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Validation Project Manager Jobs in Ohio (NOW HIRING)

RIECK SERVICES LLC

Project Manager

Dayton, OH · On-site

$100K - $108K/yr

Key Responsibilities Manage mechanical service projects from initial scope review through ... Valid driver's license and ability to travel to customer sites and project locations as needed.

Rieck Services

Project Manager

Dayton, OH · On-site

Key Responsibilities • Manage mechanical service projects from initial scope review through ... Valid driver's license and ability to travel to customer sites and project locations as needed. • ...

Rieck Services LLC

Project Manager

Dayton, OH · On-site

$100K - $108K/yr

Mechanical Services Project Manager We are seeking an experienced Mechanical Services Project ... · Valid driver's license and ability to travel to customer sites and project locations as needed ...

CARIAN

Utility Distribution Project Manager I

Akron, OH · On-site

$95 - $145/hr

Distribution Project Manager - New Jersey Location : Morristown, NJ OR Reading, PA (Office ... Review and validate project scopes and develop work plans with engineering and utility stakeholders

Marcus Thomas, LLC

Project Manager

Cincinnati, OH · On-site

$80 - $110/hr

Project Management Reports To: Senior Project Manager Locations: Ohio is the preferred hiring ... We can't issue an offer based on a planned future move without a valid address. Employment ...

Sidram Technologies

Project Manager

Ohio City, OH · On-site

Project Manager Location: Cincinnati, OH w2/c2c JD: KEY JOB RESPONSIBILITIES: * Develop and ... Requirements Documentation, Prototyping, Design, Verification, Validation, and Product Quality and ...

Sidram Technologies

Project Manager

Cincinnati, OH · On-site

Project Manager Location: Cincinnati, OH Customer: Johnson & Johnson Services, Inc JD: KEY JOB ... Requirements Documentation, Prototyping, Design, Verification, Validation, and Product Quality and ...

Marcus Thomas LLC

Project Manager

Cleveland, OH · On-site

$85 - $110/hr

Project Management Reports To: Senior Project Manager Locations: Ohio is the preferred hiring ... We can't issue an offer based on a planned future move without a valid address. Candidates must be ...

New

Rumpke Waste & Recycling

Project Manager

Bevis, OH · On-site

$85 - $120/hr

The Project Manager is responsible for leading software implementation and technology initiatives ... Lead user acceptance testing (UAT), including test case development and validation of business ...

Marcus Thomas

Project Manager

Cincinnati, OH · On-site

$90 - $120/hr

Project Management Reports To: Senior Project Manager Locations: Ohio is the preferred hiring ... We can't issue an offer based on a planned future move without a valid address. Candidates must be ...

Northeast Ohio Medical University

Project Manager

OH · On-site

$55K - $63K/yr

Posting Details Position Information Position Title Project Manager Position Type Admin ... valid medical reasons, sincerely held religious beliefs and matters of conscience. Close Date

ABM Industries, Inc.

Project Manager

Columbus, OH · On-site

The Project Manager serves as the primary point of contact for customers and is responsible for ... Valid driver's license and acceptable driving record. * Ability to travel as required to support ...

cGMP Consulting

Project Manager

Cincinnati, OH · On-site

$85 - $100/hr

About Us At cGMP Consulting, we specialize in providing expert validation, qualification, and ... Monitor progress, manage risk and coordinate resources across multiple concurrent projects. * Serve ...

Rumpke Waste & Recycling

Project Manager

Cincinnati, OH · On-site

$90 - $120/hr

The Project Manager is responsible for leading software implementation and technology initiatives ... Lead user acceptance testing (UAT), including test case development and validation of business ...

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Validation Project Manager information

What is a validation project manager?

A Validation Project Manager is a professional responsible for overseeing and coordinating validation activities in industries such as pharmaceuticals, biotechnology, or manufacturing. Their main duties include ensuring that systems, equipment, and processes meet regulatory standards and operate as intended. They manage project timelines, resources, and communication among cross-functional teams to ensure successful validation outcomes. Additionally, they maintain documentation and ensure compliance with industry regulations such as FDA or GMP. This role is crucial for maintaining product quality, safety, and regulatory compliance.

How does a validation project manager typically collaborate with cross-functional teams during a project?

A Validation Project Manager regularly collaborates with cross-functional teams such as quality assurance, regulatory affairs, engineering, and production to ensure that all validation activities meet regulatory standards and project timelines. This collaboration often involves coordinating meetings, aligning on project milestones, and facilitating clear communication to address any technical or compliance issues. Building strong working relationships across departments is crucial for anticipating challenges and ensuring a smooth validation process. Effective coordination helps to minimize delays and ensures that all documentation and testing requirements are thoroughly met.

