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Contract Cleaning Validation Engineer Jobs in Ohio

Our Business Adare Pharma Solutions is a global Contract Development and Manufacturing Organization ... Develop and execute studies for process, equipment, and cleaning validation activities related to ...

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions ... Collaborate with Procurement and Legal on vendor contracts. * Create and maintain engineering ...

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions ... Collaborate with Procurement and Legal on vendor contracts. * Create and maintain engineering ...

Validation Engineer

Cincinnati, OH ยท On-site

$80 - $100/hr

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions ... Collaborate with Procurement and Legal on vendor contracts. * Create and maintain engineering ...

This includes process, cleaning, equipment, and utility system qualifications for OTC products, cosmetics, and regulated systems. The Validation Engineer collaborates closely with Engineering ...

This includes process, cleaning, equipment, and utility system qualifications for OTC products, cosmetics, and regulated systems. The Validation Engineer collaborates closely with Engineering ...

Engineer, Validation

New Albany, OH ยท On-site

$60 - $80/hr

This includes process, cleaning, equipment, and utility system qualifications for OTC products, cosmetics, and regulated systems. The Validation Engineer collaborates closely with Engineering ...

As a Validation Engineer I , you will be responsible for the design, implementation, and execution ... Understanding of aseptic processing and clean room standards. * Proficiency in risk assessment ...

As a Validation Engineer I , you will be responsible for the design, implementation, and execution ... Understanding of aseptic processing and clean room standards. * Proficiency in risk assessment ...

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Contract Cleaning Validation Engineer information

What is a contract cleaning validation engineer?

Contract Cleaning Validation Engineers are professionals who specialize in ensuring that cleaning procedures in manufacturing environments, especially in industries like pharmaceuticals and biotechnology, meet regulatory and quality standards. They are typically hired on a contract basis to validate and document that cleaning processes effectively remove contaminants and residues from equipment and facilities. Their work includes developing and executing cleaning validation protocols, analyzing test results, and preparing reports for regulatory compliance. These engineers play a crucial role in maintaining product safety and quality, and their expertise helps companies pass regulatory inspections. Contract Cleaning Validation Engineers often work with cross-functional teams and need strong knowledge of industry guidelines such as those from the FDA and EMA.

What are the key skills and qualifications needed to thrive as a contract cleaning validation engineer?

To thrive as a Contract Cleaning Validation Engineer, you need a strong background in chemical engineering, microbiology, or a related field, along with experience in cleaning validation within regulated industries. Familiarity with validation protocols, regulatory standards (such as FDA or EU GMP), and statistical analysis software is typically required. Attention to detail, problem-solving skills, and effective communication are crucial for documenting processes and collaborating with cross-functional teams. These skills ensure cleaning processes are compliant, reproducible, and safe, which is vital for product quality and regulatory approval.

What are some common challenges faced by a contract cleaning validation engineer during a project?

Contract Cleaning Validation Engineers often encounter challenges such as aligning cleaning protocols with both client requirements and regulatory standards, managing tight project timelines, and navigating complex equipment or facility layouts. Additionally, collaborating effectively with client teams and other contractors is crucial to ensure that validation documentation is accurate and comprehensive. Staying up-to-date with evolving industry regulations and best practices is also essential to delivering successful validation outcomes.

What is the difference between Contract Cleaning Validation Engineer vs Quality Assurance Specialist?

AspectContract Cleaning Validation EngineerQuality Assurance Specialist
CredentialsValidation certifications, engineering backgroundQA certifications, quality management training
Work EnvironmentPharmaceutical, biotech, or cleanroom facilitiesManufacturing, production, or laboratory settings
Employer & IndustryContract-based roles in regulated industriesIn-house or consulting roles in various industries
Search & Comparison IntentFocus on cleaning validation processesFocus on overall quality assurance practices

The Contract Cleaning Validation Engineer primarily specializes in validating cleaning processes within regulated environments like pharmaceuticals and biotech. In contrast, a Quality Assurance Specialist oversees broader quality systems, including audits and compliance. While both roles require understanding of industry standards, the validation engineer focuses on specific cleaning validation tasks, whereas the QA specialist manages overall quality assurance programs.

What are popular job titles related to Contract Cleaning Validation Engineer jobs in Ohio?

For Contract Cleaning Validation Engineer jobs in Ohio, the most frequently searched job titles are:

What job categories do people searching Contract Cleaning Validation Engineer jobs in Ohio look for?

The top searched job categories for Contract Cleaning Validation Engineer jobs in Ohio are:

What cities in Ohio are hiring for Contract Cleaning Validation Engineer jobs?

Cities in Ohio with the most Contract Cleaning Validation Engineer job openings:

Infographic showing various Contract Cleaning Validation Engineer job openings in Ohio as of August 2026, with employment types broken down into 1% As Needed, 67% Full Time, 27% Part Time, 2% Temporary, 2% Contract, and 1% Nights. Highlights an 99% Physical, and 1% Remote job distribution.

Validation Engineer

Stark Pharma Solutions Inc

Columbus, OH โ€ข On-site

Contractor

Posted 6 days ago


Job description

About the Company

Stark Pharma Solutions Inc. is a global consulting and staffing partner established in 2014, serving the Pharmaceutical, Medical Device, Biotech, and IT industries across the USA, Canada, and India.

We provide specialized consulting and staffing solutions across Quality & Validation, Regulatory Affairs, R&D, Manufacturing, Supply Chain, Project Management, and IT, with a focus on delivering tailored solutions that drive growth, operational excellence, and long-term client success.
Position: Validation Engineer
Location: Ohio
Duration: Long Term

Job Overview

We are seeking an experienced Validation Engineer to support Oral Solid Dosage (OSD) manufacturing operations within a cGMP pharmaceutical environment.

The role will focus on Process Validation, Cleaning Validation, and CQV activities for pharmaceutical manufacturing equipment, facilities, utilities, and processes.

Key Responsibilities

• Support Process Validation, Cleaning Validation, and CQV activities.
• Prepare, review, and execute IQ/OQ/PQ and PPQ protocols.
• Prepare validation plans, protocols, and final reports.
• Support qualification of manufacturing equipment, facilities, and utilities.
• Support cleaning validation activities, including swab and rinse sampling.
• Perform residue limit calculations for cleaning validation.
• Support equipment installation, process improvements, and technology transfers.
• Work with Manufacturing, Quality Assurance, Engineering, MS&T, and Regulatory teams.
• Ensure validation activities comply with cGMP, FDA, and EMA requirements.
• Support OSD manufacturing processes including blending, granulation, compression, encapsulation, coating, and packaging.

Required Qualifications

• Bachelor’s degree in Engineering, Life Sciences, or a related field.
• Experience as a Validation Engineer in a pharmaceutical manufacturing environment.
• Experience with OSD manufacturing processes.
• Hands-on experience with Process Validation and Cleaning Validation.
• Experience with CQV and equipment qualification.
• Strong knowledge of IQ/OQ/PQ and PPQ.
• Experience with swab and rinse sampling and residue limit calculations.
• Knowledge of cGMP, FDA, and EMA requirements.
• Strong technical writing, communication, and problem-solving skills.

How to Apply

Apply Now: Submit your updated resume to Stark Pharma Solutions Inc. for consideration.

Stark Pharma is an Equal Opportunity Employer and welcomes qualified candidates from diverse backgrounds.