Validation Engineer - Life Sciences CQV & Packaging

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

Benefits offered by this job

Competitive pay & incentives

Health & life insurance

Tuition reimbursement

401(k) with match

Paid time off & holidays

Job summary

Verista is seeking a Validation/CQV Engineer to join our team in the United States. The role involves authoring and executing validation documentation for equipment, systems, and software, while adhering to project schedules and maintaining meticulous records.

Strong communication and teamwork are essential, with a focus on GMP practices and Good Documentation. The ideal candidate holds a Bachelor’s degree or equivalent and has experience in pharmaceutical, medical device, or regulated packaging

Qualifications

• Bachelor’s Degree or equivalent required.
• Experience supporting validation, qualification, or testing activities for packaging equipment or packaging lines preferred.
• Experience in pharmaceutical, medical device, or regulated packaging operations is a plus.
• Proficiency with PC and Microsoft Office tools.
• Strong communication and teamwork abilities; detail-oriented and organized.

Responsibilities

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

Skills

Communication

Teamwork

Problem solving

Time management

Detail oriented

GMP training

Education

Bachelor's Degree

Tools

Word

Excel

PowerPoint

Job description

Verista is seeking a Validation/CQV Engineer to join our team in the United States. The role involves authoring and executing validation documentation for equipment, systems, and software, while adhering to project schedules and maintaining meticulous records.

Strong communication and teamwork are essential, with a focus on GMP practices and Good Documentation. The ideal candidate holds a Bachelor’s degree or equivalent and has experience in pharmaceutical, medical device, or regulated packaging