Stephen Lexa's Location
Carmel, IN, US
Stephen Lexa's Work
- Sr. Director - Clinical Manufacturing @ Eli Lilly and Company
- Associate Sr. Consultant, Quality @ Eli Lilly and Company
- Manager - QA BioProcess R and D @ Eli Lilly and Company
- Associate Consultant - Development Quality - Infrastructure, Governance and Improvement @ Eli Lilly and Company
- Manager, Production @ Boehringer Ingelheim
- Manager, Quality Assurance @ Boehringer Ingelheim
- Supervisor, Quality Assurance @ Boehringer Ingelheim
- Manufacturing Floor Auditor I and II, Manufacturing Quality Assurance @ Boehringer Ingelheim
- Financial Advisor @ Morgan Stanley
Stephen Lexa's Education
- University of Toledo College of Pharmacy
Bachelor of Science in Pharmaceutical Sciences (Pharmacy Administration)
2000 - 2005
Stephen Lexa's Skills
- cGMP manufacturing
- cGMP practices
- Batch Records
- Batch Release
- Batch Processing
- 21 CFR Part 11
- 21 CFR Part 210
- 21 CFR Part 211
- EU Annex 1
- FDA
Stephen Lexa's Summary
Stephen Lexa, based in Carmel, IN, US, is currently a Sr. Director - Clinical Manufacturing at Eli Lilly and Company, bringing experience from previous roles at Eli Lilly and Company and Boehringer Ingelheim, Ben Venue Laboratories. Stephen Lexa holds a 2000 - 2005 Bachelor of Science in Pharmaceutical Sciences in Pharmacy Administration @ University of Toledo College of Pharmacy. With a robust skill set that includes cGMP manufacturing, cGMP practices, Batch Records, Batch Release, Batch Processing and more, Stephen Lexa contributes valuable insights to the industry. Stephen Lexa has 3 emails on RocketReach.
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