Pharma CQV Validation Engineer - Travel Ready

CAI; Bend (OR); On-site; USD 70,000 - 100,000; Full time

Job summary

CAI is seeking a CQV Engineer to execute commissioning, qualification, and validation activities in pharmaceutical environments. The role emphasizes safety, adherence to project schedules, and thorough CQV documentation. Travel across the U.S.

and possibly internationally may be required, leveraging strong communication and collaborative skills. Ideal candidates have a bachelor’s degree in Engineering, Chemistry, or Life Sciences, 2+ years in Pharma/Life Sciences, and GMP experience.

Qualifications

• Bachelor’s degree in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for education)
• 2+ years of related experience in the Pharmaceutical/Life Sciences industry
• Essential experience in a GMP environment
• Outstanding oral and written communication skills
• Strong problem-solving abilities
• Customer-focused mindset
• Willingness and flexibility to travel throughout the U.S. and potentially internationally

Responsibilities

• Perform CQV (Commissioning, Qualification, and Validation) activities with a strong focus on safety
• Deliver CQV activities in alignment with project schedules
• Track and report progress of CQV efforts
• Assist with CQV documentation, review, and qualification of equipment design
• Coordinate testing and vendor relationships during CQV execution

Skills

Communication skills

Problem solving

Customer focus

Travel flexibility

Education

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

Job description

CAI is seeking a CQV Engineer to execute commissioning, qualification, and validation activities in pharmaceutical environments. The role emphasizes safety, adherence to project schedules, and thorough CQV documentation. Travel across the U.S.

and possibly internationally may be required, leveraging strong communication and collaborative skills. Ideal candidates have a bachelor’s degree in Engineering, Chemistry, or Life Sciences, 2+ years in Pharma/Life Sciences, and GMP experience.