Operations Support Specialist
About The Position
The Operations Support Specialist role for Beckman Coulter manages and optimizes purification production schedules in a fast-paced manufacturing environment, ensuring clear communication and effective collaboration with cross-functional teams. Operating independently, this role is responsible for ensuring efficient material flow, accurate system representation, equipment reliability, and cross-functional communication within the Reagent Manufacturing operation. This position reports to the Supervisor of Reagent Operations and is part of Reagent Operations department located in Chaska, MN, and will be on-site. In this role, you will have the opportunity to: Execute across key operational domains, including procurement, inventory and material management, equipment lifecycle 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 directly and cooperatively with cross-functional team members to troubleshoot issues and ensure emphasis on quality
Requirements
- High School degree or GED with 4+ years of experience or Associate Degree with 2+ years of experience or Bachelor's Degree with 0+ years of relevant experience
- Operated in an administrative position, supporting process flow
Nice To Haves
- Previous experience in a regulated industry preferred (e.g. FDA, ISO).
- Proven track record of good laboratory practices (GLP).
- Supported quality operations by managing inventory, equipment maintenance, and material procurement.
Responsibilities
- Manage and optimize purification production schedules in a fast-paced manufacturing environment.
- Ensure clear communication and effective collaboration with cross-functional teams.
- Ensure efficient material flow, accurate system representation, equipment reliability, and cross-functional communication within the Reagent Manufacturing operation.
- Execute across key operational domains, including procurement, inventory and material management, equipment lifecycle 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 directly and cooperatively with cross-functional team members to troubleshoot issues and ensure emphasis on quality.
Benefits
- paid time off
- medical/dental/vision insurance
- 401(k)
- bonus/incentive pay
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED
