subsequent generation of a range of trials documentation/material. About You; You’ll have experience in firing trials and/or system integration & validation You’ll ideally have experience of external trials preparation and conduct You’ll be an excellent communicator possessing the ability to communicate with stakeholders at more »
requirements for achieving vehicle system objectives. Develop and execute calibration plans and test protocols to validate functional safety features. Conduct on-road testing and validation of vehicle reaction functions. Analyse test data and performance metrics to identify areas for optimization and improvement. Work closely with Software teams to implement calibration more »
Stevenage, Hertfordshire, South East, United Kingdom
Henderson Scott
develop solutions, and integrate FPGA designs into larger systems. Utilize cutting-edge tools and technologies to optimize FPGA performance and functionality. Perform verification and validation testing to ensure the reliability and accuracy of FPGA designs. Provide support and guidance throughout the development lifecycle, from concept to production. Requirements: Bachelor's 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 »
Are you an ambitious Software Tester looking for an exciting new role within a successful company where you will be responsible for the software validation of products based on the companies sensor technology. This company provides specialist data-gathering solutions for engineering companies across a range of industries. They are more »
As a Project Manager in a Defence Programmes team, you'll play a pivotal role in managing and supporting projects related to military vehicle validation, testing, and support for UK MoD and OE manufacturers. Operating within the unique test facilities, you'll oversee a range of projects, from short-term 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 »
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 »
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 »
Stevenage, Hertfordshire, South East, United Kingdom Hybrid / WFH Options
Omega Resource Group
Use Case analysis Carry out concept assessments, and design trade studies System architecture design and functional modelling Performance assessment and systems behaviour analysis Verification, Validation, and Certification Model-based engineering techniques Work across the product lifecycle If applicable, lead a team of engineers or assist in mentorship Qualifications & Requirements – Systems 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 »
monitoring of funding requests for NHS payment scheme excluded medicines and medical devices. This will include the management and processing of prior approvals, invoice validation and development and maintenance of monitoring systems. The job description and person specification are an outline of the tasks, responsibilities and outcomes required of the more »
NHS Bedfordshire, Luton and Milton Keynes Integrated Care Board
MiDoS related aspects of patient/public/healthcare professional feedback. 11. Ensuring services populated directly on MiDoS are maintained in line with DoS validation process. 12. Championing innovation and improvements to MiDoS to support user community 13. Work closely with NHS 111/IUC and 999 providers to improve 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 »
have an awareness of Air Traffic Control systems. Key responsibilities will include; Requirements analysis and management including the generation of technical documentation Testing and Validation including the development of test plans to validate the functionality and performance of integrated systems Work in a highly technical environment whilst working on complex 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 »
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 »
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 »
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 »
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 »
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 »
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 »
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 »
Luton, Bedfordshire, South East, United Kingdom Hybrid / WFH Options
Adept Recruitment Limited
fee reimbursement (NMC & HCPC) Private medical insurance, life assurance, income protection insurance, pension scheme, personal accident insurance and professional indemnity insurance CPD and re-validation support with protection and training on a regular basis To Apply To apply for this role please forward a CV or call Jay Gibbons for more »
Employment Type: Permanent, Part Time, Work From Home
