Leading development of flagship product, CaptureNoire. A mobile photography application focused on optimizing a variety of diverse skin tones. Recipient of Pitchfeast Competition, 2nd Place and Audience Choice Award Winner 2023NILE Fund 2023INTAP Grant 2023BeNimble Pitch Competition, Inaugural Grand Prize Winner 2021https://www.ibj.com/articles/editing-suite-for-range-of-skin-tones-is-first-be-nimble-idea-stage-pitch-competition

Founder of Drea & Co, a digital marketing agencyProvides marketing and communications services, social media management, etc.

Provided marketing consultant services:Managed and authored digital content creation for commercial clients, including web copy, printed labeling and advertising materials and digital collateral. Managed and executed client social media strategy, content production and publishing. Created and executed digital launch strategy for the opening of a premiere restaurant chain. Provided photography and videography services. Managed influencer marketing campaigns on behalf of clients. Developed brand identity and marketing guidelines for commercial clients. Developed internal processes and procedures.

Regulatory Affairs and Compliance ConsultantMedical Device Manufacturing

• Conducted domestic and international audits of Approved Supplier Sites to assess manufacturing compliance with current regulations and guidelines - ISO 9001, ISO 13485, ISO 14644, etc. • Participated in the identification, approval and management of pharmaceutical material suppliers and GMP Service Providers

• Provided quality oversight during commercialization and development operations of sterile pharmaceutical product• Provided local guidance of SOPs and direction for CAPA programs while ensuring maintenance of an effective control strategy and regulatory compliance for all new molecules• Promoted a constant state of inspection/audit readiness within GMP manufacturing areas• Supported design, commissioning and qualification strategies of new and existing equipment and systems

• Supported global and domestic (FDA) medical device regulatory compliance and development• Received several Class I, II and III approvals for new medical devices in Japan• Coordinated submission and testing strategy for large scale material change• Organized implementation efforts for internal project tracking software

• Identified a worst case line of products for Ethylene Oxide residual testing• Assured sterilization and biocompatibility testing compliance per international regulatory standards, specifically ISO-10993-7