Teams at Epredia

Maintain and optimize the site quality management system for medical device products, ensuring compliance with NMPA GMP, ISO 13485, IVDR, and FDA regulations. Conduct audits, management reviews, document reviews, process mapping, SOP and work-instruction development, training, remediation, CAPA, continuous improvement, document control, and risk management. Collaborate cross-functionally to support regulatory compliance and business growth.

Sell medical and laboratory equipment across Minnesota while meeting sales quotas, developing customer relationships, identifying opportunities, coordinating installations and training, resolving service issues, supporting channel partners, documenting forecasts in Salesforce.com, monitoring competition, and attending trade shows. The role is field-based near Minneapolis and requires overnight travel up to 50%.

Administer and configure Salesforce, including users, permissions, workflows, flows, reports, dashboards, data governance, and access controls. Support CRM enhancements, testing, UAT, releases, integrations, documentation, and post-release monitoring. Maintain data quality, imports, exports, deduplication, and reporting standards. Troubleshoot user issues, deliver training, and partner with commercial, sales, marketing, IT, and CRM leadership to support global CRM operations.