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Computer Systems Validation Engineer
full-timeIndianapolis$75k - $106k

Summary

Location

Indianapolis

Salary

$75k - $106k

Type

full-time

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About this role

Are You Ready?

CAI is a 100% employee-owned professional services company established in 1996 that has grown to more than 700 people worldwide. We provide commissioning, qualification, validation, startup, project management, and other consulting services associated with operational readiness to FDA-regulated and other mission-critical industries.

Our approach is simple—we put the client’s interests first, we don’t stop until it’s right, and we do whatever it takes to get there.


Our Foundational Principles:

- We act with integrity

- We serve each other

- We serve society

- We work for our future


With employee ownership, one person’s success is everyone’s success. We work diligently to accomplish team goals and live our core values:

- Team Before Self

- Respect for Others

- Can-Do Attitude


This position could report to Rockville, MD or Frederick, MD



Key Responsibilities

Documentation & Compliance

Author GxP computer validation documentation (e.g., URS, FRS, RTM, summary reports)

Generate and execute test protocols and scripts

Ensure adherence to 21 CFR Part 11 and data integrity principles

Review and contribute to validation plans and risk assessments

System & Industry Expertise

Support CSV activities across various platforms including MES, DCS, SCADA, and batch systems

Engage with major systems and platforms such as Rockwell PharmaSuite, Rockwell Automation platforms, Emerson DeltaV, DeltaV Batch, Emerson Syncade, PI, GE, ABB, Siemens, Honeywell, PAS-X, FactoryTalk, FactoryLogix, PLM, Simatic, iFix, Wonderware

Apply knowledge of GAMP and compliance expectations (21 CFR Parts 210, 211, 11)

Utilize familiarity with S88/S95 batch control standards

Apply working knowledge of recipe authoring, batch recipe development, and S88-based recipe structures across systems such as DeltaV and Rockwell

Client Support & Technical Execution

Support client engagements with strong customer-service orientation

Perform system assessments and remediation related to data integrity

Collaborate with client teams to ensure validation compliance and delivery



Qualifications and Experience

Bachelor’s degree (BS/BA) in Computer Science, Engineering, or related field; equivalent experience may be accepted

Minimum of 3+ years of experience in computer systems validation

Experience in biotech or pharmaceutical environments preferred over medical device

In-depth understanding of GAMP guidelines and FDA regulations (21 CFR 11, 210, 211)

Familiarity with S88/S95 batch control standards

Experience with Rockwell platforms, DeltaV systems, and recipe authoring in batch environments strongly preferred

Experience with multiple automation and manufacturing execution systems is highly desirable

Data integrity assessment/remediation experience is a plus



Other Requirements

- Excellent oral and written communication skills in English

- Ability to travel domestically and internationally as required

- Willingness to work paid overtime when needed

- Must be authorized to work in the U.S. without current or future sponsorship



Critical Competencies

Influence Strategy

- Pursues opportunities based on organizational fit and strategy

- Identifies high-impact, innovative solutions


Satisfy the Customer

- Anticipates and meets client needs

- Delivers high-quality solutions and maintains satisfaction


Plan for Success

- Aligns business goals with execution plans

- Allocates resources and builds risk mitigation strategies


Pursue Execution

- Prioritizes effectively and ensures accountability

- Proactively addresses challenges


Tailor Communication

- Communicates clearly and professionally

- Adapts style for technical and non-technical audiences


Build Partnerships

- Builds cross-functional networks

- Promotes collaboration and stakeholder engagement


Influence Others

- Gains support through sound reasoning

- Promotes innovation and value


Develop Self and Others

- Demonstrates integrity and commitment to growth

- Builds effective relationships internally and externally

#LI-MV1

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$75,000 - $106,000 a year
Average base salary range - not including benefits, and potential overtime and/or Cost of Living Adjustment.

CAI Benefits:
•Comprehensive Health Insurance coverage
•24 days of Paid Time Off
•ESOP/401K - 15% Company Contribution (US Only)
•Company paid Life Insurance
•Company paid Long Term Disability
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We are an equal opportunity employer; we are proud to employ veterans and promote diversity and inclusion in our workplace. Diversity is a strength for our global company. We pledge that CAI will be operated in a way that is fair and equitable to all – our employees, our customers, and the broader society.

 

This job description is not all inclusive and you may be asked to do other duties. CAI will also consider for employment qualified applicants with criminal histories in a manner consistent with the requirements of the Fair Chance Act (FCA) / Fair Chance Ordinance (FCO). 

Other facts

Tech stack
Computer Systems Validation,GxP Documentation,Test Protocols,Data Integrity,Validation Plans,Risk Assessments,MES,DCS,SCADA,Batch Systems,GAMP Guidelines,FDA Regulations,Recipe Authoring,Client Engagement,System Assessments,Remediation

About CAI

At CAI, we are a professional services firm designed to accelerate operational readiness and excellence in critical environments. Our team of engineering, quality, and operations experts combines top-tier talent with the latest technology to deliver projects on time and within budget. We're committed to continuous improvement, real connections, and the highest standards, aiming to lead the industry and build the future.

Are you ready?

Team size: 501-1,000 employees
LinkedIn: Visit
Industry: Pharmaceutical Manufacturing

What you'll do

  • The Computer Systems Validation Engineer will author GxP computer validation documentation and generate and execute test protocols. They will also support CSV activities across various platforms and ensure validation compliance.

Ready to join CAI?

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Frequently Asked Questions

What does CAI pay for a Computer Systems Validation Engineer?

CAI offers a competitive compensation package for the Computer Systems Validation Engineer role. The salary range is USD 75k - 106k per year. Apply through Clera to learn more about the full compensation details.

What does a Computer Systems Validation Engineer do at CAI?

As a Computer Systems Validation Engineer at CAI, you will: the Computer Systems Validation Engineer will author GxP computer validation documentation and generate and execute test protocols. They will also support CSV activities across various platforms and ensure validation compliance..

Why join CAI as a Computer Systems Validation Engineer?

CAI is a leading Pharmaceutical Manufacturing company. The Computer Systems Validation Engineer role offers competitive compensation.

Is the Computer Systems Validation Engineer position at CAI remote?

The Computer Systems Validation Engineer position at CAI is based in Indianapolis, Indiana, United States. Contact the company through Clera for specific work arrangement details.

How do I apply for the Computer Systems Validation Engineer position at CAI?

You can apply for the Computer Systems Validation Engineer position at CAI directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about CAI on their website.