Senior Validation & CQV Engineer — GMP Focus, Life Sciences

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

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

401(k) Matching

Paid Time Off

Tuition Reimbursement

Life Insurance

Disability Insurance

Transit Benefits

Parental Leave

Job summary

Verista seeks a Senior Validation / CQV Engineer to author, edit, and execute validation documentation for standard equipment, systems, software, and processes as directed by project leads. You will run test scripts, maintain detailed records, and ensure compliance with GMP and Good Documentation Practice.

Candidates should have a Bachelor's degree, 5+ years in validation, strong communication, teamwork, and proficiency in Word, Excel, and PowerPoint.

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 for packaging equipment/lines is a plus.
• Experience in pharmaceutical, medical device, or regulated packaging ops is beneficial.
• Proficiency with PC and Microsoft Office tools.
• Strong communication, teamwork, problem-solving, and time-management skills.
• GMP and Good Documentation Practice training may be completed at onboarding.
• Intermediate skills with WORD (styles, tables, TOCs, track changes), basic Excel and PowerPoint.
• Strong interpersonal and clear communication capabilities.

Responsibilities

• Authoring, editing, and executing validation documentation for equipment, systems, software, and processes as directed by the project leader.
• Running test scripts and documenting results.
• Adhering to project schedules for all assigned activities.
• Maintaining clear, detailed qualification and validation records.
• Reading schematics to identify, locate, and test sensors, verify part numbers, and complete I/O testing on automated manufacturing equipment.

Skills

GMP knowledge

Good Documentation Practice

Microsoft Office

Communication

Teamwork

Problem solving

Time management

Attention to detail

Education

Bachelor’s Degree or equivalent

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Job description

Verista seeks a Senior Validation / CQV Engineer to author, edit, and execute validation documentation for standard equipment, systems, software, and processes as directed by project leads. You will run test scripts, maintain detailed records, and ensure compliance with GMP and Good Documentation Practice.

Candidates should have a Bachelor's degree, 5+ years in validation, strong communication, teamwork, and proficiency in Word, Excel, and PowerPoint.