1 to 25 of 49 Permanent Validation Jobs in Cambridgeshire

Plan, etc.).Create or review and approve CDISC-compliant datasets and corresponding documentation for electronic submission to regulatory agencies.Implement in-house data standards.Develop software validation procedures and test plans, as necessary.Create and document archives of software, outputs, and analysis files.Create and maintain department SOPs and guidelines related to clinical programming.Oversee more »

underwent a rigorous assessment that covered the whole of our business including employee benefits, charitable giving and sustainability. We believe this certification is external validation of our mission to be a force for good. The Recruitment Process Our recruitment process includes a written assessment and proofreading exercise for you to more »

pot developers in a new designated Innovation Team. Technology requirements: 5+ years experience C# .NET, with previous experience running innovation teams employing early-stage validation techniques. Hybrid (fortnightly commute to a brand-new, purpose built office in Cambridge!) Paying up to £90,000 (DOE) Condensed working week (10AM-3PM) Friday more »

and Product Development in order to oversee the QC approach and support with new and existing analytical methods in addition to helping out with validation and verification and transfer activities. Investigating and resolving any issues with availability or performance of reagents and consumables, including: root cause analysis, impact assessment and more »

fundamentals of RF/wireless system architecture and Wi-Fi/BT/Cellular protocols. Experience of RF test for device characterization and performance validation Passion for your work and accomplishments! A desire to develop yourself. Job/vacancy location: Cambridge (commutable from Newmarket, Huntingdon, St Neots, Newmarket, Royston, Bury more »

of software operating/automation systems, including, but not limited to, utility, development, and diagnostic software. They perform technical planning, system integration, verification and validation, cost, risk, supportability and effectiveness analyses for total systems. The Embedded Software Engineer will report to the Electronic and Sensor Integration Manager, Energy and will … MV & HV applications. Responsibilities: All aspects of the software development life cycle: Requirements capture Feasibility study and architecture definition Software design & implementation Integration and validation test Firmware development Design and implement embedded software Implementing hardware drivers, interfaces, abstractions, state machines, advanced signal processing algorithms, application modules and unit tests What more »

LEX is currently seeking a Verification and Validation Engineer who will actively engage in hands-on testing of the LEX diagnostic system. You will be working closely with the head of Quality and Engineering team and will be responsible for defining, designing, and executing verification and validation activities for the … read more about LEX here. You’ll develop testing strategies and methodologies with the wider LEX team to complete testing and draft verification and validation protocols. Your contributions will be crucial in ensuring the successful execution of validation and verification activities required ahead of regulatory approval and product launch. Responsibilities … include: Supporting with verification & validation to prepare the LEX System for clinical study and FDA approval. Implement verification and validation test plans and protocols for the system/product, documenting all activities within the Quality Management System (eQMS). Contribute to the development of Work Instructions and Standard Operating Procedures more »

C and RTOS applications at the core of their products and contribute to the design and development of automated systems for building, testing and, validation of the technology and products. A successful candidate must have: Degree in Electronic Engineering, Computer science or equivalent. Extensive RTOS and Linux experience Hands-on more »

here. As someone with a background in molecular biology and previous experience working on FDA approvals, you'll easily collaborate with the verification and validation team to ensure that the regulated documentation is in place to support with FDA approvals. You will receive support from the Quality Systems Manager and … control systems, offering continuous support and training to both new and existing LEX colleagues Assist in developing and implementing document templates for Verification and Validation (V&V) activities Requirements Previous skills and experience that would be useful to be successful in this role: Confident at using electronic Quality Management Systems more »

challenge the business on regulatory and prioritized projects from both a regulatory and first line risk perspective. Own and deliver the first line annual validation and monitoring plan and closely engage with second line on overall delivery. Identify and managing continuous improvement of the business control environment through ongoing assessments more »

during installation and commissioning phases, utilizing troubleshooting skills and technical experience Execute commissioning procedures to bring automation systems online, including system integration, calibration, and validation Commissioning Engineer Position Requirements Happy to travel the UK for work (part of the role) Commissioning/Installation experience Knowledge and experience of PLC'S more »

