Job Details

ID #51136333
Estado Carolina del Norte
Ciudad Durham
Full-time
Salario USD TBD TBD
Fuente BioFire Diagnostics, LLC.
Showed 2024-02-27
Fecha 2024-02-28
Fecha tope 2024-04-28
Categoría Etcétera
Crear un currículum vítae

Packaging Tech - Night Shift

Carolina del Norte, Durham, 27701 Durham USA

Vacancy caducado!

Benefits at bioMerieux: Low-cost medical, dental, and vision benefits starting day one.11 paid holidays160 hours of paid time offAnnual bonus9.5% 401k company contribution with no vesting periodTuition reimbursement up to $10,000 per calendar yearOnsite cafeteria with daily food stipendPosition Summary:Normal working hours: 7:00pm - 7:30am working a 2-2-3The 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 and cleaning of equipment used throughout the BacT/ALERT Manufacturing and Packaging processes · Additionally, this individual will be responsible for completing production batches and corresponding documentation for the associated task · AQL inspections, reworks and Material reconciliation that goes along with the batch. Primary Responsibilities: · Production: · Operate high speed manufacturing equipment, in some cases highly automated, using HMI/SCADA interfaces · Execute production activities per approved Manufacturing Directions while maintaining compliance with all job-related SOPs · Quality: · Ensure that all batch paperwork is completed in an accurate, thorough, and timely manner · Perform and document all processes and procedures in a timely manner, while maintaining compliance with all company and regulatory agency regulations · Provide assistance with the review and revision of Manufacturing Directions and SOPs necessary for the manufacture and packaging of product. · Assist with manufacturing deviation analysis, CAPA actions and other process equipment related quality concerns · Maintain all work areas in a well-organized, clean and tidy manner at all times in compliance with cGMP requirements · Operate cleaning equipment, utilize SOP and documentation to record data manually or through identified software applications. · Safety: · Comply with all safety policies and procedures at all times · Appropriately use PPE (Personal Protection Equipment) as required to perform routine and non-routine duties. · Other Duties: · Generate reports, charts and KPI's and interpret the data to identify problems, and proceed with proper decision making · Assist with executing validation protocols associated with manufacturing/packaging equipment and procedures including revalidation as scheduled or required to maintain systems in a validated state · Perform computer applications · Perform other duties as assigned by Management Knowledge, Skills, & Experience: · High School Diploma or GED Required · Certification in a Bioworks Program or equivalent is preferred · Demonstrated proficiency in the operation of high speed, highly automated, production equipment preferred. · Knowledge of and experience in following OSHA regulations (LOTO, electrical safety, etc.) preferred. · Knowledge of FDA and/or GMP regulations preferred. · Mechanical background preferred.

Vacancy caducado!

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