Full-stack bootcamp designing software systems and solutions with 800+ hours of education and application including:Object-Oriented Programming: JavaWeb Application Development: HTML, CSS, JavaScript, Spring Boot, Vue.jsDatabase Programming: JDBC, Table Design, SQL, PostgreSQL, E/R diagramsDevelopment Tools and Techniques: Agile, Unit Testing (JUnit), Integration Testing, Git, IntelliJ

• Maintained eDMS (SAP) as the company's go-to subject matter expert for 100% of Quality Systems review. • Accelerated completion of tasks through collaboration site wide to promote cross-functional teamwork, effective communication, and task prioritization for tight project deadlines. • Empowered quality system associates by providing comprehensive training on the functionalities and processes within the eDMS system, resulting in enhanced understanding of system operations.

• Lead, maintained, improved, and executed the Internal Audit Program. o Prepared internal audit documentation including schedule, attendance, audit plan, and summary reports, to ensure conformance with applicable regulation and company procedures. o Assessed previous audit findings to establish strategies and evaluated the effectiveness of the actions taken. o Assessed objective evidence to determine conformity to cGxPs, GDP, and SOP requirements, including ranking the levels of nonconformance findings.• Managed eDMS system and was a site SME regarding its operation and functionality. o Worked closely with other departments to foster cross-functional teamwork, communication, and prioritization in relation to support documentation activities. o Identified areas for continuous process improvement. o Provided final review of documents to ensure compliance regarding content and format. o Processed document change requests. o Trained quality system associates in the functions and processes in the DMS system.• Harmonized new hire training across Nitto Denko Avecia sites.• Transferred and updated quizzes associated with 50 SOPs into the company’s electronicsystem.• Updated procedures specific to quality systems department.• Issued, filed, and retrieved records and documents in compliance with cGMP and companypolicies and procedures.

• Specialized in creating new/managing the revision of pre-existing documents in TrackWise eDMS for all Andelyn Staff. • Coordinated with other departments to ensure FDA compliance with cGMP, GDP, and procedures applicable regulatory requirements for Phase I/II cellular and gene therapy products. • Assigned lot numbers for production in SAP, issues, and reviews Manufacturing Batch Records. • Assisted Training Department in management of Learning Management System. • Trained new Quality Assurance staff members in the inner workings of the document management system.

• Fast-paced wet lab-oriented environment that tested for qualitative and quantitative amounts of microorganisms in a variety of matrixes. • Adhered to company SOPs to ensure products were free of food borne illnesses that could harm consumers. • Managed multiple priorities and worked independently, in areas requiring both manual labor and administrative record keeping.

• Worked in a detail-oriented environment that ensured patient safety by inspecting vials and syringes for defects. • Adhered to current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP) as well as company Standard Operating Procedures (GDP) to provide a safe product for patients.

• Conducted and developed experiments to elucidate the function of metabolic enzymes that are predicted to be involved in the quaternary amine catabolism of methanogens in Dr. D.J. Ferguson's lab.

• Cleaned and organized glassware, maintained inventory of lab equipment and materials to ensure research productivity for Dr. D.J. Ferguson's lab.

• Engaged in biological field research surveying the monogamist behavior of male prairie voles.