Senior Validation & CQV Engineer — Life Sciences

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

Benefits offered by this job

Health Insurance

Life Insurance

Disability Insurance

Tuition Reimbursement

Paid Time Off (PTO) & Holidays

Parental Leave

Job summary

Verista is seeking a capable professional to join our Columbus, OH team to author, edit, and execute commissioning, qualification, and validation documentation for standard equipment and software. You will test packaging lines, read schematics, and maintain thorough records to support regulated operations.

The role requires strong communication, teamwork, and problem-solving skills, with GMP/GxP practices and MS Office proficiency emphasized. Equal opportunity employer with competitive benefits.

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 supporting validation, qualification, or testing activities for packaging equipment or packaging lines preferred.
• Experience working in or supporting pharmaceutical, medical device, combination product, or regulated packaging operations is a plus.
• Proficiency using PC and Microsoft Office tools.
• Outgoing personality with strong ability to communicate effectively with peers in clear, concise terms.
• Ability to work as part of a team.
• GMP and Good Documentation Practice training (may be completed at onboarding).
• Reading technical schematics to identify, locate, and test photo sensors, verify part numbers, and complete I/O testing on automated manufacturing equipment.

Responsibilities

• Author, edit, and execute commissioning, qualification and validation documentation.
• Read and interpret technical schematics and identify test points.
• Maintain clear, detailed records of qualification and validation activities.
• Run test scripts and document results.
• Adhere to project schedules for all assigned activities.

Skills

Communication

Teamwork

Attention to detail

Problem solving

Education

Bachelor's degree or equivalent

Tools

WORD

Excel

PowerPoint

Job description

Verista is seeking a capable professional to join our Columbus, OH team to author, edit, and execute commissioning, qualification, and validation documentation for standard equipment and software. You will test packaging lines, read schematics, and maintain thorough records to support regulated operations.

The role requires strong communication, teamwork, and problem-solving skills, with GMP/GxP practices and MS Office proficiency emphasized. Equal opportunity employer with competitive benefits.