third party/CMO management, compendia liaison. Data integrity and forensic data investigations. Stability programs for commercial and clinical trail stage (phase appropriate) GMP/GLP . Pharmaco-economics applied to quality functions : cost benefit analysis for QMS implementations, general cost of quality determination, standard hours etc.
Sergio Richard Wolff Ms Cqa’s Current Industry Alexion Pharmaceuticals
Sergio
Richard Wolff Ms Cqa’s Prior Industry
Becton Dickinson
|
Sanofi Aventis
|
Purdue Pharma
|
United States Army Reserve
|
Abbott Labs
|
Teva Pharmaceuticals
|
Perrigo
|
Independent Consulting
|
University Of Rhode Island
|
Pharmasol
|
American Distilling
|
Avista Pharma Solutions Now Part Of Cambrex
|
Wave Life Sciences
|
Invicro
|
Alexion Pharmaceuticals
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Work Experience
Alexion Pharmaceuticals
Sr. Auditor , Global GxP Audit Quality
Thu Feb 01 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Present
Invicro
Director of Chemistry QA
Wed Mar 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Feb 01 2024 00:00:00 GMT+0000 (Coordinated Universal Time)
Wave Life Sciences
Manager, External Quality & Compliance
Mon Feb 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed Mar 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time)
Avista Pharma Solutions Now Part Of Cambrex
Sr. Director Quality Assurance
Tue Jan 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Aug 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time)
American Distilling
Director of Quality and Regulatory Affairs
Tue May 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Jan 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time)
Pharmasol
VP Quality and Regulatory Affairs
Sun Jan 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Jan 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time)
Independent Consulting
Sr Pharmaceutical Consultant
Sun Jan 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Jan 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time)
University Of Rhode Island
Head of Quality, cGMP Facility (part time)
Sun Jan 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Jan 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time)
Perrigo
Director QA/QC
Thu Jan 01 2009 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Jan 01 2011 00:00:00 GMT+0000 (Coordinated Universal Time)
Teva Pharmaceuticals
Senior Manager Quality Technical Services
Sat Jan 01 2005 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Jan 01 2009 00:00:00 GMT+0000 (Coordinated Universal Time)
Abbott Labs
Manager Product Assurance (Stability)
Fri Jan 01 1999 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Jan 01 2005 00:00:00 GMT+0000 (Coordinated Universal Time)
United States Army Reserve
E4 -Technical Support Engineer
Thu Jan 01 1998 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Jan 01 2001 00:00:00 GMT+0000 (Coordinated Universal Time)
Purdue Pharma
Sr. Chemist and Supervisor
Sat Jan 01 1994 00:00:00 GMT+0000 (Coordinated Universal Time) — Fri Jan 01 1999 00:00:00 GMT+0000 (Coordinated Universal Time)
Sanofi Aventis
Method Development Chemist
Fri Jan 01 1993 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Jan 01 1994 00:00:00 GMT+0000 (Coordinated Universal Time)
Becton Dickinson
R&D Chemist
Wed Jan 01 1992 00:00:00 GMT+0000 (Coordinated Universal Time) — Fri Jan 01 1993 00:00:00 GMT+0000 (Coordinated Universal Time)Skills
Languages
Sergio Richard Wolff Ms Cqa Email Addresses
FAQ About Sergio Richard Wolff Ms Cqa
-
Sergio Richard Wolff Ms Cqa is located at
North Haven, Connecticut, United States -
Sergio Richard Wolff Ms Cqa is a
Experienced analytical chemist, chemical engineer and quality executive with over 20 years of cGMP experience in pharmaceuticals, biotech, nutritionals, medical devices and compounding pharmacy. Specialties: Executive site quality management including QC, QA , stability, investigations, CAPA, change control, specifications, raw material/supply chain management. Quality Systems design, implementation and validation for cGMP manufacturing. Analytical research, development and validation. Internal and external auditing, third party/CMO management, compendia liaison. Data integrity and forensic data investigations. Stability programs for commercial and clinical trail stage (phase appropriate) GMP/GLP . Pharmaco-economics applied to quality functions : cost benefit analysis for QMS implementations, general cost of quality determination, standard hours etc. Alexion Pharmaceuticals -
Sergio Richard Wolff Ms Cqa currently works in the
Alexion Pharmaceuticals -
Sergio Richard Wolff Ms Cqa specializes in
Experienced analytical chemist, chemical engineer and quality executive with over 20 years of cGMP experience in pharmaceuticals, biotech, nutritionals, medical devices and compounding pharmacy. Specialties: Executive site quality management including QC, QA , stability, investigations, CAPA, change control, specifications, raw material/supply chain management. Quality Systems design, implementation and validation for cGMP manufacturing. Analytical research, development and validation. Internal and external auditing, third party/CMO management, compendia liaison. Data integrity and forensic data investigations. Stability programs for commercial and clinical trail stage (phase appropriate) GMP/GLP . Pharmaco-economics applied to quality functions : cost benefit analysis for QMS implementations, general cost of quality determination, standard hours etc. -
Sergio Richard Wolff Ms Cqa speaks the following languages:
No languages available. -
Sergio Richard Wolff Ms Cqa has prior experience in the following industries:
Invicro , Wave Life Sciences , Avista Pharma Solutions Now Part Of Cambrex , American Distilling , Pharmasol , Independent Consulting , University Of Rhode Island , Perrigo , Teva Pharmaceuticals , Abbott Labs , United States Army Reserve , Purdue Pharma , Sanofi Aventis , Becton Dickinson -
Sergio Richard Wolff Ms Cqa has the following professional experience:
Alexion Pharmaceuticals , Invicro , Wave Life Sciences , Avista Pharma Solutions Now Part Of Cambrex , American Distilling , Pharmasol , Independent Consulting , University Of Rhode Island , Perrigo , Teva Pharmaceuticals , Abbott Labs , United States Army Reserve , Purdue Pharma , Sanofi Aventis , Becton Dickinson . -
You can view Sergio Richard Wolff Ms Cqa’s
LinkedIn profile at LinkedIn URL. -
Sergio Richard Wolff Ms Cqa’s work email addresses are
[email protected] . -
Sergio Richard Wolff Ms Cqa works at
Alexion Pharmaceuticals
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