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Cqv Engineer Jobs (NOW HIRING)

Lonza

CQV Engineer

Bend, OR · On-site

High School Diploma or GED required; engineering degree preferred. * Experience in CQV and temperature mapping. * Understanding of FDA, ICH, ISPE, and ISO guidelines. * Proficiency with Microsoft ...

NNE AS

Advanced CQV Engineer - Clayton NC

Clayton, NC · On-site

As an Advanced CQV Consultant, you are responsible for planning, executing, and delivering ... Collaborate with engineering, automation, quality, and manufacturing teams while supporting FAT ...

Veg Group

Senior Packaging CQV Engineer

Greenville, SC · On-site

Summary: We are seeking a Senior CQV / Packaging Validation Engineer to lead qualification and validation activities for a new packaging line handling liquid products in multiple bottle and cap ...

NNE AS

Advanced CQV Engineer - Clayton NC

Clayton, NC · On-site

Education & Experience Bachelor's or Master's degree in Engineering, Life Sciences, Biotechnology, Pharmaceutical Sciences, or a related field. 8+ years of CQV, Quality, Validation, or GMP consulting ...

NNE Inc.

Bachelor's or Master's degree in Engineering, Life Sciences, Biotechnology, Pharmaceutical Sciences, or a related field. * 8+ years of CQV, Quality, Validation, or GMP consulting experience within ...

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Cqv Engineer information

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How much do cqv engineer jobs pay per year?

As of Sep 12, 2026, the average yearly pay for cqv engineer in the United States is $89,183.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,500.00 and $109,000.00 per year, depending on experience, location, and employer.

What is a CQV engineer?

A CQV (Commissioning, Qualification, and Validation) Engineer is responsible for ensuring that equipment, systems, and processes within regulated industries, such as pharmaceuticals or biotechnology, meet regulatory and operational requirements. They develop and execute test protocols, troubleshoot issues, and document compliance with industry standards (e.g., FDA, GMP). Their role ensures that manufacturing facilities produce safe and effective products. CQV Engineers often collaborate with cross-functional teams, including quality, engineering, and operations.

What are the key skills and qualifications needed to thrive as a CQV engineer?

To thrive as a CQV (Commissioning, Qualification, and Validation) Engineer, you need a solid background in engineering principles, GMP regulations, and life sciences or pharmaceutical processes, often supported by a relevant degree. Familiarity with quality management systems, risk assessment tools, and software for documentation and validation such as TrackWise or Veeva is commonly required, and certifications like Six Sigma or CQV-specific credentials are valuable. Strong analytical thinking, attention to detail, effective communication, and collaboration skills set top performers apart. These competencies are essential to ensure compliance, project success, and seamless interaction with cross-functional teams in highly regulated environments.

What are some common challenges faced by CQV engineers in the pharmaceutical industry?

CQV Engineers in the pharmaceutical industry often encounter challenges such as managing strict timelines while ensuring full compliance with regulatory standards and adapting to evolving project requirements. They must coordinate with multiple departments including QA, production, and engineering to align project goals and documentation. Additionally, troubleshooting unexpected technical issues and staying updated with the latest industry guidelines can be demanding. However, overcoming these challenges is rewarding, as it directly contributes to the safe and effective delivery of life-saving products.

How much do CQV engineers make in the US?

CQV (Commissioning, Qualification, and Validation) engineers in the US typically earn between $80,000 and $130,000 annually, depending on experience, location, and industry. Senior or specialized engineers with certifications and extensive expertise can earn higher salaries, often exceeding $150,000. The role often requires knowledge of regulatory standards and validation tools.
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Cqv Engineer jobs near you
Infographic showing various Cqv Engineer job openings in the United States as of August 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 100% In-person job distribution, with an average salary of $89,183 per year, or $42.9 per hour.

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

Indianapolis, IN

Verista, Inc.
Pharmaceutical and Medicine Manufacturing • 201 - 500 employees
Learn more about Verista, Inc.external

$69K - $95K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 16 days ago

Key responsibilities

  • Support change control activities by authoring, reviewing, and managing change controls impacting systems, equipment, and processes.

  • Perform impact assessments to evaluate product quality, validated state, and regulatory impact, and support the execution of change control deliverables.

  • Participate in audits and inspections, providing subject matter expert support for change control and deviation processes.

Job description

Description

Verista's 500 experts team up with the world's most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world's most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.

Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.

Company Culture Guidelines & Values:

  • We empower and support our colleagues
  • We commit to client success at every turn
  • We have the courage to do the right thing
  • We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
  • We constantly acquire new skills and learn from our experiences to enhance our collective expertise

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

For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future.

*Verista is an equal opportunity employer.

National (US) Range
$69,300—$95,358 USD

Benefits

Why Choose Verista?

  • High growth potential and fast-paced organization with a people-focused culture
  • Competitive pay plus performance-based incentive programs
  • Company-paid Life, Short-Term, and Long-Term Disability Insurance.
  • Medical, Dental & Vision insurances
  • FSA, DCARE, Commuter Benefits
  • Supplemental Life, Hospital, Critical Illness and Legal Insurance
  • Health Savings Account
  • 401(k) Retirement Plan (Employer Matching benefit)
  • Paid Time Off (Rollover Option) and Holidays
  • As Needed Sick Time
  • Tuition Reimbursement
  • Team Social Activities (We have fun!)
  • Employee Recognition
  • Employee Referral Program
  • Paid Parental Leave and Bereavement

Verista collects and processes personal data in accordance with applicable data protection laws.  If you are a California Job Applicant, see the privacy notice for further details. 

For more information about our company, please visit us at Verista.com