Validation Engineer

ALGOBRAINZ LLC; Lebanon (IN); On-site; USD 65,000 - 95,000; Full time

Job summary

ALGOBRAINZ LLC is seeking a Validation Engineer to support pharmaceutical manufacturing and validation activities. The role focuses on ensuring equipment, processes, and computer systems meet GMP/GxP, FDA, and quality requirements.

Entry-level candidates with relevant academic or project experience and experienced professionals are encouraged to apply. The position involves collaborating with Quality, Engineering, and Manufacturing teams to execute validation, documentation, and continuous

Qualifications

• Bachelor’s degree in Engineering, Life Sciences, Pharmacy, or related field.
• 0–3+ years of validation, quality, manufacturing, or pharmaceutical experience.
• Knowledge of GMP/GxP, FDA regulations, and 21 CFR Part 11 is a plus.

Responsibilities

• Execute and support equipment, process, cleaning, and computer system validation.
• Prepare and review validation protocols, reports, and documentation.
• Support IQ/OQ/PQ and qualification activities.
• Assist with deviations, CAPAs, and change controls.
• Collaborate with Quality, Engineering, Manufacturing, and other cross-functional teams.

Skills

GMP/GxP knowledge

Validation methods

Documentation

Communication

Education

Bachelor's degree in Engineering/Life Sciences/Pharmacy

Job description

We are seeking a Validation Engineer to support pharmaceutical manufacturing and validation activities. The role involves ensuring equipment, processes, and systems meet GMP/GxP, FDA, and quality requirements. Both entry-level candidates with relevant academic/project experience and experienced professionals are encouraged to apply.

Key Responsibilities

• Execute and support equipment, process, cleaning, and computer system validation.
• Prepare and review validation protocols, reports, and documentation.
• Support IQ/OQ/PQ and qualification activities.
• Assist with deviations, CAPAs, and change controls.
• Collaborate with Quality, Engineering, Manufacturing, and other cross-functional teams.

Requirements

• Bachelor’s degree in Engineering, Life Sciences, Pharmacy, or related field.
• 0–3+ years of validation, quality, manufacturing, or pharmaceutical experience.
• Knowledge of GMP/GxP, FDA regulations, and 21 CFR Part 11 is a plus.
• Strong documentation, analytical, and communication skills.