51 to 75 of 141 Validation Jobs in the East of England

s and communities across the business advocating Equity, Diversity and Inclusion. Key technical areas of interest; Project Management and Project Planning Integration Engineers System Validation and Verification Engineers Weapon Systems/Launcher Integration Electronic/Mechanical Engineers Systems Engineers Guidance Control & Navigation Engineers Systems Architects Customer Support & Services Sales & Business more »

maintain software documentation, including functional specifications, design documents, and test plans, to ensure compliance with industry standards and regulatory requirements. Conduct system testing and validation to verify software functionality, identify issues, and implement corrective actions as needed. Provide technical support to internal teams and external customers, troubleshooting software-related issues more »

and staff development Carry out regular staff reviews and appraisals.Carry out staff performance management activities.Management of associated lab facilities to enable system and subsystem validation and integration testing for new and existing products.What do I need to qualify for this job?Detailed knowledge of software development process for safety related more »

Associate Director Clinical Biomarkers, Oncology EMU Are you interested in developing, integrating, and implementing innovative biomarker strategies for Oncology clinical development programs, including validation and integration of biomarker assays into clinical trials? If so, the Clinical Biomarker Lead role within Experimental Medicine Unit (EMU) could be an ideal opportunity to more »

selection of innovative technology solutions for effectiveness and modernization. Maintain and improve existing processes, documentation, technology, and software systems for efficiency, includes testing and validation enhancements and fixes. Understand and apply principles of technical delivery and ensure compliance with Security, Quality and Regulatory standards. Learn to analyze data to enable more »

satisfactory completion of training and administer user ID for access to POCT devices. Assist with result verification for newly implemented POCT devices. Complete batch validation for new reagent lots, as directed by the POCT Coordinator. Assist with health and safety, risk assessment and control of substances hazardous to health (COSHH 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 »

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 »

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 »

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 »

ideally in the areas of testing frameworks, build scripts and CI/CD automation Keywords: Verilog, SystemVerilog, FPGA, IC, Xilinx, RTL, simulation, synthesis, verification, validation, I2C, SPI, USB, AMBA, mixed signal, firmware Another top job from ECM, the high-tech recruitment experts. Even if this job's not quite right more »

and maintain data management documentation, including case report forms, data matrices and data management plans in accordance with research-specific project timelines. Conduct data validation checks and implement quality control measures to ensure the accuracy and completeness of datasets. Configure and manage electronic data capture systems (EDC) and clinical data 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 »

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 »

currently involved in designing hardware platforms with custom SoC and FPGAs at the heart. These platforms serve as powerful tools for software development and validation, used by both internal developers and external collaborators. This is a permanent role based on-site in Cambridge, currently visa sponsorship is not available for 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 »

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 »

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 »

configuration & testing Knowledge of Prince 2 methodology ISTQB Foundation (CTFL) certificationKnowledge of ISO-IEC-IEEE 29119 and/or TMMiKnowledge of ITIL v3 Service Validation & TestingUse of formal Test Management tools (e.g Quality centre or Spira)Proficiency in working in a matrix organisation, managing test managers, testers and business users more »

issue for design phase to commissioning. As part of the commissioning team the incumbent will be responsible of process commissioning activities, systemisation, development, and validation of commissioning procedures. Participate and provide input for all planning coordination, scheduling, safety, and progress review meetings. Typical duties will include systemisation of the plant more »

commissioning team the incumbent will be responsible for a team of process commissioning system engineers, the management of process commissioning activities, systemisation, development and validation of commissioning procedures. Participate and provide input for all planning coordination, scheduling, safety, and progress review meetings. Typical duties will include leading systemisation of the more »

and Digitalisation Projects Equipment Obsolescence Upgrades Manufacturing Process Software Upgrades Your Role: You will lead, develop and supervise a team of Project Engineers and Validation Engineers, providing guidance, training, and support as needed. You will foster a collaborative and innovative team culture that encourages creativity, accountability, and excellence. Serve as more »

discipline with 10+ years post-PhD industry experienceExpert scientific knowledge and experience in the areas of Inflammation and autoimmunity/inflammation is required.Familiarity with validation of drug targets and the exploratory drug development process. Proven biopharmaceutical industry experience developing and leading innovative therapeutic programs and advancing complex technologies.7 years of 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 »

Digital IC Design Engineer based in Cambridgeshire Proven experience in digital IC design Experience in Verilog RTL/System Verilog Testing/Verification and Validation experience For more information or to apply for the Contract Digital IC Design Engineer based in Cambridgeshire, please contact Shammi Choudhury -/01582 878818 quoting more »