Engineer
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QRC Group
Juncos
Summary
The engineer will conduct root cause investigations and manage corrective and preventive actions within a GMP-regulated environment. They are responsible for applying engineering principles to optimize production processes and perform technical report writing.
Job Description
We are seeking an Engineer with experience working with packaging equipment, process characterization, validation, monitoring, and optimization techniques and Expertise in identifying and managing Corrective and Preventive Actions (CAPAs), in a GMP-regulated environment .
- Proficiency in technical report writing.
- Strong problem-solving skills and experience conducting root cause investigations.
- Proficiency in statistical analysis and Design of Experiments (DOE) methodologies.
- Ability to apply engineering principles to solve technical issues in a production environment.
- Availability to support non-standard shifts, including extended hours, nights, weekends, and holidays.
- Shift: 1st or 2nd
Requirements
- Master’s degree or Bachelor’s degree in Engineering & 2 years of Engineering experience
- Fully Bilingual (English & Spanish)
- Availability to support non-standard shifts, including extended hours, nights, weekends, and holidays.
- Shift: 1st or 2nd
QRC group is a life science firm dedicated to provide services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.
Our services and solutions include:
Process and Laboratory Investigation
• Corrective and Preventive Action (CAPA)
• Change Control
• Training
• Document Management Control
• QA Laboratory
• Methodology Transfer and Validation
• Instrument Calibration
• Validation and Training in Chromatographic Data Acquisition System
• Cleaning Validation
• Automation Engineering
• Quality Systems
Founded
2005
Company size
51-200 employees
Industry
Staffing and Recruiting
Org type
Privately Held
Headquarters
Caguas, PR
QRC group is a life science firm dedicated to provide services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.
Our services and solutions include:
Process and Laboratory Investigation
• Corrective and Preventive Action (CAPA)
• Change Control
• Training
• Document Management Control
• QA Laboratory
• Methodology Transfer and Validation
• Instrument Calibration
• Validation and Training in Chromatographic Data Acquisition System
• Cleaning Validation
• Automation Engineering
• Quality Systems
Founded
2005
Company size
51-200 employees
Industry
Staffing and Recruiting
Org type
Privately Held
Headquarters
Caguas, PR
