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Localisation: Salt Lake City, UT, États-Unis
Type de Contrat: Unfixed Term
Fonction: Supply Chain
At BioFire Diagnostics, LLC. we make the world a healthier place by providing molecular solutions that lessen the time to medical results and empower healthcare professionals to make better diagnostic decisions.
We are proud to be part of the bioMérieux family and the 5,000+ team members across 12 sites and subsidiaries in North America committed to our mission to help save lives around the globe through the power of diagnostics.
Come be a part of our team and our mission as a Production Coordinator!
The Production Coordinator organizes and prepares work within a manufacturing group. Follows a production schedule to coordinate and organize resources necessary for production work orders and to ensure production flows smoothly and efficiently. Creates production batch records, prints/prepares labels, and gathers assigned materials lots for production orders. Participates in cycle counts, delivery of QC samples, and delivery/transaction of R&D materials. Ensures comprehensive compliance for proper documentation of batch records and material requirements for the production staff. Interfaces between production departments and with production schedulers, materials management, QA, and R&D to properly prepare the production orders per schedule requirements. Communicates any potential scheduling issues to the affected groups, and works with the production schedulers and scheduling manager to resolve scheduling issues. Monitors inventory status of production sub-assemblies critical to the manufacturing process, and communicates potential shortages to the production scheduler. Collects, reviews, and inputs data into databases. Has knowledge of commonly used concepts, practices and procedures within cGMP reagent manufacturing. Normally receives general instruction on routine work and detailed instruction on new assignments. The Production Coordinator may participate in process improvements and other documentation efforts. Performs work in compliance with company policy and within the guidelines of BioFire Diagnostics Quality System.
Principal Job Duties and Responsibilities:
Training & Education: High School Diploma required. Bachelor’s degree in a Biology/Chemistry or Supply Chain field is preferred.
Experience: Prior cGMP/FDA/ISO manufacturing experience is required. Prior experience in manufacturing reagents is preferred. Demonstrated working knowledge of PCR is preferred.
Skills: Must have a demonstrated understanding of inventory control and electronic MRP systems and intermediate proficiency using Excel and other Microsoft applications. Must be able to assign and transcribe numerical data associated with assigning and tracking lot numbers. Must be able to use mathematical skills to assess materials availability and assignment to job orders and assess inventory, throughput and yield performance. Must be able to communicate clearly and effectively and have strong attention to detail, organizational, and multitasking skills.
Physical Requirements: Must be able to perform duties wearing a Powered Air Purifying Respirator (PAPR).