GMP Validation Engineer - Early Career Growth

GxP Associates; California; On-site; USD 70,000 - 90,000; Full time

Job summary

GxP Associates seeks a motivated Validation Engineer to support validation activities for equipment, systems, processes, and facilities in a regulated environment. This early-career role offers growth in GMP compliance, qualification documentation, and regulated manufacturing operations.

You will assist with IQ/OQ/PQ, develop and execute validation protocols, and collaborate with Quality, Engineering, Manufacturing, IT, and Operations to ensure compliance and readiness for inspections.

Qualifications

• Bachelor's degree required in engineering, life sciences, pharma, or related field.
• 0-3 years in validation, qualification, manufacturing, or regulated industry.
• Basic GMP understanding.
• Familiarity with IQ/OQ/PQ preferred.
• Strong writing and documentation skills.
• Analytical and problem-solving abilities.
• Ability to work cross-functionally.

Responsibilities

• Support validation activities for equipment, processes, facilities, and systems.
• Assist development and execution of validation protocols and reports.
• Support IQ, OQ, PQ and other qualification activities.
• Review and maintain validation docs per procedures.
• Support risk assessments, traceability, and deviations related to validation.
• Assist with change controls and corrective actions.
• Participate in equipment commissioning, testing, and qualification.
• Ensure GMP compliance in validation activities.

Skills

GMP knowledge

IQ/OQ/PQ concepts

Technical writing

Analytical skills

Cross-functional collaboration

Documentation skills

Education

Bachelor's degree in Engineering, Life Sciences, Pharmaceutical Sciences, or a related field

Job description

GxP Associates seeks a motivated Validation Engineer to support validation activities for equipment, systems, processes, and facilities in a regulated environment. This early-career role offers growth in GMP compliance, qualification documentation, and regulated manufacturing operations.

You will assist with IQ/OQ/PQ, develop and execute validation protocols, and collaborate with Quality, Engineering, Manufacturing, IT, and Operations to ensure compliance and readiness for inspections.