Senior Validation Engineer - Equipment & QA Impact

United Therapeutics Corporation; Jacksonville (FL); Hybrid; USD 110,000 - 140,000; Full time

Benefits offered by this job

Medical/Dental/Vision insurance

401(k) and ESPP

Paid time off & parental leave

Job summary

United Therapeutics Corporation in Jacksonville, FL is seeking a Senior Validation Engineer, Equipment (LBE) to support the full equipment lifecycle across Manufacturing, Quality Control, and Quality Assurance. You will develop, review, and execute validation protocols and final reports, serving as a liaison to ensure alignment with regulatory and quality standards.

The role requires a Bachelor’s degree in science or engineering and 5+ years in validation within a medical device/cGMP

Qualifications

• Bachelor’s degree in science or engineering required.
• 5+ years of validation experience in medical device/cGMP environment.
• Strong understanding of validation lifecycle principles and regulatory requirements.

Responsibilities

• Develop, execute, review validation protocols and reports for equipment, systems, and processes.
• Coordinate validation activities and act as technical resource within validation areas.
• Perform root cause analysis and implement corrective actions for validation issues.
• Review and support change control activities from a validation perspective.
• Assist in audits and ensure documentation aligns with GMP/GLP/QSR standards.

Skills

Validation lifecycle

Cross-functional collaboration

Root cause analysis

Documentation review

QA guidance

GMP compliance

Education

Bachelor’s Degree in science or engineering

Tools

Kaye/Ellab validation datalogger

Statistical tools

Job description

United Therapeutics Corporation in Jacksonville, FL is seeking a Senior Validation Engineer, Equipment (LBE) to support the full equipment lifecycle across Manufacturing, Quality Control, and Quality Assurance. You will develop, review, and execute validation protocols and final reports, serving as a liaison to ensure alignment with regulatory and quality standards.

The role requires a Bachelor’s degree in science or engineering and 5+ years in validation within a medical device/cGMP