Data Quality Analyst– Regulatory Affairs
Johnson & Johnson MedTech
Mar 2023 - Jun 2024 (1 year 4 months)
• Archived 51,989 products by developing strategies through MDRIM to mitigate regulatory supply chain risks of medical products • Created predictive models by extracting unstructured data through SQL to track product activity across the licenses in different regions • Worked in tandem with MedTech RA and Regional leads to create possible replacements to avoid shipment delay due to product ineligibility • Analyzed user login activity to modify RAMP access based on eligibility, resulting in monthly savings of $9,570 • Streamlined regulatory processes by migrating relevant RA actions to RAMP to prioritize critical issues for the legacy request manager initiative