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Computer System Validation Remote Jobs in Indiana

Zifo

Veeva QMS Consultant

Bloomington, IN · On-site +1

**This role is open to remote candidates who have availability to travel to the client in Bloomington ... Computer Systems Validation is required for this role * Strong knowledge of GxP Requirements, GLP ...

Zifo

Veeva QMS Consultant

Bloomington, IN · On-site +1

**This role is open to remote candidates who have availability to travel to the client in Bloomington ... Computer Systems Validation is required for this role * Strong knowledge of GxP Requirements, GLP ...

S&S's Customer Information Systems

A valid passport is needed for travel About Systems & Software: Systems and Software (S&S), a ... Computer Systems, is a software development company headquartered in Winooski, VT, that was ...

Harris

A valid passport is needed for travel About Systems & Software: Systems and Software (S&S), a ... Computer Systems, is a software development company headquartered in Winooski, VT, that was ...

Harris

A valid passport is needed for travel About Systems & Software: Systems and Software (S&S), a ... Computer Systems, is a software development company headquartered in Winooski, VT, that was ...

Harris

Travel is required as needed, approximately 10%. Candidates must hold a current, valid passport and ... Bachelor's degree in Geographic Information Systems, Computer Science, Geography, or a related ...

Harris

Travel is required as needed, approximately 10%. Candidates must hold a current, valid passport and ... Bachelor's degree in Geographic Information Systems, Computer Science, Geography, or a related ...

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All JobsComputer System Validation Remote JobsComputer System Validation Remote Jobs in Indiana

Computer System Validation Remote information

See Indiana salary details

$27.3K

$89.1K

$153.3K

How much do computer system validation remote jobs pay per year?

As of Jun 21, 2026, the average yearly pay for computer system validation remote in Indiana is $89,136.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,500.00 and $108,100.00 per year, depending on experience, location, and employer.

What is computer system validation (CSV) in a remote job context?

Computer system validation (CSV) is a process used to ensure that IT systems and software used in regulated industries (such as pharmaceuticals or healthcare) work as intended and comply with relevant regulations. In a remote job context, CSV professionals perform validation tasks, documentation, and system testing from an offsite location, often collaborating with teams via digital tools. This remote work typically involves reviewing validation protocols, writing reports, and ensuring compliance with standards like FDA 21 CFR Part 11, all while leveraging secure online platforms to communicate and manage documentation.

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

To excel as a Computer System Validation Remote professional, you need a solid understanding of regulatory compliance (such as FDA 21 CFR Part 11), risk management, and validation lifecycle processes, often supported by a degree in computer science, engineering, or a related field. Familiarity with validation software, quality management systems (QMS), and documentation tools is typically required, along with certifications like GAMP or Six Sigma being advantageous. Strong attention to detail, analytical thinking, and effective remote communication are crucial soft skills for this role. These competencies ensure validated systems meet compliance standards, minimize risks, and support seamless collaboration in a regulated, distributed environment.

What is the difference between Computer System Validation Remote vs Computer System Validation on-site?

AspectComputer System Validation RemoteComputer System Validation on-site
Work EnvironmentPerforms validation tasks remotely, often from home or a different location from the client site.Works directly at the client or company site, conducting validation activities in person.
Required CredentialsTypically requires certifications like GxP, 21 CFR Part 11, and validation experience, applicable in both settings.Same certifications as remote roles, with additional familiarity with on-site equipment and facilities.
Industry UsageCommon in industries like pharmaceuticals and biotech where remote oversight is feasible.Traditional in regulated industries requiring on-site validation activities.

Both roles require similar certifications and industry knowledge, but the main difference lies in the work environment—remote versus on-site. Remote validation offers flexibility, while on-site validation involves direct interaction at the facility.

What are some common challenges faced by Computer System Validation professionals working remotely, and how can they be addressed?

Remote Computer System Validation (CSV) professionals often encounter challenges such as coordinating validation activities across distributed teams and ensuring secure access to sensitive documentation. Effective communication and use of collaborative tools are crucial for managing documentation reviews, test execution, and issue resolution. Establishing clear validation protocols and regular virtual check-ins with cross-functional teams can help maintain compliance and project momentum. Additionally, leveraging secure cloud-based validation platforms can streamline approvals and maintain data integrity while working remotely.
What are the most commonly searched types of Computer System Validation jobs in Indiana? The most popular types of Computer System Validation jobs in Indiana are:
What are popular job titles related to Computer System Validation Remote jobs in Indiana? For Computer System Validation Remote jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Computer System Validation Remote jobs in Indiana look for? The top searched job categories for Computer System Validation Remote jobs in Indiana are:
What cities in Indiana are hiring for Computer System Validation Remote jobs? Cities in Indiana with the most Computer System Validation Remote job openings:
Computer System Validation Remote jobs near you
Infographic showing various Computer System Validation Remote job openings in Indiana as of June 2026, with employment types broken down into 72% Full Time, and 28% Temporary. Highlights an 100% Remote job distribution, with an average salary of $89,136 per year, or $42.9 per hour.

