Medical Device QA Technician II

Confluent Medical Technologies, Inc.

Chattanooga (TN)

On-site

USD 48,000 - 65,000

Full time

3 days ago
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Job summary

Confluent Medical Technologies, Inc. is seeking a Quality Assurance Technician II in Chattanooga, TN. The role focuses on reviewing quality docs for release, supporting calibration and QMS processes, and applying statistics to improve manufacturing outcomes.

You will participate in audits, assist in root cause investigations, and may supervise inspection staff. Strong Excel skills, Minitab knowledge, and familiarity with ISO 9001/13485 are highly valued.

Qualifications

  • High-school diploma; college degree preferred.
  • Experience in medical device industry a plus.
  • Proficient in Excel and MS Office with strong data handling skills.
  • Familiarity with ISO 9001/13485, FDA 820 or related quality tools is beneficial.
  • Statistical knowledge (Six Sigma, QMS) is an asset.

Responsibilities

  • Reviews manufacturing and quality documentation for product release to Shipping.
  • Supports calibration management activities and QMS compliance.
  • Plans and conducts evaluations and adapts standard techniques.
  • Performs root cause investigations and supports audits.
  • May supervise inspectors or operators on specific assignments.
  • Participates in KPI achievement and safety adherence.
  • Contributes to DCOs, ECOs, and validation activities.
  • Maintains accurate records and documentation.

Skills

Excel proficiency
Microsoft Office suite
Minitab knowledge
Statistics understanding
Problem solving
Documentation skills
Attention to detail
Confidentiality
Multi-tasking
Customer service focus

Education

High-school diploma
College degree preferred
ISO 9001/13485 & FDA training

Tools

Minitab
Statistical methods

Job description

Confluent Medical Technologies, Inc. is seeking a Quality Assurance Technician II in Chattanooga, TN. The role focuses on reviewing quality docs for release, supporting calibration and QMS processes, and applying statistics to improve manufacturing outcomes.

You will participate in audits, assist in root cause investigations, and may supervise inspection staff. Strong Excel skills, Minitab knowledge, and familiarity with ISO 9001/13485 are highly valued.

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