Lee Tang Email & Phone Number

Irving, Tx, Us

• Providing thought-leadership and guiding teams through the digital product transformation journey to transition from project to product centric organization• Mentoring/coaching senior business and DTS leaders on product and agile mindset to enable them as effective leaders in digital product space• Coaching product teams on how to define and monitor outcomes and value realization• Monitoring effectiveness of product management practices and driving continuous improvement

Chicago, Us

• Led the delivery of multi-cloud strategy for GE Healthcare with emphasis on leveraging infrastructure as code• Led the delivery of Infrastructure Asset Management, Cost, Security, Inventory Reporting analytics• Collaborated with internal sub business teams; translating business needs into a cohesive roadmap that maximizes ROI

Chicago, Us

• Led the completed migration of Healthcare applications on GE Predix to a Docker Swarm solution on AWS - est. $1M+ reduction in Predix costs (YoY)• Led the delivery of Workforce Optimization platform that optimizes Field Service Engineers and their assigned systems - est. $2-4M+ in increase FE capacity• Led a defunct cloud team that focused on building a platform as a service on AWS using Kubernetes, Docker, and Infrastructure as Code• Assessing business problems and providing custom software solution proposal as well as standing in for Scrum Master and UX Designer responsibilities

Chicago, Us

•Leading User and Customer experience strategy and governance for US and Canada service business•Leading team to design and build customer solution prototypes•Product Owner of Service Operations and Customer Insights platform to help manage and grow a $2.4B service business – est. $3M benefits•Led functional testing, training, and deployment strategy for IT platform to serve our 2K+ field service engineers – est. $20M benefits•Product Manager from small to large websites, web applications, and mobile applications for our service teams and customers•Design Thinking coach/facilitator to lead groups through design workshops and boot camps so they can be empowered design methodologies•Creating and leading usability testing lab that will increase solution usability

Chicago, Us

Regulatory Affairs IT program - $4M+ Critical IT platform that provides governance over Regulatory Affairs medical device registrations:• Part of $50M FDA mandated Product Controllership program that enabled FDA UDI compliance• Manages all NPI registrations for over 60+ regulated countries• Big Data and analytics enabled through BI integrations Supplier Quality IT Program - $1.2M+ Supplier Quality IT program that enhanced the tracking and rating of external suppliers• Data Consolidation of 6 systems through BI integrations• Provides predictive actionable data of external suppliers part quality and overall quality before it reaches an unacceptable level•Led gathering & managing requirements to comply with FDA Unique Device Identification (UDI) regulations (in compliance).•Partnered with project manager for on time system releases and program milestones (10+ releases).•Implemented a productivity system to reduce time to create training & increase on boarding efficiency (2x training efficiency).•Systems testing strategy and Mobile & Collaboration tools adoption leader

Chicago, Us

The Clinical Research Associate (CRA) supports the Business Research Managers (RMs) through monitoring and coordinating of clinical research studies to ensure research is compliant with Good Clinical Practices and other applicable regulations and company procedures.• Support RMs in performing initial contact and participates in the assessment and selection of qualified investigators for inclusion in research.• Support RMs in completing Pre-Selection, Initiation, Monitoring, and Closeout site visits, or coordinate contractors in their performance of these activities as needed. Track required documentation from study site.• Review and approve study documentation such as protocols, informed consents, amendments, case report forms, and study reports.• Support RMs with initiation of research and site training.• Ensure compliant recording and reporting of any adverse events occurring during research.• Interface with Regulatory Agencies as required.• Ensure overall regulatory compliance of investigational sites with applicable regulations. • Review clinical history file for completeness throughout research process.• Assist with the coordination and conducting of the Research Review meetings.

Princeton, New Jersey, Us

• Responsible for the coordinating and tracking the activities of various operating groups to meet study deadlines and assisting the study director/supervisor in all administrative aspects of analytical studies.• Writing/drafting protocols, sample analysis plan/outline, addendums/amendments, toxicology support reports, validation reports, and sample analysis reports.• Handle routine quality assurance matters and client communications and provide input on assessing new report formats and procedures.• Review and compile data for analytical reports, formats text, data tables, and figures to department conventions or client specifications.• Development of Excel macros to aid in data mining and report writing. • Provide user support and training for Watson Bioanalytical LIMS

• Assisting in FDA 510(K) approval for an IVD assay.• Design and implement experiments relating to IVD assay validation in ISO & cGMP environment.• Proficient at extraction and purification of various sample sources.• Preventive maintenance on various machines and equipment (e.g. Magnapure, thermocyclers)• Document, maintain, and analyze experiment data (e.g. RT PCR CTs & RFUs)• Assisting in FDA 510(K) approval for an IVD assay.• Design and implement experiments relating to IVD assay validation in ISO & cGMP environment.• Proficient at extraction and purification of various sample sources.• Preventive maintenance on various machines and equipment (e.g. Magnapure, thermocyclers)• Help develop electronic document system using web based software

Milwaukee, Wi, Us

• Project Leader for two projects that were presented at the national Neuroscience Conference• Actively managed daily operations such as current project experiments and SOP, purchasing, inventory, resource allocation, maintaining communication between multiple labs on collaborative projects, and negotiating deals with biotech representatives. • Served as liaison between system users and technical support group.• Trained and Managed 12 undergraduate students based upon project needs• Given presentations with an attendance of 20 or more which includes both laymen and experts

Master Of Science (Ms), User Experience Design

Mba, Emphasis In It Management And International Business

Masters, Biotechnology

Bs, Biomedical Sciences