Senior Validation Engineer — GMP & CQV for Life Sciences

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

Benefits offered by this job

Health Savings Account

Company-paid Life Insurance

Paid Time Off

Tuition Reimbursement

Team Social Activities

Job summary

Verista, a leading life science solutions provider in Columbus, OH, is seeking professionals to author and execute validation documentation for standard equipment and software. You will run test scripts, document results, and ensure alignment with project schedules while maintaining precise records.

The role favors candidates with 5+ years of experience in commissioning, qualification, and validation in regulated packaging environments, plus proficiency in MS Office tools.

Qualifications

• Bachelor’s Degree or equivalent required.
• 5+ years of experience authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/software.
• Experience in validation/qualification/testing for packaging equipment or lines preferred.
• Experience in regulated pharmaceutical/medical device packaging operations is a plus.
• Proficiency with PC and Microsoft Office tools.

Responsibilities

• Author, edit, and execute commissioning, qualification and validation documentation for standard equipment/systems/software.
• Run test scripts and document results.
• Adhere to project schedules for all assigned activities.
• Maintain clear, detailed records of qualification and validation.
• Read schematics to identify, locate, and test sensors and verify part numbers on automated equipment.

Skills

Communication skills

Organizational skills

Time management

Detail-oriented

Team collaboration

Problem solving

Education

Bachelor’s degree or equivalent

Tools

Word

Excel

PowerPoint

Job description

Verista, a leading life science solutions provider in Columbus, OH, is seeking professionals to author and execute validation documentation for standard equipment and software. You will run test scripts, document results, and ensure alignment with project schedules while maintaining precise records.

The role favors candidates with 5+ years of experience in commissioning, qualification, and validation in regulated packaging environments, plus proficiency in MS Office tools.