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QG

QRC Group

Process Engineers

Caguas, PRPresencialContratoTiempo completo

Publicado 14 sept 2026

We are seeking a Process Engineer with pharma-medical device experience as well as validations life-cycle experience (write/execute/analyze/close) to support the daily operations:
  • Root cause analysis
  • Investigation experience for QN/CAPAclosures
  • Experience with manual and automated systems/lines


Requirements

  • Bachelor's Degree in Engineering (Mechanical, Chemical, Industrial, Biomedical, or related field).
  • Strong experience in the Medical Device industry (required).
  • Pharmaceutical industry experience (preferred).
  • Demonstrated experience with validation life cycle activities (design, execute, analyze, and close protocols/reports).
  • Experience performing root cause analysis and implementing solutions.
  • Experience supporting investigations, QN, and CAPA closures.
  • Experience working with manual and automated manufacturing systems/production lines.
  • Ability to work effectively in a fast-paced manufacturing environment.
  • Standard site schedule; flexible to support 24/7 operation including shifts, weekends, and  holidays as operational demands requireBilingual (English and Spanish) required.
  • Availability to work in Texas.


Resumen del puesto

Tipo de empleo

Tiempo completo

Habilidades requeridas

Validation lifecycle management (design, execute, analyze, close protocols/reports)Validation protocol and report authoringRoot cause analysisQuality investigations (QN)CAPA management and closureAutomated manufacturing systems operation and troubleshootingManual manufacturing systems operation and troubleshootingMedical device industry knowledgePharmaceutical industry knowledge (preferred)Working effectively in fast-paced manufacturing environments24/7 shift flexibility and production supportBilingual communication (English and Spanish)

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