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 »
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 »
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 »
Peterborough, Cambridgeshire, East Anglia, United Kingdom
Claremont Consulting
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 »
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 »
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 »
using tools like Altium. Troubleshoot technical challenges within the electromechanical system. Ensure documentation of electronics design is up-to-date throughout the Verification and Validation (V&V) process. Manage relationships with external providers, including component suppliers and PCBA manufacturers. Support other areas of the business as needed. Qualifications To be 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 »
detailed commissioning activities for 132kV, 33kV, and 11kV systems including primary transformers, grid transformers, switchgear, relays, AVCs, and SCADA systems. Conduct rigorous testing and validation of all equipment to ensure compliance with design specifications and operational standards. Diagnose and resolve technical issues encountered during the commissioning process, working closely with 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 »
Join an innovative and well-funded company as Verification and Validation Engineer, contributing to the development and refinement of cutting-edge diagnostic systems. Your role will be pivotal in perfecting the electronics design of the product as they move towards launch. You'll work closely with the team and collaborate … with an external electronics team to ensure smooth knowledge transfer, design integrity, and technical evaluations. Position Overview They are looking for a Verification and Validation Engineer to join the team. You will be responsible for defining, designing, and executing verification and validation activities, ensuring our diagnostic systems meet regulatory requirements … and are ready for product launch. Key Responsibilities Support verification and validation processes to prepare the system for clinical studies and FDA approval. Implement test plans and protocols, documenting all activities within the Quality Management System (eQMS). Develop Work Instructions and Standard Operating Procedures (SOPs). Collaborate with Engineering more »
A leading manufacturer of industrial off-highway diesel engines is currently looking for a Validation Engineer to join the team at their site based in Peterborough. The position is paying up to £30.62 per hour based on a 37 hour week. As a Validation Engineer, you will report to the … Validation Engineering Manager. You will have responsibility for conducting testing on validation test beds to sign-o... 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 »
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 »
of the most sophisticated, innovative, and successful Life Sciences companies. Our 750 consultants are working on innovative activities in engineering, production, quality (QA, QC, validation), R&D, and regulatory affairs across Belgium, Switzerland, Germany, Denmark France, and Canada. Thanks to our excellent team, we support manufacturers in all stages of 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 »
of the most sophisticated, innovative, and successful Life Sciences companies. Our 750 consultants are working on innovative activities in engineering, production, quality (QA, QC, validation), R&D, and regulatory affairs across Belgium, Switzerland, Germany, Denmark France, and Canada. Thanks to our excellent team, we support manufacturers in all stages of 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 »
