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Csv Analyst Jobs (NOW HIRING)

Familiarity with various data formats like XML, XSD, JSON, and CSV. * Analytical Skills: Strong analytical and problem-solving skills for root cause analysis and issue resolution. Desirable ...

... csv/.xls). • Use Excel tools to transform and prepare structured datasets. • Track data quality ... analysis, IT asset management, or database administration. • Strong analytical thinking and ...

Analyze and clean data to support accurate modeling and reporting. * Maintain and validate Models ... Build and manage import templates for data onboarding (.csv/.xls). * Use Excel tools to transform ...

Quality Control Analyst II

Fort Worth, TX · On-site

$23 - $31/hr

Pay Rate Low: 28.00 | Pay Rate High: 35.00 Exciting Quality Control Analyst II (Contract ... CSA/CSV experience is highly preferred. Key Responsibilities: * Coordinate PM, calibration, PV, and ...

Familiarity with various data formats like XML, XSD, JSON, and CSV. * Analytical Skills: Strong analytical and problem-solving skills for root cause analysis and issue resolution. Desirable ...

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Csv Analyst information

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$35.5K

$99.2K

$127K

How much do csv analyst jobs pay per year?

As of Jul 23, 2026, the average yearly pay for csv analyst in the United States is $99,157.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,000.00 and $126,500.00 per year, depending on experience, location, and employer.

What are some common challenges a CSV Analyst faces when working with large datasets, and how can these be managed?

CSV Analysts often encounter issues such as handling inconsistent data formatting, missing values, and large file sizes that can slow down processing. To manage these challenges, it's important to use robust data cleaning tools and scripting languages like Python or R, which can automate repetitive tasks and efficiently process large volumes of data. Collaborating closely with data engineers or IT teams can also help address technical bottlenecks and ensure data integrity across projects.

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

To thrive as a CSV (Computer System Validation) Analyst, you need a solid understanding of validation principles, regulatory compliance (such as FDA 21 CFR Part 11), and life sciences processes, usually supported by a degree in a relevant field like IT or life sciences. Familiarity with validation tools, electronic documentation systems, and quality management software is typically required, along with knowledge of GxP guidelines. Attention to detail, analytical thinking, and strong communication skills help ensure successful system validation and effective collaboration with stakeholders. These competencies are crucial to maintain data integrity, regulatory compliance, and operational efficiency in highly regulated environments.

What is a CSV Analyst?

A CSV Analyst is a professional who specializes in working with CSV (Comma-Separated Values) files, which are commonly used for storing and exchanging tabular data. Their role involves importing, cleaning, analyzing, and interpreting data from CSV files using various tools such as Excel, Python, or specialized data analysis software. CSV Analysts help organizations make data-driven decisions by extracting valuable insights from raw data. They also ensure data quality and integrity throughout the analysis process.

What is the difference between Csv Analyst vs Data Analyst?

AspectCsv AnalystData Analyst
Required CredentialsTypically requires a degree in data science, statistics, or related fields; proficiency in Excel, SQL, and data visualization toolsSimilar credentials; often includes degrees in data analysis, statistics, or related disciplines; skills in Excel, SQL, and visualization
Work EnvironmentPrimarily works with CSV files, databases, and data management tools; often in finance, healthcare, or marketing sectorsWorks with various data formats, reports, and dashboards across multiple industries
Employer & Industry UsageUsed by organizations needing CSV data processing, such as data warehouses and analytics firmsWidely used across industries for data interpretation, reporting, and decision-making

While both Csv Analysts and Data Analysts handle data analysis tasks, Csv Analysts focus more on processing and managing CSV files specifically, whereas Data Analysts work with a broader range of data formats and analytical tools. The roles often overlap, but Csv Analysts tend to specialize in data extraction and cleaning from CSV sources.

More about Csv Analyst jobs
Infographic showing various Csv Analyst job openings in the United States as of July 2026, with employment types broken down into 66% Full Time, 4% Part Time, and 30% Contract. Highlights an 61% Physical, 5% Hybrid, and 34% Remote job distribution, with an average salary of $99,157 per year, or $47.7 per hour.
Assoc Director, BI&T Compliance & CSV

Assoc Director, BI&T Compliance & CSV

Bristol Myers Squibb

Devens, MA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 28 days ago


Bristol Myers Squibb rating

8.2

Company rating: 8.2 out of 10

Based on 51 frontline employees who took The Breakroom Quiz

28th of 74 rated pharmaceutical


Job description

Working with Us
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.

