2,126 to 2,150 of 2,475 Validation Jobs in the UK

downstream processes. • Develop Quality Plans for the implementation of new processes, enhancements, or continuous improvements to existing processes • Prepare documentation, plan, schedule, and execute validation activities of the QMS software utilizing a risk-based approach. Ensure compliance to medical device industry regulations, including 21 CFR Part 11, EU GMP Annex … processes. • Support Regulatory audits/inspections as a Subject Matter Expert (SME). Your Profile: • Minimum 5 years of related experience in QMS Software Validation with a Bachelor's degree; or 3 years of related experience with a Master's degree. NOTE: A diploma, certificate or other evidence of formal ...

downstream processes. • Develop Quality Plans for the implementation of new processes, enhancements, or continuous improvements to existing processes • Prepare documentation, plan, schedule, and execute validation activities of the QMS software utilizing a risk-based approach. Ensure compliance to medical device industry regulations, including 21 CFR Part 11, EU GMP Annex … processes. • Support Regulatory audits/inspections as a Subject Matter Expert (SME). Your Profile: • Minimum 5 years of related experience in QMS Software Validation with a Bachelor's degree; or 3 years of related experience with a Master's degree. NOTE: A diploma, certificate or other evidence of formal ...

downstream processes. • Develop Quality Plans for the implementation of new processes, enhancements, or continuous improvements to existing processes • Prepare documentation, plan, schedule, and execute validation activities of the QMS software utilizing a risk-based approach. Ensure compliance to medical device industry regulations, including 21 CFR Part 11, EU GMP Annex … processes. • Support Regulatory audits/inspections as a Subject Matter Expert (SME). Your Profile: • Minimum 5 years of related experience in QMS Software Validation with a Bachelor's degree; or 3 years of related experience with a Master's degree. NOTE: A diploma, certificate or other evidence of formal ...

downstream processes. • Develop Quality Plans for the implementation of new processes, enhancements, or continuous improvements to existing processes • Prepare documentation, plan, schedule, and execute validation activities of the QMS software utilizing a risk-based approach. Ensure compliance to medical device industry regulations, including 21 CFR Part 11, EU GMP Annex … processes. • Support Regulatory audits/inspections as a Subject Matter Expert (SME). Your Profile: • Minimum 5 years of related experience in QMS Software Validation with a Bachelor's degree; or 3 years of related experience with a Master's degree. NOTE: A diploma, certificate or other evidence of formal ...

downstream processes. • Develop Quality Plans for the implementation of new processes, enhancements, or continuous improvements to existing processes • Prepare documentation, plan, schedule, and execute validation activities of the QMS software utilizing a risk-based approach. Ensure compliance to medical device industry regulations, including 21 CFR Part 11, EU GMP Annex … processes. • Support Regulatory audits/inspections as a Subject Matter Expert (SME). Your Profile: • Minimum 5 years of related experience in QMS Software Validation with a Bachelor's degree; or 3 years of related experience with a Master's degree. NOTE: A diploma, certificate or other evidence of formal ...

downstream processes. • Develop Quality Plans for the implementation of new processes, enhancements, or continuous improvements to existing processes • Prepare documentation, plan, schedule, and execute validation activities of the QMS software utilizing a risk-based approach. Ensure compliance to medical device industry regulations, including 21 CFR Part 11, EU GMP Annex … processes. • Support Regulatory audits/inspections as a Subject Matter Expert (SME). Your Profile: • Minimum 5 years of related experience in QMS Software Validation with a Bachelor's degree; or 3 years of related experience with a Master's degree. NOTE: A diploma, certificate or other evidence of formal ...

systems, and potentially SAP. Ensure data quality, governance, and lineage tracking throughout the project. Required Skills ETL/ELT pipeline design and data validation frameworks. Advanced Python (pandas, numpy, boto3) and SQL (complex queries, optimisation). Experience with AWS Glue , Step Functions , and event-driven architectures . Knowledge of vector … databases , embeddings, and semantic search strategies. Familiarity with document parsing libraries (PyPDF2, pdfplumber, Textract) and OCR tools. Understanding of data governance , schema validation, and master data management. Strong grasp of real-time vs batch processing trade-offs . Beneficial Experience CockroachDB deployment and management. PySpark or similar for large-scale ...

