MRB Administrator

ESAB USA

  • USA, IL
  • 30+ days ago
  • $45,772–$52,653 Per Year
  • Autofill and Review
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Skills

  • Communication Skillsunmatched
  • Computer Systemsunmatched
  • Corrective Actionunmatched
  • Credit Processingunmatched
  • Cross-Functionalunmatched
  • Data Entryunmatched
  • Detail Orientedunmatched
  • English Languageunmatched
  • Establish Prioritiesunmatched
  • GMP (Good Manufacturing Practices)unmatched
  • Maintain Complianceunmatched
  • Manufacturingunmatched
  • Mathematicsunmatched
  • Medical Equipmentunmatched
  • Microsoft Excelunmatched
  • Microsoft Officeunmatched
  • Microsoft Outlookunmatched
  • Microsoft Wordunmatched
  • Multitaskingunmatched
  • Presentation/Verbal Skillsunmatched
  • Problem Solving Skillsunmatched
  • Quality Managementunmatched
  • Regulatory Requirementsunmatched
  • Returns Processingunmatched
  • Root Cause Analysisunmatched
  • Team Playerunmatched
  • Test & Measurement Equipmentunmatched
  • Time Managementunmatched
  • Vendor/Supplier Evaluationunmatched
  • Vendor/Supplier Selectionunmatched
  • Willing to Travelunmatched
  • Writing Skillsunmatched

Description

Job Description:

Material Review Board (MRB) Administrator

Location: 1111 Lakeside Drive | Gurnee, IL 60031-4099 Company: Ohio Medical

Position Overview

The MRB Administrator plays a critical role in maintaining product quality and compliance by overseeing all nonconforming materials from initial identification through final disposition. This position ensures timely resolution of material issues, facilitates cross-functional collaboration, and supports supplier communication to uphold GMP standards.

Key Responsibilities

Responsibilities include, but are not limited to:

  • Facilitate and lead Material Review Board (MRB) meetings, ensuring timely follow-up and resolution of action items

  • Document and retain accurate meeting minutes and decisions

  • Identify nonconforming or potentially nonconforming stock and initiate appropriate containment actions

  • Conduct preliminary root cause analysis and coordinate supplier returns or corrective actions

  • Communicate with suppliers regarding identified nonconformances and manage return or credit processes

  • Ensure compliance with internal quality procedures and regulatory requirements throughout the disposition process

Qualifications

Professional Experience

  • 1-2 years of experience in a GMP-regulated manufacturing environment; medical device industry preferred

  • Working knowledge of inspection, measuring, and test equipment

  • Proficiency in Microsoft Office Suite (Word, Excel, Outlook)

Education

  • High school diploma or equivalent required

Language Skills

  • Fluency in English required

  • Spanish proficiency preferred but not mandatory

Travel Requirements

  • This position does not require travel

Personal Attributes & Skills

  • Strong verbal and written communication skills

  • High attention to detail and accuracy

  • Basic math skills (addition and subtraction using whole numbers)

  • Competent in data entry and review using computer systems

  • Problem-solving ability in standardized situations

  • Collaborative mindset with the ability to work effectively in team settings

  • Capable of managing multiple tasks and prioritizing effectively in a fast-paced environment

Pay Range:

$45,772.00-$52,653.00

Numbers & Facts

LocationUSA, IL
Salary$45,772–$52,653 Per Year

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