Primary Duties Prioritize answering customer inquiries, both internal and external, per established guidelines and documents in ERP system; consult as appropriate with Clinical Applications Specialists, peers, Management, Global Customer Support and Lab IT Specialists. Provide consistent follow up to ensure customer satisfaction and meet minimum key performance indicators

Our mission is to help fight sepsis by providing a rapid Antibiotic Susceptibility Testing solution. The primary purpose of this position is to develop image processing related tools and algorithms to perform signal analysis and classification. The work product will be used internally as well as in production, in the medical device space. PRIMARY DUTIES Design, analyze, i

Work as a technical lead on Sensor Team projects to make fundamental improvements in sensor performance and capabilities Acquire deep understanding of current product chemistry Embrace systems mindset to understand how the sensor interfaces with other subsystems of the VITEK Reveal platform including hardware, software, and microbiology. Develop characterization methods t

As a key team member working alongside the Senior Director, Accounting, this role focuses on assisting in the creation of financial reports for our parent company. You'll contribute to producing accurate and timely financial results, internal management reports, and maintaining internal control processes. Collaborate with various finance and business teams to ensure the p

The operation of high speed equipment used in the production and packaging of VITEK 2 cards in a cGMP environment. Perform or assist in setup, operation, inspection, maintenance, troubleshooting and cleaning equipment. Responsible for completing production batches and corresponding documentation, AQL inspections, reworks, and material reconciliation. Contribute to buildin

1. Perform all work in compliance with company policy and within the guidelines of BFDX's Quality System. 2. Responsible for wet and freeze dried reagent formulations, sub assemblies, and finished goods. 3. Operates Production Equipment. 4. Maintains records in compliance with regulatory requirements, current Good Manufacturing Practices, and Standard Operating Procedures

The Site Manufacturing Controller (SMC) is the Finance Business Partner for the Site Director and sits on the Site Leadership Team. The SMC supports the Site Director and Leadership Team in decision making to maximize value, is responsible for all financial activities and processes from budgeting, to reporting, to forecasting, and represents the site financially to the Re

he Quality Assurance (QA) department provides Quality support across various company departments. The department is organized into distinct subunits, consisting of Metrology, Document Control, Reagent Quality, Instrument Quality, Servicing Quality, and Incoming Material QC. Depending on the sub unit, this individual may review quality records, inspect manufactured product

he Quality Assurance (QA) department provides Quality support across various company departments. The department is organized into distinct subunits, consisting of Metrology, Document Control, Reagent Quality, Instrument Quality, Servicing Quality, and Incoming Material QC. Depending on the sub unit, this individual may review quality records, inspect manufactured product

Enter data into the CAL/PM software Scan calibration certificates into the Cal/PM software Perform Level 1 Calibrations (Pipette, Pressure, Calipers) Perform second person verification of calibration Escort suppliers into restricted areas to perform on site calibration Review and approve calibration and preventative maintenance forms Perform contamination swabbing Schedul

Enter data into the CAL/PM software Scan calibration certificates into the Cal/PM software Perform Level 1 Calibrations (Pipette, Pressure, Calipers) Perform second person verification of calibration Escort suppliers into restricted areas to perform on site calibration Review and approve calibration and preventative maintenance forms Perform contamination swabbing Schedul

This is a full time exempt position. The Quality Engineer I is responsible for assisting with the maintenance of technical aspects of the Quality Management System, including investigations, validations, corrective actions, risk management, and continuous improvement efforts. This person will be working with BioFire employees outside of Quality Assurance on a day to day b

This is a full time exempt position. The Quality Engineer I is responsible for assisting with the maintenance of technical aspects of the Quality Management System, including investigations, validations, corrective actions, risk management, and continuous improvement efforts. This person will be working with BioFire employees outside of Quality Assurance on a day to day b

This is a full time exempt position. The Quality Engineer I is responsible for assisting with the maintenance of technical aspects of the Quality Management System, including investigations, validations, corrective actions, risk management, and continuous improvement efforts. This person will be working with BioFire employees outside of Quality Assurance on a day to day b

Perform all work in compliance with company policy and within the guidelines of BioFire Diagnostics' Quality System. Observe for signs of crime and suspicious activities and report to the proper company departments. Secure premises by completing patrols internal and external to the buildings and document activities in a written log and/or electronic application due at the