• Marketing lead on upstream platform development projects for new assay development• Constructed of the point-of-care portfolio 5-year strategy with extensive market segmentation, channel distribution, competitive differentiation, product positioning, and customer insight• Product management of on-market rapid PCR infectious disease product lines (SARS-CoV-2, Flu A+B, RSV, Strep A)• Drive and coordinate new product /product line extensions on an international basis

• Global management of IVD Drugs of Abuse (DOA) devices throughout the product lifecycle, gathering and prioritizing product and customer requirements, defining product positioning, and working closely with Quality, Engineering, Manufacturing, Finance, and Regulatory to deliver high quality products.• Manage the packaging and labeling process, review and approve product claims for Toxicology & DOA collateral and facilitate translations and updates needed to support new product registration requirements.• Develop sales tools, customer communications, product literature, brochures, and web libraries.• Assist in the strategy and development of new products based on market opportunity and competitive analysis, working closely with R&D, Regulatory, and Quality to ensure the highest quality product reflective of the voice of the customer, utilizing phased gate product development.• Support field representatives by attending sales meetings, training, industry conferences and trade shows.• Focus on expansion of product growth for the Hospital, Clinical, Workplace, and Physician Office Laboratory marketplaces.• Work with global teams to create businesses cases for new product introduction, including North America, Europe, Asia-Pac, LATAM, Middle East, and Africa.• Function as an SME for entirety of product portfolio.• Manage and foster partnerships with third parties based on overall business expansion strategy.

• Support, troubleshoot and document complaints and inquiries on a variety of FDA approved IVD-instrument based products testing for cardiac markers, anticoagulation, lipids, hemoglobin, DOA, blood-gases and diabetes.• Experience with recall and medical device correction notifications including completion of CAPA Activities. • Escalation of complaints regarding potential MDRs for further investigation.• Proposed and implemented a new training program for 2 Alere product lines by creating new technical materials and presentations for incoming trainees.Special Project: Salesforce Validation, December 2015 – July 2016.• Selected as a member of a 4 person focus group to validate a new and improved instance of Salesforce CRM for Alere, Inc. as part of the complaint handling system per global quality objectives.• Considered a subject matter expert on Salesforce functionality, reporting, and complaint review.• Created all training materials & presentations. After launch, the updated CRM has proven effective and was released to 8 different complaint handling sites internationally.

• Liaison between health care professionals to ensure and manage optimal flow of the unit.• Team lead during hospital's transition from paper to electronic medical records (EMRs), training Physicians on the newly implemented software for more efficient patient care.

• Performed patient assessments including vitals, histories, and all other pre-hospital care. • Assessed all medical gear, assigned vehicles and equipment to ensure safe operations.• Vice President of VTRS