Duties/Responsibilities

  • Lead the Campus IT Compliance and CSV team
    • Promote a safe and compliant environment and mindset.
    • Select, develop, coach, and manage the Devens Campus IT Compliance and CSV team.
    • Set goals, objectives, and contributions of the Campus IT Compliance and CSV team.
    • Drive continuous improvement of team productivity and KPIs.
    • Ensure the team delivers critical projects on time.
    • Act as a liaison between site stakeholders and enterprise/business application teams to ensure business continuity is maintained.
    • Manage service providers and ensure alignment with contractual SLAs.
    • Engage and support PBRG teams in support of the BMS culture.
  • Act as the Computer System Validation (CSV) process owner onsite
    • Provide guidance to Digital Plant and site functional groups on CSV process implementation.
    • Participate actively with other groups to analyze and address process deficiencies.
    • Support the BMS Data Integrity and Quality Risk Management programs.
  • Lead campus-wide IT compliance support and project execution
    • Ensure appropriate support for GxP business operations across the Devens campus.
    • Define, implement, and track Service Level Agreements (SLA) for supported business-critical activities.
    • Collaborate with Devens Digital Plant leaders to address issues and develop plans to reduce support volumes across the site.
    • Manage organizational adoption of BMS standard processes and systems, including ServiceNow, and continuously enhance processes to simplify support requirements.
    • Foster business and enterprise partner relationships to ensure a high customer satisfaction rating.
    • Represent Digital Plant during internal audits and regulatory inspections.
    • Ensure that procedures, guidance documents, and other GxP-related documents are maintained in a high state of compliance and audit readiness.
    • Ensure the validation, implementation, and change management of regulated IT systems used across the site are conducted in compliance with applicable regulatory requirements.
    • Participate actively with other groups to analyze and address process deficiencies, working collaboratively with peers in Validation, Manufacturing, Engineering, Quality, and Digital Plant.
    • Effectively track project progress to address priorities, meet schedules, maximize productivity, reduce costs, and increase efficiencies.
    • Provide updates to management through established tools and project dashboards.
  • Pursue innovative solutions.
    • Periodically review, specify, and revise regulated IT systems supporting site operations.
    • Follow industry trends and innovation, finding new technical solutions to meet evolving business needs.
    • Evaluate vendor recommendations and lessons learned from other BMS sites.

Requirements

  • Bachelor's degree in Engineering, Information Technology, Computer Science, or related field, with a minimum of 12 years of experience in pharmaceutical quality operations, quality assurance, quality systems, computer system validation, and/or IT compliance roles.
  • Proven leadership skills and track record of success in managing regulated IT compliance and validation initiatives.
  • Demonstrated leadership skills in coaching, managing, and mentoring staff members, including effective team selection and personnel management.
  • Expertise in 21 CFR 210, 211, and 11, and GAMP standards for validation of automated systems is required; a high level of understanding and experience in computer system validation and qualification principles is required.
  • Knowledge of Quality principles, system development lifecycles, and QA methodologies, such as ISO 9001.
  • Experience with IT oversight of electronic systems supporting GMP operations is required.
  • Demonstrated ability to work effectively with US FDA and other regulatory agencies.
  • Substantial knowledge of QSR, GMP, FDA, GAMP, ISO, ICH, and other applicable standards and guidance regimes.
  • Experienced documentation and technical writing skills.
  • Excellent technical troubleshooting abilities.
  • Demonstrated creative problem-solving skills.
  • Ability to lead highly effective teams both at a local site level and across the network.
  • Strong collaboration and cross-functional leadership skills to drive continuous improvement, promote knowledge sharing, and implement best practices across the network.

If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Compensation Overview:

Devens - MA - US: $176,720 - $214,137

The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.

Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:

  • Health Coverage: Medical, pharmacy, dental, and vision care.

  • Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).

  • Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.

Work-life benefits include:

Paid Time Off

  • US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)

  • Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays

Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.

All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.

*Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as "Transforming patients' lives through science ", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information:https://careers.bms.com/california-residents/

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.

R1603585 : Assoc Director, BI&T Compliance & CSV

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Bristol-Myers Squibb logo

About Bristol-Myers Squibb

Sourced by ZipRecruiter

Bristol-Myers Squibb is a world-renowned global Biopharmaceutical company headquartered in New York, NY, US. Established in 1887, the company has more than 130 years’ worth of history dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. The company operates in the healthcare industry and thrives on providing a range of pharmaceutical products and services for various medical fields, like oncology, cardiovascular diseases, and immunoscience. Notably, Bristol-Myers Squibb is known for its commitment to relentless research and innovative drug development, which has led to breakthroughs like Opdivo, one of the first immunotherapies.

Industry

Scientific research and development services and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

New York, NY, US