1 to 25 of 32 Permanent Validation Jobs in Yorkshire

product to design specifications. Ensure suitable documentation and training has been devised and is available to complete all tasks required in the manufacture and validation of Product. Conduct any analytical or empirical studies required to support proposed changes. Liaison directly with Customers and or Suppliers as required by the function. more »

functions within the Digital Forensics Unit (DFU). You will also assist in the development and maintenance of Technical Standard Operating Procedures (SOPs) and validation techniques within the DFU, ensuring that all processes maximise evidential yield. The successful candidate will be responsible for assisting the Quality Manager in maintaining a more »

Experience with ARM processors, Xilinx/Altera(Intel) VHDL FPGA design. Understanding of Design for Manufacture. Understanding of RF design techniques. Experience of product validation and certification for international markets. Remuneration: £50,000 - £60,000 Pension 30 days holidays + bank holidays If you are interested in this position please more »

Engineering, Production, Internal sales and Quality teams, the role is varied and would suit someone with a broad technical background. Responsibilities will include technical validation as part of new product introduction, liaising with external test houses and preparation of technical documentation. Previous automotive or lighting industry experience would be an more »

of coding best practices and design patterns and experience with code and data versioning, dependency management, code quality and optimisation, error handling, logging, monitoring, validation and alerting. You have experience in writing well tested object-oriented Python. You have experience with using CI/CD tooling to analyse, build, test more »

. Broad manufacturing knowledge of different materials and processes in particular sheet metal forming and bending , machined metal, plastic injection moulding. Proficient in design validation and analysis Experience of material selection for ideal product realisation. Experienced in Design for Manufacture (DFM). Product Data Management (PDM) and engineering change management. more »

A working knowledge and practical experience using LC-MS/MS. Key Words: Small Molecule | Study Manager | Team Lead | Bioanalysis | GLP | GCP | Method Development | Validation | Sample Analysis | Regulatory Compliance | LC-MS/MS Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People more »

the suggested solutions Deep experience in not only CPQ with touchpoints to CRM (Salesforce preferably) but also quote to contract lifecycle (Contract authoring, contract validation, renewal, amendments, recurring Billing etc.) Exposure to SaaS Billing automation tool is preferable plus (like Oracle RMCS/OBRM, Zuora, Billing Platform, Stripe, Salesforce, SAP more »

a full-time staff position based in our Chesterfield office, with an excellent salary and benefits package. Responsibilities/Duties Leading the build, configuration, validation, and delivery of cutting-edge digital manufacturing systems. Liaising with customers to gather and translate project and process improvement requirements into functional design and detailed … and ASP.Net Core. Designing and developing production reports in AVEVA Historian and AVEVA PI System. Providing technical and automation operational support to Engineering, Manufacturing, Validation and Facilities departments. Co-ordinating and supporting project commissioning activities. Enforcing technical and project execution best practices. Mentoring and training of junior engineers. Working closely more »

Role Overview We are seeking a Lead Test Engineer to Support the verification and validation of the ABD Solutions autonomy stack. This will involve the development of highly automated test equipment to automatically verify all parts of the autonomy stack. These include functional, functional safety, and cyber security requirements. This … techniques and measured to overcome complex challenges. This is a hands-on, fast-paced, collaborative development environment. What will you be doing? Own the Validation and Verification Strategy for ABDS products, leading planning effort for each phase of the V&V life cycle. Derive test cases to demonstrate the functionality more »

of coding best practices and design patterns and experience with code and data versioning, dependency management, code quality and optimisation, error handling, logging, monitoring, validation and alerting. You have experience in writing well tested object-oriented Python. You have experience with using CI/CD tooling to analyse, build, test more »

a fine chemical or pharmaceutical industry role. HPLC and GC experience. - Experience of working in a GMP environment/method development experience/cleaning validation experience. To Apply: For more information, or to apply for this QC Analyst position please contact James Horne on 0191 370 6483 or email jhorne more »

What Are We Looking For? RSE Controls, a subsidiary of Saftronics, is looking to recruit a Senior Software Design Engineer that will be responsible for the development, commissioning and support of automation and control systems. RSE Controls are a specialist more »

to identify trends and drive improvements Compliance. Oversight and management of vendor management program for ensuring supply compliance Oversight and management of computer systems validation program to ensure compliance Oversight and management of regional data privacy program to ensure compliance Representation of company at client meetings, regulatory audits, and other more »

