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

Sourcing Project Manager is responsible for conducting all sourcing activities and managing suppliers for specific assigned categories in accordance with the prescribed sourcing regulations and procedures. The Sourcing Category Project works in conjunction with Engineering Project Managers and Program Management to meet Company manufacturing objectives and increase produc

The primary purpose of this position is to direct Reagents Manufacturing at the St Louis Operations site to ensure that disposable diagnostic product is manufactured per company and Regulatory requirements. This requires the ability to direct the activities of multiple shifts, develop teamwork between departments to ensure consistent product flow, maintain a safety and qu

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

Support and sustain Instrument Manufacturing activities and facilitate efficient operations within the production environment, optimize existing processes and ensure established production goals are achieved. Collaborates with engineers and technicians to ensure the successful design, development, testing and implementation of both product and process changes in support o

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

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

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