What are the key skills and qualifications needed to thrive as a validation project manager, and why are they important?

To thrive as a Validation Project Manager, you need expertise in regulatory compliance, project management, and validation protocols, often supported by a degree in engineering, life sciences, or a related field. Familiarity with validation software, quality management systems (QMS), and certifications like PMP or Six Sigma are commonly required. Exceptional organizational, leadership, and communication skills help coordinate cross-functional teams and manage complex timelines. These skills are crucial to ensure validated processes comply with industry standards, mitigate risks, and deliver successful project outcomes.

What is the difference between Validation Project Manager vs Quality Assurance Specialist?

AspectValidation Project ManagerQuality Assurance Specialist
CertificationsGMP, ISO, PMPISO, Six Sigma, GMP
Work EnvironmentRegulated industries like pharma, biotechManufacturing, software, healthcare
Primary FocusEnsuring validation processes and protocolsMaintaining quality standards and procedures
Employer UsagePharmaceutical, biotech, medical device companiesManufacturers, software firms, healthcare providers

The Validation Project Manager primarily oversees validation activities, ensuring compliance with industry standards, while the Quality Assurance Specialist focuses on maintaining overall quality standards across processes. Both roles require similar certifications and are common in regulated industries, but their core responsibilities differ in scope and focus.

What are popular job titles related to Validation Project Manager jobs in Ohio?

For Validation Project Manager jobs in Ohio, the most frequently searched job titles are:

What job categories do people searching Validation Project Manager jobs in Ohio look for?

The top searched job categories for Validation Project Manager jobs in Ohio are:

What cities in Ohio are hiring for Validation Project Manager jobs?

Cities in Ohio with the most Validation Project Manager job openings:

Validation Project Manager jobs near you
Infographic showing various Validation Project Manager job openings in Ohio as of August 2026, with employment types broken down into 84% Full Time, 13% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 84% Physical, 2% Hybrid, and 14% Remote job distribution.

Validation Engineer

Validation & Engineering Group, Inc

Cincinnati, OH • On-site

Full-time

Re-posted 24 days ago

Key responsibilities

  • Lead full validation lifecycle activities including FAT, SAT, CSV, equipment integration, and startup.

  • Develop User Requirement Specifications (URS) and create engineering documentation.

  • Manage equipment commissioning, qualification, and ensure compliance with safety, regulatory, and GMP standards.

Job description

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

  • Validation Engineer

Description:

The role demands deep technical expertise across the full validation lifecycle — including URS development, FAT/SAT execution, and Computer System Validation (CSV) — as well as hands-on experience with systems and controls integration. The candidate will drive end-to-end project implementation: from equipment design and installation through startup, commissioning, and qualification.

Key Responsibilities:

  • Develop User Requirement Specifications (URS).
  • Lead full validation lifecycle activities: FAT, SAT, CSV, equipment integration, and startup.
  • Drive process design for new equipment and ensure product design requirements are met.
  • Execute commissioning and qualification activities for new and existing equipment.
  • Provide technical oversight to ensure equipment meets safety, regulatory, and operational standards.
  • Manage suppliers and external vendors on capital projects, controlling scope, cost, and lead time.
  • Collaborate with Procurement and Legal on vendor contracts.
  • Create and maintain engineering documentation (URS, assembly instructions, bill of process, etc.).
  • Optimize equipment design for manufacturability, cost reduction, maintainability, and efficiency.
  • Lead design reviews, risk assessments, and FMEA to ensure reliability and performance.
  • Ensure compliance with all safety regulations and quality policies, procedures, and GMP standards.
  • Apply statistical analysis and SPC systems to support data-driven decision-making.
  • Manage multiple priorities and maintain equipment qualification schedules.

Qualifications:

  • Bachelor's degree in Engineering or Science.
  • Minimum 4 years of engineering experience in pharmaceutical and/or medical device industries.
  • Demonstrated experience across the full validation lifecycle (URS, FAT, SAT, CSV).
  • Proven track record supporting full project implementation: design, installation, startup, commissioning, and qualification.
  • Strong experience executing capital projects within GMP-regulated manufacturing environments.
  • Familiarity with GMP, ISO standards, Lean Manufacturing, and FDA-regulated environments.
  • Ability to work independently and lead solutions under general direction.
  • Strong organization, and communication skills

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.