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Csv Manager Jobs (NOW HIRING)

The CSV Engineer I is responsible for ensuring that GxP computerized systems at Forge Biologics are ... Manage system change control, deviations, and CAPAs related to validated systems, ensuring ...

For more information, please visit www.resilience.com The CSV Engineer III independently plans ... Lead the qualification and lifecycle management of automated equipment and GxP computer systems (e ...

We offer IT solutions across the disciplines of program/project management, applications ... IT CSV Lead. Location: Raritan, NJ Duration: 3 months + to start and positively will get extended ...

CSV Engineer (6mo. Contract-to-Hire) Location: Baltimore, MD Company Join a premier global Contract ... Plan, coordinate, and execute assigned projects by effectively using Project Management ...

The CSV Engineer I is responsible for ensuring that GxP computerized systems at Forge Biologics are ... Manage system change control, deviations, and CAPAs related to validated systems, ensuring ...

Execute on implementation tasks, work prioritization and support escalation management activities ... Working knowledge of the CSV lifecycle, including system risk assessment, protocol development and ...

Execute on implementation tasks, work prioritization and support escalation management activities ... Working knowledge of the CSV lifecycle, including system risk assessment, protocol development and ...

For more information, please visit www.resilience.com The CSV Engineer III independently plans ... Lead the qualification and lifecycle management of automated equipment and GxP computer systems (e ...

The CSV Engineer I is responsible for ensuring that GxP computerized systems at Forge Biologics are ... Manage system change control, deviations, and CAPAs related to validated systems, ensuring ...

Ability to manage multiple activities * The ability to communicate with fellow project team members ... depth CSV experiences including as a Validation lead Essential The ability to communicate with ...

Sr. CSV Validation Engineer

Lexington, MA · On-site

$115K - $140K/yr

Ability to manage multiple activities * The ability to communicate with fellow project team members ... depth CSV experiences including as a Validation lead Essential The ability to communicate with ...

CSV Engineer Location: Raritan, NJ(Hybrid) Mandatory - Validation experience with ERP applications ... JIRA, SAP Solution Manager, XRAY and Change Record review • Should be experienced in Test scripts ...

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Csv Manager information

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$29K

$104.6K

$118K

How much do csv manager jobs pay per year?

As of Jul 14, 2026, the average yearly pay for csv manager in the United States is $104,575.00, according to ZipRecruiter salary data. Most workers in this role earn between $114,000.00 and $116,500.00 per year, depending on experience, location, and employer.

What are some common challenges faced by a CSV Manager in maintaining regulatory compliance across multiple projects?

A CSV (Computer System Validation) Manager often manages several projects simultaneously, each with unique regulatory requirements. One major challenge is ensuring that all validation documentation remains current and audit-ready, despite frequent software updates or process changes. Additionally, coordinating with cross-functional teams such as IT, Quality Assurance, and Operations can be demanding, as priorities and timelines may differ. Staying updated with evolving industry regulations and effectively training team members are also essential to maintaining consistent compliance.

What is a CSV Manager?

A CSV Manager is a software tool or professional responsible for handling, organizing, and processing CSV (Comma-Separated Values) files. These files are commonly used for storing and exchanging data in a simple text format, making them popular for data imports and exports in various applications. A CSV Manager ensures that the data within these files is correctly formatted, validated, and sometimes transformed for compatibility with databases or other systems. They may also automate workflows involving large amounts of CSV data to improve efficiency and accuracy.

What is the difference between Csv Manager vs Data Analyst?

AspectCsv ManagerData Analyst
Required CredentialsExperience with CSV data management, basic database skillsDegree in statistics, data science, or related field; proficiency in data analysis tools
Work EnvironmentData management teams, IT departmentsBusiness analysis teams, research departments
Employer & Industry UsageUsed in industries handling large CSV datasets, such as logistics and financeUsed across industries for interpreting data, reporting, and decision-making

The Csv Manager primarily focuses on managing and organizing CSV data files, ensuring data integrity and accessibility. In contrast, a Data Analyst interprets data, creates reports, and provides insights. While both roles work with data, Csv Managers specialize in data handling, whereas Data Analysts focus on analysis and interpretation.

What are the key skills and qualifications needed to thrive as a CSV Manager, and why are they important?

To thrive as a CSV (Computer System Validation) Manager, you need a strong background in GxP regulations, validation methodologies, and a degree in life sciences, engineering, or a related field. Familiarity with validation lifecycle documentation, risk assessment tools, and regulatory standards like FDA 21 CFR Part 11 is typically required. Outstanding project management, attention to detail, and strong communication skills make a CSV Manager stand out in ensuring compliance and leading cross-functional teams. These competencies are crucial for ensuring validated systems meet regulatory requirements and support business operations in highly regulated industries.
More about Csv Manager jobs
What cities are hiring for Csv Manager jobs? Cities with the most Csv Manager job openings:
What states have the most Csv Manager jobs? States with the most job openings for Csv Manager jobs include:
Infographic showing various Csv Manager job openings in the United States as of July 2026, with employment types broken down into 4% Locum Tenens, 1% As Needed, 74% Full Time, 3% Part Time, 8% Contract, and 10% Summer. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $104,575 per year, or $50.3 per hour.
CSV Engineer I

Other

Medical, Dental, Vision, Retirement, PTO

Re-posted 20 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: 

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. 

Work Environment and Physical Demands  

This position works in both a laboratory environment and typical 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. Ability to identify small details within the field of vision, distinguish between different colors, and accurately identify objects within a specific area. 

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.