Process Engineers

QRC Group, LLC; Caguas (PR); On-site; USD 70,000 - 100,000; Full time

Job summary

QRC Group, LLC in Caguas, Puerto Rico is seeking a Process Engineer with pharma-medical device experience to support daily operations and validations lifecycle.

You will perform root cause analyses, investigations, and CAPA closures for both manual and automated manufacturing lines, with a fast-paced environment and 24/7 flexibility as needed.

Qualifications

• Bachelor's Degree in Engineering (Mechanical, Chemical, Industrial, Biomedical, or related field).
• Strong experience in the Medical Device industry (required).
• Pharmaceutical industry experience (preferred).
• 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.
• Bilingual (English and Spanish) required.

Responsibilities

• Perform root cause analysis and implement corrective actions on manufacturing processes.
• Lead investigations and support CAPA closures for QN events.
• Support validation activities across manual and automated production lines.

Skills

Root cause analysis

Investigation experience

Validation lifecycle

Manual and automated systems

Pharma/medical device experience

Education

Bachelor's Degree in Engineering

Job description

Caguas, Puerto Rico | Posted on 08/17/2026

We are seeking a Process Engineer with pharma-medical device experience aswell as validations life-cycle experience (write/execute/analyze/close) tosupport the daily operations:

• Rootcause analysis
  
• Investigationexperience for QN/CAPAclosures
  
• Experiencewith 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.