Senior CQV Validation Engineer - Pharma & GMP Expert

CAI; Madison (WI); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Health Insurance

PTO 24 days

Life Insurance

Long Term Disability

Job summary

CAI is seeking an experienced CQV Engineer for projects in the pharmaceutical and life sciences sectors in the United States. The role focuses on commissioning, qualification, and validation activities with a strong emphasis on safety and regulatory compliance.

Candidates should have a BS/BA in Engineering, Chemistry, or Life Sciences and at least 3 years of GMP experience, plus excellent communication skills and a willingness to travel nationally or internationally.

Qualifications

• Bachelor’s degree required in Engineering, Chemistry, or Life Sciences (relevant experience can substitute).
• 3+ years of related experience in Pharmaceutical/Life Sciences.
• Essential GMP experience in a regulated environment.
• Outstanding oral and written communication skills.

Responsibilities

• Perform CQV activities with safety focus; deliver CQV in line with project schedules.
• Support generation and review of CQV and related documents; SOPs and plans.
• Assist with planning CQV activities; allocate resources and coordinate support.
• Coordinate testing with project contractors and equipment vendors.

Skills

CQV

GMP

Communication

Travel readiness

Education

Bachelor’s degree in Engineering/Chemistry/Life Sciences

Job description

CAI is seeking an experienced CQV Engineer for projects in the pharmaceutical and life sciences sectors in the United States. The role focuses on commissioning, qualification, and validation activities with a strong emphasis on safety and regulatory compliance.

Candidates should have a BS/BA in Engineering, Chemistry, or Life Sciences and at least 3 years of GMP experience, plus excellent communication skills and a willingness to travel nationally or internationally.