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Steve Weis

Analytical, structured and systematic pharmaceutical quality professional with extensive and diverse industry experience encompassing Research and Development (R&D),... | Antioch, Illinois, United States

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Steve Weis’s Emails sw****@as****.org

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Steve Weis’s Location Antioch, Illinois, United States

Steve Weis’s Expertise Analytical, structured and systematic pharmaceutical quality professional with extensive and diverse industry experience encompassing Research and Development (R&D), Active Pharmaceutical Ingredients (API) and Drug Product (DP) quality operations. Detail- and data-oriented, leveraging knowledge of manufacturing, packaging, storage/distribution, and laboratory management to facilitate site and contractor quality management. Foster consistency in processes, procedures, and practices. Adept communicator, collaborator, and leader, aligning with stakeholder to build consensus, and deliver on high standards across quality management. Areas of expertise: Quality Assurance (QA) Good Manufacturing Practices (GMP) Supplier and Contractor Quality Management Global Regulations Root Cause Analysis CAPA Active Pharmaceutical Ingredients (API) Drug Product (DP) Audit Validation and Qualification DP and API Manufacturing Packaging Operations Stability Warehousing and Distribution Supply Chain Quality Agreements Change Management Continuous Improvement Six Sigma and DMAIC Quality Control (QC) Laboratory Method Development Raw Material, API and DP Testing

Steve Weis’s Current Industry Melinta Therapeutics

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Work Experience

Melinta Therapeutics

Director, Product Quality Assurance and Compliance

Mon Feb 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Present

Pfizer

Senior Manager, Business Development Quality, External Supply Quality

Tue Oct 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time) — Fri May 01 2020 00:00:00 GMT+0000 (Coordinated Universal Time)

Pfizer

Senior Manager, Contractor Quality Lead, External Supply Quality

Sat Apr 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Dec 01 2020 00:00:00 GMT+0000 (Coordinated Universal Time)

Hospira Pfizer

Senior Quality Manager, Supplier Quality, Pharma Chemicals

Tue Sep 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Apr 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time)

Hospira

Senior Quality Program Manager, Global Supplier Quality, APIs

Sat Sep 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Apr 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time)

Hospira

Senior Quality Program Manager

Sat Oct 01 2011 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Sep 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time)

Hospira

Quality Program Manager

Sat Apr 01 2006 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Oct 01 2011 00:00:00 GMT+0000 (Coordinated Universal Time)

Hospira

Quality Analyst

Wed Oct 01 2003 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Apr 01 2006 00:00:00 GMT+0000 (Coordinated Universal Time)

Pharmacia

Manager, GMP Documentation

Sat Dec 01 2001 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed Oct 01 2003 00:00:00 GMT+0000 (Coordinated Universal Time)

Progressive Validation

Senior Validation Consultant

Sun Oct 01 2000 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Dec 01 2001 00:00:00 GMT+0000 (Coordinated Universal Time)

Sanofi Synthelabo

Manager, Quality Assurance

Thu Apr 01 1999 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Oct 01 2000 00:00:00 GMT+0000 (Coordinated Universal Time)

Sanofi Synthelabo

Quality Assurance Specialist

Sat Nov 01 1997 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Mar 01 1999 00:00:00 GMT+0000 (Coordinated Universal Time)

Mallinckrodt

Supervisor, Product Release

Fri Mar 01 1996 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Nov 01 1997 00:00:00 GMT+0000 (Coordinated Universal Time)

Mallinckrodt

Analytical Research Chemist

Wed Jul 01 1992 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Dec 01 1994 00:00:00 GMT+0000 (Coordinated Universal Time)

Skills

Languages

Steve Weis Email Addresses

sw****@as****.org Work Email

sw****@as****.org Personal Email

sw****@me****.com Personal Email

FAQ About Steve Weis

Steve Weis is located at
Antioch, Illinois, United States

Steve Weis is a
Analytical, structured and systematic pharmaceutical quality professional with extensive and diverse industry experience encompassing Research and Development (R&D), Active Pharmaceutical Ingredients (API) and Drug Product (DP) quality operations. Detail- and data-oriented, leveraging knowledge of manufacturing, packaging, storage/distribution, and laboratory management to facilitate site and contractor quality management. Foster consistency in processes, procedures, and practices. Adept communicator, collaborator, and leader, aligning with stakeholder to build consensus, and deliver on high standards across quality management. Areas of expertise: Quality Assurance (QA) Good Manufacturing Practices (GMP) Supplier and Contractor Quality Management Global Regulations Root Cause Analysis CAPA Active Pharmaceutical Ingredients (API) Drug Product (DP) Audit Validation and Qualification DP and API Manufacturing Packaging Operations Stability Warehousing and Distribution Supply Chain Quality Agreements Change Management Continuous Improvement Six Sigma and DMAIC Quality Control (QC) Laboratory Method Development Raw Material, API and DP Testing Melinta Therapeutics

Steve Weis currently works in the
Melinta Therapeutics

Steve Weis specializes in
Analytical, structured and systematic pharmaceutical quality professional with extensive and diverse industry experience encompassing Research and Development (R&D), Active Pharmaceutical Ingredients (API) and Drug Product (DP) quality operations. Detail- and data-oriented, leveraging knowledge of manufacturing, packaging, storage/distribution, and laboratory management to facilitate site and contractor quality management. Foster consistency in processes, procedures, and practices. Adept communicator, collaborator, and leader, aligning with stakeholder to build consensus, and deliver on high standards across quality management. Areas of expertise: Quality Assurance (QA) Good Manufacturing Practices (GMP) Supplier and Contractor Quality Management Global Regulations Root Cause Analysis CAPA Active Pharmaceutical Ingredients (API) Drug Product (DP) Audit Validation and Qualification DP and API Manufacturing Packaging Operations Stability Warehousing and Distribution Supply Chain Quality Agreements Change Management Continuous Improvement Six Sigma and DMAIC Quality Control (QC) Laboratory Method Development Raw Material, API and DP Testing

Steve Weis speaks the following languages:
No languages available.

Steve Weis has prior experience in the following industries:
Pfizer , Pfizer , Hospira Pfizer , Hospira , Hospira , Hospira , Hospira , Pharmacia , Progressive Validation , Sanofi Synthelabo , Sanofi Synthelabo , Mallinckrodt , Mallinckrodt

Steve Weis has the following professional experience:
Melinta Therapeutics , Pfizer , Pfizer , Hospira Pfizer , Hospira , Hospira , Hospira , Hospira , Pharmacia , Progressive Validation , Sanofi Synthelabo , Sanofi Synthelabo , Mallinckrodt , Mallinckrodt .