Materials Management Compliance & Process Improvement Specialist
Lonza
- Location
- Houston, Texas, United States
- Job type
- Full-time
Required skills
- TrackWise
- Microsoft Word
- Microsoft Excel
About the role
Relevant cGMP pharmaceutical/biotech experience; demonstrated experience authoring controlled procedures and owning deviations/CAPAs; strong technical writing; proficiency with Microsoft Word and Excel; experience with electronic quality and document management systems; Bachelor's degree or equivalent; onsite in Houston.
About Lonza
A global partner to the pharmaceutical and biotech industries.
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