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Csv Engineer Jobs in Ohio (NOW HIRING)

The CSV Engineer I is responsible for ensuring that GxP computerized systems at Forge Biologics are validated in compliance with regulatory standards (21 CFR Part 11, EU Annex 11, GAMP 5). This role ...

For more information, please visit www.resilience.com The CSV Engineer III independently plans, executes, and leads validation activities across facility, utility, process, cleaning, automation, and ...

For more information, please visit www.resilience.com The CSV Engineer III independently plans, executes, and leads validation activities across facility, utility, process, cleaning, automation, and ...

The CSV Engineer I is responsible for ensuring that GxP computerized systems at Forge Biologics are validated in compliance with regulatory standards (21 CFR Part 11, EU Annex 11, GAMP 5). This role ...

The CSV Engineer I is responsible for ensuring that GxP computerized systems at Forge Biologics are validated in compliance with regulatory standards (21 CFR Part 11, EU Annex 11, GAMP 5). This role ...

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions ... FAT, SAT, CSV, equipment integration, and startup. * Drive process design for new equipment and ...

Automation Engineer Location: New Albany, OH Position Summary Seeking a mid-level Automation ... Collaborate with Packaging, Warehouse, Quality, CSV, IT/OT teams, vendors, and system integrators.

OH ยท On-site

$100K - $131K/yr

CSV and Automation Validation Please share your resumes chaitanya@itminds.net/949 -210-9861

Partner with Quality Assurance, Computer System Validation (CSV), Packaging, Manufacturing, and IT ... Apply engineering principles and practices across automation, controls, robotics, and integrated ...

Partner with Quality Assurance, Computer System Validation (CSV), Packaging, Manufacturing, and IT ... Apply engineering principles and practices across automation, controls, robotics, and integrated ...

Partner with Quality Assurance, Computer System Validation (CSV), Packaging, Manufacturing, and IT ... Apply engineering principles and practices across automation, controls, robotics, and integrated ...

Partner with Quality Assurance, Computer System Validation (CSV), Packaging, Manufacturing, and IT ... Apply engineering principles and practices across automation, controls, robotics, and integrated ...

Automation Engineer Location: New Albany, OH We are seeking a mid-level Automation Engineer to ... Knowledge of cGMP, 21 CFR Part 11, CSV, and data integrity requirements * Experience working with ...

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Showing results 1-20

Csv Engineer information

See Ohio salary details

$33.7K

$93K

$128.7K

How much do csv engineer jobs pay per year?

As of Aug 1, 2026, the average yearly pay for csv engineer in Ohio is $93,026.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,100.00 and $109,000.00 per year, depending on experience, location, and employer.

What engineer makes 500,000 a year?

Highly experienced engineers in specialized fields such as software engineering, data engineering, or systems architecture can earn salaries of $500,000 or more annually, especially with senior roles, bonuses, and stock options. These roles often require advanced skills, certifications, and extensive industry experience.

How much does a CSV engineer make?

A CSV engineer's salary typically ranges from $70,000 to $120,000 annually, depending on experience, location, and industry. Skills in data management, scripting, and familiarity with database tools can influence earning potential.

What is a CSV Engineer job?

A CSV (Computer System Validation) Engineer is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals and medical devices, comply with regulatory requirements. They develop validation protocols, perform testing, document results, and ensure adherence to industry standards like FDA 21 CFR Part 11 and GAMP 5. Their goal is to confirm that software and hardware systems function correctly, maintain data integrity, and meet compliance requirements.

What does a CSV engineer do?

A CSV engineer specializes in designing, developing, and maintaining systems that process and manage data stored in CSV (comma-separated values) format. They often work with data integration, scripting, and database tools to ensure accurate data handling and transformation for analysis or application use.

What are the common challenges faced by a CSV Engineer in the pharmaceutical or medical device industry?

CSV Engineers in the pharmaceutical or medical device industry often face the challenge of keeping up with evolving regulatory requirements and ensuring all computerized systems remain compliant throughout their lifecycle. Managing comprehensive documentation, coordinating with multiple departments, and troubleshooting complex system changes can add to the workload. Successful CSV Engineers are proactive about staying informed of regulatory updates, are highly organized, and collaborate closely with Quality Assurance, IT, and operations teams. This dynamic environment offers the opportunity to learn continuously, develop expertise in validation best practices, and advance into leadership or specialized quality roles.

What is the salary of a CSV engineer?

The salary of a CSV engineer typically ranges from $70,000 to $120,000 annually, depending on experience, location, and industry. Skilled professionals with expertise in data processing, scripting, and database management tend to earn higher salaries.

