Location: Salt Lake City, UT, United States
Position Type: Unfixed Term
Job Function: Supply Chain
Principal Job Duties and Responsibilities:
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 2!
The Production Coordinator 2 manages product movement across all work centers in Reagent Manufacturing and QC to ensure product flow is not disrupted. Responsible for NCR movement and visibility, coordinates with manufacturing work centers, engineering, QA, QC, BioMath, etc. to ensure NCRs and RNDs are completed in a timely manner. Participates with Continuous Improvement team for NCR/RND process improvement projects. Tracks and manages visibility of validation lots. Communicates product movement, NCR/RND status, and validation lot status across shifts and within scheduling team. Assists with the management and filling of internal orders. Manages Buffer 1A scheduling and coordination within BioFire and participates in communication with the vendor related to the production schedule. 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 coordinate product movement. Communicates any potential scheduling issues to the affected groups, and works with the production schedulers and scheduling manager to resolve scheduling issues. Collects, reviews, and inputs data into databases. Normally receives general instruction on routine work and detailed instruction on new assignments. The Production Coordinator 2 may participate in process improvements and other documentation efforts.
PLEASE NOTE: The working schedule will be every other Wednesday + Sunday – Tuesday from 6:00 PM – 6:00 AM.
Training & Education: High School Diploma required. Bachelor’s degree in a Biology/Chemistry or Supply Chain field is preferred.
Experience: 2 years of cGMP/FDA/ISO manufacturing experience is required. Prior experience in manufacturing reagents 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).