Senior Validation Engineer - Life Sciences CQV Specialist

Veristainc; Columbus (OH); On-site; USD 79,000 - 129,000; Full time

Benefits offered by this job

Competitive pay

401(k) Employer Matching

Paid Time Off

Tuition Reimbursement

Health Insurance

Dental Insurance

Vision Insurance

Flexible Spending Accounts

Commuter Benefits

Life Insurance

Job summary

Verista is seeking a Senior Validation / Senior CQV Engineer in the United States (Columbus, OH) to author, edit, and execute validation documentation for equipment, systems, and software within packaging operations. You will run test scripts, maintain records, and ensure project schedules are met, contributing to GMP-compliant processes.

The role requires a Bachelor’s degree and 5+ years in validation, with strong communication and teamwork skills to support life sciences clients.

Qualifications

• Bachelor’s Degree or equivalent required.
• 5+ years of experience authoring, editing, and executing technical commissioning, qualification and validation documentation.
• Experience supporting validation, qualification, or testing for packaging equipment/lines preferred.
• Experience in pharmaceutical, medical device, or regulated packaging operations is a plus.
• Proficiency with PC and Microsoft Office tools.
• Strong communication, teamwork, and problem-solving skills.
• Excellent organizational and time management skills.
• GMP and Good Documentation Practice training (may be on onboarding).
• Intermediate Word skills with large technical documents.
• Basic Excel and PowerPoint skills.
• Strong interpersonal and clear communication capabilities.

Responsibilities

• Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/software,
• Running test scripts and documenting results
• Adherence with project schedule for all assigned activities
• Maintaining clear, detailed records qualification and validation
• Reading technical schematics to identify, locate, and test photo sensors, verify part numbers, and complete I/O testing on automated manufacturing equipment

Skills

Communication

Teamwork

Problem-solving

Attention to detail

Time management

GMP training

Organizational skills

Clear communication

Education

Bachelor’s Degree or equivalent

Tools

MS Word

Excel

PowerPoint

Microsoft Office

Job description

Verista is seeking a Senior Validation / Senior CQV Engineer in the United States (Columbus, OH) to author, edit, and execute validation documentation for equipment, systems, and software within packaging operations. You will run test scripts, maintain records, and ensure project schedules are met, contributing to GMP-compliant processes.

The role requires a Bachelor’s degree and 5+ years in validation, with strong communication and teamwork skills to support life sciences clients.