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Senior Computer System Validation Csv Jobs in Indiana

Senior MES Engineer

Fishers, IN

$97.80K - $134.30K/yr

Senior MES Engineer Summary INCOG BioPharma is seeking a highly motivated individual with subject ... Provide technical support to Computer System Validation (CSV) activities, including MES ...

Senior MES Engineer

Fishers, IN · On-site

$97.80K - $134.30K/yr

Description Senior MES Engineer Summary INCOG BioPharma is seeking a highly motivated individual ... Computer System Validation (CSV) activities, including MES qualification and data integrity ...

Senior MES Engineer

Fishers, IN

$94.10K - $129.20K/yr

Senior MES Engineer Summary INCOG BioPharma is seeking a highly motivated individual with subject ... Computer System Validation (CSV) activities, including MES qualification and data integrity ...

Senior MES Engineer

Fishers, IN · On-site

$94.10K - $129.20K/yr

Senior MES Engineer Summary INCOG BioPharma is seeking a highly motivated individual with subject ... Computer System Validation (CSV) activities, including MES qualification and data integrity ...

Requirements * 3+ years of Computer System Validation (CSV) experience with process control, SCADA and automation systems, MES and data integration systems (Emerson DeltaV and/or Syncade experience ...

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Senior Computer System Validation Csv information

What are the key skills and qualifications needed to thrive as a Senior Computer System Validation (CSV) professional, and why are they important?

To excel as a Senior Computer System Validation (CSV) professional, you need deep knowledge of regulatory compliance (such as FDA 21 CFR Part 11), validation lifecycle methodologies, and a background in computer science, engineering, or life sciences. Familiarity with validation management tools, risk assessment software, and quality management systems (QMS) is typically required, along with certifications like GAMP or Six Sigma being highly valued. Outstanding analytical skills, attention to detail, and strong communication abilities set high performers apart in this role. These competencies ensure validated systems meet regulatory requirements, maintain data integrity, and support quality operations in regulated industries.

What are some common challenges Senior Computer System Validation (CSV) professionals face when working on large-scale projects?

Senior CSV professionals often encounter challenges such as coordinating validation activities across multiple departments, managing evolving regulatory requirements, and ensuring thorough documentation throughout the project lifecycle. They also need to balance project timelines with the need for comprehensive testing and risk assessments. Effective communication and collaboration with IT, QA, and business stakeholders are essential to address issues proactively and ensure compliance in complex, regulated environments.

What is a Senior Computer System Validation (CSV) specialist?

A Senior Computer System Validation (CSV) specialist is an experienced professional responsible for ensuring that computer systems used in regulated industries—such as pharmaceuticals, biotechnology, or medical devices—meet compliance standards. This involves planning, executing, and documenting validation activities to demonstrate that systems consistently perform according to predefined specifications and regulatory requirements. Senior CSV specialists often lead validation projects, manage teams, and interact with regulatory auditors, making sure that systems are reliable, secure, and compliant with guidelines like FDA 21 CFR Part 11 and GxP. Their expertise helps organizations avoid compliance issues, data integrity problems, and costly system failures.

What is the difference between Senior Computer System Validation Csv vs Computer System Validation Specialist?

AspectSenior Computer System Validation CsvComputer System Validation Specialist
CertificationsGxP, 21 CFR Part 11, CSV certificationsGxP, 21 CFR Part 11, CSV certifications
Work EnvironmentRegulated industries like pharma, biotech, medical devicesRegulated industries like pharma, biotech, medical devices
ResponsibilitiesLeading validation projects, ensuring compliance, mentoringExecuting validation activities, documentation, testing

While both roles require similar certifications and work in regulated environments, the Senior Computer System Validation Csv typically involves leading projects and overseeing compliance efforts, whereas the Computer System Validation Specialist focuses on executing validation tasks and documentation. The senior role often requires more experience and leadership responsibilities.

What are the most commonly searched types of Computer System Validation Csv jobs in Indiana? The most popular types of Computer System Validation Csv jobs in Indiana are:
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Quality Assurance - Computer System Validation (CSV)

Quality Assurance - Computer System Validation (CSV)

Elanco

Clinton, IN

$18.25 - $24/hr

Full-time

Retirement, PTO

Posted 20 days ago


Elanco rating

7.8

Company rating: 7.8 out of 10

Based on 25 frontline employees who took The Breakroom Quiz

39th of 70 rated pharmaceutical


Job description

At Elanco (NYSE: ELAN) - it all starts with animals!

As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose - all to Go Beyond for Animals, Customers, Society and Our People.

At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you'll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.

Making animals' lives better makes life better - join our team today!

Your Role:Quality Assurance - Computer System Validation (CSV)

As theQuality Assurance - Computer System Validation (CSV), you will be part of the Quality organization supporting Clinton Manufacturing Operations. In this role, you will provide quality oversight for computerized systems used in GxP operations, ensuring compliance with global regulatory requirements and data integrity standards. You will partner with IT, Automation, Engineering, and Production teams to maintain validated systems and integrate compliant digital solutions across the site.

Your Responsibilities:

  • Provide quality oversight for the lifecycle of computerized systems, ensuring compliance with GAMP 5, 21 CFR Part 11, and Data Integrity standards

  • Review and approve Computer System Validation (CSV) documentation including Validation Plans, IQ/OQ/PQ protocols, and summary reports

  • Lead investigations for CSV-related deviations, system failures, and data integrity issues, including root cause analysis

  • Partner cross-functionally with IT, Engineering, Automation, and Operations to implement and maintain compliant computerized systems

  • Support continuous improvement of site Quality Systems through SOP development, training, coaching, and change control management

What You Need to Succeed (minimum qualifications):

  • Education: Bachelor's Degree in Science, Technology, Engineering, Computer Science, or a related technical discipline (or equivalent experience)

  • Required Experience: Minimum 10 years of experience in a GxP regulated environment (Pharmaceutical, Biotech, or Medical Device), including at least 3-5 years of experience in Computer System Validation (CSV) or Computer System Quality Assurance (CSQA)

  • Top 2 Skills: Strong knowledge of Data Integrity and computerized system validation regulations (21 CFR Part 11, Annex 11, ALCOA++), and ability to influence and coach cross-functional technical teams on compliance requirements

What will give you a competitive edge (preferred qualifications):

  • Professional certifications such as CISA (Certified Information Systems Auditor) or CSQE (Certified Software Quality Engineer)

  • Experience supporting Data Integrity audits and regulatory inspections

  • Experience with regulated system platforms such as SAP, Veeva, MES, or LIMS

  • Experience implementing risk-based validation approaches aligned with GAMP 5

  • Experience supporting manufacturing or laboratory systems in regulated environments

Additional Information:

  • Location: Clinton, IN - Onsite Manufacturing Facility

Don't meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles!

Elanco Benefits and Perks:

We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include:

  • Multiple relocation packages

  • Two weeklong shutdowns (mid-summer and year-end) in the US (in addition to PTO)

  • 8-week parental leave

  • 9 Employee Resource Groups

  • Annual bonus offering

  • Flexible work arrangements

  • Up to 6% 401K matching

Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status

Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against jobrelated criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.


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