Validation Engineer

Piper Companies is looking for an Analytical Validation Engineer to support commissioning and decommissioning activities for a major pharmaceutical company in the Raritan, NJ area.Responsibilities for the Analytical Validation Engineer include: Experience in Pharmaceutical Laboratory Operations Must be familiar and have experience with laboratory...

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. We are seeking a talented, dedicated individual...

Role: CSV Engineer Location: Raritan, NJ Roles and Responsibilities: 7+ years of CSV experience with exposure in SAP ECC/S4 HANA system validation, Solman/ChaRM change control process, JIRA/XRAY/qTEST tools for validation required. Working Knowledge of regulations: 21 CFR Part 11 and Annex 11 Understanding of quality risk-management concepts (ICH Q9) and...

Role: CSV Engineer Location: Raritan, NJ Roles and Responsibilities:7+ years of CSV experience with exposure in SAP ECC/S4 HANA system validation, Solman/ChaRM change control process, JIRA/XRAY/qTEST tools for validation required.Working Knowledge of regulations: 21 CFR Part 11 and Annex 11Understanding of quality risk-management concepts (ICH Q9) and adept...

Role: CSV Engineer Location: Raritan, NJ Roles and Responsibilities:7+ years of CSV experience with exposure in SAP ECC/S4 HANA system validation, Solman/ChaRM change control process, JIRA/XRAY/qTEST tools for validation required.Working Knowledge of regulations: 21 CFR Part 11 and Annex 11Understanding of quality risk-management concepts (ICH Q9) and adept...

Role: CSV Engineer Location: Raritan, NJ Roles and Responsibilities:7+ years of CSV experience with exposure in SAP ECC/S4 HANA system validation, Solman/ChaRM change control process, JIRA/XRAY/qTEST tools for validation required.Working Knowledge of regulations: 21 CFR Part 11 and Annex 11Understanding of quality risk-management concepts (ICH Q9) and adept...

Role: CSV Engineer Location: Raritan, NJ Roles and Responsibilities: 7+ years of CSV experience with exposure in SAP ECC/S4 HANA system validation, Solman/ChaRM change control process, JIRA/XRAY/qTEST tools for validation required. Working Knowledge of regulations: 21 CFR Part 11 and Annex 11 Understanding of quality risk-management concepts (ICH Q9) and...

Job Title: MBR EngineerLocation: Raritan, NJJob Description:Position Overview: As a Senior MES PAS-X MBR Modeler you will play a critical role in the design, implementation, and maintenance of our MBR using Werum PAS-X V2/V3. You will ensure compliance with industry standards and regulations while optimizing production processes.Key Responsibilities:·...

Job Title: MBR EngineerLocation: Raritan, NJJob Description:Position Overview: As a Senior MES PAS-X MBR Modeler you will play a critical role in the design, implementation, and maintenance of our MBR using Werum PAS-X V2/V3. You will ensure compliance with industry standards and regulations while optimizing production processes.Key Responsibilities:·...

Job Title: MBR EngineerLocation: Raritan, NJJob Description:Position Overview: As a Senior MES PAS-X MBR Modeler you will play a critical role in the design, implementation, and maintenance of our MBR using Werum PAS-X V2/V3. You will ensure compliance with industry standards and regulations while optimizing production processes.Key Responsibilities:·...

Johnson & Johnson is recruiting for a Manager of Engineering in Quality, Compliance, and Labs (QCL) headquartered in Raritan, NJ. Remote work options may be considered on a case-by-case basis and if approved by the Company. Applicants must be willing to work on Eastern Time zone schedule. At Johnson & Johnson, we believe health is everything. Our...

Minimum 7 years in CSV required. Experience in Validation and Testing (UAT, Regression Testing) Experience in leading application profile, operational requirements, business process and other project knowledge, as required, to provide the Services Experience creating detailed reports The deliverables will be created in Pharmaceutical SDLC template...

Minimum 7 years in CSV required. Experience in Validation and Testing (UAT, Regression Testing) Experience in leading application profile, operational requirements, business process and other project knowledge, as required, to provide the Services Experience creating detailed reports The deliverables will be created in Pharmaceutical SDLC template...

Responsibilities: 3+ years' Experience in Validating MES or Manufacturing an Lab systems. Experienced in CSV activities in Manufacturing related applications like SAP Systems, MES systems or Lab related systems in the manufacturing space. Perform review for GxP systems to ensure compliance with regulatory requirements. Working knowledge on end-to-end...