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Quality Validation Analyst Jobs in Ohio (NOW HIRING)

Belcan

Quality Engineer

Cincinnati, OH · On-site

$50 - $60/hr

Quality Engineer Pay Rate: $50-60/hr Duration: 24-month contract Location: Cincinnati, OH Zip Code ... Analysis, Test Method Validation, IQ, OQ, PQ, FAI) of new supplier manufactured components.

R.W. Screw Products, Inc.

Quality Engineer

Massillon, OH · On-site

$65K - $85K/yr

Root Cause Analysis and Corrective Actions: Identify quality issues through data analysis and ... Product & Process Validation: Collaborate with sales, engineering, production, and materials that ...

Arhaus

Quality Analyst

Boston Heights, OH · On-site

The Quality Analyst is responsible for assisting with the preparation of routine product and ... Must have a valid driver's license. * Employee is regularly required to stand, walk, and sit; use ...

Amphenol TPC Wire & Cable

Data Quality Engineer

Macedonia, OH · On-site

$103K - $124K/yr

Perform root cause analysis on data issues across source systems, pipelines, and downstream applications. * Own cross-system data quality validation, ensuring data integrity is enforced at ingestion ...

TPC Wire and Cable

Data Quality Engineer

Macedonia, OH · On-site

$103K - $124K/yr

Perform root cause analysis on data issues across source systems, pipelines, and downstream applications. * Own cross-system data quality validation, ensuring data integrity is enforced at ingestion ...

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Quality Validation Analyst information

What does a quality validation analyst do?

A Quality Validation Analyst is responsible for ensuring that products, processes, or systems meet established quality standards and regulatory requirements. They design and execute validation tests, analyze data, document results, and recommend improvements to maintain compliance and product integrity. Their work is crucial in industries like pharmaceuticals, manufacturing, and software, where validated processes are required for safety and efficiency. Quality Validation Analysts often collaborate with engineering, production, and quality assurance teams to resolve issues and optimize procedures.

What are the key skills and qualifications needed to thrive as a quality validation analyst?

To thrive as a Quality Validation Analyst, you need expertise in quality assurance methodologies, data analysis, and process validation, often supported by a degree in life sciences, engineering, or a related field. Familiarity with tools such as LIMS (Laboratory Information Management Systems), validation software, and knowledge of regulatory standards like GMP or ISO is crucial. Strong attention to detail, analytical thinking, and effective communication make someone stand out in this role. These skills ensure that products and processes meet stringent quality standards, maintain compliance, and minimize errors in regulated environments.

How does a quality validation analyst typically collaborate with other departments to ensure compliance and product quality?

Quality Validation Analysts work closely with cross-functional teams such as manufacturing, engineering, and regulatory affairs to ensure that products and processes meet established standards. They often participate in meetings to discuss validation protocols, review test results, and address any discrepancies or non-conformities. Effective communication and documentation are essential, as analysts must clearly convey findings and recommendations to both technical and non-technical stakeholders. This collaborative approach helps maintain compliance and continuous improvement across the organization.

What is the difference between Quality Validation Analyst vs Quality Assurance Specialist?

AspectQuality Validation AnalystQuality Assurance Specialist
CertificationsOften requires certifications like CQE or Six SigmaSimilar certifications, often including ISO or Six Sigma
Work EnvironmentPrimarily in labs, manufacturing, or regulated industriesInvolved in process audits, documentation, and compliance
Job FocusValidates products or processes meet specificationsEnsures overall quality processes and standards are followed

Both roles focus on quality but differ in scope. The Quality Validation Analyst primarily verifies that products or processes meet specific standards, often through testing and validation. The Quality Assurance Specialist oversees broader quality systems, audits, and compliance. Understanding these differences helps in choosing the right career path or job search focus.

Is a quality validation analyst a good job?

