Clean in manufacturing/clean room environments and labs where PPEs or other gowning and entrance/exit procedures must be followed. Responsible for cleaning entryways, hallways, bathrooms, offices, and indoor/outdoor common areas. Cleaning floors includes vacuuming, sweeping, moping, and using a floor scrubber. Clean and disinfect restrooms including urinals/toilets, count

Microbiologist is responsible for review of finished good lot performance data to ensure all lots meet current specifications. Performs performance testing and additional testing for assigned lot as needed. Uses good aseptic lab practices, is responsible for timely and accurate testing of VITEK2 finished good cards to ensure they meet all defined acceptance criteria and m

Primary Duties 1. Serve as the internal primary point of contact with US Key Accounts. 2. Prioritize the US Key Account orders, communicate expiring pricing, expiring scheduling agreements and about the products availability when back orders / allocations occur and ensure their follow up (allocation, priorities & management). 3. Communicates with internal departments, mai

This marketing role manages all aspects of current and future bioMerieux Molecular Panels product development for some dedicated clinical areas, from voice of customer collection, to concept design and to development. This position works closely with system and software Global Marketing team, with Global Marketing Market Data & Insights, R&D, projects and programs, Global

Be a key business partner to support business transformation, build and promote the IS project portfolio of a business related domain for which they are accountable of the execution. Primary Responsibilities Relationship Management Act as leader with all IS resources involved in project deliveries by providing guidance and supervisory support to the project ensuring align

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

As part of the Industrialization department, the Process Engineer will develop and/or manage process improvement projects to support the manufacturing of in vitro diagnostics. Within this role the Process Engineer will be required to interface with Manufacturing, Quality Control, Quality Assurance, R&D, Purchasing, Supply Chain, HSE, and other functions as required, to en

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

Normal working hours 7 00pm 7 30am working a 2 2 3 The Process Technician position is responsible for the operation of high speed equipment used in the production and packaging of BacT/ALERT bottles and/or preparing and formulating the liquid reagents that fill the finished BacT/ALERT bottle in a cGMP compliant manner. The position may perform or assist in the setup, insp

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

The Process Technician position is responsible for the operation of high speed equipment used in the production and packaging of BacT/ALERT bottles and/or preparing and formulating the liquid reagents that fill the finished BacT/ALERT bottle in a cGMP compliant manner. The position may perform or assist in the setup, inspection, preventive maintenance, troubleshooting, an

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

The MES Data Administrator role is to be part of the Operational Technology team which supports configuration, enhancement, interface, and operation of the Manufacturing Execution System (MES) as well as maintenance of our Manufacturing network and current and future software applications that support our manufacturing operations. Primary Responsibilities Plan, design, de