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KBI: US - Global Finite Scheduler, Senior

$99.14k - $136.32k

KBI BioPharma

Overview Position Summary: Responsible for creating and maintaining Finite Production Schedule for assigned site(s) by using a Finite Scheduling software. Responsible for internal alignment and communication of the Production Schedule to all departments involved. Responsible for scheduling and making active work orders in systems of record to signal material picking in the Warehouse and for Support to build PARs. Responsible for scheduling maintenance and metrology activities at assigned site(s). Responsible for assisting, creating, and displaying metrics for the rest of the Global Supply Chain and assisting Planning as needed. Responsibilities Creating and optimizing schedules: Create, track, maintain and optimize short‑term schedules for production by balancing demand with production sequencing and resource efficiency. Work with Manufacturing and Planning Leadership teams on running simulations and scenarios for enhanced decision making. Participate in theoretical capacity evaluations to firm up the cadence, changeover time, shutdown, maintenance windows that derive the total theoretical annual batch count that impacts the budget and financial commitments, and that help track capacity utilization. Incorporating feedback and alignment reached through the S&OE and S&OP processes to ensure feedback about changes to plans are incorporated into schedules in a timely manner and work with teams like material planners, warehouse, quality, and maintenance to ensure alignment and meet company objectives. Ensuring that work orders driving material needs are aligned with the active schedule. Modeling operations: Model different steps of operations, capacity type, buffer type, and wait time constraints and conducting simulations. Perform other work‑related duties as assigned. Qualifications Minimum education required: Bachelor’s degree Minimum experience required: 8+ years preferably as a MFG Operator or Production Control Planner or a combination of education & experience Minimum knowledge required: general cGMP MFG operations (Chromatography, TFF, Automated Systems, etc…) Minimum skills required: Technical writing Proficiency with Microsoft Office Programs Familiarity with SAP, LIMS, MES (Syncade) and other PLC systems Experience in a Scheduler role, preferably within a GMP (Good Manufacturing Principles) environment. Ability to collaborate with functional leaders to support production optimization recommendations. Good communication and presentation skills. Ability to present ideas in a clear and concise manner. Analytical skills with the ability to measure and report metrics and help to identify issues through peers and manager through root cause analysis. Salary & Benefits Salary Range: $99,142 - $136,321. The role offers an annual bonus structure, comprehensive medical, dental and vision coverage, paid PTO and holidays, 401K matching with 100% vesting in 60 days, and employee recognition programs. EEO Statement KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its workforce. All qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability, or veteran status, are strongly encouraged to apply. #J-18808-Ljbffr

Vacancy posted 4 days ago
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