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Internship Computer System Validation Csv Jobs in Lancaster, TX

Deloitte

System Test and Validation Lead

Dallas, TX · 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

Dallas, TX · 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

Dallas, TX · 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 ...

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Internship Computer System Validation Csv information

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$28

$49

$71

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

As of Aug 30, 2026, the average hourly pay for internship computer system validation csv in Lancaster, TX is $49.11, according to ZipRecruiter salary data. Most workers in this role earn between $36.92 and $61.06 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.

What job categories do people searching Internship Computer System Validation Csv jobs in Lancaster, TX look for?

The top searched job categories for Internship Computer System Validation Csv jobs in Lancaster, TX are:

What cities near Lancaster, TX are hiring for Internship Computer System Validation Csv jobs?

Cities near Lancaster, TX with the most Internship Computer System Validation Csv job openings:

Internship Computer System Validation Csv jobs near you
Infographic showing various Internship Computer System Validation Csv job openings in Lancaster, TX as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 12% Part Time, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $102,146 per year, or $49.1 per hour.

Computer System Validation-Pharmaceutical

Fort Worth, TX

PharmEng Technology
See more jobs at PharmEng Technologyexternal

Full-time

Re-posted 28 days ago

Job description

Title: Computer Validation Specialist-PQM Location: Fort Worth, TX Company: PharmEng Technology Inc. PharmEng Technology is a full service consulting firm that serves the pharmaceutical, medical devices and biotechnology industries in North America and internationally. Since 1997, the company has provided industry recognized consulting services assisting clients in the rapid commercialization of new product from drug discovery, strategic planning to process scale up.

PharmEng has immediate opening for candidates with experience in Process Validation Engineer. Essential Functions and Responsibilities Proficient in Validation and Qualification aspects of systems. If required, creates and documents Validation Plan, Quality Plan, IQ Report, OQ Report, and Validation Summary Reports.

Drive continuous improvement of the quality system to meet and sustain compliance with internal and external regulatory requirements Conduct Quality reviews to evaluate if processes and deliverables fulfill the requirements for quality, to uncover errors or deficiencies in processes and deliverables, and to identify strengths and opportunities for improvement Follow up resolution of identified quality exposures and escalation to line management if critical situations are not resolved in due course Contribute to business decisions in the decisions in the definition and assessment of IT requirements Support the development and delivery of training in quality matters Drive and facilitate create of relevant of system SOPs. Prepare and follow internal authority inspections. Prepare, or review and approve major system documentation to ensure consistency with quality standards and quality deliverables.

Coordination documentation, testing and change management activities to ensure compliance with business and regulatory needs Develop PQM resources for projects and services and monitor their performance to ensure adherence with agreed quality systems. Forecast demand and plan for IT PQM related to projects, provide task estimating and ICE roadmap to PMs, monitor and manage project risk and compliance Ownership IT CAPA and CCR Process for the responsible functional areas. Minimum Qualifications: Bachelor's of Science and a minimum of 5 years experience in IT in pharmaceutical industry with expert knowledge of current regulations Ability to interact with all levels of the organization Influence and leadership capability, and credibility within the business Strong organization skills Strong written and verbal communication skills Excellent written and spoken English Thank you for your interest in our organization.

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