Computer Systems Validation

Job Description: Pay Range $55hr - $62hr 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...

Job Title : Senior Computer Systems Validation (CSV Skillset) Location : Raritan, NJ (Onsite) Duration: 6 months Contract Job Description: Experience in computer systems validation, GXP regulatory knowledge and good documentation methods and CSA approaches and risk-based validation required. Prior experience in SAP ECC/S4 HANA system validation,...

Job Title : Senior Computer Systems Validation (CSV Skillset)Location : Raritan, NJ (Onsite)Duration: 6 months ContractJob Description:Experience in computer systems validation, GXP regulatory knowledge and good documentation methods and CSA approaches and risk-based validation required. Prior experience in SAP ECC/S4 HANA system validation, Solman/ChaRM...

Job Title : Senior Computer Systems Validation (CSV Skillset)Location : Raritan, NJ (Onsite)Duration: 6 months ContractJob Description:Experience in computer systems validation, GXP regulatory knowledge and good documentation methods and CSA approaches and risk-based validation required. Prior experience in SAP ECC/S4 HANA system validation, Solman/ChaRM...

Job Title : Senior Computer Systems Validation (CSV Skillset) Location : Raritan, NJ (Onsite) Duration: 6 months Contract Job Description: Experience in computer systems validation, GXP regulatory knowledge and good documentation methods and CSA approaches and risk-based validation required. Prior experience in SAP ECC/S4 HANA system validation,...

Job Title : Senior Computer Systems Validation (CSV Skillset) Location : Raritan, NJ (Onsite) Duration: 6 months Contract In order to make an application, simply read through the following job description and make sure to attach relevant documents. Job Description: Experience in computer systems validation, GXP regulatory knowledge and good documentation...

The Opportunity QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers...

**_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...

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...

What would you consider to be the top 3, non-negotiable skills that you'll be looking for when reviewing candidate resumes?: -Proficiency with Computer Systems in General, in particular with purchase order systems, market research operational systems. -Working with stakeholders to discuss and understand issues as they occur so they can be...

Responsibilities: 7+ years of experience in Computer System Validation. Reviewing and approving validation deliverables of GxP regulated Computerized Systems to ensure full compliance with Health Authority regulatory requirements and adherence to company policies and procedures by supporting computer validation projects and base business support teams....

MBR Engineer Location: Raritan, NJ Hybrid Working Model Position Overview: As a Senior MES Client-X MBR Modeler you will play a critical role in the design, implementation, and maintenance of our MBR using Werum Client-X V2/V3. You will ensure compliance with industry standards and regulations while optimizing production processes. Key Responsibilities:...

MBR Engineer Location: Raritan, NJ Hybrid Working Model Position Overview: As a Senior MES Client-X MBR Modeler you will play a critical role in the design, implementation, and maintenance of our MBR using Werum Client-X V2/V3. You will ensure compliance with industry standards and regulations while optimizing production processes. Key...

Responsibilities: Minimum 7 years' Experience in the Validating IT software systems like Quality Management System in Life Sciences industry Experience in FDA and/or Global regulated environment with good understanding of GxP standards like CFR 820 and Risk based validation. Experience in validating Global Risk and Compliance...

Would you like to be a part of a team that plays a critical role in providing quality patient care and improving lives? Come join us at LabCorp! LabCorp is seeking a Warehouse Associate to join our team in Raritan, NJ. This position will be responsible for fulfilling customer orders of medical lab supplies and products. What to Expect Place orders for...

Hybrid - Onsite 3 days a week Neuroscience Operations Specialist Top 3 skills: -Proficiency with Computer Systems in General, in particular with purchase order systems, market research operational systems. -Working with stakeholders to discuss and understand issues as they occur so they can be solved -Understanding system processes and requirements to...

Hybrid - Onsite 3 days a week Neuroscience Operations Specialist Top 3 skills: -Proficiency with Computer Systems in General, in particular with purchase order systems, market research operational systems. -Working with stakeholders to discuss and understand issues as they occur so they can be solved -Understanding system processes and...

Senior Quality Engineer, Medical DevicesOur client has engaged GForce to identify a Senior Quality Engineer with in-depth understanding of medical device quality system requirements, with specific experience in applying the following: Medical Device product risk management, Medical devices process validation, and Medical Device Design...

Senior Quality Engineer, Medical Devices Our client has engaged GForce to identify a Senior Quality Engineer with in-depth understanding of medical device quality system requirements, with specific experience in applying the following: Medical Device product risk management, Medical devices process validation, and Medical Device Design Control. ...

Senior Quality Engineer, Medical DevicesOur client has engaged GForce to identify a Senior Quality Engineer with in-depth understanding of medical device quality system requirements, with specific experience in applying the following: Medical Device product risk management, Medical devices process validation, and Medical Device Design...