Senior Validation Engineer - Pharma CQV, Travel

Energy Jobline ZR; Houston (TX); On-site; USD 90,000 - 130,000; Full time

Job summary

CAI is a professional services company delivering CQV, commissioning, qualification, and validation services to the Pharmaceutical/Life Sciences industry. The role focuses on executing CQV activities with emphasis on safety, aligning with project schedules, and tracking progress across multiple projects.

Ideal candidates have a GMP background, strong communication skills, and are willing to travel across the United States and internationally as needed.

Qualifications

• Bachelor’s degree in Engineering, Chemistry, or Life Sciences.
• 3+ years of related experience in Pharmaceutical/Life Sciences.
• Essential GMP environment experience.
• Outstanding oral and written communication skills.
• Willingness and flexibility to travel throughout the U.S. and potentially internationally.

Responsibilities

• Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on safety.
• Deliver CQ activities in alignment with project schedules
• Track and report progress of CQV efforts
• Support the and review of CQ procedures for client projects
• Review and revise qualification-related documents, including SOPs, master plans, and execution plans
• Assist with CQV review and qualification of equipment design
• Support planning of commissioning spares and consumables
• Allocate project resources for efficient execution
• Coordinate support and logistics during CQV execution
• Support execution of design reviews, equipment shakedown, commissioning, FATs, IQ, OQ, and PQ activities
• Coordinate with project contractors and equipment vendors to execute required testing

Skills

CQV Execution

Documentation

Project Planning

Testing & Vendor Mgmt

Communication

Education

Bachelor’s degree in Engineering, Chemistry, or Life Sciences

Job description

CAI is a professional services company delivering CQV, commissioning, qualification, and validation services to the Pharmaceutical/Life Sciences industry. The role focuses on executing CQV activities with emphasis on safety, aligning with project schedules, and tracking progress across multiple projects.

Ideal candidates have a GMP background, strong communication skills, and are willing to travel across the United States and internationally as needed.