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Entry Level Oq Evaluator Jobs (NOW HIRING)

Tjoapack

Validation Writer

Clinton, TN · On-site

Your primary responsibility is entry level Technical Writing- authoring product-specific Master ... Perform technical evaluations of packaging components and processes. * Assess and document the ...

Tjoapack

Validation Writer

Clinton, TN · On-site

Your primary responsibility is entry level Technical Writing- authoring product-specific Master ... Perform technical evaluations of packaging components and processes. * Assess and document the ...

medplast

Quality - Quality Engineer I

Vega Baja, PR

$60K - $78K/yr

Quality Engineer I Position Description/Responsibilities: Entry-level to intermediate Quality ... Support validation activities (IQ/OQ/PQ) with approved protocols for sustaining projects.

medplast

Quality - Quality Engineer I

Vega Baja, PR

$60K - $78K/yr

Quality Engineer I Position Description/Responsibilities: Entry-level to intermediate Quality ... Support validation activities (IQ/OQ/PQ) with approved protocols for sustaining projects.

medplast

Quality - Quality Engineer I

Vega Baja, PR

$60K - $78K/yr

Quality Engineer I Position Description/Responsibilities: Entry-level to intermediate Quality ... Support validation activities (IQ/OQ/PQ) with approved protocols for sustaining projects.

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Entry Level Oq Evaluator information

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$65.5K

$106.5K

How much do entry level oq evaluator jobs pay per year?

As of Aug 30, 2026, the average yearly pay for entry level oq evaluator in the United States is $65,471.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,500.00 and $79,500.00 per year, depending on experience, location, and employer.

What are the most commonly searched types of Oq Evaluator jobs?

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Entry Level Oq Evaluator jobs near you
Infographic showing various Entry Level Oq Evaluator job openings in the United States as of August 2026, with employment types broken down into 92% Full Time, 6% Part Time, and 2% Contract. Highlights an 93% Physical, and 7% Remote job distribution, with an average salary of $65,471 per year, or $31.5 per hour.

6505 - Validation Engineer / CQV Engineer - Change Control & Deviations

Verista, Inc.

Indianapolis, IN • On-site

Full-time

Posted 3 days ago

New

Job description

We are seeking a CQV Engineer to support change control and deviation management activities. This role will play a critical part in maintaining compliance, supporting quality systems, and ensuring manufacturing changes are properly assessed, documented, and executed in a regulated cGMP environment.

The ideal candidate will have hands-on experience in change management and CQV lifecycle support within pharmaceutical or medical device manufacturing.

Validation Engineer / CQV Engineer Responsibilities:

Change Control Management

  • 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, which could include tracking/ updating to  documentation

CQV & Compliance Support

  • Analytical Development
  • Maintain alignment with cGMP and Good Documentation Practices (GDP)
  • Support impact assessments and execution activities related to changes
  • Review and approve technical documentation as required
  • Participate in audits and inspections, providing SME support for change control and deviation processes

Cross-Functional Collaboration

  • Interface with Analytics, Quality Assurance, , and Engineering teams 
  • Support continuous improvement initiatives related to quality systems and CQV processes
  • Communicate project status, risks, and issues to stakeholders
Requirements:
  • Bachelor's degree in Chemistry, Engineering, Life Sciences, or related field
  • 1-3 years of experience in CQV, Validation, or Quality Engineering in a regulated industry - Entry-level candidates encouraged to apply
  • Strong experience with:
    • Change control systems
    • cGMP and GDP environments
  • Familiarity with analytical testing and Chemistry  is highly preferred
  • Experience supporting validation lifecycle activities (IQ/OQ/PQ) is a plus
  • Strong technical writing and documentation skills
  • Excellent communication and cross-functional collaboration abilities
  • Onsite job requirement in Indianapolis, IN

Apply