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Raritan, New Jersey

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Today

Job Details: Role Overview: Request for Technology Quality Manufacturing and MES Services - 100% allocation / North America (Onshore). Must have: Strong CSV and Quality expertise with ability to independently lead validation activities across the SDLC for GxP systems with minimal supervision. 7-10 years of relevant experience. Proven experience with Manufacturing, MES, and Data Platform Applications, including support for global and regional GxP computerized systems. Deep knowledge of GxP compl

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SAP CSV (Computer System Validation)

Hybrid in Ohio City, Ohio

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9d ago

Job Title: SAP CSV (Computer System Validation) Workstream Lead Location: Ohio (Travel up to 50%) Duration: 6 Months (with potential for long-term extension) Travel: Up to 50% Industry: Life Sciences Experience leading validation activities for large-scale SAP implementations or transformations. Strong documentation and project leadership skills. Required Experience: SAP, CSV, GxP Validation, Customer-Facing Leadership Skills Job Description We are seeking an experienced CSV (Computer System V

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Contract

Depends on Experience

Validation Engineer/Technician with CSV / CQV Focus

Worcester, Massachusetts

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30+d ago

Arthur Lawrence is looking for a Validation Engineer/Technician with CSV / CQV Focus one of our clients in Worcester, MA. Please find the job description below and send us your updated resume if interested: Must-Have Skills: Experience in validation, calibration, or CQV within a pharmaceutical or regulated environment Strong knowledge of GMP and 21 CFR Part 11 compliance, including CSV (Computerized System Validation) Hands-on experience with equipment qualification (IQ/OQ/PQ), process validati

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Contract

$40+

CSV Consultant 68928

Raritan, New Jersey

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Today

CSV Consultant We have an Immediate need for a CSV Consultant for our client. The ideal candidate must be able to support Business Separation activities for Large global and regional GxP Computerized systems are required. We are looking for candidates with experience in reviewing system test and user acceptance test scripts, Traceability matrix and Design Specs Experience in QA Methodologies, designing, reviewing and approving Test Plans, systems and UAT test scripts and Test procedures. No su

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Contract

$50.00 - 55.00

Sr. Computerized System Validation (CSV) Manager

Remote

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24d ago

We are Looking for a Senior Computerized System Validation (CSV) Manager with CRO industry experience. This a full-time permanent hire position with our client. In this role you can work fully remote (anywhere in USA). In this role as a Senior Computerized System Validation (CSV) Manager, you will lead the transformation of CSV practices within the organization. In this role as a Senior Computerized System Validation (CSV) Manager you will ensure validation processes are risk-based, efficient, a

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Full-time

Depends on Experience

CSV Engineer

Columbus, Ohio

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Today

Job Summary: The CSV Engineer is responsible for ensuring that GxP computerized systems at the client site are validated in compliance with regulatory standards (21 CFR Part 11, EU Annex 11, GAMP 5). This role directly supports gene therapy manufacturing operations by leading validation activities for key systems, including Veeva QMS, BMRAM, analytical lab instruments, and the Metasys Client. By maintaining data integrity and system compliance, the CSV Engineer plays a critical part in ensuring

Full-time

CSV Engineer

Raritan, New Jersey

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Today

Roles & Responsibilities Lead end-to-end CSV activities (inventory assessment remediation disposition) Support business separation for large GxP systems Define & implement risk-based validation strategies Review & approve test plans, UAT scripts, validation documents Ensure compliance with regulatory & quality standards Provide guidance, escalation & leadership to validation teams Collaborate with global & remote teams Education & Experience : 7-10 years in CSV / Validation roles Experience in P

Full-time

CSV Engineer

New Jersey

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Today

Summary : CSV Validation Engineer is responsible for authoring and executing validation test scripts to support regulated systems within a GxP life sciences environment. This role will focus on validating ERP Master Data Governance processes and Data Lake platforms, ensuring compliance with regulatory requirements and data integrity standards. Roles & Responsibilities: Author, review, and execute validation test scripts (IQ/OQ/PQ) for GxP computerized systems Support validation activities for E

Full-time

CSV Engineer

Newark, Delaware

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Today

Job Summary: We are looking for a Computer System Validation (CSV) Engineer to support our client in Newark, DE. In this role, you will be responsible for ensuring that computerised systems used in regulated environments are validated and compliant with industry standards. You will work closely with IT, Quality, and business teams to support validation activities and maintain system compliance throughout its lifecycle. Roles & Responsibilities: Lead and support CSV activities for GxP systems, in

Full-time

CSV Engineer

Pennsylvania

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Today

Job Summary: The CSV Engineer / Validation Engineer will be responsible for ensuring computerized systems in a regulated pharmaceutical environment comply with GxP, 21 CFR Part 11, GAMP 5, EU Annex 11, ISO 9001, and SOX requirements. The role involves supporting validation activities using a risk-based approach aligned with CSA principles, ensuring systems are audit-ready, and maintaining compliance throughout the system lifecycle. The position also requires hands-on involvement in documentatio

