CQV Engineer (New Grad) – Onsite in Columbus

Verista, Inc.; Columbus (OH); On-site; USD 65,000 - 95,000; Full time

Benefits offered by this job

Competitive pay

Life Insurance

Disability Insurance

Tuition Reimbursement

Paid Time Off

Holidays

Sick Time

Parental Leave

Health Savings Account

Team Social Activities

Employee Referral Program

Job summary

Verista is seeking an experienced CQV professional to lead commissioning, qualification and validation activities for process equipment at our Columbus, OH site. You will develop testing strategies, author validation documents and ensure compliance with GMP standards while coordinating with project teams.

The role emphasizes collaborative problem solving, precise documentation, and adherence to project timelines in a fast-paced life sciences environment.

Qualifications

• Bachelor’s degree required; STEM degree highly preferred.
• Experience leading CQV activities for Process Equipment.
• Proficiency with GMP and documentation practices.
• Willingness to work onsite in Columbus, OH.

Responsibilities

• Author, edit and execute commissioning, qualification and validation documentation for equipment and systems as part of a project team.
• Develop and document testing strategies, test scripts and acceptance criteria.
• Review and document risk assessments and testing results.
• Maintain detailed qualification records and ensure alignment with project schedules.

Skills

CQV leadership

Strong communication

Team collaboration

Problem solving

Attention to detail

GMP experience

Education

Bachelor’s Degree in STEM

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Job description

Verista is seeking an experienced CQV professional to lead commissioning, qualification and validation activities for process equipment at our Columbus, OH site. You will develop testing strategies, author validation documents and ensure compliance with GMP standards while coordinating with project teams.

The role emphasizes collaborative problem solving, precise documentation, and adherence to project timelines in a fast-paced life sciences environment.