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Part Time Computer System Validation Csv Jobs in Massachusetts

Domino's Franchise

Customer Service Rep(03712)

North Adams, MA · On-site

$15 - $20.50/hr

As a CSR you will receive training on our computer system and will gain confidence through working ... For job openings on your schedule - part time or full time - give us a try. You must be 18 years of ...

Steve Madden

Stock Associate

Somerville, MA

$16.25 - $20.75/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.

Steve Madden

Shoe Stylist

Wrentham, MA · 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.

Steve Madden

Stock Associate

Wrentham, MA

$16.50 - $20.75/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.

Steve Madden

Shoe Stylist

Wrentham, MA

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.

Steve Madden

Cashier

Somerville, MA

$12.75 - $17.50/hr

Cashier (P/T) The Cashier is responsible for listening and responding appropriately to customer ... 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.
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Part Time Computer System Validation Csv jobs near you
Infographic showing various Part Time Computer System Validation Csv job openings in Massachusetts as of July 2026, with employment types broken down into 100% Part Time. Highlights an 100% In-person job distribution.

IRT/RTSM Script Writer

Dark Horse Consulting Group

Boston, MA • On-site

Part-time

Posted 13 days ago

Job description

We are seeking an experienced IRT/RTSM Script Writer to support our clients in the life sciences industry with IRT/RTSM design and implementation. This role will focus on IRT (Interactive Response Technology) design support, test script writing, and testing support for clinical trials. The ideal candidate will bring experience working closely with cross-functional clinical study teams, IRT/RTSM vendors, and external partners to ensure test scripts align with IRT design and clinical trial objectives. This is a part-time role.

Key Responsibilities
IRT/RTSM Design and Implementation Support
• Oversee IRT/RTSM design and implementation from user requirement specifications through Go-Live, ensuring alignment with clinical study protocol and functional requirements.
• Participate in client meetings, design sessions, and sandbox testing with the ability to suggest solutions for client problems.
• Develop and manage project plans to ensure timely completion of scripts, incorporating key milestones and activity timelines.
• Communicate IRT/RTSM implementation project status, accomplishments, risks, and issues to stakeholders.
• Identify, escalate, and drive resolution of project-related risks and challenges.
• Support Computer System Validation (CSV) activities for IRT/RTSM.
• Leverage templates and AI to develop scripts for IRT/RTSM User Acceptance Testing (UAT) and EDC integration.
• Provide live UAT testing support.

Qualifications & Experience
• Proven experience writing IRT test scripts for User Acceptance Testing.
• Knowledge of IRT/RTSM solutions, clinical trial design of Phase I-IV clinical trials, & clinical distribution strategies.
• Experience collaborating with IRT/RTSM vendors and cross-functional client teams to ensure seamless study execution.
• Ability to work in a fast-paced environment with the possibility of last-minute schedule changes.
• Available to work flexible hours though primarily standard East Coast business hours.
• Bachelor’s degree and 3 years of script writing experience required.