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Csv Manager Jobs in Indiana (NOW HIRING)

Responsible for management of the automation systems across the facility (building/process/laboratory). Ensures the site's compliance with internal GMP's, CSV and external regulatory requirements. At ...

Senior MES Engineer

Fishers, IN

$97K - $134K/yr

... and ongoing management of Manufacturing Execution System (MES) platforms to ensure seamless ... Provide technical support to Computer System Validation (CSV) activities, including MES ...

Senior MES Engineer

Fishers, IN · On-site

$97K - $134K/yr

... and ongoing management of Manufacturing Execution System (MES) platforms to ensure seamless ... CSV) activities, including MES qualification and data integrity assessments. • Work closely with ...

Automation Engineer

Indianapolis, IN · On-site

$92K - $139K/yr

Ensures the site's compliance with internal GMP's, CSV and external regulatory requirements. At ... to manage a diverse portfolio of projects. • Lead, plan, and execute automation projects from ...

Senior MES Engineer

Fishers, IN · On-site

$94K - $129K/yr

... and ongoing management of Manufacturing Execution System (MES) platforms to ensure seamless ... CSV) activities, including MES qualification and data integrity assessments. · Work closely with ...

Senior MES Engineer

Fishers, IN · On-site

$94K - $129K/yr

... and ongoing management of Manufacturing Execution System (MES) platforms to ensure seamless ... CSV) activities, including MES qualification and data integrity assessments. · Work closely with ...

Showing results 21-40

Csv Manager information

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?

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.
What are popular job titles related to Csv Manager jobs in Indiana? For Csv Manager jobs in Indiana, the most frequently searched job titles are:
What cities in Indiana are hiring for Csv Manager jobs? Cities in Indiana with the most Csv Manager job openings:
Infographic showing various Csv Manager job openings in Indiana as of July 2026, with employment types broken down into 100% Full Time. Highlights an 55% In-person, 6% Hybrid, and 39% Remote job distribution.

Principal Informatics Engineer - Lilly Medicine Foundry

Eli Lilly and Company

Indianapolis, IN • Hybrid

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 28 days ago


Eli Lilly and Company rating

8.8

Company rating: 8.8 out of 10

Based on 63 frontline employees who took The Breakroom Quiz

11th of 86 rated pharmaceutical


Job description

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work-but it's work worth doing. If you're driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.


Lilly recently announced a $4.5 billion investment to create the Lilly Medicine Foundry, a new center for advanced manufacturing and drug development. The first-ever facility of its kind, combining research and manufacturing in a single location, the Medicine Foundry will allow Lilly to further develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental impact.

What You'll Be Doing:

As an Informatics Engineer, you will partner with the Process Translation and Analytical Laboratories functional areas and site, group, and global IT teams to implement and support digital laboratory solutions that enable the Foundry's operational objectives. Your scope includes key lab systems such as Laboratory Information Management Systems (LIMS), Laboratory Execution Systems (LES), Electronic Lab Notebooks (ELN), Chromatography Data Systems (CDS), and Environmental Monitoring (EM) platforms.

You will be driving and supporting system design, configuration, validation, and release - serving as an IT domain expert (SME) for analytical laboratory IT systems at the Foundry.

How You'll Succeed:

System Implementation & Configuration

  • Lead system design and configuration sessions with analytical lab SMEs for LIMS, LES, ELN, and CDS platforms, translating business and scientific processes into validated technical solutions.

  • Develop and implement Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols in compliance with 21 CFR Part 11 and EU Annex 11.

  • Lead data integrity requirements across lab systems and ensure audit readiness for regulatory inspections.

  • Coordinate instrument integration and data flows between lab equipment and LIMS/LES platforms.

  • Support site deployment and upgrade of analytical laboratory IT systems throughout the facility's startup and operational phases.

Validation & Compliance

  • Produce and maintain Computer System Validation (CSV) documentation, standard operating procedures (SOPs), and validation plans in alignment with applicable regulatory frameworks.

  • Ensure systems remain in a validated state and lead their lifecycle through releases, recapitalization, and retirement.

  • Build and maintain awareness of regulatory, legal, and quality requirements impacting the quality control laboratory, ensuring solution requirements comply.

Collaboration & Readiness

  • Collaborate with site and global IT system teams to ensure operational readiness of laboratory systems supporting the Foundry's release objectives.

  • Act as a key IT SME for analytical laboratory IT systems, organizing and educating peers on system use and best practices.

  • Support audits and provide oversight for management reviews, laboratory metrics, equipment records, and laboratory documentation.

Location & Work Flexibility
This role will initially be located out of Indianapolis, IN. Once constructed the permanent location will be based at our new Lilly Medicine Foundry in nearby Lebanon, IN. We offer a flexible hybrid work model, with three days onsite and two days working remotely each week, supporting both collaboration and worklife balance.

Your Basic Qualifications:

  • Bachelor of Science degree in IT, Chemistry, Pharmacy, Science, Engineering, or related field.

  • 3+ years of relevant experience in information technology, engineering, computer system validation, quality control support, or a related area.

  • Experience with Computer System Validation (CSV) methodology.

Additional Skills / Preferences:

  • Strong working knowledge of analytical laboratory IT systems including:

  • LIMS: LabVantage, LabWare

  • ELN: Benchling, Signals Notebook, or equivalent

  • CDS: Empower, or equivalent

  • LES/MES: L7, MODA, or equivalent

  • Solid knowledge of CSV process and electronic records/electronic signatures (ERES) requirements.

  • Experience working in a GMP-regulated environment (pharmaceutical, biotech, or equivalent).

  • Demonstrated ability to prepare and implement IQ/OQ/PQ protocols and associated documentation.

  • Experience with API/middleware integration and instrument connectivity between lab equipment and informatics platforms.

  • Understanding of data integrity frameworks applicable to GMP lab environments.

  • Familiarity with Agile or iterative delivery methodologies in a regulated setting.

  • Demonstrated learning agility and curiosity; ability to analyze, anticipate, and resolve complex issues through sound problem-solving.

  • Ability to accurately translate business and scientific processes into IT requirements and solutions.

  • Effective communicator across diverse forums and audiences, including technical peers, QA, and business customers.

  • Certification in relevant IT areas (e.g., ITIL, cloud, AI) is a plus.

Location & Work Flexibility
This role will initially be located out of Indianapolis, IN. Once constructed the permanent location will be based at our new Lilly Medicine Foundry in nearby Lebanon, IN. We offer a flexible hybrid work model, with three days onsite and two days working remotely each week, supporting both collaboration and worklife balance.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.


Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.


Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women's Initiative for Leading at Lilly (WILL).


Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is

$126,000 - $224,400

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

#WeAreLilly


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About Eli Lilly

Sourced by ZipRecruiter

Eli Lilly, based in Indianapolis, IN, US, is one of the pioneers in the pharmaceutical industry with a rich history dating back to 1876. This global pharmaceutical company focuses on discovering, developing, manufacturing and selling pharmaceutical products in approximately 120 countries. The company's product categories include endocrinology, oncology, cardiovascular, neuroscience, and immunology. Having invested over $9 billion in research and development in the past decade, Eli Lilly is also committed to creating high-quality medicines that meet real needs. As a recipient of several awards and recognitions, Eli Lilly is known for its focus on life-saving research and drug development. Their mission is to make medicines that help people live longer, healthier, and more active lives.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Indianapolis, IN, US

Year founded

1876