Inventory Operations Support Specialist

Danaher•Chaska, MN
•Onsite

About The Position

The Operations Support Specialist role at Beckman Coulter Diagnostics manages and optimizes purification production schedules in a fast-paced manufacturing environment. The position supports efficient material flow, accurate system representation, equipment reliability, and effective communication across the Reagent Manufacturing operation. The role operates independently and works closely with cross-functional teams. It is part of the Reagent Operations department in Chaska, Minnesota, and is on-site. The position reports to the Supervisor of Reagent Operations. The role covers procurement, inventory and material management, equipment lifecycle management, and administrative processes such as document control. It also supports compliance with FDA Quality System Regulations (QSR), Good Manufacturing Practices (GMP), and ISO requirements, while applying basic analytical skills or scientific methods to daily work and collaborating to troubleshoot issues with a focus on quality.

Requirements

  • High school degree or GED with at least 4 years of experience, or an associate degree with at least 2 years of experience, or a bachelor's degree with at least 0 years of relevant experience.
  • Experience operating in an administrative position supporting process flow.

Nice To Haves

  • Experience in a regulated industry, such as FDA- or ISO-regulated environments.
  • A proven track record of good laboratory practices (GLP).
  • Experience supporting quality operations through inventory management, equipment maintenance, and material procurement.

Responsibilities

  • Manage and optimize purification production schedules in a fast-paced manufacturing environment.
  • Support efficient material flow and accurate representation of operations in systems.
  • Support equipment reliability and lifecycle management.
  • Execute procurement, inventory and material management, and administrative processes such as document control.
  • Assure compliance with FDA Quality System Regulations (QSR), Good Manufacturing Practices (GMP), and ISO regulatory requirements.
  • Apply basic analytical skills or scientific methods to perform daily tasks.
  • Work cooperatively with cross-functional team members to troubleshoot issues and maintain an emphasis on quality.

Benefits

  • Paid time off.
  • Medical insurance.
  • Dental insurance.
  • Vision insurance.
  • 401(k).
  • Bonus or incentive pay.
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