What are the key skills and qualifications needed to thrive in the Csv Engineer position, and why are they important?

To thrive as a CSV Engineer (Computer System Validation Engineer), you need a solid understanding of validation principles, regulatory compliance (such as FDA 21 CFR Part 11), and a relevant degree in life sciences, engineering, or information technology. Familiarity with validation lifecycle documentation, risk assessment tools, and industry-standard systems like SAP, LIMS, and TrackWise is highly valued, as are certifications such as GAMP or Six Sigma. Strong attention to detail, analytical thinking, and excellent communication skills help CSV Engineers collaborate efficiently with cross-functional teams and ensure thorough documentation. These skills are crucial to guarantee that computerized systems in regulated industries meet compliance requirements, supporting product quality and patient safety.

What are the most commonly searched types of Csv Engineer jobs in Ohio? The most popular types of Csv Engineer jobs in Ohio are:
Infographic showing various Csv Engineer job openings in Ohio as of July 2026, with employment types broken down into 100% Contract. Highlights an 100% In-person job distribution, with an average salary of $93,026 per year, or $44.7 per hour.

CSV Engineer I

Forge Biologics

Columbus, OH โ€ข On-site

Other

Medical, Dental, Vision, Retirement, PTO

Re-posted 8 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 ofย H.O.P.E.ย We areย hardworking, showing up each day with determination and grit. We areย open, creating a space where ideas flow freely, and every voice is valued. We areย purpose-driven, with every task directly tied to changing lives. And we areย 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:ย 

The CSV Engineer I is responsible for ensuring that GxP computerized systems at Forge Biologics are validated in compliance with regulatory standards (21 CFR Part 11, EU Annex 11, GAMP 5). This role directly supports gene therapy manufacturing operations by leading validation activities for key systems including Veeva QMS, BMRAM, analytical lab instruments, and the Metasys BMS. By maintaining data integrity and system compliance, the CSV Engineer plays a critical part in ensuring product quality, patient safety, and regulatory inspection readiness.

Responsibilities:

  • Author, review, and execute validation deliverables for GxP computerized systems, including Validation Plans, Requirements Specifications (URS/FS/DS), IQ/OQ/PQ protocols, Trace Matrices, and Validation Summary Reports.
  • Supports computer system validation efforts for Veeva Vault QMS, BMRAM (laboratory information management), analytical lab instruments (e.g., HPLC, UHPLC, PCR instruments, plate readers etc), ERP System (NetSuite).
  • Perform risk assessments to determine validation approach and ensure appropriate testing of system functionality, data integrity, and audit trail review.
  • Manage system change control, deviations, and CAPAs related to validated systems, ensuring compliance with Forge's quality system.
  • Collaborate with IT, QA, Lab Operations, and Facilities teams to support system upgrades, patches, and periodic reviews while maintaining validated state.

Qualifications:

  • Bachelor's degree in Computer Science, Engineering, Life Sciences, or related field (or equivelant experience).
  • 2+ years of experience in Computer System Validation (CSV) within a GxP regulated environment (pharmaceutical, biotech, or medical device).
  • Working knowledge of GAMP 5, 21 CFR Part 11, EU Annex 11, and data integrity principles (ALCOA+).
  • Experience validating at least one of the following: Veeva Vault QMS, BMRAM, laboratory instrumentation (e.g., Waters, Agilent, Chromeleon, Softmax or similar), or a building management system (BMS) like Metasys.
  • Strong technical writing skills and ability to execute protocols with minimal supervision.
  • Ability to work onsite (in Columbus, Ohio) 3-4 days/week on average.

Preferred Skills:

  • Experience with Veeva Vault platform (QMS or QualityDocs) and BMRAM configuration or validation.
  • Hands-on validation of laboratory instruments (e.g., HPLC, UV-Vis,)including software like Empower or Chromeleon.
  • Familiarity with Metasys BMS or similar environmental monitoring systems in a GxP facility.
  • Experience with electronic execution systems such as Veeva Vault Manager or similar.
  • Experience supporting regulatory inspections (FDA, EMA) and responding to CSV-related observations.

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.ย 

Work Environment and Physical Demandsย ย 

This position works in both a laboratory environment andย typicalย office environment where the physical work demands will vary depending on the specific tasks and duties required of the job. The employee will be stationary (standing/sitting) for extended periods of time. Employees regularly wear personal protective equipment based on the task being performed. Must be able to work in a confined space, such as a clean room or laboratory environment.ย Ability toย identifyย small detailsย within the field of vision, distinguish betweenย different colors, and accuratelyย identifyย objects within a specific area.ย 

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.ย 

We've Got You Covered:ย 

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 youย andย 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.