CQV Engineer Consultant - Diverse Life Sciences Projects

ELIQUENT Life Sciences, Inc.; California (MO); Hybrid; USD 85,000 - 125,000; Full time

Job summary

ELIQUENT Life Sciences, Inc. is seeking CQV Engineers to support commissioning, qualification, and validation across the United States.

This project-based consulting role involves developing protocols for equipment, utilities, and facilities, while ensuring SOP alignment and regulatory compliance. You will work with diverse client teams across the West Coast, Midwest, and East Coast, contributing to successful project deliveries and maintaining high quality.

Qualifications

• BS in Engineering, Science or equivalent technical degree.
• Solid understanding of GMP regulations and industry standards.
• Experience in commissioning, qualification, and validation within pharmaceutical/medical device industries.

Responsibilities

• Develop and execute CQV protocols for equipment, utilities, and facilities.
• Contribute to SOP development and ensure regulatory compliance.
• Collaborate with project teams to integrate CQV activities into project timelines.
• Provide updates through technical presentations on validation status.
• Uphold GMP standards and regulatory guidelines in project execution.
• Identify risks and develop mitigation strategies for CQV activities.

Skills

GMP knowledge

Communication skills

Independent & team work

CQV experience

Education

BS in Engineering, Science or equivalent technical degree

Job description

ELIQUENT Life Sciences, Inc. is seeking CQV Engineers to support commissioning, qualification, and validation across the United States.

This project-based consulting role involves developing protocols for equipment, utilities, and facilities, while ensuring SOP alignment and regulatory compliance. You will work with diverse client teams across the West Coast, Midwest, and East Coast, contributing to successful project deliveries and maintaining high quality.