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Part Time Computer System Validation Csv Jobs in Maryland

Validation Intern

Rockville, MD ยท On-site

$35/hr

Our team ensures that equipment, systems, and processes used in the development and production of ... Pharmaceutical & Biotechnology Internship Type: Part-Time or Full-Time, Paid Internship Duration: 2 ...

Shoe Stylist (P/T) The Shoe Stylist is responsible for applying selling techniques to merchandise ... Ability to process information or merchandise through the computer system and POS register system.

$60 - $65/hr

Proficient in computer systems including Casamba and PointClickCare preferred Certificates ... Valid, unrestricted driver's license * Ability to pass a criminal background check Skills ...

Shoe Stylist

Towson, MD ยท On-site

Shoe Stylist (P/T) The Shoe Stylist is responsible for applying selling techniques to merchandise ... Ability to process information or merchandise through the computer system and POS register system.

Shoe Stylist (P/T) The Shoe Stylist is responsible for applying selling techniques to merchandise ... Ability to process information or merchandise through the computer system and POS register system.

Stock Associate

National Harbor, MD

$15.25 - $19.25/hr

Stock Associate (P/T) The Stock Associate is responsible for verifying merchandise receipts ... Ability to process information or merchandise through the computer system and POS register system.

Shoe Stylist (P/T) The Shoe Stylist is responsible for applying selling techniques to merchandise ... Ability to process information or merchandise through the computer system and POS register system.

Stock Associate

Clarksburg, MD ยท On-site

$15.50 - $19.50/hr

Stock Associate (P/T) The Stock Associate is responsible for verifying merchandise receipts ... Ability to process information or merchandise through the computer system and POS register system.

Shoe Stylist (P/T) The Shoe Stylist is responsible for applying selling techniques to merchandise ... Ability to process information or merchandise through the computer system and POS register system.

Stock Associate

Towson, MD

$14.25 - $18.25/hr

Stock Associate (P/T) The Stock Associate is responsible for verifying merchandise receipts ... Ability to process information or merchandise through the computer system and POS register system.

Shoe Stylist (P/T) The Shoe Stylist is responsible for applying selling techniques to merchandise ... Ability to process information or merchandise through the computer system and POS register system.

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Part Time Computer System Validation Csv information

What is the difference between Part Time Computer System Validation Csv vs Part Time Quality Assurance Specialist?

AspectPart Time Computer System Validation CsvPart Time Quality Assurance Specialist
CertificationsGxP, 21 CFR Part 11, CSV-specific trainingGxP, ISO, QA certifications
Work EnvironmentPharmaceutical, biotech, or healthcare industries focusing on computer systemsManufacturing, healthcare, or biotech industries focusing on product quality
Primary FocusValidating computer systems, ensuring compliance with regulationsMonitoring quality processes, audits, and compliance
Common UsageRegulatory submissions, validation documentationQuality audits, process improvements

While both roles involve compliance and industry standards, Part Time Computer System Validation Csv specifically focuses on validating computer systems to meet regulatory requirements, whereas Part Time Quality Assurance Specialist oversees overall quality processes and compliance. The CSV role is more technical and system-specific, while QA specialists handle broader quality assurance tasks across various processes.

How does a part-time Computer System Validation (CSV) specialist typically collaborate with cross-functional teams in regulated industries?

As a part-time CSV specialist, you will often work closely with quality assurance, IT, and operations teams to ensure that computer systems meet regulatory and compliance standards. Collaboration usually involves participating in validation planning sessions, reviewing documentation, and providing input during system implementation or upgrades. Even in a part-time capacity, effective communication and flexibility are crucial, as you may need to coordinate your schedule with project milestones and key team meetings. This collaborative environment provides valuable exposure to different departments and helps you build a versatile skill set.

What is a Part Time Computer System Validation (CSV) specialist?

