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Cqv Engineer Jobs in Ohio (NOW HIRING)

CAI

Senior Validation Engineer

Cincinnati, OH · On-site

$87K - $94K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

SmartIPlace

Automation Engineer

Columbus, OH · On-site

We are seeking a mid-level Automation Engineer to play a pivotal role in designing, implementing ... Lead commissioning and qualification (CQV) processes. Ensure technologies and processes are ...

IT MINDS L.L.C.

OH · On-site

$100K - $131K/yr

Job Title: Sr. Cold Room Automation Engineer Location: Ohio (Hybrid - 50% Onsite) Duration: 12 ... Strong CQV, Validation, Commissioning, and Startup experience * Knowledge of PLC, HMI, SCADA, OT ...

ATS Automation

Senior Automation Engineer

Lewis Center, OH · On-site

$98K - $129K/yr

Support Commissioning, Qualification, and Validation (CQV) activities for the cold room systems ... Serve as a recognized Engineering Subject Matter Expert (SME) for cold room systems, establishing ...

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Showing results 21-40

All JobsCqv Engineer JobsCqv Engineer Jobs in Ohio

Cqv Engineer information

See Ohio salary details

$31.4K

$84.8K

$135K

How much do cqv engineer jobs pay per year?

As of Sep 5, 2026, the average yearly pay for cqv engineer in Ohio is $84,786.00, according to ZipRecruiter salary data. Most workers in this role earn between $63,200.00 and $103,600.00 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.

What are popular job titles related to Cqv Engineer jobs in Ohio?

For Cqv Engineer jobs in Ohio, the most frequently searched job titles are:

What job categories do people searching Cqv Engineer jobs in Ohio look for?

The top searched job categories for Cqv Engineer jobs in Ohio are:

Cqv Engineer jobs near you
Infographic showing various Cqv Engineer job openings in Ohio as of August 2026, with employment types broken down into 74% Full Time, and 26% Contract. Highlights an 100% In-person job distribution, with an average salary of $84,786 per year, or $40.8 per hour.

6507 - Document Controller / Associate CQV Engineer

Verista, Inc.

West Chester, OH • On-site

$58K - $84K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

New

Key responsibilities

  • Manage the creation, review, approval, revision, and archival of controlled documents within the electronic document management system (EDMS).

  • Coordinate document reviews and approvals with cross-functional teams and track documents through the approval process.

  • Perform quality checks of documentation for completeness, accuracy, formatting, and compliance with Good Documentation Practices (GDP).

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 an experienced Document Controller to support document management and control activities within a regulated pharmaceutical manufacturing environment. This individual will be responsible for maintaining accurate, compliant, and controlled documentation while supporting Quality, Engineering, Validation, Manufacturing, and other cross-functional teams.

Document Controller Responsibilities
  • Manage the creation, routing, review, approval, issuance, revision, and archival of controlled documents within the electronic document management system (EDMS).
  • Utilize Veeva to manage document workflows, approvals, revisions, and document lifecycle activities.
  • Ensure controlled documents are accurate, current, properly formatted, and maintained in accordance with established procedures and cGMP requirements.
  • Support document control activities for SOPs, work instructions, specifications, protocols, reports, forms, and other GxP documentation.
  • Coordinate document reviews and approvals with Quality, Engineering, Validation, Manufacturing, and other stakeholders.
  • Track documents through the approval process and follow up with document owners and reviewers to ensure timely completion.
  • Maintain document histories, revision records, effective dates, and appropriate archival of superseded documentation.
  • Perform quality checks of documentation for completeness, accuracy, formatting, and compliance with Good Documentation Practices (GDP).
  • Assist with document retrieval and preparation for internal audits, regulatory inspections, and project activities.
  • Support continuous improvement of document control processes and procedures.
Requirements
  • Previous Document Control experience within the pharmaceutical, biotechnology, or other highly regulated life sciences industry required.
  • Hands-on experience with Veeva, preferably Veeva Vault QualityDocs or a similar Veeva document management application, required.
  • Knowledge of cGMP and Good Documentation Practices (GDP).
  • Experience managing controlled documents and electronic document workflows.
  • Strong attention to detail with excellent organizational and time-management skills.
  • Ability to manage multiple documents, priorities, and deadlines simultaneously.
  • Strong written and verbal communication skills with the ability to work effectively across multiple functional groups.
  • Proficiency with Microsoft Office applications.
  • Ability to work onsite in West Chester, Ohio.

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
$58,550—$84,905 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