GMP Validation Engineer for Life Sciences Equipment

Verista; Columbus (OH); On-site; USD 70,000 - 118,000; Full time

Benefits offered by this job

Growth potential

Competitive pay

Life insurance

Health insurance

Dental insurance

Vision insurance

401(k) matching

Paid time off

Tuition reimbursement

Parental leave

Job summary

Verista in the life sciences sector is seeking a Validation/CQV Engineer to author, edit, and execute commissioning, qualification, and validation documentation for standard equipment and processes.

The role requires a Bachelor's degree, strong teamwork, documentation discipline, and experience with GMP and validated testing. Ohio/Columbus area; US salary ranges apply with competitive benefits.

Qualifications

• Bachelor’s Degree or equivalent required.
• Prior experience supporting validation, qualification, or testing activities for packaging equipment or packaging lines preferred.
• Experience in pharmaceutical/medical device/regulatory 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 with styles, tables, and track changes; basic Excel/PowerPoint.

Responsibilities

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

Skills

Communication

Teamwork

GMP

Documentation

Attention to detail

Problem-solving

Time management

Interpersonal skills

MS Office

Education

Bachelor’s degree

Tools

WORD

Excel

PowerPoint

Job description

Verista in the life sciences sector is seeking a Validation/CQV Engineer to author, edit, and execute commissioning, qualification, and validation documentation for standard equipment and processes.

The role requires a Bachelor's degree, strong teamwork, documentation discipline, and experience with GMP and validated testing. Ohio/Columbus area; US salary ranges apply with competitive benefits.