Medical Device Manufacturing Technician (Cleanroom)

Validation & Engineering Group

United States

Vor Ort

USD 42.000 - 58.000

Vollzeit

14 Tage+
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Benefits dieser Stelle

Cleanroom environment

Zusammenfassung

Validation & Engineering Group is seeking Manufacturing Technicians to support production operations for a medical device manufacturing facility in Austin, Texas. The role involves hands-on work in a controlled cleanroom environment, following SOPs, GDP and ISO 13485 aligned quality procedures to assist embolic device production.

Ideal candidates have experience in regulated manufacturing environments with strong attention to detail and the ability to document production activities accurately.

Qualifikationen

  • High school diploma or equivalent required; technical degree or relevant training is a plus.
  • Experience in medical device/pharma/biotech or other regulated manufacturing environments preferred.
  • Strong attention to detail and ability to perform repetitive precision tasks.
  • Familiarity with GMP/GDP ISO 13485 FDA regulations or other regulated manufacturing requirements preferred.

Aufgaben

  • Perform hands on manufacturing and production activities in a controlled cleanroom environment.
  • Follow established manufacturing procedures, work instructions, SOPs and safety requirements.
  • Complete production and batch documentation accurately and in accordance with GDP.
  • Maintain cleanroom standards, gowning, hygiene, contamination control and housekeeping.

Kenntnisse

Attention to detail
Manual dexterity
Procedural compliance
PPE and cleanroom discipline

Ausbildung

High school diploma or equivalent
Technical degree or relevant training

Jobbeschreibung

Validation & Engineering Group is seeking Manufacturing Technicians to support production operations for a medical device manufacturing facility in Austin, Texas. The role involves hands-on work in a controlled cleanroom environment, following SOPs, GDP and ISO 13485 aligned quality procedures to assist embolic device production.

Ideal candidates have experience in regulated manufacturing environments with strong attention to detail and the ability to document production activities accurately.

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