Process Improvement Engineer II - Cleanroom Validation

RXinsider LTD.; Sugar Land (TX); On-site; USD 90,000 - 150,000; Full time

Job summary

Quva seeks a Process Improvement Engineer II to lead cross‑functional teams in pharmaceutical development, drive formulation and process efficiency projects, and support deviations investigations and tech transfers across sites. You will develop validations, write technical assessments, and contribute to readiness for growth and compliance.

The role includes building the TX site airflow visualization program, coordinating sterility, quality, operations, and R&D inputs to meet FDA expectations

Qualifications

• BS/MS/PhD in a relevant field.

Responsibilities

• Lead cross-functional teams on complex project improvements.

Skills

GMP/ICH/QbD knowledge

Process development

Scale-up / tech transfer

Data analysis

Project management

Cross-functional leadership

Technical writing

Airflow visualization

Education

BS/MS/PhD in Pharmaceutical Sciences or related field

Tools

MS Office

Electronic documentation systems

Job description

Quva seeks a Process Improvement Engineer II to lead cross‑functional teams in pharmaceutical development, drive formulation and process efficiency projects, and support deviations investigations and tech transfers across sites. You will develop validations, write technical assessments, and contribute to readiness for growth and compliance.

The role includes building the TX site airflow visualization program, coordinating sterility, quality, operations, and R&D inputs to meet FDA expectations