Pharma CQV Validation Engineer

CAI; Boulder (CO); On-site; USD 87,152 - 94,600; Full time

Job summary

CAI, a leading professional services company, is seeking candidates for a role focusing on CQV (Commissioning, Qualification, and Validation) activities in the Pharmaceutical/Life Sciences sector. The ideal candidate will have a Bachelor's degree in a relevant field and at least 2 years of experience in a GMP environment. With a commitment to operational excellence, this position involves critical documentation, project planning, and collaboration with vendors to ensure compliance and quality throughout project execution. Join a team dedicated to improving the human experience and making impactful contributions.

Qualifications

• 2+ years of related experience in Pharmaceutical/Life Sciences industry.
• Essential experience in a GMP environment.
• Willing to travel throughout the U.S. and internationally.

Responsibilities

• Perform CQV activities with a focus on safety and compliance.
• Support the generation and review of C&Q procedures.
• Coordinate project resources and logistics during CQV execution.

Skills

Communication

Problem-Solving

Customer Focus

Project Management

Education

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

Job description

CAI, a leading professional services company, is seeking candidates for a role focusing on CQV (Commissioning, Qualification, and Validation) activities in the Pharmaceutical/Life Sciences sector. The ideal candidate will have a Bachelor's degree in a relevant field and at least 2 years of experience in a GMP environment. With a commitment to operational excellence, this position involves critical documentation, project planning, and collaboration with vendors to ensure compliance and quality throughout project execution. Join a team dedicated to improving the human experience and making impactful contributions.