25 Permanent Validation Jobs in Yorkshire

support to help members to develop their domain expertise. The Software Architect is responsible for defining the solution and system architecture (including models, decisions, validation, evolution and delivery support), working with the customer and any subcontractors to identify, trade-off and design the overall architecture. Architects assist with the overall 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 »

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 »

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 »

SME in designing & building the Data Warehouse Customising ETL procedures, data mappings, and transformations to coordinate data integration Documenting solutions, tools and processes Implementing validation procedures to ensure high quality of data Collaboration with internal stakeholders About You 3+ years of experience within Data Engineering Ability to work autonomously in 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 »

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 Hannah Oakley on 01246 457711 or email hoakley@ckgroup.co.uk. 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 Key Skills Attention to detail Ability to Plan and organize workload Ability to think creatively and apply new and innovative ideas to bring business more »

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 »

and drive this. Key responsibilities include - * Oversee the administration of change (including documentation). * Supporting change requests ensuring prioritisation, impact, risk, deployment plans and validation steps are understood and documented * Reporting of change KPIs * Communicating change * Working with all the relevant stakeholders and ensure service levels are maintained as your 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 »

smoothly and timely. Create and maintain product 3D CAD and technical drawings using SolidWorks. Ensure all products comply with relevant Technical Standards. Perform product validation tests as required. Coordinate tooling projects with external suppliers. Implement and roll out technical/engineering change processes across all departments. Liaise with third party 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 »

with SQL Server. You must have a thorough knowledge of manual testing procedures and structured test methods and processes. Experience of producing automated regression, validation and performance test suites. Proven experience of testing complex user interfaces. Detailed knowledge of both manual and automated testing methods. Experience of testing database applications. 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 »

reimbursement (NMC or HCPC) - Private medical insurance, life assurance, income protection insurance, pension scheme, personal accident insurance and professional indemnity insurance - Registration/Re-validation support and reimbursement - All bonuses and uplifts are dependent on practicing at the required level and maintenance of quality standards. - Role Summary As a disability more »

SRG is working with a pharmaceutical company in Leeds. We are looking for a QC Validation Analyst to join the team on a contract until December 2025. A fantastic opportunity to strengthen your skills within a pharmaceutical environment working with experienced team members. Job Title: QC Validation analyst Vacancy type … routine analysis of raw materials, in-process samples, and finished products using various analytical techniques including HPLC, UV and GC. Develop, execute, and manage validation protocols and strategies for analytical methods, equipment, and processes in compliance with regulatory requirements and industry standards. Conduct quality control tests to ensure product consistency … with relevant experience Minimum of 1 year of experience in a quality control or analytical laboratory setting (HPLC, GC). Minimum of 1 year validation experience and writing you own protocols. Excellent attention to detail and organisational skills. Ability to work independently and as part of a team. If you 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 »

quality engineering support to other areas within the business. Assisting with design verification and validation. Providing support to inspection teams. Providing support to process validation (IQ, OQ, PQ). Non- conformance investigations. Risk management. Post-market assessment. Reviewing and approving design changes. Ensuring that processes and procedures are compliant. Assisting … of test protocols. Creation and review of technical reports and documentation. Lead cross function teams for improvement projects. Assisting in the completion of the Validation Master Plan. Auditing (internal and external). Equipment maintenance and calibration. Root cause analysis investigations. NCRs CAPA Compliant investigation. Requirements: Educated to degree level in more »

frontend and backend technologies Version Control (Github/bitbucket) Experience working with RESTful APIs and integrating backend services In-depth experience with security, form validation, XSS prevention, database security, session management, input validation and other OWASP guidelines Proven experience in developing scalable web applications using Laravel and other web technologies more »

ContentsLocationAbout the jobBenefitsThings you need to knowApply and further informationLocationLondon York Porton DownAbout the jobJob summaryThe Food, Water and Environmental (FW&E) Microbiology Laboratories are specialist microbiology laboratories within UKHSA. Based in 3 sites across the country, the laboratories are more »

Identify and report potential issues related to design of electronics & electronic performance using reporting tools. Identify & document test cases for New Product Development (design validation testing) Carry out design validation testing on NPD’s. Support the definition of project scope & requirements. Produce product architectures to support cross functional development. Create 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 »

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 »