Validation Engineer / CQV

this is only for US Citizens and GC

Job Summary

We are seeking a Junior Validation Engineer to support validation, qualification, and calibration activities within a pharmaceutical manufacturing environment. This is an excellent opportunity for candidates with 1–2 years of experience in validation, CQV, or regulated industries who are looking to grow their career in pharmaceutical manufacturing and compliance.

Responsibilities

• Support equipment validation, qualification, and calibration activities
• Assist with execution of IQ/OQ/PQ protocols and validation documentation
• Ensure compliance with GMP and 21 CFR Part 11 requirements
• Support Computerized System Validation (CSV) activities
• Assist in validation of autoclaves, CIP skids, isolators, parts washers, and other manufacturing equipment
• Collaborate with Quality, Manufacturing, and Engineering teams to resolve validation issues
• Maintain accurate documentation and support audit readiness

Qualifications

• 1–2 years of experience in Validation, CQV, Calibration, or CSV
• Basic understanding of GMP and pharmaceutical compliance requirements
• Familiarity with IQ/OQ/PQ documentation and validation lifecycle
• Pharmaceutical, biotech, or regulated industry experience preferred
• Strong communication and problem-solving skills
• Bachelor’s degree in Engineering, Life Sciences, or related field preferred

Location: Albany, NY