Assists in set up on all stations and benches as assigned. Checks documentation to assure that the correct data forms are present and contain the correct identifying information lot#, product name, date, etc. Performs all production per schedule by processing through the production steps as described by procedures. Documents all necessary information on the DHR forms. All

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

Business Analyst Interns partner with software teams to research, plan, test, and maintain critical solutions for various software applications. This will require you to provide high quality customer service to internal parties and develop strong relationships with partners inside the business. You will support technical teams with an understanding of various application

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

We are seeking an experienced and highly skilled Sr Data Engineer to join us. This role requires a seasoned professional with a deep understanding of automated data pipelines, cloud infrastructure, databases, and workflow engines. The ideal candidate will have a minimum of 5 years of technical lead experience in the medical device field and at least 7 years of experience

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