Alexandra Eldredge Email & Phone Number

Atlanta, Ga, Us

Atlanta, Georgia, United States

Atlanta, Georgia, United States

Greater Atlanta Area

Fort Lauderdale, Florida

Provide field support, including case coverage and troubleshooting, for the EnSite Velocity and EnSite Precision Cardiac Mapping Systems. Maintain knowledge of electrophysiology and Abbott EP products as a part of case support. Provide field support, including case, clinic, and on-demand coverage and troubleshooting, for St. Jude Medical/Abbott cardiac rhythm management devices, including pacemakers, implantable cardioverter-defibrillators, cardiac resynchronization therapy devices, and… Show more Provide field support, including case coverage and troubleshooting, for the EnSite Velocity and EnSite Precision Cardiac Mapping Systems. Maintain knowledge of electrophysiology and Abbott EP products as a part of case support. Provide field support, including case, clinic, and on-demand coverage and troubleshooting, for St. Jude Medical/Abbott cardiac rhythm management devices, including pacemakers, implantable cardioverter-defibrillators, cardiac resynchronization therapy devices, and implantable loop recorders. Maintain knowledge of cardiac rhythm management and Abbott CRM products as part of case and clinical support. Provide technical and educational support to physicians, health care professionals, and patients on Abbott Atrial Fibrillation and Cardiac Rhythm Management products. EnSite NavX, EP Product, and CRM certified. Show less

Alpharetta, Georgia

Extensive experience working in regulated manufacturing environment with ISO Class 8 clean rooms and compliance with 21 CFR 820, ISO 13285:2003, SOR/98-282 (Health Canada), and other international requirements.Initiated and documented project design reviews per the company’s Design Control procedures.Developed, wrote and edited technical documentation such as Device Master Records (DMRs); process documentation such as work instructions, finished product specifications, and raw… Show more Extensive experience working in regulated manufacturing environment with ISO Class 8 clean rooms and compliance with 21 CFR 820, ISO 13285:2003, SOR/98-282 (Health Canada), and other international requirements.Initiated and documented project design reviews per the company’s Design Control procedures.Developed, wrote and edited technical documentation such as Device Master Records (DMRs); process documentation such as work instructions, finished product specifications, and raw material specifications; and regulatory documentation. Wrote and executed design verification and process validation protocols per the requirements of the company’s quality system, including Validation Master Plans (MVPs), Operational Qualifications (OQ) and Performance Qualifications (PQ), Aging and Stability studies, and Design Verification Testing. Collected and analyzed qualification data. Wrote validation/verification reports to include results, data analysis, and conclusions.Created product and process risk management documentation (e.g. Design/Process Failure Modes and Effects Analysis, Design Input/Output Document, and Master Quality Plan) within quality system.Redesigned Instructions for Use (IFU) label for a company product as part of a cost-reduction project.Organized the removal of project/product documentation from the quality system, and executed documentation change notifications to remove identified inactive projects/products. Show less

Provisioned and upgraded company mobile devices, completed documentation, and shipped equipment. Provided customer support to LexisNexis and Reed Elsevier employees. Responsible for implementing summer BlackBerry upgrade project and providing support.