Medical Device Lab Technician: Precise Testing & Data

Socket.dev

Chicago (IL)

On-site

USD 28,000 - 41,000

Full time

3 days ago
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Job summary

Nemera is seeking a detail-oriented technician to perform testing on medical devices in our Chicago laboratory using analytical equipment.

You will analyze results, document findings, and help implement new testing methods while maintaining a clean, organized workspace and managing consumables. You will report deviations and ensure compliance with GMP and FDA regulations throughout the workflow.

Qualifications

  • Bachelor’s degree in a scientific field.
  • Experience in a laboratory environment.
  • Self-motivated with good communication skills.
  • Excellent organization skills.
  • Strong attention to detail.
  • Ability to work independently and as part of a team.
  • Proficient with the MS Suite.

Responsibilities

  • Perform various testing on medical devices utilizing analytical equipment.
  • Analyse and interpret test results, ensuring data is within specification limits.
  • Document and report test findings and observations, maintaining accurate records according to documentation requirements.
  • Participate in the implementation of new testing methods and protocols.
  • Contribute to maintaining the cleanliness and orderliness of the laboratory.
  • Manage the stock of laboratory consumables.
  • Report any deviations, errors, failures, or OOS results and participate in the follow-up actions.
  • Comply with the Good Practices applicable to the laboratory.

Skills

Self-motivation & communication
Attention to detail
Organization
Independent & team work
MS Suite
Laboratory experience

Education

Bachelor’s degree in a scientific field

Tools

MS Suite

Job description

Nemera is seeking a detail-oriented technician to perform testing on medical devices in our Chicago laboratory using analytical equipment.

You will analyze results, document findings, and help implement new testing methods while maintaining a clean, organized workspace and managing consumables. You will report deviations and ensure compliance with GMP and FDA regulations throughout the workflow.

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