Rianda Steck
Global Pharmacovigilance Quality Audit & Inspection Readiness Expert at Sanofi
- Role
- Pharmacovigilance Audit & Inspection Readiness Expert - Global Pharmacovigilance Quality at Sanofi
- Location
- Morristown, NJ, US
- LinkedIn followers
- 500 followers
About Rianda Steck
With over 16 years of experience in the global biopharmaceutical industry, I have built a strong foundation across both manufacturing and quality functions. This includes 10 years in a GMP vaccine manufacturing environment, spanning Aseptic Filling and Visual Inspection Operations, Project Management, Continuous Improvement, Quality Control, and Quality Assurance — followed by 6+ years in Global Quality, supporting Medical and Pharmacovigilance processes through Quality Assurance, Deviation Management, Quality Risk Management, and Audit & Inspection Readiness.
Experience
Pharmacovigilance Audit & Inspection Readiness Expert - Global Pharmacovigilance Quality
Jan 2025 — Present · Morristown, NJ, US
Education
King's College
Bachelor of Science (BS), Biology, General
2003 — 2007
Skills
- Quality Assurance
- Biotechnology
- Deviations
- Cross-Functional Team Leadership
- Aseptic Technique
- Validation
- Visual Inspection
- Cgmp Practices
- Logistics
- 21 Cfr Part 11
- Process Improvement
- Continuous Improvement
- Gxp
- Aseptic Processing
- Usp
- Vaccines
- Lims
- Change Control
- Lean Manufacturing
- Right First Time
- Cgmp Manufacturing
- Batch Records
- Trackwise
- Quality System
- Pharmaceutical Industry
- Sop
- Fda
- Quality Control
- Gmp
- Manufacturing
- Capa
- Management
- Pharmaceutics
- Project Management
- Technical Writing
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