Electronics Engineering, Computer Science, or related field. Key Skills: Experience in analyzing, designing, constructing, and testing electronic circuits. Proficiency with electronic test equipment and validation methodologies. Strong understanding of analogue and digital circuit design. Proficiency in schematic and PCB design tools. Excellent analytical and problem-solving skills. Knowledge of communication more »

to represent mixed signal design elements in the wider system. Help validate new silicon chips – engineering effort is needed to write a suite of validation tests that can be used to check the correct operation of custom silicon both in terms of electrical performance and functionality. Such tests would require more »

build physical hardware development platforms, based around Arm’s custom system-on-chip (SoC) and FPGAs. The platforms are used for software development and validation activities for both our external partners/customers and our internal development teams. Responsibilities: System Verification: Develop and maintain SoC verification testbench in SystemVerilog. Experience more »

skills Outstanding written and verbal communication Preferred Qualifications Knowledge of RISC-V ISA, including vector extension Experience in CPU design, Silicon bring up and validation of CPU features Proficiency in computer/SoC architecture and performance trade-offs Strong understanding of power management, physical design concepts Knowledge of ML concepts more »

following areas: Key Account and Product Management Quality Management Mechanical Engineering Mechanical Design Electronics Engineering Mechatronics Engineering Software Engineering (industrial automation, embedded) Verification and Validation Engineering Cellular Origins Cellular Origins is part of TTP Group, an employee-owned business. It is based on the TTP Campus, within purpose-built sustainable more »

perspective regarding the design of clinical trial protocolsOversee, develop and maintain study-specific documentation, including Data Management Plans, eCRF specifications, CRF Completion Guidelines, Data Validation Guidelines, Data Transfer Specifications, Coding Guidelines, Post Production Database Change Control Documentation, Database Audit and Lock ProceduresOversee and participate in the process of data review more »

CK Group are recruiting for a Validation Manager on behalf of a growing Cell Therapy CDMO to be based at their site in Cambridge on a permanent basis. The Role: Reporting to the Head of Quality, you will be responsible for leading the Validation function by building the team and … with manufacturing and lab equipment, facilities, utilities, laboratory, and computer systems are completed, in accordance with GMP requirements Responsibilities : Manage a team and ensure validation master plans (VMPs), protocols and procedures are established To prepare and maintain validation plans (VPs) and identifying validation requirements. Assist in the authoring of User … Requirement Specifications, DQ/IQ/OQ/PQ protocols, and reports for validation purposes. Working with external companies and project teams to ensure activities that require specialist knowledge are completed Executing validation protocols for equipment, facilities and utilities Your Background: Degree (or equivalent) in a Science or related discipline more »

NPU System Performance Modelling Engineer in Cambridge, UK About Neubla As pioneers of innovative neural computing, Neubla is transforming the future of computing by bringing the enormous potential of neural computing to the highest performance in most data-intensive applications. more »

Performance Tools Engineer in Cambridge, UK About Neubla As pioneers of innovative neural computing, Neubla is transforming the future of computing by bringing the enormous potential of neural computing to the highest performance in most data-intensive applications. Neubla is more »

the implementation of those algorithms in C or C++, for execution on Signaloid's compute engine.Be responsible for designing and implementing a testing and validation strategy for the Statistical Electronic Design Automation Tools you implement.After a year in this role, based on your demonstrated performance, you will have the opportunity more »

customer requests, demands, and comments to our Lincoln location and as the project progresses, you will be crucial to ensure that development, verification, and validation are successful. You will develop into the Subject Matter Expert (SME) for the project acting as the main point of contact for stakeholder queries. The more »

Engineer to develop physical hardware development platforms, based around custom system-on-chip (SoC) and FPGAs. The platforms are used for software development and validation activities for both our external partners/customers and our internal development teams. Responsibilities: The specification, development, and commissioning of new hardware platforms. Leading the more »

challenge the business on regulatory and prioritized projects from both a regulatory and first line risk perspective. Own and deliver the first line annual validation and monitoring plan and closely engage with second line on overall delivery. Identify and managing continuous improvement of the business control environment through ongoing assessments more »

forefront of embedded IP and system design. We build physical hardware development platforms, to FPGA in support of software development, pre-silicon, and IP validation, as well as a number of design profiling use cases. To ensure accurate modelling of incoming designs, we must constantly develop new and innovative prototyping more »