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Process Simulate Jobs in Columbus, OH (NOW HIRING)

Knowledge of validation principles across multiple disciplines, which may include computerized systems, aseptic process simulation, and/or process validation. * Experience in the application of pre ...

Knowledge of validation principles across multiple disciplines, which may include computerized systems, aseptic process simulation, and/or process validation. * Experience in the application of pre ...

... simulations, as well as manage data for lab experiments related to chemical and biochemical effects of electric field and other advanced food, biological and environmental processes. It is expected ...

Experience in the full life cycle of Integrated Circuit Design including processes such as, Simulation, Synthesis, Layout, and Fabrication * Experience in the full FPGA development flow including RTL ...

Experience with planning model design, control parameters, and scenario simulations. Strong analytical, data mining, and large-volume data processing skills. Experience working with cross-functional ...

Experience with planning model design, control parameters, and scenario simulations. Strong analytical, data mining, and large-volume data processing skills. Experience working with cross-functional ...

Experience with gaming consoles, simulation platforms, or real-time control systems * Experience in ... If you would like more information about how your data is processed, please contact us. apply for ...

Research Scientist

Columbus, OH · On-site

$80 - $120/hr

Strong and proven background in molecular dynamics simulations * Experience working with novel preservation technologies such as ohmic heating and moderate electric field processing * Knowledge of ...

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Process Simulate information

See Columbus, OH salary details

$13

$24

$46

How much do process simulate jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for process simulate in Columbus, OH is $24.61, according to ZipRecruiter salary data. Most workers in this role earn between $16.97 and $28.56 per hour, depending on experience, location, and employer.

What is a Process Simulate?

A Process Simulate engineer specializes in using simulation software—such as Siemens Process Simulate—to design, validate, and optimize manufacturing processes in a virtual environment. Their main tasks include creating digital models of production lines, testing various process scenarios, and identifying improvements before physical implementation. This helps manufacturers save time, reduce costs, and minimize errors by addressing issues early in the design phase. Process Simulate engineers often collaborate closely with production, quality, and design teams to ensure efficient and error-free manufacturing workflows.

How does a Process Simulate specialist typically collaborate with engineering and production teams during a project?

A Process Simulate specialist works closely with both engineering and production teams to develop, test, and optimize manufacturing processes in a virtual environment before implementation on the shop floor. This collaboration involves regular meetings to review simulation results, gather feedback on proposed process changes, and ensure alignment with production goals and constraints. Effective communication is key, as the specialist must translate technical simulation data into actionable insights for engineers and operators. Such teamwork helps identify potential bottlenecks, improve efficiency, and reduce costly errors during actual production ramp-up.

What are the key skills and qualifications needed to thrive as a Process Simulate specialist, and why are they important?

To excel as a Process Simulate Specialist, you need a strong background in industrial engineering, manufacturing processes, and 3D simulation, often supported by a relevant engineering degree. Proficiency in Siemens Process Simulate software, knowledge of PLC programming, and familiarity with CAD systems are essential technical requirements. Strong analytical thinking, problem-solving, and effective communication skills set top performers apart in this field. These capabilities are crucial for accurately modeling, optimizing, and communicating complex manufacturing processes, ensuring efficiency and reducing production risks.

What is the difference between Process Simulate vs Process Engineer?

AspectProcess SimulateProcess Engineer
Primary RoleUses simulation software to model manufacturing processesDesigns, develops, and optimizes manufacturing processes
Skills & CertificationsCAD/CAM, simulation software proficiency, technical engineering backgroundProcess design, project management, engineering certifications
Work EnvironmentTypically in software labs or engineering officesFactories, manufacturing plants, engineering offices
Industry UsageUsed by manufacturing and automation companies for process validationEmployed in manufacturing, automotive, aerospace industries for process development

While Process Simulate focuses on modeling and testing manufacturing processes virtually, Process Engineers are responsible for designing and implementing these processes in real-world settings. Both roles require technical expertise, but Process Simulate emphasizes simulation skills, whereas Process Engineers focus on practical process development and optimization.

What job categories do people searching Process Simulate jobs in Columbus, OH look for?

The top searched job categories for Process Simulate jobs in Columbus, OH are:

Infographic showing various Process Simulate job openings in Columbus, OH as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 16% Part Time, 4% Contract, and 1% Nights. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $51,179 per year, or $24.6 per hour.

Validation Engineer I

Forge Biologics

Columbus, OH • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 10 days ago


Job description

Forge Your Future with Us:

At Forge Biologics, we believe in turning bold ideas into life-changing realities. Our mission is simple yet powerful: to enable access to life-changing gene therapies and help bring them from ideas into reality. We partner with scientists, physicians, biotech and pharma innovators, and patient communities — all united by one goal: improving lives. If you're driven by purpose and excited to make a tangible impact, this is where your journey begins.

Our team works out of The Hearth, a state-of-the-art, 200,000-square-foot cGMP facility in Columbus, Ohio. Here, you won't just watch innovation happen — you'll be part of it. Whether you're scaling AAV manufacturing, collaborating on cutting-edge therapies, or supporting complex technical projects, you'll play a key role in bringing hope to patients with genetic diseases.

