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.
Numbers & Facts
Location
Caguas, Puerto Rico
Website
https://qrcgroup.com/
Skills
Analysis Skillsunmatched
Biomedicineunmatched
Biotech and Pharmaceuticalunmatched
Corrective and Preventative Action (CAPA) Systemsunmatched
English Languageunmatched
Manufacturingunmatched
Manufacturing Systemsunmatched
Mechanical Engineeringunmatched
Medical Equipmentunmatched
Operational Supportunmatched
Operationsunmatched
Process Engineeringunmatched
Protocol Analysisunmatched
Root Cause Analysisunmatched
Spanish Languageunmatched
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