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Internship Computer System Validation Csv Jobs in Towson, MD

Workforce Genetics

CSV Engineer

Baltimore, MD

Implement Computer System Assurance (CSA) Methodologies: Lead the transition from traditional, documentation-heavy Computer System Validation (CSV) to a right-sized, risk-based CSA approach ...

CAI

Computer Systems Validation Engineer

Baltimore, MD

$75K - $106K/yr

... computer validation documentation (e.g., URS, FRS, RTM, summary reports) Generate and execute test ... System & Industry Expertise Support CSV activities across various platforms including MES, DCS ...

CAI

Computer Systems Validation Engineer

Baltimore, MD · On-site

$75K - $106K/yr

... computer validation documentation (e.g., URS, FRS, RTM, summary reports) Generate and execute test ... System & Industry Expertise Support CSV activities across various platforms including MES, DCS ...

CAI

Computer Systems Validation Engineer

Baltimore, MD · On-site

$75K - $106K/yr

... computer validation documentation (e.g., URS, FRS, RTM, summary reports) Generate and execute test ... System & Industry Expertise Support CSV activities across various platforms including MES, DCS ...

Deloitte

System Test and Validation Lead

Baltimore, MD · On-site +1

Bachelor's degree in business, information systems, computer science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment ...

Deloitte

System Test and Validation Lead

Baltimore, MD · On-site +1

Bachelor's degree in business, information systems, computer science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment ...

Deloitte

System Test and Validation Lead

Baltimore, MD · On-site +1

Bachelor's degree in business, information systems, computer science, engineering, or equivalent experience; 6+ years of experience in computer system validation in a life sciences environment ...

Eliassen Group

Computer Systems Analyst

Woodlawn, MD · On-site

$35 - $42/hr

Write functional and system requirements covering web front-end, database, web services, RESTful ... Familiarity with prompt engineering for generating and validating test cases, acceptance criteria ...

Eliassen Group

Computer Systems Analyst

Woodlawn, MD · On-site

$35 - $42/hr

Write functional and system requirements covering web front-end, database, web services, RESTful ... Familiarity with prompt engineering for generating and validating test cases, acceptance criteria ...

Avista Realtime Systems LLC

Be Seen First

SCADA & Controls Technician Intern

Elkridge, MD · On-site

$32 - $35/hr

Support diagnostics, troubleshooting, and system validation Minimum Education Requirement ... Computer Engineering Technology * Industrial Automation * Mechatronics * Electronics Technology

Avista Realtime Systems LLC

Be Seen First

SCADA & Controls Technician Intern

Elkridge, MD · On-site

$32 - $35/hr

Support diagnostics, troubleshooting, and system validation Minimum Education Requirement ... Computer Engineering Technology * Industrial Automation * Mechatronics * Electronics Technology

DigiFlight, Inc.

System Engineer V

Fort George G Meade, MD · On-site

$140 - $180/hr

Familiar with data formats such as CSV, JSON, PCAP and XML * Understanding of tactical datalinks ... Chemistry, Computer Science, Information Systems, Mathematics, and Physics Our People DigiFlight ...

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Internship Computer System Validation Csv information

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How much do internship computer system validation csv jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for internship computer system validation csv in Towson, MD is $49.63, according to ZipRecruiter salary data. Most workers in this role earn between $37.31 and $61.73 per hour, depending on experience, location, and employer.

What is an internship in computer system validation (CSV)?

An Internship in Computer System Validation (CSV) is a temporary position, typically for students or recent graduates, that provides hands-on experience in ensuring that computer systems used in regulated industries (like pharmaceuticals or healthcare) meet required standards and regulations. Interns assist with validating software and hardware, documenting processes, and ensuring compliance with industry guidelines such as FDA 21 CFR Part 11 or EU Annex 11. This role helps interns understand the lifecycle of computer systems in a regulated environment and prepares them for careers in quality assurance, compliance, or IT within highly regulated sectors.

What are the typical responsibilities of an intern in computer system validation (CSV)?

As a Computer System Validation (CSV) intern, you can expect to assist with tasks such as reviewing and drafting validation documentation, executing test scripts, and collecting evidence to ensure compliance with regulatory requirements. You may also support the maintenance of validation records and participate in team meetings to discuss project progress or findings. These responsibilities are crucial in ensuring that computer systems used in regulated industries, like pharmaceuticals or healthcare, function as intended and meet quality standards. Working closely with senior validation specialists, you'll gain hands-on experience with industry guidelines and learn how cross-functional teams collaborate to achieve compliance.

What are the key skills and qualifications needed for an internship in computer system validation (CSV)?

To thrive as an Internship Computer System Validation CSV specialist, you need foundational knowledge in computer science, life sciences, or engineering, along with an understanding of regulatory standards like GxP or FDA 21 CFR Part 11. Familiarity with validation documentation, software testing tools, and quality management systems is typically required. Attention to detail, analytical thinking, and effective communication are crucial soft skills for interpreting requirements and collaborating with cross-functional teams. These skills ensure compliance, data integrity, and the successful validation of computerized systems in regulated environments.

