Lead Validation Engineer CQV — On‑Site Life Sciences

BioPharma Consulting JAD Group; College Station (TX); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Administrative shift

1-year contract

Job summary

BioPharma Consulting JAD Group seeks a Validation Engineer to lead lifecycle activities for product launches and technology transfers at the FDBT site. You will execute CD/CQ/PQ/PR, collaborate with cross-functional teams, and ensure right-first-time validation aligned with regulatory needs.

The role requires strong technical writing, on-site availability, and expertise in validation documentation and vendor oversight. Proficiency in Kneat and Microsoft Office is beneficial.

Qualifications

• Bachelor's degree in Engineering or Science required.
• 7+ years of validation experience in life sciences.
• Experience creating full validation lifecycle documentation.
• On-site role with no remote work.

Responsibilities

• Execute validation lifecycle activities (CD/CQ/PQ/PR).
• Develop and review URS, FRS, DS, IQ/OQ/PQ protocols.
• Coordinate vendor validation activities and deviations.
• Produce final validation reports and summaries.

Skills

Cross-functional leadership

Technical writing

Project planning

CSV knowledge

Regulatory understanding

Independent troubleshooting

Multitasking

Mentoring teammates

Education

Bachelor's degree in Engineering or Science

Tools

Kneat electronic validation

Word

Excel

PowerPoint

Job description

BioPharma Consulting JAD Group seeks a Validation Engineer to lead lifecycle activities for product launches and technology transfers at the FDBT site. You will execute CD/CQ/PQ/PR, collaborate with cross-functional teams, and ensure right-first-time validation aligned with regulatory needs.

The role requires strong technical writing, on-site availability, and expertise in validation documentation and vendor oversight. Proficiency in Kneat and Microsoft Office is beneficial.