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KBI Biopharma

CDMO delivering cell line development

Manufacturing Senior Scheduler

Production Planning & SchedulingConfirmed live in the last 24 hours
Full-timeDurham, NC, USANo salary listedIn-person

About the Job

Requirements

  • An associate's degree is required.
  • A minimum of five years' experience in manufacturing, production planning, scheduling, supply chain, operations, or a related field is preferred.
  • Direct experience supporting biopharmaceutical manufacturing operations is strongly preferred.
  • Demonstrated experience developing or managing resource-constrained production schedules is preferred.
  • Experience supporting multi-product manufacturing environments is preferred.

Responsibilities

  • Own and maintain the Manufacturing production schedule as the single source of truth for daily, weekly, one-month, and three-month production planning.
  • Develop integrated finite schedules that align manufacturing activities with equipment and facility availability, staffing and skill requirements, materials, maintenance, Quality/QC, environmental monitoring, and other operational dependencies.
  • Facilitate cross-functional scheduling with Manufacturing, MS&T, Supply Chain, Quality, QC, Facilities, Maintenance, and other stakeholders to ensure production readiness and alignment.
  • Identify and manage constraints and scheduling conflicts by assessing impacts to production, resources, equipment, facilities, materials, staffing, and manufacturing commitments.
  • Develop schedule recovery and mitigation plans for equipment downtime, material delays, process deviations, maintenance activities, staffing constraints, facility outages, and other disruptions.
  • Coordinate materials and manufacturing support requirements, ensuring raw materials, consumables, work orders, environmental monitoring, testing, and other support activities are aligned with the production schedule.
  • Integrate maintenance, calibration, facility activities, and shutdowns into the production schedule to minimize disruption to Manufacturing operations.
  • Maintain and improve scheduling standards and assumptions, including process durations, equipment occupancy, setup/teardown, cleaning, room turnover, hold times, and changeovers, using actual execution data to improve schedule accuracy.
  • Support capacity planning and scenario analysis by evaluating production cadence, equipment and facility constraints, staffing requirements, new programs, campaign changes, and other factors affecting Manufacturing capacity.
  • Develop and communicate scheduling KPIs and trends, including schedule adherence, production attainment, capacity utilization, constraints, and schedule changes, to support data-driven decision-making and continuous improvement.
  • Escalate significant scheduling risks and unresolved conflicts to Manufacturing leadership with clear impacts, options, tradeoffs, and recommended actions.

About the Company

KBI Biopharma

CDMO delivering cell line development

KBI Biopharma is a CDMO that accelerates the development of biological medicines by providing rapid cell line generation and process development for preclinical programs. It uses established mammalian and microbial expression systems (such as CHO K1, CHO S, CHO DG44, HEK293, and DXB11 E. coli) to create production cell lines and develop integrated manufacturing processes. Compared with competitors, it wins on speed, end-to-end capability, and flexibility across multiple platforms to move projects quickly from discovery to preclinical milestones for a diverse client base. Its goal is to reduce risk, shorten development timelines, and expand global access to life-saving biologic therapies.

Company size
1,001-5,000
Company stage
Late Stage VC
Total funding
$109.5M
Headquarters
Durham, NC
Founded
1996

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