MedTech Quality Control Specialist

Becton Dickinson

Columbus (NE)

On-site

USD 45,000 - 65,000

Full time

14 days+

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Job summary

Becton, Dickinson, and Company in Columbus, NE is seeking a Quality Assurance professional to safeguard product quality and compliance across manufacturing operations. The role emphasizes supporting audits, line QC, and continuous improvement with data-driven actions.

Responsibilities include assisting in training, applying sampling plans, maintaining GMP documentation, and collaborating with cross-functional teams to resolve quality issues and prevent defects.

Qualifications

  • High School diploma or GED required; an Associate's degree is preferred.
  • Experience with product and process specifications is a plus.
  • Familiarity with GMP and quality systems is desirable.
  • Candidates should be able to read and interpret drawings/specifications.
  • Proficiency with Excel/Word/PowerPoint is expected.

Responsibilities

  • Provide guidance and input to manufacturing and management for quality issues.
  • Aide in the training of associates to ensure compliance with quality systems.
  • Support product complaint investigations and corrective actions.
  • Contribute with continuous improvement activities (Kaizens, blitz, validations).
  • Trend quality metrics and investigate problem areas for corrective action.
  • Develop/assist in creating visual instructions and proper filing of documentation.

Skills

Quality procedures
Documentation & records
Team collaboration
Problem solving
Communication skills

Education

High School diploma/GED
Associates degree preferred

Tools

Excel
Word
PowerPoint
Inspection equipment

Job description

Becton, Dickinson, and Company in Columbus, NE is seeking a Quality Assurance professional to safeguard product quality and compliance across manufacturing operations. The role emphasizes supporting audits, line QC, and continuous improvement with data-driven actions.

Responsibilities include assisting in training, applying sampling plans, maintaining GMP documentation, and collaborating with cross-functional teams to resolve quality issues and prevent defects.

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