CQV Validation Engineer — Life Sciences (Entry-Level)

Verista, Inc.; Indianapolis (IN); On-site; USD 69,000 - 95,000; Full time

Benefits offered by this job

Competitive pay

Health, Dental & Vision insurance

401(k) Retirement Plan

Paid Time Off

Tuition Reimbursement

Team Social Activities

Employee Recognition

Employee Referral Program

Parental Leave

Job summary

Verista, Inc. is seeking a CQV Engineer to support change control and deviation management within a regulated cGMP environment.

The role focuses on ensuring manufacturing changes are properly assessed, documented, and executed, with collaboration across Analytics, Quality, and Engineering teams. The ideal candidate will have hands-on CQV lifecycle experience and strong technical writing skills, plus onsite availability in Indianapolis, IN.

Qualifications

• Bachelor’s degree in a relevant field is required.
• 1–3 years of CQV, Validation, or Quality Engineering experience in a regulated industry.
• Experience with change control systems in cGMP and GDP environments is preferred.
• Strong technical writing and documentation skills are essential.
• Excellent communication and cross-functional collaboration abilities are required.

Responsibilities

• Author, review, and manage change controls impacting systems, equipment, and processes.
• Perform impact assessments including product quality, validated state, and regulatory impact.
• Collaborate with Scientists, Quality, Analytics, and Engineering teams to ensure timely, compliant changes.
• Support execution of change control deliverables and related CQV & Compliance tasks.
• Participate in audits and inspections, providing SME support for change control and deviation processes.

Skills

Change control systems cGMP GDP

Analytical testing familiarity

IQ/OQ/PQ validation lifecycle

Technical writing & documentation

Cross-functional collaboration

Education

Bachelor’s degree in Chemistry, Engineering, Life Sciences, or related field

Job description

Verista, Inc. is seeking a CQV Engineer to support change control and deviation management within a regulated cGMP environment.

The role focuses on ensuring manufacturing changes are properly assessed, documented, and executed, with collaboration across Analytics, Quality, and Engineering teams. The ideal candidate will have hands-on CQV lifecycle experience and strong technical writing skills, plus onsite availability in Indianapolis, IN.