Life Sciences Operations & Materials Coordinator

Radiometer

Chaska (MN)

On-site

USD 36,000 - 39,000

Full time

4 days ago
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Job summary

Beckman Coulter Diagnostics, a Danaher operating company, seeks an Operations Support Specialist to optimize purification production schedules in a fast-paced manufacturing environment in Chaska, MN. The role requires independent work and collaboration with cross-functional teams on material flow and equipment reliability.

Reporting to the Supervisor of Reagent Operations, you will support document control, regulatory compliance (FDA QSR, GMP, ISO), and administrative processes while applying

Qualifications

  • High School degree or GED with 4+ years of experience.
  • Associate Degree with 2+ years of experience.
  • Bachelor's Degree with 0+ years of relevant experience.
  • Experience supporting process flow in an administrative role.
  • Experience in a regulated industry (FDA/ISO) is a plus; GLP experience preferred.

Responsibilities

  • In this role you will optimize purification production schedules and ensure clear cross-functional communication.
  • Manage material flow, equipment reliability, and document control within Reagent Manufacturing.
  • Coordinate with procurement, inventory and QA to maintain compliance with QSR, GMP, and ISO.
  • Support daily operations through data analysis and collaboration with the Supervisor of Reagent Operations.

Skills

Cross-functional communication
Analytical skills
Procurement
Inventory management
Documentation control
Regulatory compliance

Education

High School or GED
Associate Degree
Bachelor's Degree

Job description

Beckman Coulter Diagnostics, a Danaher operating company, seeks an Operations Support Specialist to optimize purification production schedules in a fast-paced manufacturing environment in Chaska, MN. The role requires independent work and collaboration with cross-functional teams on material flow and equipment reliability.

Reporting to the Supervisor of Reagent Operations, you will support document control, regulatory compliance (FDA QSR, GMP, ISO), and administrative processes while applying

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