What sets Forge apart is our culture of H.O.P.E. We are hardworking, showing up each day with determination and grit. We are open, creating a space where ideas flow freely, and every voice is valued. We are purpose-driven, with every task directly tied to changing lives. And we are engaged, energized by the challenges we face and the milestones we achieve together.

At Forge, your growth matters. We're committed to helping you expand your skills, take on new challenges, and develop your career through mentorship, hands-on learning, and opportunities for advancement. Our people are our greatest investment, and we're proud to see team members grow with us.

If you're ready to use your talent to help deliver hope to patients around the world, join us — and be part of something bigger than yourself.

About The Role: 

As a Validation Engineer I, you will be responsible for the design, implementation, and execution of equipment validation activities to ensure the compliance, quality, and efficacy of our manufacturing processes. You will work closely with cross-functional teams to develop and execute validation strategies, provide technical expertise in equipment validation, and ensure adherence to regulatory requirements.

Responsibilities:

  • Bachelor's or degree in Engineering, Biotechnology, Pharmaceutical Sciences, or a related field (or equivalent experience).
  • Experience in equipment validation within a regulated industry.
  • Experience in qualifying a wide range of equipment, including Isolators, Filling & Capping equipment, Biological Safety Cabinets (BSCs), Controlled Temperature Units (CTUs), bioreactors, incubators, chromatography systems, and centrifuges.
  • Understanding of aseptic processing and clean room standards.
  • Proficiency in risk assessment methodologies.
  • Understanding of cGMPs (current Good Manufacturing Practices).
  • Excellent analytical, problem-solving, and decision-making skills, with meticulous attention to detail.
  • Effective communication and collaboration abilities, with the capacity to work cross-functionally and influence stakeholders at various levels of the organization.
  • Strong project management skills, with the ability to prioritize and manage multiple validation projects concurrently.
  • Ability to work in a cleanroom environment while wearing appropriate gowning and PPE up to 50% of the time.

Qualifications:

  • Bachelor's or degree in Engineering, Biotechnology, Pharmaceutical Sciences, or a related field (or equivalent experience).
  • Experience in equipment validation within the pharmaceutical or biotechnology industry.
  • Experience in qualifying a wide range of equipment, including Isolators, Filling & Capping equipment, Biological Safety Cabinets (BSCs), Controlled Temperature Units (CTUs), bioreactors, incubators, chromatography systems, and centrifuges.
  • Experience with aseptic processing and clean room standards.
  • Proficiency in risk assessment methodologies.
  • Strong understanding of cGMPs (current Good Manufacturing Practices).
  • Excellent analytical, problem-solving, and decision-making skills, with meticulous attention to detail.
  • Effective communication and collaboration abilities, with the capacity to work cross-functionally and influence stakeholders at various levels of the organization.
  • Strong project management skills, with the ability to prioritize and manage multiple validation projects concurrently.
  • Ability to work in a cleanroom environment while wearing appropriate gowning and PPE up to 50% of the time.

Preferred Skills:

  • Experience in the Cell & Gene Therapy Industry.
  • Knowledge of validation principles across multiple disciplines, which may include computerized systems, aseptic process simulation, and/or process validation.
  • Experience in the application of pre-clinical, clinical, and commercial cGMPs.

This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities and activities may change, or new ones may be assigned. 

Work Environment and Physical Demands  

This position is performed in a temperature-controlled laboratory or office environment and requires regular standing, hand manipulation, and use of laboratory equipment. The role may involve lifting or moving materials up to 25 pounds and occasional reaching or handling at various heights. Appropriate personal protective equipment (PPE) must be worn when working with chemicals, biological materials, or in controlled environments.

Forge Biologics is an equal opportunity employer dedicated to building an inclusive and diverse workforce. Forge Biologics, provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. 

We've Got You Covered: 

At Forge Biologics, we believe our people deserve to be taken care of – in and out of the workplace. We've built a comprehensive compensation and benefits package designed to help you thrive, grow, and feel valued every step of the way:

Health from day one

  • Health, dental and vision insurance start your first day – with 90% of premiums covered for you and your family.

Time to recharge

  • A competitive paid time off plan – because rest fuels innovation.
  • 12 weeks of fully paid parental leave so you can focus on family when it matters most.

Rewarding your impact

  • Annual bonus opportunities for all full-time team members.
  • 401(k) with company match to help you plan for the future.
  • Special employee discounts, including childcare and dependent care savings.

Your wellness, supported

  • Onsite fitness facility at The Hearth.
  • Mental health counseling and financial planning services through our Employee Assistance Program.
  • Employer-paid short and long-term disability coverage to protect your peace of mind.

Fuel for your workday

  • A fully stocked kitchen with free snacks and beverages – we keep you energized and ready for what's next.

Grow with us

  • Ongoing professional development resources, training, and mentorship programs to help you build your care and grow within Forge.