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14 minutes ago
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manufacturing qsr cleanroom iso 13485 cgmp
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πŸ“‹ Description

  • Performs moderately complex assembly of medical devices according to Federal QSR, ISO 13485, lot
  • Performs in-process inspection of components and assemblies to verify quality conformance.
  • Records information on lot history records and performs component accountabilities.
  • Sets up and operates manufacturing equipment.
  • Maintains cleanroom standards, practices, and housekeeping according to standard operating
  • Cleans supplies and manufacturing equipment and work areas.

🎯 Requirements

  • High School or equivalent with 1+ year clean room assembly experience or manufacturing experience
  • Basic math skills.
  • Able to comprehend spoken and written English.
  • Effective verbal and written communication skills.
  • Able to pay close attention to detail.
  • High manual dexterity.

🎁 Benefits

  • A collaborative teamwork environment where learning is constant, and performance is rewarded.
  • The opportunity to be part of the team that is revolutionizing the treatment of some of the world's
  • Generous benefits package for eligible employees: medical, dental, vision, life, AD&D, short
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