Full-Time

Master Scheduler

Nextern

Nextern

Contract medical device development and manufacturing

No salary listed

Maple Grove, MN, USA

In Person

Category
Operations & Logistics (1)
Required Skills
ERP
Requirements
  • Ability to develop and maintain capacity-balanced master production schedules across multiple client programs and product lines.
  • Ability to translate forecasts, purchase orders, and contractual delivery commitments into executable production plans within an enterprise resource planning/materials requirements planning system.
  • Knowledge of material availability, labor and equipment capacity, component lead times, inventory targets, bills of material, routings, lot sizes, safety stock, and planning parameters.
  • Ability to model production capacity, identify constraints and capacity gaps, and develop recovery options such as overtime, resequencing, or subcontracting.
  • Ability to support rough-cut capacity planning, scenario analysis, and Sales and Operations Planning.
  • Ability to maintain accurate planning master data and planning dashboards and key performance indicators.
  • Knowledge of applicable medical device quality and regulatory requirements, including 21 CFR Part 820 and ISO 13485.
  • Ability to incorporate inspection, validation, disposition holds, traceability, and Device History Record documentation requirements into production scheduling.
Responsibilities
  • Develop, publish, and maintain the site master production schedule across multiple client programs and product lines while balancing demand, capacity, and inventory targets.
  • Convert client forecasts, purchase orders, and contractual delivery commitments into an executable, capacity-balanced build plan within the enterprise resource planning/materials requirements planning system.
  • Run and interpret materials requirements planning outputs, and release, reschedule, and prioritize work orders to align material availability, labor, and equipment capacity with the master production schedule.
  • Maintain planning parameters, including lead times, lot sizes, safety stock, bills of material, and routing data.
  • Manage the planning time fence and change-control process by evaluating schedule impacts before committing new orders, engineering changes, or expedite requests.
  • Model and monitor production capacity by line and work center, identify gaps and constraints, and propose recovery options such as overtime, resequencing, or subcontracting.
  • Partner with Manufacturing and New Product Introduction to translate development and pilot-scale programs into full commercial-scale production schedules.
  • Escalate material or capacity shortfalls that put client delivery commitments at risk, including recovery plans and revised dates.
  • Serve as the scheduling point of contact for Program Management, Procurement, Manufacturing, and Quality regarding delivery status, risks, and priorities.
  • Participate in daily tier meetings and weekly operations and Sales and Operations Planning reviews, providing visibility into schedule adherence, backlog, and at-risk orders.
  • Communicate schedule changes, priorities, and constraints across departments and to client-facing teams.
  • Reconcile demand signals from multiple clients against available capacity and materials as part of the Sales and Operations Planning process.
  • Own the accuracy of planning-related master data, including bills of material, routings, lead times, and planning codes, within the enterprise resource planning/materials requirements planning system.
  • Build and maintain planning dashboards and key performance indicators for on-time delivery, schedule adherence, past-due backlog, and inventory turns.
  • Identify and implement continuous improvements to planning workflows by applying lean principles to reduce variability and manual rework.
  • Ensure production plans and schedule changes are executed in compliance with 21 CFR Part 820, ISO 13485, and applicable client and regulatory requirements.
  • Coordinate with Quality to incorporate inspection, validation, and disposition holds into the production schedule without compromising delivery commitments.
  • Maintain traceability of planning decisions and schedule changes consistent with Device History Record and documentation requirements.

Nextern provides contract engineering and manufacturing services for medical devices across the product lifecycle, collaborating with OEMs, clinicians, and innovators from concept through commercialization. It offers four integrated pillars—Medical Device Product Development, Medical Device Manufacturing, NPX Precision Technologies, and Nextern Consulting Services—covering electromechanical systems, catheters, guidewires, pulse generators, and nitinol components with NPX laser cutting and welding. The company differentiates itself with an end-to-end, globally distributed model and a revenue structure tied to manufacturing output, aligning success with its partners’ commercial performance. Its goal is to enable medical device commercialization by delivering scalable, globally distributed manufacturing and lifecycle support across markets like peripheral vascular, interventional cardiology, structural heart, neuromodulation, and electrophysiology.

Company Size

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Company Stage

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Total Funding

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Headquarters

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Founded

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Simplify Jobs

Simplify's Take

What believers are saying

  • June 22, 2026 consulting launch opens higher-margin regulatory and quality services.
  • Corey Kranz joined in 2026 as COO, strengthening global operations and supply chain execution.
  • Nextern's 2026 site map shows manufacturing capacity in Costa Rica, Vietnam, and China.

What critics are saying

  • Employee reviews flag weak management, poor communication, and headcount cuts in 2025.
  • Nextern depends on OEM program wins; any customer loss quickly hits manufacturing revenue.
  • China, Vietnam, and Costa Rica operations expose Nextern to tariff, logistics, and regulatory shocks.

What makes Nextern unique

  • Nextern spans development, manufacturing, consulting, and precision components across five global sites.
  • John Hastings became CEO on September 29, 2025, adding seasoned medtech operating leadership.
  • Its Maple Grove headquarters centralizes product development, bio-simulation, and commercialization support.

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Benefits

Health Insurance

Dental Insurance

Health Savings Account/Flexible Spending Account

401(k) Retirement Plan

401(k) Company Match

Paid Holidays

Paid Vacation

Gym Membership

Disability Insurance

Life Insurance

Training Programs

Company Social Events