Analytical Validation Engineer

**_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...

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...

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...

Experienced Package Engineer Opportunity Relevant Experience And Skills 3+ years of Package Engineering experience, preferably in the regulated medical device industry Proficiency in glass vials, labels, folding cartons, corrugated materials, and transport packaging Strong written and verbal communication skills Analytical, problem-solving, and critical...

Company InformationLegend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell and natural killer (NK)...

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. The Engineering Manager in QCL will lead a team of engineers to...

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 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...

Company Information Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell and natural killer (NK)...

Company Information Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell and natural killer (NK)...

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...

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:...

Job Description Have you got the right qualifications and skills for this job Find out below, and hit apply to be considered.We're looking for a skilled Senior Quality Engineer to help maintain our commitment to excellence. As a Senior Quality Engineer, you will be responsible for implementing and maintaining the effectiveness of our Quality System, ensuring...

Job Description For a complete understanding of this opportunity, and what will be required to be a successful applicant, read on.Responsibilities of this engineering grade level inherently include and expand upon the responsibilities established for lower engineering grade levels.Responsible for compliance with applicable policies and procedures.Plans and...

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...

Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell and natural killer (NK) cell-based...

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....

10+ years' experience in Global Regulatory affairs, CMC submissions. Knowledge on Insights and regulatory affairs. Develop the detailed project plan Kickoff the project with full project team including IT, Validation and Business participants Collaborate with multiple squad resources, and other Product Teams and Technical Services (as needed) Conduct the...