CQV Validation Lead – Pharma & Life Science

FITS LLC; Wilson (NC); On-site; USD 90,000 - 120,000; Full time

Job summary

FITS LLC in the United States seeks a Validation and Commissioning & Qualification support specialist in Engineering. The role focuses on CQV plan development, coordinating cross-functional teams, and ensuring CQV readiness and documentation.

The ideal candidate will have a life science or engineering degree, pharma validation exposure, and bilingual Spanish/English communication. Administrative shift and MS Office proficiency are required.

Qualifications

• Bachelor's degree in Life Science or Engineering.
• Exposure to Validation Life Cycle in pharma.
• Bilingual Spanish and English preferred.

Responsibilities

• Develop CQV plans with the client project scheduler and meet milestones.
• Lead weekly CQV/Eng/CM/USER coordination meetings; manage org chart.
• Ensure HSE and startup activities including LOTO and CQV readiness.
• Oversee deviation management, change control, and vendor management.
• Create and review CQ test plans and specs for approvals.
• Develop training materials and maintain CQV documentation.
• Manage scheduling and resource levels at system and area level.

Skills

CQV Experience

Validation Life Cycle

Bilingual (Spanish & English)

MS Office

Education

Bachelor’s Degree in Life Science or Engineering

Tools

MS Office

Job description

FITS LLC in the United States seeks a Validation and Commissioning & Qualification support specialist in Engineering. The role focuses on CQV plan development, coordinating cross-functional teams, and ensuring CQV readiness and documentation.

The ideal candidate will have a life science or engineering degree, pharma validation exposure, and bilingual Spanish/English communication. Administrative shift and MS Office proficiency are required.