Manufacturing SchedulerPlanner

Job summary

The Manufacturing Production Scheduler develops maintains and manages the finite production schedule in support of Manufacturing operations. The incumbent is the primary owner of the near-term manufacturing schedule and ensures production requirements equipment availability personnel constraints material readiness maintenance activities facility support and other critical dependencies are integrated into an executable production plan.

The Production Scheduler partners closely with Manufacturing Manufacturing Sciences and Technology (MS&T) Supply Chain Quality QC Facilities Maintenance and other support functions to ensure schedule accuracy identify and resolve constraints assess the impact of schedule changes and support reliable execution of manufacturing operations.

The incumbent maintains short- and medium-term production visibility facilitates routine scheduling discussions develops recovery scenarios when disruptions occur and escalates risks with clear impact assessments and recommended options.

Job Responsibilities

• Develop maintain and continuously improve a finite scheduling system in support of daily weekly and longer-term Manufacturing operations.
• Serve as the primary owner and single source of truth for the near-term Manufacturing production schedule.
• Maintain an integrated production schedule that reflects process requirements equipment availability facility constraints personnel and skill requirements material readiness maintenance activities and other critical manufacturing dependencies.
• Ensure program requirements and scheduling assumptions accurately reflect support upstream and downstream manufacturing processes through coordination with Manufacturing and MS&T.
• Maintain appropriate scheduling horizons including:
• Detailed daily and weekly execution schedules
• Rolling 1-month finite production schedule
• 3-month production look-ahead
• Longer-term constraint and capacity visibility as required
• Facilitate weekly production scheduling meetings with Manufacturing and key cross-functional stakeholders to review upcoming activities constraints schedule changes production readiness and required actions.
• Coordinate schedule changes with Manufacturing MS&T Supply Chain Quality QC Facilities Maintenance and other support functions as appropriate.
• Assess the impact of proposed or unplanned schedule changes on subsequent manufacturing activities equipment utilization facility availability staffing materials maintenance windows and overall production commitments.
• Identify scheduling conflicts and operational constraints proactively and work with cross-functional teams to develop mitigation or recovery plans.
• Develop and communicate schedule recovery scenarios following equipment downtime material delays process deviations maintenance activities staffing constraints or other production disruptions.
• Escalate unresolved scheduling conflicts and risks to Manufacturing leadership with clear identification of impacts options tradeoffs and recommended actions.
• Support coordination and creation of material work orders and material plans required for support upstream and downstream manufacturing activities.
• Partner with Supply Chain and Manufacturing to ensure required raw materials consumables and other production materials are available in accordance with scheduled dates.
• Integrate preventive maintenance corrective maintenance calibration Facility Response activities shutdowns and other facility or equipment support activities into the production schedule to minimize impact to Manufacturing operations.
• Coordinate with Manufacturing leadership to identify personnel shift coverage and critical skill requirements associated with scheduled manufacturing activities.
• Incorporate relevant Quality and QC dependencies into the schedule including sampling testing release activities environmental monitoring and other required manufacturing support activities where appropriate.
• Create and manage manufacturing support requests associated with scheduled operations including environmental monitoring or other cross-functional support requirements.
• Maintain and periodically review standard scheduling assumptions including process durations equipment occupancy setup and teardown requirements room turnover cleaning activities hold times changeovers and other process dependencies.
• Compare actual manufacturing execution against scheduling assumptions and update scheduling standards as process knowledge and operational performance improve.
• Support scenario modeling and what-if analysis for new programs campaign changes increased production cadence equipment constraints facility outages and other changes affecting Manufacturing capacity.
• Support development of production capacity assessments and identify emerging bottlenecks or constraints within the near- and medium-term manufacturing horizon.
• Develop maintain and communicate Manufacturing scheduling Key Performance Indicators and trends.

Responsibility

Develop/Maintain/Improve finite schedule for Manufacturing Operations

Support material plan requests

Coordination of facility maintenance events

Minimum Requirements

• Associates degree required; bachelors degree in supply chain engineering operations management life sciences business or a related discipline preferred

• A minimum of five years experience in manufacturing production planning scheduling supply chain operations or a related field preferred

• Direct experience supporting biopharmaceutical manufacturing operations strongly preferred

• Demonstrated experience developing or managing resource-constrained production schedules preferred

• Experience supporting multi-product manufacturing environments preferred

Nothing in this job description restricts managements right to assign or reassign duties and responsibilities to this job at any time.

KBI Biopharma Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore 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.

I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma Inc. to hire me. If I am hired I understand that either KBI Biopharma Inc. or I can terminate my employment at any time and for any reason with or without cause and without prior notice. I understand that no representative of KBI Biopharma Inc. has the authority to make any assurance to the contrary.

I attest with my signature below that I have given to KBI Biopharma Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma Inc. to contact references provided for employment reference checks. If any information I have provided is untrue or if I have concealed material information I understand that this will constitute cause for the denial of employment or immediate dismissal.