Veeva QMS Consultant

Zifo

Bloomington, IN • On-site, Remote

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 23 days ago

Job description

**This role is open to remote candidates who have availability to travel to the client in Bloomington, IN on a regular basis**


Zifo is seeking a highly skilled and detail-oriented Veeva QMS consultant to support the implementation, optimization, and ongoing management of Quality Management Systems (QMS) within a regulated scientific environment. This role will focus on leveraging Veeva Vault QMS solutions to ensure compliance, streamline processes, and enhance operational efficiency across quality and regulatory functions.

The ideal candidate combines strong scientific domain knowledge with technical expertise in QMS platforms and Veeva Vault applications.

Responsibilities:

  • Lead the implementation, configuration, and support of QMS applications, with a focus on Veeva Vault QMS.
  • Collaborate with cross-functional stakeholders (Quality, Regulatory, R&D, IT) to gather requirements and translate them into system solutions.
  • Ensure compliance with industry regulations (e.g., GxP, FDA, ISO standards) through proper system design and usage.
  • Provide subject matter expertise on QMS processes including CAPA, Change Control, Deviations, Audits, and Document Management.
  • Configure and maintain Veeva Vault modules to support business processes and regulatory requirements.
  • Conduct system validation activities, including documentation, testing, and change control.
  • Support data migration, system upgrades, and integrations with other enterprise systems.
  • Deliver end-user training and provide ongoing support to ensure effective system adoption.
  • Identify opportunities for process improvement and system optimization.
  • Participate in audits and inspections, providing system-related support and documentation.

Requirements

  • QMS Certification (e.g., ASQ, ISO-related certifications, or equivalent).
  • Veeva Certification, specifically related to Veeva Vault (QMS preferred).
  • Proven experience working with Quality Management Systems (QMS) in regulated environments.
  • Hands-on experience with Veeva Vault QMS, including configuration and administration.
  • Strong understanding of GxP compliance requirements and validation processes (CSV/CSA).
  • Experience with quality processes such as CAPA, Change Control, Deviations, and Audits.
  • Excellent analytical, problem-solving, and communication skills.

Qualifications

  • Bachelor or Master's degree in Life sciences or Computer Sciences
  • 5+ years' experience with Computer Systems Validation is required for this role
  • Strong knowledge of GxP Requirements, GLP and GMP regulations, 21 CFR part 11, 210, 211, EU Annex 11, 15 requirements
  • QMS Certification (e.g., ASQ, ISO-related certifications, or equivalent).
  • Veeva Certification, specifically related to Veeva Vault (QMS preferred).
  • Proven experience working with Quality Management Systems (QMS) in regulated environments.
  • Hands-on experience withVeeva Vault QMS, including configuration and administration.
  • Strong understanding of GxP compliance requirements and validation processes (CSV/CSA).
  • Experience with quality processes such as CAPA, Change Control, Deviations, and Audits.
  • Excellent analytical, problem-solving, and communication skills.

Benefits

CURIOSITY DRIVEN, SCIENCE FOCUSED, EMPLOYEE BUILT. Our culture is unlike any other, one where we debate, challenge ourselves, and interact with all alike. We are a curious bunch, characterized by our passion to learn and spirit of teamwork. Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing QC, Medical Devices, specialty chemicals and other research-based organizations. Our team's knowledge of science and expertise in technology help Zifo better serve our customers around the globe, including 18 of the Top 20 Biopharma companies. 

We look for Science - Biotechnology, Pharmaceutical Technology, Biomedical Engineering, Microbiology etc. We possess scientific and technical knowledge and bear professional and personal goals.  While we have a "no doors" policy to promote free access within, we do have a tough door to walk in. We search with a two-point agenda - technical competency and cultural adaptability. 

We offer a competitive compensation package including accrued vacation, medical, dental, vision, 401k with company matching, life insurance, and flexible spending accounts.  

If you share these sentiments and are prepared for the atypical, then Zifo is your calling! 

Zifo is an equal opportunity employer, and we value diversity at our company.  We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. 

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