Lead Compliance Analyst to ensure the provision of accurate and timely regulatory submissions to Ofgem. You will also be accountable for the extraction and validation of connections data in preparing of all regulatory returns. Along with a competitive salary between £31,906 - £36,854 we also offer great benefits such … in other business areas to determine project information •Maintaining accurate data on the connections projects within the connections systems. •Support with data extraction and validation routines •Coordination of the cancellation of projects which are outside of project milestones. •Data assurance routines in line with Ofgem process. •Development of reports within … Management of existing reports within both the PowerBi and CRM Oracle reporting tool Key Competencies •Creation of analytical reports using tools like Power Bi •Validation of data to aid decision making processes •Utilising reporting software to improve outputs •Strong planning and organisation skills to ensure timely submission of information •Collaborative more »

slides for examination by others. In order to achieve the required turnaround times the work must be performed with both speed and accuracy. Technical validation and designated clinical authorisation of results as determined by specialist area Communication of complex, technical information to users of the service Use of LIMS to … slides for examination by others. In order to achieve the required turnaround times the work must be performed with both speed and accuracy. Technical validation and designated clinical authorisation of results as determined by specialist area Communication of complex, technical information to users of the service Use of LIMS to more »

summary Working across Communicable Diseases the post holder will contribute to maintaining data quality throughout. This will be achieved by generating data reports for validation at specified intervals and in line with Trust reporting requirements. From these reports, the post holder will be required to identify any trends/problems … all required reports within set reporting timescales. The post holder will support the supervisor and other members of the management team by undertaking data validation checks and corrections where necessary, but where appropriate they will empower admin teams to validate their own error reports. The post holder will also take more »

Job summary We have a rare and exciting opportunity to join a newly created in-house Data Quality Validation Team, that will be responsible for the validation of all patient pathways. The Trust is making a significant investment in the team with the creation of 17 new posts. This is … a new model and provides a chance to be part of shaping the future of validation in preparation for the new EPR (Electronic Patient Record). You will be joining the Team at an exciting time and will take a lead role in ensuring that the Trust has high quality … team, the Trust and the wider NHS. Main duties of the job The main duties of the role centre around the undertaking of data validation and updating data within Trust systems, primarily within the PAS (Patient Administration System. Expediting patients for further action. You will identify any themes in data more »

of coding best practices and design patterns and experience with code and data versioning, dependency management, code quality and optimisation, error handling, logging, monitoring, validation and alerting. You have experience in writing well tested object-oriented Python. You have experience with using CI/CD tooling to analyse, build, test more »

the department, as well as being a point of contact for queries from the team. They do this by conducting regular, professional audits and validation of the work of the department and feeding results back to the team to improve our practice. Main duties of the job The successful applicant more »

customers to identify areas for improvement through the use of automation and data analytics technology. Providing technical and automation operational support to Engineering, Manufacturing, Validation and Facilities departments. Co-ordinating and supporting project commissioning activities. Mentoring and training of junior engineers. Researching new technologies and trends in Industrial Automation and more »

Act, Freedom of Information Act) and their application. Understanding of a wide range of data quality issues and the application of the appropriate data validation techniques. Expert knowledge of a variety of analytical tools and techniques, including but not limited to SQL, Python, Excel, PowerBI, R. The post holder will more »

the setting up and chairing of specification workstream working groups ? Managing processes to ensure the analysis, evaluation and testing of options, including assessment and validation of proposals In addition, the Specification Manager will be expected to work flexibly to support the delivery of business requirements. A quality competency we are more »

be considered as the role can offer hybrid working if preferred. Main duties of the role will be to coordinate and lead Computer System Validation (CSV) activities to ensure computerised and automation systems and software are in full compliance with regulatory requirements, company policies and procedures. Serve as the subject … with all relevant Safety, Health and Environmental (SHE), Good Manufacturing Practice (GMP), Data Integrity (DI), quality and best practice requirements Preparation and approval of validation documentation or management of the process (fulfilling the Quality Assurance role) in accordance with the relevant processes (e.g. Quality Management System) To monitor project and … or support activities to ensure systems are fit for purpose, that significant risks are identified and mitigated, and that the approach and rigor of validation is in proportion to the risks the systems present to regulated business processes To provide and or facilitate quality assurance oversight for the automation of more »

completion of tasks either by execution or work of other team members. • Be accountable for measurement system planning, development, and work with quality on validation for assigned programs. This includes FAIR, PPAP, equipment selection (including capacity), fixturing, CMM programs, gauges, documentation, and other supporting elements to ensure a thorough and … interpretation, GD&T, Design for Manufacturing/Assembly (DFMA), and process documentation. • Working knowledge and expertise in new product and process introduction (NPPI) and validation (PPAP, FAIR, PFMEA/DFMEA, MSA, etc). Experience in medical or aerospace environments are ideal. • Basic lean and/or industrial engineering knowledge and more »