Full-time

CSV Engineer

Indiana

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Today

Job Summary: The CSV (Computer System Validation) Engineer will be responsible for ensuring that computerized systems used in a pharmaceutical/GMP-regulated environment are validated and compliant with regulatory standards, including 21 CFR Part 11. The role requires strong expertise in GAMP 5 methodology, validation lifecycle processes, and experience with automation and control systems. This is an onsite position based in Bloomfield, Indiana. Roles & Responsibilities: Execute and manage com

Full-time

Sr. CSV Engineer

Chesterbrook, Pennsylvania

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Today

Job Summary: Seeking a Sr. CSV Engineer with 10+ years of experience in pharmaceutical compliance, Computerized System Validation (CSV), and GxP-regulated environments. The ideal candidate should have expertise in compliance regulations including 21 CFR Part 11, GxP, GAMP 5, SOX IT, Quality Management, Document Management, and Change Management. Experience with testing tools such as Client-ALM, JIRA, X-Ray, Agile methodologies, and exposure to global delivery models is required. Roles & Res

Full-time

CSV Engineer

Indianapolis, Indiana

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Today

Roles & Responsibilities: Author equipment qualification and validation packages Plan coordination with equipment manufacturer or supplier for preventative maintenance Technical review and execution of qualification/validation protocols Execution of CSV initiatives Apply knowledge of quality principles, GMPs, federal regulations and standard procedures to deliverables Initiate CSV change controls on equipment Experience: Experience Required: 2-4 Years Experience in executing equipment validati

Full-time

CSV Engineer

Redwood City, California

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Today

Summary: Our client is looking for an experienced and well-rounded CSV (Computer System Validation) Consultant to support multiple ongoing projects within a pharmaceutical environment. The ideal candidate must have hands-on experience with Veeva platforms and data migration projects in regulated pharma environments. Roles & Responsibilities: Validating Veeva platforms within a pharmaceutical company Developing UAT documents and writing test scripts Managing change controls including creation, e

Full-time

CSV Validation Engineer

Nashville, Tennessee

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Today

Job Summary: Responsible for supporting equipment and process validation activities within a regulated environment, ensuring compliance with GMP, FDA, and Food/Consumer industry standards. The role focuses on validation lifecycle execution, risk-based approaches, and cross-functional collaboration to maintain product quality and regulatory compliance. Roles & Responsibilities: Develop, execute, and report IQ/OQ/PQ protocols. Perform equipment and process validation activities (e.g., mixing, pack

Full-time

CSV Engineer

Pittsburgh, Pennsylvania

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Today

Job Summary: CSV Engineer to support commissioning and validation activities for a newly built Cell & Gene Therapy R&D and manufacturing facility in Pittsburgh, PA. The role focuses on reviewing validation deliverables, ensuring compliance with regulatory standards (21 CFR Part 11, GAMP 5), and coordinating with commissioning teams handling facilities, utilities, MES, EMS, CMMS, and related systems. The consultant will work within environments using Kneat, Microsoft Office, and automation platfo

Full-time

CSV Engineer

South Plainfield, New Jersey

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Today

Responsibilities: Creates Computer System Validation (CSV) deliverables (Validation Plan, Requirements Specifications, Protocols, Summary Reports, Trace Matrices, SOPs, Risk assessments). Collaborates with Business Users, System Owner, Global IT teams and Business Analysts to define validation requirements and plans. Providing leadership, oversight, and training related to validation activities to multi-functional teams. Generate and execute validation protocols (IQ/OQ/PQ) using Good Documentati

Full-time

Senior Computer System Validation (CSV) Consultant - Concord, NC (Onsite)

Concord, North Carolina

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11d ago

Job Title: Senior Computer System Validation (CSV) Consultant - Concord, NC (Onsite) Location: Concord, NC (Onsite) Duration: 12 Months Visa: Open to All Work Authorisations Experience: 46 Years (Strong Communication Skills Required) Industry: Pharmaceutical / Life Sciences / Healthcare Job Summary We are seeking an experienced Senior Computer System Validation (CSV) Consultant to support validation and compliance initiatives for MES and other GMP-regulated systems within a pharmaceuti

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Contract, Third Party

Depends on Experience

CSV Engineer

Hillsboro, Oregon

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Today

Job Description: We are seeking an experienced Computer Systems Validation (CSV) Engineer with strong communication skills and a true consultant mindset. The ideal candidate will have solid experience in pharma validation environments and hands-on exposure to manufacturing and automation systems. Requirements: Bachelor's degree in computer science, Engineering, Life Sciences, or related field. 5+ years of experience in CSV/CSA frameworks (GAMP) within the Pharma industry. Hands-on experien

Full-time

CSV Engineer

San Francisco, California

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Today

Job Summary: CSV Consultant responsible for leading Computer System Validation (CSV) and applying Computer Software Assurance (CSA) principles for SAP S/4HANA with a focus on the Quality Management (QM) module. The role involves validation of QM processes, ensuring GxP compliance, managing QA/testing activities, and supporting regulatory and audit requirements in a regulated environment. Roles & Responsibilities: Lead Computer System Validation (CSV) for SAP S/4HANA (QM module focus). pply Compu

Full-time

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