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QRC Group

Process Engineers

Caguas, PRВ офисеКонтрактПолная занятость

Опубликовано 14 сент. 2026 г.

Эта вакансия опубликована на ES

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.


Кратко о роли

Тип работы

Полная занятость

Требуемые навыки

Validation lifecycle (design, write, execute, analyze, close protocols/reports)Root cause analysisInvestigations and CAPA management (QN/CAPA closures)Working with manual manufacturing systems/production linesWorking with automated manufacturing systems/production linesMedical device industry experience and regulatory awarenessPharmaceutical industry knowledge (preferred)Protocol and technical report writingImplementing corrective and preventive actionsProcess troubleshooting and problem solving in manufacturingAbility to operate effectively in a fast-paced, 24/7 manufacturing environment (shift flexibility)Bilingual communication (English and Spanish)

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