Steve Weis Email & Phone Number
Director, Product Quality Assurance and Compliance @ Melinta Therapeutics
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Steve Weis Location
- Antioch, IL, US
Steve Weis Work
- Director, Product Quality Assurance and Compliance @ (February 2021 - Present)
- Senior Manager, Contractor Quality Lead, Contract Operations Quality Assurance @ (April 2017 - December 2020)
- Senior Manager, Business Development Quality, External Supply Quality @ (October 2019 - May 2020)
- Senior Quality Manager, Supplier Quality, Pharma Chemicals @ Hospira Pfizer (September 2015 - April 2017)
- Senior Quality Program Manager, Global Supplier Quality, Apis @ (September 2012 - April 2017)
- Senior Quality Program Manager @ (October 2011 - September 2012)
- Quality Program Manager @ (April 2006 - October 2011)
- Quality Analyst @
- Manager, GMP Documentation @ (December 2001 - October 2003)
- Senior Validation Consultant @ Progressive Validation (October 2000 - December 2001)
- Supervisor, Product Release @ (March 1996 - November 1997)
- Analytical Research Chemist @ (July 1992 - December 1994)
- Manager, Quality Assurance @
- Quality Assurance Specialist @
Steve Weis Education
- Webster University
Master of Arts (Management)
1989-1991 - Quincy University
Bachelor of Science
1980-1984 -
(General Studies)
1976-1980
Steve Weis Skills
- Six Sigma
- Quality Management
- Quality System Compliance
- Procedure Writing
- Quality Operations
- Good Documentation Practices
- Parenteral
- Analytical Methods Development
- Equipment Qualification
- Computer System Validation
- GMP
- Annual Product Quality Review
- GxP
- Change Control
- Supplier Quality
- Validation
- Process Improvement
- Quality Assurance
- Cleaning Validation
- Active Pharmaceutical Ingredients
- Documentation Management
- Quality System
- SOP development
- Pharmaceuticals
- Quality Auditing
- Document Management
- Stability
- FDA GMP
- Batch Release
- Laboratory Controls
- Regulatory Submissions
- Excipients
- Distribution Center Operations
- Operational Excellence
- Instrument Qualification
- Quality Control
- Pharmaceutical Industry
- Incoming Quality Assurance
- Technology Transfer
- Continuous Improvement
- LIMS
- CAPA
- Analytical Method Validation
- FDA
- Batch Records
- Sop
- 21 CFR Part 11
- R&d
- Solid Oral Dosage Forms
- Good Distribution Practices
- Product Quality
Steve Weis Summary
- Steve Weis, based in Antioch, IL, US, is currently a Director, Product Quality Assurance and Compliance at Melinta Therapeutics. Steve Weis brings experience from previous roles at Pfizer, Hospira Pfizer and Hospira. Steve Weis holds a 1989 - 1991 Master of Arts in Management @ Webster University. With a robust skill set that includes Six Sigma, Quality Management, Quality System Compliance, Procedure Writing, Quality Operations and more. Steve Weis has 2 emails and 1 mobile phone numbers on RocketReach.
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Top Melinta Therapeutics Employees
Ting Chen
Head of Regulatory Affairs
Florham Park, NJ, US
Craig Counseller
Key Account Manager
Delhi charter Township, MI, US
William Waverczak
Associate Director, Clinical Operations
Parsippany-Troy Hills, NJ, US
Sandra George
Clinical Trial Manager
Simsbury, CT, US
Tiffani Wallace
Senior Key Account Manager
Ann Arbor, MI, US
Katie Klaveano
Key Account Manager
Kirkland, WA, US
Jim Summers
Key Account Manager
Madison, WI, US
Barbara Taylor
Sr. Regional Sales Director
Decatur, GA, US
John Meyer
Director IT
Downers Grove, IL, US
Sameer Late
Director, Regulatory Affairs
Philadelphia, PA, US
Yusheng Wu
Research Associate Director
New Haven, CT, US
Antonie Horton
Associate Director Regulatory Affairs
Texas, United States
Jamal Brown
Sr. Director, GMP QA & Compliance
Parsippany-Troy Hills, NJ, US
Mark Redell
VP Medical Affairs
Phoenix, AZ, US
Eugenia Madar
Senior Financial Analyst
Grayslake, IL, US
Jeff Hull
Senior Director of Market Access, National Accounts
Nashville, TN, US
Pooja Chopra
Director, Technical Operations
Philadelphia, PA, US
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