Senior Validation Engineer - CQV for Life Sciences

Verista, Inc.; North Carolina; On-site; USD 79,000 - 129,000; Full time

Benefits offered by this job

Life/Disability Insurance

Medical/Dental/Vision Insurance

401(k) Matching

Paid Time Off

Tuition Reimbursement

Parental Leave

Job summary

Verista, Inc. is seeking a Senior Validation / CQV Engineer in the United States to author, edit, and execute commissioning, qualification, and validation documentation for standard equipment, systems, software, and processes as part of a project team.

You will run test scripts, maintain detailed records, and ensure adherence to schedules while collaborating with peers in regulated packaging environments. A Bachelor’s degree and 5+ years of CQV experience, GMP training, and proficiency with

Qualifications

• Bachelor’s Degree or equivalent required.
• 5+ years authoring, editing, and executing validation docs.
• Experience with packaging equipment/lines preferred.
• Experience in pharmaceutical, medical device, or regulated packaging is a plus.
• Proficiency with PC and Microsoft Office tools.
• Outgoing personality with clear, concise communication.
• Strong teamwork and problem-solving abilities.
• GMP and Good Documentation Practice training (may be completed at onboarding).
• Intermediate Word and basic Excel/PowerPoint skills.

Responsibilities

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

Skills

Communication

Teamwork

Detail-oriented

Problem solving

Time management

Education

Bachelor's degree or equivalent

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Job description

Verista, Inc. is seeking a Senior Validation / CQV Engineer in the United States to author, edit, and execute commissioning, qualification, and validation documentation for standard equipment, systems, software, and processes as part of a project team.

You will run test scripts, maintain detailed records, and ensure adherence to schedules while collaborating with peers in regulated packaging environments. A Bachelor’s degree and 5+ years of CQV experience, GMP training, and proficiency with