CQV validation engineer

We are seeking an Entry-Level CQV (Commissioning, Qualification & Validation) Engineer to support commissioning, qualification, and validation activities for manufacturing equipment, clean utilities, and facilities in a GMP-regulated pharmaceutical or biotechnology environment. This role offers an excellent opportunity for recent graduates or early-career engineers to gain hands‑on experience in validation and compliance.

• Assist with commissioning and qualification of manufacturing equipment, clean utilities, and facility systems.
• Support execution of Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols.
• Prepare, review, and maintain validation protocols, reports, and supporting documentation.
• Participate in equipment startup, testing, and verification activities.
• Assist in documenting deviations, change controls, and corrective actions (CAPA).
• Ensure validation activities comply with GMP/cGMP
  , FDA regulations, and company quality standards.
• Collaborate with Engineering, Manufacturing, Quality Assurance, and Validation teams.
• Support risk assessments and validation impact evaluations.
• Maintain organized, inspection-ready documentation.
• Participate in continuous improvement initiatives related to validation and equipment performance.

• Bachelor's degree in Chemical Engineering, Mechanical Engineering, Biomedical Engineering, Biotechnology, Industrial Engineering, or a related engineering discipline.
• 0–3 years of experience through internships, co-ops, or full-time roles in pharmaceutical, biotechnology, medical device, or regulated manufacturing environments.
• Basic understanding of validation concepts and the equipment qualification lifecycle.
• Strong technical writing and documentation skills.
• Excellent analytical, organizational, and problem-solving abilities.
• Proficiency with Microsoft Office (Word, Excel, PowerPoint).