downstream processes. • Develop Quality Plans for the implementation of new processes, enhancements, or continuous improvements to existing processes • Prepare documentation, plan, schedule, and execute validation activities of the QMS software utilizing a risk-based approach. Ensure compliance to medical device industry regulations, including 21 CFR Part 11, EU GMP Annex … processes. • Support Regulatory audits/inspections as a Subject Matter Expert (SME). Your Profile: • Minimum 5 years of related experience in QMS Software Validation with a Bachelor's degree; or 3 years of related experience with a Master's degree. NOTE: A diploma, certificate or other evidence of formal ...

downstream processes. • Develop Quality Plans for the implementation of new processes, enhancements, or continuous improvements to existing processes • Prepare documentation, plan, schedule, and execute validation activities of the QMS software utilizing a risk-based approach. Ensure compliance to medical device industry regulations, including 21 CFR Part 11, EU GMP Annex … processes. • Support Regulatory audits/inspections as a Subject Matter Expert (SME). Your Profile: • Minimum 5 years of related experience in QMS Software Validation with a Bachelor's degree; or 3 years of related experience with a Master's degree. NOTE: A diploma, certificate or other evidence of formal ...

downstream processes. • Develop Quality Plans for the implementation of new processes, enhancements, or continuous improvements to existing processes • Prepare documentation, plan, schedule, and execute validation activities of the QMS software utilizing a risk-based approach. Ensure compliance to medical device industry regulations, including 21 CFR Part 11, EU GMP Annex … processes. • Support Regulatory audits/inspections as a Subject Matter Expert (SME). Your Profile: • Minimum 5 years of related experience in QMS Software Validation with a Bachelor's degree; or 3 years of related experience with a Master's degree. NOTE: A diploma, certificate or other evidence of formal ...

downstream processes. • Develop Quality Plans for the implementation of new processes, enhancements, or continuous improvements to existing processes • Prepare documentation, plan, schedule, and execute validation activities of the QMS software utilizing a risk-based approach. Ensure compliance to medical device industry regulations, including 21 CFR Part 11, EU GMP Annex … processes. • Support Regulatory audits/inspections as a Subject Matter Expert (SME). Your Profile: • Minimum 5 years of related experience in QMS Software Validation with a Bachelor's degree; or 3 years of related experience with a Master's degree. NOTE: A diploma, certificate or other evidence of formal ...

downstream processes. • Develop Quality Plans for the implementation of new processes, enhancements, or continuous improvements to existing processes • Prepare documentation, plan, schedule, and execute validation activities of the QMS software utilizing a risk-based approach. Ensure compliance to medical device industry regulations, including 21 CFR Part 11, EU GMP Annex … processes. • Support Regulatory audits/inspections as a Subject Matter Expert (SME). Your Profile: • Minimum 5 years of related experience in QMS Software Validation with a Bachelor's degree; or 3 years of related experience with a Master's degree. NOTE: A diploma, certificate or other evidence of formal ...

downstream processes. • Develop Quality Plans for the implementation of new processes, enhancements, or continuous improvements to existing processes • Prepare documentation, plan, schedule, and execute validation activities of the QMS software utilizing a risk-based approach. Ensure compliance to medical device industry regulations, including 21 CFR Part 11, EU GMP Annex … processes. • Support Regulatory audits/inspections as a Subject Matter Expert (SME). Your Profile: • Minimum 5 years of related experience in QMS Software Validation with a Bachelor's degree; or 3 years of related experience with a Master's degree. NOTE: A diploma, certificate or other evidence of formal ...

downstream processes. • Develop Quality Plans for the implementation of new processes, enhancements, or continuous improvements to existing processes • Prepare documentation, plan, schedule, and execute validation activities of the QMS software utilizing a risk-based approach. Ensure compliance to medical device industry regulations, including 21 CFR Part 11, EU GMP Annex … processes. • Support Regulatory audits/inspections as a Subject Matter Expert (SME). Your Profile : • Minimum 5 years of related experience in QMS Software Validation with a Bachelor’s degree; or 3 years of related experience with a Master’s degree. NOTE: A diploma, certificate or other evidence of formal ...

disciplines. Systems Engineer essential skills Strong experience across the systems engineering lifecycle Requirements capture and management, including use of DOORS System design, verification and validation experience Background working with multi disciplined engineering teams Ability to produce clear, concise technical documentation Degree level qualification in a relevant engineering discipline Eligible … your application to our client in conjunction with this vacancy only. Key skills: Systems Engineer, Systems Engineering, Product Development, Requirements Management, DOORS, Verification and Validation, Cyber, Information Assurance, Defence ...

