Develop and maintain software solutions for medical devices across desktop, web, and cloud environments. Collaborate closely with cross functional teams to gather requirements and develop software solutions. Refactor and optimize existing code to improve performance, reliability, and maintainability. Engage in the complete software development lifecycle, from design to de

The Associate Engineer Electrical is a technical position expected to play a collaborative role in the electrical engineering design activities developing complex medical diagnostic equipment. Through his or her expertise, this individual contributes to the proof of concept, definition, development and support of specific components and services, throughout the lifecycle

Perform all aspects of electronic design from the initial feasibility stage to manufacturing release for use in medical diagnostic equipment. Using knowledge of schematic design, EMC, analysis, debug, and PCB layout, support and sustain instrument manufacturing activities to facilitate efficient operations within the production environment, optimize existing processes, an

This role will perform calibrations, act as a calibration SME, and provide backup for the Group Lead as needed. This role required interdepartmental collaboration to ensure timely and effective calibration execution without impact to the Production schedule. Normal working hours are Sunday Thursday from 11 00pm 7 30am. Primary Responsibilities Serve as the backup for the

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

Perform all work in compliance with company policy and within the guidelines of BioFire Diagnostics' Quality System. Perform moderately complex repairs involving manual to semi automated manufacturing and/or packaging equipment. Perform basic routine preventative and scheduled maintenance on manual to semi automated production equipment, which may include the replacement

Perform all work in compliance with company policy and within the guidelines of BioFire Diagnostics' Quality System. Perform moderately complex repairs involving manual to semi automated manufacturing and/or packaging equipment. Perform basic routine preventative and scheduled maintenance on manual to semi automated production equipment, which may include the replacement

Perform all work in compliance with company policy and within the guidelines of BioFire Diagnostics' Quality System. Perform moderately complex repairs involving manual to semi automated manufacturing and/or packaging equipment. Perform basic routine preventative and scheduled maintenance on manual to semi automated production equipment, which may include the replacement

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

and Overall Objective of the Job Ensures that Manufacturing existing processes maintain a high level of sustainable performance by continuously reviewing and refining them regarding efficiency, quality improvement, cost reduction and customer satisfaction increase with respect to HSE culture. May manage a team depending on the site size. Main Accountabilities Creates and

QC Technologist works in a cGMP environment performing quality control testing for commercial and diagnostics products. Responsibilities include conducting testing of reagents and IVD materials as well as personnel swabs. In addition, responsibilities include working with the Manufacturing, Technology Transfer and other departments for data collections and validations for

Main Accountabilities Assists in the definition, proof of concept, design, development, implementation and/or support of technical or business solutions by performing specific research activities or developments within the scope of the assigned activity. Assumes responsibility for the identification of errors and related problem solving to identify the necessary activitie

The Sr Marketing Manager, Strategic Partnerships is a downstream marketing role in the NA region that drives the creation and launch of molecular products across all relevant segments. The Marketing Manager will ensure competitive differentiation by demonstrating the value of molecular solutions to all customer key stakeholders and decision makers. This Sr Marketing Manag

Complete initial data review of lot performance for finished good lots Responsible for assigned lot updates, including database entries Complete initial review of investigation use only (IUOs) and adhesive kit match (AKM) lots Performance testing per procedure and schedule (as needed) Troubleshoot performance testing issues with assistance from management. Perform failure

Using good GMP practices, is responsible for timely and accurate inspection and testing of incoming chemicals and analysis of in process product components prior to the release to manufacturing, ensuring compliance with internal specifications. This position must prioritize to ensure schedule is met. Identifies and documents nonconforming materials and maintains trending