ZipRecruiter

Log In

1

Internship Computer System Validation Csv Jobs in Largo, FL

TekWissen LLC

Quality Assurance Engineer

Tampa, FL · On-site

$25 - $35/hr

... computer systems, validation, and laboratory instruments. * Contribute to continuous improvement ... Exposure to computerized system validation (CSV). * Experience in biologics, pharmaceutical, or ...

Lonza

ERP Head (SAP)

Tampa, FL · On-site

$210 - $320/hr

GxP Compliance & Computer Systems Validation (CSV) GxP Compliance & Computer Systems Validation (CSV): Manage the ERP environment in strict compliance with life science quality regulations; ensure ...

Deloitte

System Test and Validation Lead

Tampa, FL · 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

Tampa, FL · 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

Tampa, FL · 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 ...

Lonza

OT Engineer

Tampa, FL

Familiarity with Computer System Validation (CSV), GAMP 5, and 21 CFR Part 11 requirements. * Strong troubleshooting, analytical, and problem-solving skills. * Ability to collaborate effectively with ...

Lonza

OT Engineer

Tampa, FL · On-site

Familiarity with Computer System Validation (CSV), GAMP 5, and 21 CFR Part 11 requirements. * Strong troubleshooting, analytical, and problem-solving skills. * Ability to collaborate effectively with ...

Lonza

OT Engineer

Tampa, FL · On-site

Familiarity with Computer System Validation (CSV), GAMP 5, and 21 CFR Part 11 requirements. * Strong troubleshooting, analytical, and problem-solving skills. * Ability to collaborate effectively with ...

Lonza

ERP Head (SAP)

Tampa, FL

GxP Compliance & Computer Systems Validation (CSV): Manage the ERP environment in strict compliance with life science quality regulations; ensure all system lifecycle phases, data migrations, and ...

Lonza

ERP Head (SAP)

Tampa, FL · On-site

GxP Compliance & Computer Systems Validation (CSV): Manage the ERP environment in strict compliance with life science quality regulations; ensure all system lifecycle phases, data migrations, and ...

Karls Technology

Be Seen First

Computer Technician

Tampa, FL · On-site

$40K - $48K/yr

... smart TVs, home security systems). You will also assist in setting up, configuring and ... Possess a valid driver's license, maintain valid insurance, a good driving record, have a reliable ...

New

next page

Showing results 1-20

All JobsComputer System Validation Csv JobsInternship Computer System Validation Csv JobsInternship Computer System Validation Csv Jobs in Largo, FL

Internship Computer System Validation Csv information

See Largo, FL salary details

$25

$44

$64

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

As of Aug 25, 2026, the average hourly pay for internship computer system validation csv in Largo, FL is $44.28, according to ZipRecruiter salary data. Most workers in this role earn between $33.27 and $55.05 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 are popular job titles related to Internship Computer System Validation Csv jobs in Largo, FL?

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

Internship Computer System Validation Csv jobs near you

Quality Assurance Engineer

Tampa, FL • On-site

TekWissen LLC
Recruiting and Staffing Services • 501 - 1,000 employees
Learn more about TekWissen LLCexternal

$25 - $35/hr

Temporary

Re-posted 29 days ago

Job description

Overview:  
 
TekWissen group is a workforce management provider throughout the USA and many other countries in the world. Our client is a leading biotechnology company that combines technological expertise with world-class manufacturing and scientific insight to support the delivery of innovative medicines for a wide range of diseases. Specializing in pharmaceutical ingredients, bioscience, biopharmaceuticals, custom manufacturing, and cell and gene therapy, the company provides comprehensive services across the pharmaceutical, biotech, and life sciences sectors. It supports every stage of drug development, from early research to commercial production, and offers solutions in biologics, small molecules, and specialty ingredients. Committed to quality and innovation, the company serves as a critical partner in advancing therapeutic solutions and streamlining complex manufacturing processes, with a global presence that ensures access to scalable, flexible, and compliant technical expertise.
 
 
Job Title:        Quality Assurance Engineer
Location:        Tampa, FL - 33634
Duration:        12 months 
Job Type:        Temporary Position
Work Type:    Onsite
 
 
Summary
 
The QA Engineer is responsible for ensuring the timely development, review, and approval of engineering, validation, and lifecycle documentation in compliance with corporate procedures, SOPs, cGMP standards, and industry best practices. This role supports validation activities across the full lifecycle and ensures the facility remains inspection-ready and compliant.
Work Model: 100% On-site.
 
Responsibilities:
  • Review and approve engineering and validation documentation, including IQ, OQ, PQ, and PPQ protocols, validation master plans, risk assessments, calibration, and periodic reviews.
  • Collaborate with plant and external engineering teams to ensure new installations, systems, and commissioning documentation comply with cGMP requirements.
  • Support the full Validation Lifecycle from design through operational improvements and revalidation programs.
  • Represent QA in cross-functional teams supporting production facility build-outs and laboratory move activities (commissioning, validation, CSV).
  • Create, review, and approve SOPs, Change Controls, CAPAs, deviations, forms, reports, and other quality system documentation.
  • Partner with internal and external stakeholders to provide quality validation support aligned with project and regulatory requirements.
  • Interface with Manufacturing, Packaging, Engineering, MSAT, PD, and QA/QC teams to resolve process issues and implement changes.
  • Conduct risk identification and management throughout the product lifecycle using risk management tools.
  • Support deviation investigations related to manufacturing equipment, utilities, automation, computer systems, validation, and laboratory instruments.
  • Contribute to continuous improvement initiatives within GMP Validation and Change Control programs.
  • Participate in internal, client, and regulatory audits.
  • Ensure the site maintains cGMP compliance and inspection readiness.
  • Establish, maintain, trend, and report Quality KPIs and metrics.
  • Participate in Management Review, Quality Review Board, Deviation Review Board, and Change Review Board meetings.
  • Perform additional duties as assigned by the Senior Manager of QA Operations.
Required Qualifications
  • Strong knowledge of cGMP regulations and compliance requirements.
  • Hands-on experience with validation processes (IQ, OQ, PQ, PPQ).
  • Experience reviewing and approving validation and engineering documentation.
  • Proficiency in Change Control, CAPA, Deviations, and Quality Systems documentation.
  • Understanding of Validation Lifecycle and revalidation processes.
  • Experience supporting audits (internal, client, regulatory).
  • Risk management knowledge and application in GMP environments.
  • Cross-functional collaboration and stakeholder management skills.
  • Strong analytical, documentation, and problem-solving skills.
  • Experience supporting facility start-up, commissioning, or laboratory relocations.
  • Exposure to computerized system validation (CSV).
  • Experience in biologics, pharmaceutical, or medical device manufacturing environments.
  • Knowledge of KPI tracking, trending, and quality metrics reporting.
  • Continuous improvement mindset and experience in quality system enhancement initiatives.
TekWissen® Group is an equal opportunity employer supporting workforce diversity.

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Our global footprint covers six countries: United States, Canada, Australia, India, United Kingdom and the Philippines. This allows us to work in close partnership with organizations and manage everything from global talent needs with demanding resourcing strategies, to single sites with lower recruitment volumes.

TekWissen® is an equal opportunity employer supporting workplace diversity. 

TekWissen logo

About TekWissen

Sourced by ZipRecruiter

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Industry

Recruiting and staffing services

Company size

501 - 1,000 Employees

Headquarters location

Ann Arbor, MI, US

Year founded

2009

Social media

Twitter

View All TekWissen Jobs