QG
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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