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

AspectInternship Computer System Validation CsvComputer System Validation Specialist
CredentialsTypically pursuing or recent graduate, basic understanding of validationRelevant certifications (e.g., GAMP, ISPE), experience preferred
Work EnvironmentInternship setting, supervised, entry-level tasksFull-time role, independent responsibilities in regulated industries
Industry UsageUsed in pharmaceutical, biotech, and medical device companies for trainingUsed for maintaining compliance, validating systems in regulated environments

In summary, the Internship Computer System Validation Csv is an entry-level position focused on learning and supporting validation tasks, while the Computer System Validation Specialist is a more experienced role responsible for ensuring system compliance and validation in regulated industries.

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For Internship Computer System Validation Csv jobs in Towson, MD, the most frequently searched job titles are:

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Internship Computer System Validation Csv jobs near you
Infographic showing various Internship Computer System Validation Csv job openings in Towson, MD as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 15% Part Time, and 2% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $103,222 per year, or $49.6 per hour.

CSV Engineer

Workforce Genetics

Baltimore, MD

Contractor

Re-posted 28 days ago

Key responsibilities

  • Interact with QA, IT, and business area users to generate user requirements and understand system functionality and use with respect to computerized systems and data integrity

  • Validate and qualify computerized manufacturing PLC-based and Windows-based systems in GXP environments

  • Write and review validation documentation, including Validation Plans, User Requirements, IQ/OQ/PQ Protocols, and Summary Reports

Job description

CSV Engineer (6mo. Contract-to-Hire)

Location: Baltimore, MD


Company

Join a premier global Contract Development and Manufacturing Organization (CDMO) that is rapidly expanding its state-of-the-art sterile manufacturing footprint in Baltimore. This organization is a strategic partner to leading pharmaceutical and biotech companies, specializing in the end-to-end development and commercialization of complex injectable products. With a reputation for scientific excellence and a commitment to Quality by Design, they offer a dynamic, client-facing environment where technical experts lead the transition of life-saving therapies from the lab to commercial scale.


Job Summary

The CSV Engineer will interact with QA, IT, and business area users to generate user requirements and understand system functionality and use with respect to computerized systems and data integrity. Maintain current system functionality and use to ensure cGMP regulatory compliance. Perform periodic reviews and remediation activities for validated systems.


What You'll Do

  • Possess strong knowledge of validation and related practices, including governmental regulations (e.g., 21CFR Part 11, EU Annex 11)
  • Plan, coordinate, and execute assigned projects by effectively using Project Management methodologies
  • Act as a subject matter expert on computer validation lifecycle processes, articulating these to clients and regulatory bodies
  • Validate and qualify computerized manufacturing PLC-based and Windows-based systems in GXP environments
  • Write and review validation documentation, including Validation Plans, User Requirements, IQ/OQ/PQ Protocols, and Summary Reports
  • Perform global computerized system risk assessments and vendor evaluations
  • Drive project execution and serve as a coach/mentor to project teams to promote continuous improvement and professional growth
  • Implement Computer System Assurance (CSA) Methodologies: Lead the transition from traditional, documentation-heavy Computer System Validation (CSV) to a right-sized, risk-based CSA approach, leveraging critical thinking to focus formal testing efforts on high-risk GxP functionalities, patient safety, and data integrity.
  • Qualify Standalone GxP Software from Scratch: Manage the complete end-to-end validation lifecycle for new, bespoke, or custom-built standalone software platforms (including GAMP Class 5 applications) without relying on pre-existing vendor frameworks.
  • Perform Right-Sized Software Risk Assessments: Conduct strategic risk modeling and Failure Mode and Effects Analysis (FMEA) to distinguish high-risk GxP functions from low-risk features, establishing documented justifications to optimize the testing burden and avoid unnecessary verification.
  • Bridge Information Technology and Automation Networks: Translate complex network architectures, server security setups, and firewall configurations into GxP-compliant validation test protocols.
  • Establish Data Integrity and Digital Readiness Strategy: Drive the site's transition from legacy paper-based recording systems to electronic data acquisition and chartless recording, ensuring robust controls for audit trails, user access interfaces, and electronic records.\
  • Defend and Justify Validation Scoping: Act as the strategic owner of the CSV/CSA framework, demonstrating the confidence and technical expertise to justify and defend risk-based testing strategies to cross-functional stakeholders and regulatory bodies during audits.


What You'll Bring

  • Bachelor's degree required
  • At least 7 years of experience in computer systems validation and 21 CFR Part 11 / Annex 11 within GMP/GLP industries
  • Comprehensive knowledge of the computer validation lifecycle process
  • Fluency with SAP, PLCs, and laboratory computer systems
  • Proficiency in Microsoft Word, Outlook, and Excel


Work Environment & Role Demands

In this role, you will be expected to organize and coordinate complex tasks, solving issues independently using sound judgment. You should be comfortable working in a fast-paced environment with frequent interruptions. The position requires strong visual acuity and eye/hand coordination for keyboard use and traversing laboratory areas. You will primarily work on-site with minimal travel, occasionally working around extreme temperatures or noise above conversation levels. Regular and predictable attendance is essential to support our laboratory operations.