Validation Engineer II, Pharmaceutical CQV

Job overview

The Validation Engineer II role is onsite in Houston, TX. Compensation is not specified. The position supports critical validation activities in a pharmaceutical and biopharmaceutical manufacturing environment. The engineer develops and executes commissioning, qualification, and validation work for equipment, utilities, facilities, and controlled temperature units. The role helps maintain validated systems and compliant operations through data review, deviation investigation, corrective actions, documentation, and collaboration with Manufacturing, Quality Assurance, Engineering, and Research and Development.

What you'll do

• Develop, review, and execute CQV deliverables
• perform IQ, OQ, and PQ for equipment, utilities, facilities, and controlled temperature units
• support temperature mapping
• ensure compliance with cGMP, ICH guidelines, and FDA regulations
• analyze validation data
• investigate deviations and support root cause analysis
• implement CAPAs and change controls
• prepare protocols and reports
• support audits
• maintain compliant documentation and validated state.

What we're looking for

Skills & competencies

validation engineer ii

commissioning qualification validation

cqv

iq oq pq

pharmaceutical

biopharmaceutical

temperature mapping

cgmp

houston tx

katalyst healthcares & life sciences

onsite

Work arrangement

• Weekend coverage required

Why this role

Combines CQV execution, temperature mapping, regulated documentation, and cross-functional pharmaceutical manufacturing support.

About the employer

Katalyst Healthcares & Life Sciences is hiring for this role. Industry: Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology). Sector: 54.