CQV Engineer Consultant — GMP Validation Lead

ELIQUENT Life Sciences, Inc.; North Carolina; On-site; USD 90,000 - 130,000; Full time

Job summary

ELIQUENT Life Sciences seeks CQV Engineers to drive commissioning, qualification, and validation for pharmaceutical and medical device projects. You will develop CQV protocols, SOPs, and integrate CQV activities with project teams. Strong communication, GMP knowledge, and ability to travel across the U.S.

are essential. We welcome project-based consultants at various experience levels to support a growing pipeline nationwide.

Qualifications

• BS in Engineering, Science or equivalent technical degree.
• Solid understanding of GMP regulations and industry standards.
• Experience in commissioning, qualification, and validation within the pharmaceutical and/or medical device industry.
• Excellent communication and interpersonal skills.
• Ability to work independently and collaboratively in a dynamic team environment.
• Willingness to travel to clients across the U.S.

Responsibilities

• Develop and execute commissioning, qualification, and/or validation protocols for equipment, utilities, and/or facilities in accordance with industry regulations and client specifications.
• Contribute to the development and revision of SOPs related to CQV processes and ensure SOPs comply with regulatory requirements and industry best practices.
• Work collaboratively with project teams to integrate CQV activities into project timelines.
• Provide regular updates through technical presentations on the status of validation activities to project teams and stakeholders.
• Uphold high standards of quality in project execution, ensuring compliance with GMP and regulatory guidelines.
• Identify and assess risks associated with CQV activities and develop mitigation strategies.

Skills

Communication skills

Interpersonal skills

Analytical thinking

Problem solving

Teamwork

Willingness to travel

Education

BS in Engineering/Science or equivalent

Job description

ELIQUENT Life Sciences seeks CQV Engineers to drive commissioning, qualification, and validation for pharmaceutical and medical device projects. You will develop CQV protocols, SOPs, and integrate CQV activities with project teams. Strong communication, GMP knowledge, and ability to travel across the U.S.

are essential. We welcome project-based consultants at various experience levels to support a growing pipeline nationwide.