Andrea P. Richardson
Program Manager at Bristol-Myers Squibb Company
- Role
- Program Manager at Bristol Myers Squibb
- Location
- Union, NJ, US
- LinkedIn followers
- 500 followers
About Andrea P. Richardson
Sr. Project/Program Manager with 33 years of experience managing multi-million dollar SDLC projects in IT infrastructure and cybersecurity, enterprise applications (e.g, SAP, business intelligence), master data management, data lake ingestion and visualization, IT operations and large manufacturing engineering projects in pharmaceutical industry. Lean Six Sigma “Green Belt”. Strong experience in validation, compliance and risk assessment.CERTIFICATIONS:Project Management Professional (PMP)Certified SAFe® 5 Practitioner (SAFe)Certified ScrumMaster (CSM)Certified Scrum Product Owner (CSPO)Certified Information Systems Auditor (CISA)- Non-Practicing StatusInformation Technology Infrastructure Library (ITIL Certification)Lean Six Sigma “Green Belt”Security Clearance: “Public Trust”
Experience
Program Manager
Mar 2026 — Present · New Brunswick, NJ, US
Leading a strategic digital transformation initiative within commercial manufacturing at Bristol Myers Squibb, focused on modernizing Quality Management System (QMS) capabilities and integrations. Currently managing the migration of change control processes from a highly customized Veeva QMS implementation to a standardized, out-of-the-box Veeva QMS solution, with seamless integration to Veeva RIM. This transformation reduces technical debt, simplifies future system upgrades, and eliminates manual data re-entry by enabling automated data flow between QMS and regulatory systems.
Education
Rutgers University–New Brunswick
Graduate Certificate ("Mini-MBA"), Finance Essentials
2011 — 2011
University of Virginia
B.S., Electrical Engineering
Skills
- Six Sigma
- Gxp
- Quality Auditing
- Quality Assurance
- 21 Cfr Part 11
- Project Management
- Corrective and Preventive Action (Capa)
- Software Documentation
- Sdlc
- Continuous Improvement
- Process Improvement
- Gamp
- Computer System Validation
- Quality System
- V&V
- Pharmaceutical Industry
- Business Process Improvement
- Sop
- Fda
- Gmp
- Validation
- U.s. Title 21 Cfr Part 11 Regulation
- Capa
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