A quality validation analyst is a valuable role in industries like pharmaceuticals, manufacturing, and healthcare, focusing on ensuring products meet quality standards through testing and documentation. The job typically requires attention to detail, knowledge of validation processes, and may involve using specialized software or tools. It offers opportunities for career growth and often requires certifications such as CQV or GMP training.
Infographic showing various Quality Validation Analyst job openings in Ohio as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 16% Part Time, 6% Contract, and 1% Nights. Highlights an 81% Physical, 1% Hybrid, and 18% Remote job distribution.

Quality Validations Specialist

Aurora, OH • On-site

Natural Essentials
201 - 500 employees
Learn more about Natural Essentialsexternal

Other

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Quality Validation Specialist.

The Validation Specialist is responsible for performing complex validation and qualification activities for critical equipment, utilities and processes used in cGMP. The position requires frequent travel between the Manufacturing Facility and the Distribution Facility. Hours are 7:00 a.m. to 3:30 p.m.; overtime may be required and hours may be adjusted during peak periods. This is a salaried exempt role.

Duties and Responsibilities:
  • Write and execute validation and re‑validation protocols and reports (IQ/OQ/PQ) for validation of new and existing processes, equipment, systems, etc.
  • Write detailed validation reports and analyze complex quality data.
  • Plan and execute cleaning validation activities.
  • Perform and/or coordinate cleaning studies, spray coverage testing, cleaning verification swabbing, and rinse sampling.
  • Provide technical input for control strategies for introduction of new products as it relates to Cleaning Validation.
  • Maintain the Cleaning Validation equipment and product matrix.
  • Analyze statistical data to verify acceptable criteria.
  • Maintain revalidation schedules to ensure the facility remains in a validated state.
  • Write and review SOPs related to qualification activities.
  • Provide technical support/troubleshooting for process and equipment issues.
  • Attend production and team meetings, as required.
  • Troubleshoot and rectify complex issues.
  • Maintain close contact with manufacturing and laboratory departments to assure effective communication on validity issues.
  • Apply CGMP guidelines to all aspects of validation.
  • Investigate and resolve deviations associated with validation studies.
  • Author technical documents such as protocols, reports, deviations, gap analyses, risk assessments, etc.
  • Provide technical and/or investigational support in troubleshooting and resolving manufacturing equipment issues.Perform periodic review of equipment and systems.
  • Critically review data to ensure completeness, accuracy and compliance.
  • Apply CGMP and CGDP to all areas of work.
Required Knowledge, Skills, and Abilities:
  • Strong organization and communication skills; high level of personal/departmental accountability and responsibility.
  • Ability to manage multiple priorities and tasks in a dynamic environment.
  • Ability to exercise judgment to determine appropriate corrective actions.
  • Ability to exercise judgment for defined practices and policies in selecting methods and techniques for obtaining solutions.
  • Minimum of four (4) years of relevant GMP metrology, validation, or process engineering experience.
  • Previous FDA experience is a plus.
  • Detail oriented with strong written and verbal communication skills.
  • Ability to work independently, within prescribed guidelines, or as a team member.
  • Experience with Google Suite and Microsoft Office applications.
  • Bachelor’s Degree in Engineering or a related degree.
Working Conditions and Physical Effort:
  • Regularly able to lift and/or move up to 10 pounds, frequently up to 25 pounds, and occasionally up to 50 pounds.
  • Standing, sitting, or walking for more than 8 hours a day.
  • Able to work in high heat and humidity or cold and dry conditions indoors/outdoors.
  • Full range of motion to lift, carry, walk, climb around equipment and facilities.
  • Work in elevated positions on ladders, lifts, and platforms.
  • Work involves moderate exposure to unusual elements such as extreme temperatures, dirt, dust, fumes, smoke, unpleasant odors, and/or loud noises.
  • Routine use of standard office equipment such as computers, phones, photocopiers, filing cabinets, and fax machines.
  • Wearing PPE as necessary for the job.

Reports to Director of Quality Assurance.

Job Type:

Full‑time.

Pay:

Compensation based on experience.

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