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Associate Production Scheduler

Vericel Corporation

Burlington, MAOnsitePosted 38 days ago$85,000 - $100,000/year
Full TimeEntry LevelOperations & Supply ChainBiotechnology
Original posting ↗

Summary

The Associate Production Scheduler supports the development and execution of daily, weekly, and monthly production schedules across the Cambridge and Burlington sites. The role independently prepares, finalizes, and communicates the next-day schedule for assigned product lines and operational activities, while partnering with the Production Scheduling Supervisor and other scheduling team members on weekly and monthly plans.

Job description

The Scheduler analyzes demand, capacity, resource availability, equipment, material and cellular inventory, quality requirements, and competing priorities; applies judgment to address routine scheduling issues; and recommends options when constraints or changes may affect the manufacturing plan.

Duties and Responsibilities

  • Independently prepare, finalize, and communicate the next-day production schedule for assigned product lines and operational activities using OpCenter APS (formerly Preactor), consistent with approved production plans and established scheduling parameters.
  • Partner with the Production Scheduling Supervisor and other scheduling team members to develop and maintain weekly and monthly production plans across the Cambridge and Burlington sites.
  • Analyze customer orders, demand priorities, available capacity and resources, equipment, Quality Control and Quality Assurance readiness, materials, cellular inventory, and cross-functional dependencies to support effective scheduling decisions.
  • Apply independent judgment within established parameters to resolve routine scheduling conflicts, evaluate alternatives, propose schedule adjustments, and implement approved changes; escalate issues requiring cross-functional prioritization or decisions beyond the role's authority.
  • Support the development and maintenance of capacity and resource-utilization models, perform scenario analyses, and provide data-supported findings and recommendations to the Production Scheduling Supervisor and operational stakeholders.
  • Monitor schedule execution and assess the effects of deviations, downtime, shortages, or other changes; recommend recovery options and schedule updates to help protect the manufacturing plan.
  • Coordinate daily schedule alignment with Manufacturing, Quality Control, Quality Assurance, Materials Management, and other stakeholders; communicate schedule changes, tradeoffs, and operational impacts and obtain the inputs needed for execution.
  • Recommend improvements to scheduling processes, OpCenter APS, and connected applications, and participate in defining requirements, testing enhancements, and developing useful reports and metrics.
  • Support assigned scheduling projects, operational initiatives, and sales-order activities using ERP, scheduling, and CRM systems, ensuring accurate data and timely completion.
  • Perform other duties as assigned.

Basic Qualifications

  • Bachelor’s degree in business, supply chain, life sciences, or a related field with 1–2 years of relevant experience; or an associate degree or biotechnology certificate with 2–3 years of relevant experience; or a high school diploma/GED with 4–5 years of relevant experience.
  • Experience in a cGMP biotechnology or pharmaceutical manufacturing environment is strongly preferred.
  • Experience using ERP, MES, CRM, production-planning, or scheduling systems.
  • Microsoft Dynamics 365, MFG/Pro, SAP, OpCenter Execution Pharma, or OpCenter APS is preferred.
  • Excellent communication skills; written and verbal.
  • Familiarity with Microsoft Office.

Preferred Qualifications

  • Experience with electronic scheduling in an EBR-based environment.
  • Autologous cell therapies experience.
  • Experience with materials planning in a complex manufacturing environment.

Requirements

  • Bachelor’s degree in business, supply chain, life sciences, or a related field with 1–2 years of relevant experience; or an associate degree or biotechnology certificate with 2–3 years of relevant experience; or a high school diploma/GED with 4–5 years of relevant experience.
  • Experience in a cGMP biotechnology or pharmaceutical manufacturing environment is strongly preferred.
  • Experience using ERP, MES, CRM, production-planning, or scheduling systems.
  • Microsoft Dynamics 365, MFG/Pro, SAP, OpCenter Execution Pharma, or OpCenter APS is preferred.
  • Excellent communication skills; written and verbal.
  • Familiarity with Microsoft Office.
  • Experience with electronic scheduling in an EBR-based environment.
  • Autologous cell therapies experience.
  • Experience with materials planning in a complex manufacturing environment.

Benefits

  • Bonus
  • Incentive pay
  • Equity
  • Benefits

Company overview

Vericel Corporation is a leading biotechnology company specializing in advanced cell therapies for sports medicine and severe burn care markets. Founded in 1989 and headquartered in Cambridge, Massachusetts, the company develops and commercializes patient-specific expanded cellular therapies that repair injuries and restore lives. Vericel markets two FDA-approved autologous cell therapy products in the United States: Carticel for cartilage defects in the knee and Epicel for permanent skin replacement in severe burn patients. The company also holds exclusive North American commercial rights to NexoBrid, a biological orphan product for eschar removal in thermal burns. Vericel's innovative approach combines biology with medical technologies to create highly differentiated cell therapies and specialty biologics. With a focus on regenerative medicine, the company is advancing treatments for cartilage repair, burn care, and other severe conditions through rigorous scientific methods and clinical research.

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