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Diana Rivera Location
Round Lake, IL, US
Diana Rivera Work
2021 -now Manager, Regulatory Affairs CMC, Medical Devices and Combination Products @
2013 -2021 Sr. Quality Assurance Mgr @
2011 -2013 R and D Quality Assurance @
2008 -2011 Project Manager @
2001 -2008 Quality Assurance @
Diana Rivera Education
Chicago Medical School
MS (Biochemistry)
1995-1999
Diana Rivera Skills
Quality Management
Design Control
Clinical Trials
Computer System Validation
HPLC
GMP
Hardware Diagnostics
ISO 13485
GxP
Biotechnology
Change Control
Regulatory Affairs
Software Documentation
Life Sciences
Validation
Medical Devices
Quality Assurance
Corrective and Preventive Action Capa
Regulatory Requirements
Quality System
Lifesciences
V&V
Quality Auditing
GCP
Cross Functional Team Leadership
Document Management
Manufacturing
Clinical Development
u.s. Food and Drug Administration Fda
Regulatory Submissions
Microbiology
Project Management
Standard Operating Procedure Sop
Quality Control
Pharmaceutical Industry
Technology Transfer
GLP
LIMS
CAPA
FDA
R&d
Sop
21 CFR Part 11
Biopharmaceuticals
u.s. Food and Drug Administration
Standard Operating Procedure
Corrective and Preventive Action
Diana Rivera Summary
Diana Rivera, based in Round Lake, IL, US, is currently a Manager, Regulatory Affairs CMC, Medical Devices and Combination Products at AbbVie. Diana Rivera brings experience from previous roles at AbbVie, Abbott Laboratories and Abbott Diagnostics. Diana Rivera holds a 1995 - 1999 MS in Biochemistry @ Chicago Medical School. With a robust skill set that includes Quality Management, Design Control, Clinical Trials, Computer System Validation, HPLC and more. Diana Rivera has 2 emails and 1 mobile phone numbers on RocketReach.
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