CQV Engineer: Change Control & Deviations (Onsite Indy)

veristainc; Indianapolis (IN); On-site; USD 69,000 - 103,000; Full time

Benefits offered by this job

Competitive pay

Medical, Dental & Vision insurances

401(k) Retirement Plan (Employer Match

Paid Time Off

Tuition Reimbursement

Job summary

Verista is seeking a CQV Engineer to support change control and deviation management in a regulated cGMP environment. The role emphasizes validation lifecycle activities (IQ/OQ/PQ) and strong technical writing within a collaborative team.

The ideal candidate will have 1–3 years of CQV/Validation experience and bachelor's degree in Chemistry, Engineering, Life Sciences, or a related field. Onsite work is required in Indianapolis, IN, with opportunities to impact product quality and compliance.

Qualifications

• Bachelor's degree in Chemistry, Engineering, Life Sciences, or related field.
• 1-3 years of CQV, Validation, or Quality Engineering in a regulated industry.
• Experience supporting validation lifecycle activities (IQ/OQ/PQ).
• Strong technical writing and documentation skills.
• Excellent communication and cross-functional collaboration abilities.

Responsibilities

• Author, review, and manage change controls impacting systems, equipment, and processes.
• Perform impact assessments, including evaluation of product quality, validated state, and regulatory impact.
• Collaborate with cross-functional teams (Scientists, Quality) to ensure timely and compliant change implementation.
• Support execution of change control deliverables, including tracking/updating documentation.

Skills

Change control systems

cGMP GDP environments

Technical writing

Cross-functional collaboration

Analytical testing knowledge

Education

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

Job description

Verista is seeking a CQV Engineer to support change control and deviation management in a regulated cGMP environment. The role emphasizes validation lifecycle activities (IQ/OQ/PQ) and strong technical writing within a collaborative team.

The ideal candidate will have 1–3 years of CQV/Validation experience and bachelor's degree in Chemistry, Engineering, Life Sciences, or a related field. Onsite work is required in Indianapolis, IN, with opportunities to impact product quality and compliance.