Pharma Quality Engineer - Onsite El Paso

Legalpmpartners; El Paso (TX); On-site; USD 76,000 - 83,000; Full time

Job summary

Legalpmpartners in El Paso, TX, is seeking a Quality Engineer to support pharmaceutical manufacturing operations on-site. The role collaborates with Manufacturing, Validation, Engineering, and Quality Assurance to resolve quality issues and ensure FDA, cGMP compliance.

You will handle deviations, CAPAs, change control reviews, and risk assessments. The ideal candidate has a Bachelor’s degree in Engineering and 3+ years in GMP-regulated environments, with strong analytical and documentation

Qualifications

• Bachelor’s degree in Engineering (Chemical, Mechanical, Industrial, Biomedical, or related).
• 3+ years in Quality Engineering, Manufacturing Quality, Validation, or similar GMP-regulated field.

Responsibilities

• Provide Quality Engineering support to manufacturing processes, equipment, and facilities.
• Investigate deviations, non-conformances, and quality issues using root cause analysis.
• Develop and support CAPAs, including implementation and verification.
• Assess change controls for impact on product quality and validated systems.
• Support equipment qualification and process validation activities.
• Participate in quality risk assessments and FMEA.
• Analyze quality metrics to identify trends and improvement opportunities.
• Collaborate with cross-functional teams to reduce defects and improve processes.
• Review SOPs, specifications, and validation records for compliance.

Skills

Root cause analysis

Quality engineering

Documentation

Microsoft Office

Education

Bachelor’s degree in Engineering

Tools

Electronic quality management systems

Job description

Legalpmpartners in El Paso, TX, is seeking a Quality Engineer to support pharmaceutical manufacturing operations on-site. The role collaborates with Manufacturing, Validation, Engineering, and Quality Assurance to resolve quality issues and ensure FDA, cGMP compliance.

You will handle deviations, CAPAs, change control reviews, and risk assessments. The ideal candidate has a Bachelor’s degree in Engineering and 3+ years in GMP-regulated environments, with strong analytical and documentation