Medical Device Supply Chain Planner I

Abbott

Houston (TX)

On-site

USD 51,000 - 101,000

Full time

14 days+
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Job summary

Abbott in Temecula, CA, is seeking a scheduling professional to develop detailed subassembly plans, release work orders in ERP, and update Kanban quantities to support build plans.

You will review forecast data and backorder reports, prioritize manufacturing jobs, manage safety stock with purchasing, and keep material master data accurate.

The role requires strong communication, teamwork, and the ability to work in a fast-paced, regulated medical-device environment.

Qualifications

  • Bachelor's Degree in Supply Chain or related field.
  • Minimum 1 year of planning experience.
  • Experience in a medical device manufacturing environment preferred.
  • Experience in a broader enterprise/cross-division model preferred.
  • Ability to work in a highly matrixed and diverse environment.
  • Strong communication and time-management skills.

Responsibilities

  • Develops a detailed scheduling plan for subassemblies aligned to top-level build plans.
  • Releases work orders in ERP and updates Kanban quantities to support plans.
  • Reviews forecast data and backorder reports to prioritize and expedite jobs.
  • Manages safety stock with Purchasing and updates material master data.
  • Collaborates across functions to minimize obsolete or expiring inventory.

Skills

Verbal communication
Written communication
Multitasking
Attention to detail
Teamwork
Organization

Education

Bachelor's degree in Supply Chain or related field

Tools

ERP systems
Kanban

Job description

Abbott in Temecula, CA, is seeking a scheduling professional to develop detailed subassembly plans, release work orders in ERP, and update Kanban quantities to support build plans.

You will review forecast data and backorder reports, prioritize manufacturing jobs, manage safety stock with purchasing, and keep material master data accurate.

The role requires strong communication, teamwork, and the ability to work in a fast-paced, regulated medical-device environment.

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