Senior CQV Engineer - Pharma Validation Lead

Verista, Inc.; Columbus (OH); On-site; USD 70,491 - 109,900; Full time

Benefits offered by this job

Competitive pay

Health savings account

Paid time off

Tuition reimbursement

Disability insurance

Job summary

Verista, Inc. in Columbus, OH, is seeking CQV professionals to support pharmaceutical manufacturing projects. The team delivers validation and commissioning services, ensuring compliant, validated facilities and systems.

Candidates should have strong communication, teamwork, and problem-solving skills, with experience in GMP environments and CQV activities. Onsite work in the Indianapolis metropolitan area may be required, with travel up to 50% anticipated.

Qualifications

• Bachelor’s Degree or equivalent required.
• 4 - 6 years of demonstrated role relevant experience.
• Experience leading CQV activities specific to pharmaceutical manufacturing requirements.
• Proficiency using PC and Microsoft Office tools.

Responsibilities

• Complete user interface testing, software verification, and alarm testing on automated systems.
• Develop, review, and execute testing documentation.
• Make recommendations for design or process modification based on test results.

Skills

Effective communication

Team mentoring

Problem solving

Interpersonal skills

Client liaison

GMP awareness

Education

Bachelor's degree or equivalent

Tools

Microsoft Office

Word

Excel

PowerPoint

Job description

Verista, Inc. in Columbus, OH, is seeking CQV professionals to support pharmaceutical manufacturing projects. The team delivers validation and commissioning services, ensuring compliant, validated facilities and systems.

Candidates should have strong communication, teamwork, and problem-solving skills, with experience in GMP environments and CQV activities. Onsite work in the Indianapolis metropolitan area may be required, with travel up to 50% anticipated.