or a related field. Key Requirements: Essential: Experience in analyzing, designing, constructing, and testing electronic circuits. Proficiency in using electronic test equipment for circuit validation and investigation. Strong understanding of both analog and digital circuit design. Proficiency in schematic and PCB design tools for generating manufacturing files. Sole British Citizenship more »
Cambridge, Cambridgeshire, East Anglia, United Kingdom
Langham Recruitment Limited
and partition in-house designs and IP from third parties and wrap with modelling logic to represent mixed signal design element. Asist with the validation of new silicon chips with a mix between CI/CD automation and manual tests through electrical test equipment. Qualifications and Experience: Strong experience in more »
Cambridge, Cambridgeshire, East Anglia, United Kingdom
Langham Recruitment Limited
and partition in-house designs and IP from third parties and wrap with modelling logic to represent mixed signal design element. Asist with the validation of new silicon chips with a mix between CI/CD automation and manual tests through electrical test equipment. Qualifications and Experience: Strong experience in more »
Cambridge, Cambridgeshire, United Kingdom Hybrid / WFH Options
Signaloid
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 Uncertainty Quantification in Materials Modeling applications you implement.After a year in this role, based on your demonstrated performance, you will have the more »
Blackfield Associates are partnered with a CDMO client based in the Cambridge area looking for a Validation Manager on a permanent basis. The Validation Manager will be leading the validation function to be able to execute report activities within the framework of GMP - Annex 11 & 15 in compliance with QMS … requirements. In addition, they will be supporting multiple validation projects, liaising with the project departments and the associated departments to ensure work is completed in a timely manner. Other responsibilities include: Ensuring Validation Master Plans (VMPs), protocols, and procedures are established to facilitate the delivery of validation activities to the … require regulatory standards. Oversee User Requirement Specifications, DQ/IQ/OQ/PQ protocols, and reports for validation purposes. Supervise validation testing performed by vendors to ensure work is accurate, critically review results and work with vendors to report deviations. Manage requalification of systems and equipment in accordance with more »
development stages. Integrate and partition in-house designs and third-party IP, incorporating modeling logic to represent mixed signal design elements. Contribute to the validation of new silicon chips by engineering a suite of validation tests assessing electrical performance and functionality. These tests will combine CI/CD automation with 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 »
against acceptance criteria as described in user stories and requirement documentation Promote full business engagement in the Agile development process. Support User Acceptance Testing Validation, Release and Deployment: Understand the approach for validating the solution and work with the Development team to ensure that work is of a consistent high more »
devices/IVD sectors, particularly in mechanical engineering. Responsibilities: As a Product Development Engineer, you will play a vital role in the verification and validation (V&V) process for two upcoming product lines. Your duties will involve testing a diverse range of devices, creating effective test methods and fixtures, and more »
new designated Innovation Team. Technology requirements: 5+ years experience C# .NET, wither commercial Kubernetes expertise, 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 »
Cambridge, Cambridgeshire, East Anglia, United Kingdom
Russell Taylor Group Ltd
and business Assist in investigations, review and presentation of resource developments that would improve analytical methodology Contribute to development, compilation and presentation of method validation packages in line with accreditation requirements. Support organics department in areas requiring advanced expertise in analytical chemistry Assist quality team in scheduled audits Respond to … of new instruments, the purchasing of consumables, etc. The Person: Will hold a Degree in a relevant Science based discipline Significant Method Development, Method Validation experience in a UKAS 17025 setting (essential); working with ICP-MS/ICP - OES Will have strong interpersonal skills and able to interact with Customers 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 »
range of compilers and toolchains and tackle software performance challenges. Responsibilities as Staff DevOps Engineer : Maintaining a board farm of hardware devices used for validation and benchmarking. Crafting, maintaining and extending the automated testing and benchmarking infrastructure. Extending existing software to suit our needs or writing new glue between systems. more »
development of physical hardware development platforms, based around custom system-on-chip (SoC) and FPGAs. These platforms are then used for software development and validation activities for both external partners/customers and internal development teams. Responsibilities as Principal Board Design Engineer : Specification, development, and commissioning of new hardware platforms. more »
Hobson Prior is seeking an individual with strong analytical and technical skills to assist in the development and validation of analytical methodologies for biomarker discovery. This role is based in Cambridge and is a permanent position. Please note that to be considered for this role you must have the right 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 »
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 »
experience would be an advantage to this role: • At least 2 years’ experience in at least one of the following: Analytical method development and validation Risk assessment/Quality by Design. Vendor management of third party CMOs/CROs or experience working at a third party CMO or CRO. API more »
onto the QMS as necessary. Working alongside CMO’s and in-house specialists to support the production scaling activities. Create and implement QC and validation protocols, ensuring that regulatory processes are followed meticulously. Report any QC pass and fails, monitoring any non-conformance closely and taking corrective action. Strictly adhere more »
be responsible for: the data management of clinical trials developing and maintaining a clinical database (experience with OpenClinica is a plus!) the design and validation of CRF specifications the data strategy through risk assessments related to data management This role is for you if you possess: data management experience within 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 »
As the selected Principal Hardware Engineer , you’ll join a small, but expert team where you’ll work on the design, development and validation of future communication products. Responsibilities for the role of Principal Hardware Engineer will include: Requirement specification and liaison with key stake holders throughout projects Design, development … of validation of high-speed application processors and supporting multiple high-speed interfaces Full lifecycle support of the current and future product lines Product compliance testing and product support As the selected Principal Hardware Engineer, your skills and experience should include: Experience designing boards to support high-speed processors Knowledge more »
My client is a deep-tech electronics company that produces advanced solutions combining mechanical, optical and software. Their products have already been used worldwide and are looking to expand further. They've grown by more than 11% in the last more »