A Part Time Computer System Validation (CSV) specialist is a professional who works on a part-time basis to ensure that computer systems used in regulated industries, such as pharmaceuticals or medical devices, meet compliance standards. Their responsibilities include planning, executing, and documenting validation activities to confirm that systems function as intended and adhere to regulatory requirements. These specialists often work with quality assurance, IT, and regulatory teams to maintain data integrity and support audits. Their part-time status allows organizations to access specialized expertise while managing costs.

What are the key skills and qualifications needed to thrive as a Part Time Computer System Validation (CSV) Specialist, and why are they important?

To excel as a Part Time Computer System Validation (CSV) Specialist, you need a solid background in computer science, life sciences, or engineering, along with knowledge of regulatory requirements such as FDA 21 CFR Part 11 and GxP guidelines. Familiarity with validation lifecycle documentation, risk management tools, and systems like SAP or LIMS, as well as certifications like PMP or Six Sigma, is highly valuable. Strong attention to detail, analytical thinking, and effective communication skills set outstanding CSV specialists apart. These competencies ensure validated systems meet compliance standards, maintain data integrity, and support safe, efficient business operations.
What are the most commonly searched types of Computer System Validation Csv jobs in Maryland? The most popular types of Computer System Validation Csv jobs in Maryland are:
What are popular job titles related to Part Time Computer System Validation Csv jobs in Maryland? For Part Time Computer System Validation Csv jobs in Maryland, the most frequently searched job titles are:
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Infographic showing various Part Time Computer System Validation Csv job openings in Maryland as of July 2026, with employment types broken down into 100% Part Time. Highlights an 100% In-person job distribution.

Validation Intern

Quality Agents, LLC

Rockville, MD โ€ข On-site

$35/hr

Full-time, Part-time, Internship

Re-posted 17 days ago


Job description

Company Overview:
Quality Agents, LLC provides expert validation and quality assurance services to the pharmaceutical and biotechnology industries. Our team ensures that equipment, systems, and processes used in the development and production of drug products meet current Good Manufacturing Practices (cGMP) and regulatory standards.
Position Summary:
We are seeking a motivated Validation Intern to support our validation team in delivering high-quality services to clients in the pharmaceutical and biotech industries. This internship offers hands-on experience with equipment qualification, system validation, and documentation preparation in regulated manufacturing environments. Interns will work under the guidance of experienced validation professionals and gain exposure to real-world validation projects.
Key Responsibilities:
  • Assist in preparing validation documents, including protocols, reports, and data summaries.
  • Support the execution of equipment and utility qualification activities at client sites.
  • Observe and help conduct temperature mapping studies using validation tools (e.g., data loggers).
  • Learn to interpret engineering drawings (P&IDs, isometric and As-built diagrams).
  • Help review and organize validation data and test results.
  • Participate in troubleshooting and investigation activities under supervision.
  • Collaborate with internal teams and client personnel to support project timelines and deliverables.

Learning Opportunities:
  • Exposure to cGMP environments and regulatory expectations (FDA, EMA, ICH).
  • Understanding of validation approaches for pharmaceutical equipment, facilities, and systems.
  • Introduction to validation tools and instrumentation, including Kaye Validators and wireless data loggers.
  • Hands-on training in technical writing and documentation practices in a regulated setting.

Preferred Qualifications:
  • Currently pursuing a degree in Engineering, Life Sciences, Chemistry, or a related technical field.
  • Strong interest in pharmaceutical/biotech industries and quality systems.
  • Basic proficiency in Microsoft Word, Excel, PowerPoint.
  • Strong written and verbal communication skills.
  • Ability to work independently and as part of a team.
  • Detail-oriented with strong organizational skills.

Nice to Have:
  • Familiarity with validation or lab instrumentation (e.g., data loggers, sensors).
  • Exposure to technical documentation or laboratory notebook keeping.
  • Experience using basic statistical tools or Excel-based data analysis.

Location: Various Client Sites (Travel May Be Required)
Industry: Pharmaceutical & Biotechnology
Internship Type: Part-Time or Full-Time, Paid Internship
Duration: 2-6 Months