Senior CQV Engineer: Onsite, Travel-Ready GMP Expert

Verista; Durham (NC); On-site; USD 70,491 - 109,900; Full time

Benefits offered by this job

Competitive pay

Performance-based incentives

Health insurance

401(k) matching

Paid time off

Employee referral program

Job summary

Verista is seeking a Senior CQV Engineer to join our team in the Raleigh/Durham area. You will lead CQV activities for pharmaceutical manufacturing, design validation plans, conduct risk assessments, and maintain thorough documentation to support audits.

The role requires 4–6 years of CQV experience, GMP exposure, and strong communication with clients. You will work onsite with a dedicated team, contribute to project planning, and mentor junior engineers while ensuring completion within the

Qualifications

• Must be able/willing to work onsite in the Raleigh/Durham metropolitan area.
• Willingness to travel 10-50% is required.
• Bachelor’s Degree or equivalent required.
• Ability to mentor and guide less experienced team members.
• Proven ability to communicate effectively with clients and report to management.
• 4-6 years of demonstrated CQV experience in pharmaceutical manufacturing.
• Experience in GMP regulated environment and Good Documentation Practice.

Responsibilities

• Designing validation plans for CQV projects.
• Conducting risk assessments with understanding of equipment, systems, and software.
• Maintaining detailed records of qualification and validation activities for audits.
• Designing and executing studies for process parameter definition and verification.
• Authoring and executing commissioning, qualification, and validation documentation.
• Running test scripts and documenting results, ensuring adherence to project schedules.
• Communicating requirements clearly to client organizations at multiple levels.

Skills

CQV leadership

GMP experience

Client communication

Team mentoring

Problem solving

Education

Bachelor’s Degree or equivalent

Tools

Microsoft Office

Job description

Verista is seeking a Senior CQV Engineer to join our team in the Raleigh/Durham area. You will lead CQV activities for pharmaceutical manufacturing, design validation plans, conduct risk assessments, and maintain thorough documentation to support audits.

The role requires 4–6 years of CQV experience, GMP exposure, and strong communication with clients. You will work onsite with a dedicated team, contribute to project planning, and mentor junior engineers while ensuring completion within the