IT CSV Analyst at Tryton TC LLC

Waltham, Massachusetts, United States -

Full Time

Start Date

Immediate

Expiry Date

07 Jan, 26

Salary

0.0

Posted On

09 Oct, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Computer System Validation, GxP Regulations, Risk Assessments, Test Plans, Documentation, Analytical Skills, Communication Skills, Cross-Functional Teams, Validation Tools, Cloud-Based Validation, Data Integrity, Cybersecurity Principles, ERP Systems, LIMS, MES, Agile Methodologies

Industry

Insurance

Description

Description Job Summary: We are seeking a detail-oriented and experienced IT CSV Analyst to support the validation of computerized systems in compliance with regulatory requirements such as FDA 21 CFR Part 11, EU Annex 11, GAMP 5, and other GxP standards. The role involves developing, executing, and maintaining validation documentation to ensure that systems are fit for intended use and compliant with quality standards. Key Responsibilities: Develop and maintain Computer System Validation (CSV) documentation including: Validation Plans (VP) User Requirements Specifications (URS) Functional Specifications (FS) Risk Assessments Test Plans, IQ/OQ/PQ Protocols Traceability Matrices Validation Summary Reports (VSR) Work closely with IT, QA, business stakeholders, and vendors to ensure compliance with regulatory and internal requirements. Review and assess change controls, deviations, and CAPAs related to computerized systems. Ensure systems are developed and maintained in accordance with GAMP 5 guidelines. Support audits and inspections by regulatory authorities and clients. Participate in system implementation projects, ensuring validation activities are integrated into the project lifecycle. Maintain documentation and validation lifecycle in alignment with data integrity principles (ALCOA+). Conduct periodic reviews of validated systems to ensure ongoing compliance. Requirements Bachelor’s degree in Computer Science, Information Technology, Life Sciences, or related field. Minimum 3–5 years of experience in IT CSV, QA, or compliance roles in a regulated environment (pharma, biotech, or medical devices). Strong knowledge of GxP regulations, including 21 CFR Part 11, EU Annex 11, and GAMP 5. Familiarity with SDLC (Software Development Life Cycle) and validation in Agile/Waterfall methodologies. Experience with ERP, LIMS, MES, TrackWise, or other GxP-regulated systems is a plus. Strong documentation, analytical, and communication skills. Ability to work independently and in cross-functional teams. Preferred Skills: Experience with validation tools or eQMS systems (e.g., Veeva, MasterControl, Kneat). Knowledge of cloud-based validation and SaaS compliance. Understanding of data integrity and cybersecurity principles in a regulated environment. Working Conditions: Mostly remote with occasional visits to Waltham, MA Some travel may be required for system implementations or audits.

Responsibilities

The IT CSV Analyst will develop, execute, and maintain validation documentation to ensure compliance with regulatory requirements. This includes working closely with IT, QA, and business stakeholders to support audits and inspections.