CQV Validation Engineer – Change Control & Compliance

Veristainc; Indianapolis (IN); On-site; USD 69,000 - 95,000; Full time

Benefits offered by this job

Competitive compensation

Full benefits

401(k) with match

Tuition reimbursement

Paid time off

Job summary

Verista in Indianapolis, IN is seeking a CQV Engineer to support change controls, validation lifecycle, and regulatory compliance in a regulated cGMP environment.

The role requires 1–3 years of CQV/Validation experience, strong technical writing, and outstanding communication abilities. You will work onsite with a collaborative team of scientists, QA, and engineering to drive quality improvements and ensure audit readiness.

Qualifications

• Bachelors degree in a science/engineering field and CQV/Validation experience in a regulated industry.
• 13 years of CQV, Validation, or Quality Engineering experience; entry-level candidates encouraged to apply.
• Strong experience with change control systems and cGMP/GDP environments.
• Familiarity with analytical testing and chemistry is highly preferred.
• Experience supporting IQ/OQ/PQ and validation lifecycle activities is a plus.
• Strong technical writing and documentation skills; excellent communication.
• Onsite job requirement in Indianapolis, IN.

Responsibilities

• Author, review, and manage change controls impacting systems, equipment, and processes.
• Support CQV lifecycle activities and ensure cGMP/GDP compliance.
• Collaborate with scientists, Quality Assurance, and Engineering to implement changes.

Skills

Change control

cGMP

GDP

Analytical testing

IQ/OQ/PQ

Technical writing

Communication

Validation lifecycle

Team collaboration

Education

Bachelors degree in Chemistry, Engineering, Life Sciences, or related field

Job description

Verista in Indianapolis, IN is seeking a CQV Engineer to support change controls, validation lifecycle, and regulatory compliance in a regulated cGMP environment.

The role requires 1–3 years of CQV/Validation experience, strong technical writing, and outstanding communication abilities. You will work onsite with a collaborative team of scientists, QA, and engineering to drive quality improvements and ensure audit readiness.