prem data environments, and integrate diverse datasets from external vendors, trading systems and internal sources. The role also involves implementing automated data validation processes, optimising data quality and performance, and ensuring high availability across all systems. Working closely with the portfolio manager, researchers and engineers, you will enable data-driven … expertise in Python and modern ETL frameworks Experience designing and maintaining cloud-based data pipelines (e.g. AWS, Airflow, Snowflake) Deep understanding of data modelling, validation, and pipeline resilience Familiarity with financial or alternative datasets preferred ...

prem data environments, and integrate diverse datasets from external vendors, trading systems and internal sources. The role also involves implementing automated data validation processes, optimising data quality and performance, and ensuring high availability across all systems. Working closely with the portfolio manager, researchers and engineers, you will enable data-driven … expertise in Python and modern ETL frameworks Experience designing and maintaining cloud-based data pipelines (e.g. AWS, Airflow, Snowflake) Deep understanding of data modelling, validation, and pipeline resilience Familiarity with financial or alternative datasets preferred ...

ensure compliance with security, GDPR, and audit requirements across all interfaces. Collaboration: Partner with the Data Lead to ensure secure and accurate data flow, validation, and reconciliation. Essential Skills & Experience SC Clearance is MANDATORY for this role. 7-10 years' experience in integration architect roles on ERP/HCM programmes … delivering integration strategies in a large-scale enterprise environment. Demonstrated ability to mobilise and deliver multiple integrations in parallel. Familiarity with data transformation, validation, and data reconciliation processes. Strong stakeholder management with IT, vendors, and business owners. Next Steps This is an Inside IR35 contract with a high likelihood ...

perception, and high-level planning. Configure and extend robotic middleware and interfaces (e.g., ROS 2 or similar) Contribute to and leverage simulation, modelling, and validation of robotic systems in virtual environments (e.g., Nvidia Isaac, Gazebo) and physical labs. Collaborate with cross-disciplinary teams to combine software, hardware, and intelligence. Contribute … frameworks, navigation, or multi-sensor integration. Familiarity with real-time communication protocols (EtherCAT, CAN, Modbus) or PLCs. Strong Mechatronics understanding Exposure to simulation and validation tools for robotic systems. Knowledge of Machine Learning principles for perception or control. Offices and Lab located in Oxford. Hybrid working c.3 days in office ...

maintain robust ETL/ELT pipelines for structured and unstructured data Hands-on experience with AWS Glue and AWS Step Functions Implementation of data validation, data quality frameworks, and reconciliation checks Strong error handling, monitoring, and retry strategies in production pipelines Experience with incremental data processing patterns (CDC, watermarking, upserts … data processing best practices SQL (advanced): complex queries, performance tuning, and query optimization Data Quality & Governance Data profiling and ongoing quality assessment Schema validation and evolution strategies Data lineage tracking and observability Understanding of Master Data Management (MDM) concepts Domain Knowledge Product catalog data models and hierarchies E-commerce data ...

maintain robust ETL/ELT pipelines for structured and unstructured data Hands-on experience with AWS Glue and AWS Step Functions Implementation of data validation, data quality frameworks, and reconciliation checks Strong error handling, monitoring, and retry strategies in production pipelines Experience with incremental data processing patterns (CDC, watermarking, upserts … data processing best practices SQL (advanced): complex queries, performance tuning, and query optimization Data Quality & Governance Data profiling and ongoing quality assessment Schema validation and evolution strategies Data lineage tracking and observability Understanding of Master Data Management (MDM) concepts Domain Knowledge Product catalog data models and hierarchies E-commerce data ...

vendor management Act as the single point of contact for technology projects, ensuring on-time, on-budget delivery Oversee compliance activities including system validation and change control Partner with global IT teams to leverage existing platforms and capabilities Engineering & Operational Leadership Support engineering strategy, CAD oversight, and design reviews Lead … laboratories Skills & Attributes Excellent stakeholder engagement and communication Ability to bridge functional business needs with IT/engineering solutions Skilled in system validation and change control processes Strong leadership capability in matrix organisations Able to influence, motivate and guide teams through change Strong documentation, analytical and problem-solving skills ...

vendor management Act as the single point of contact for technology projects, ensuring on-time, on-budget delivery Oversee compliance activities including system validation and change control Partner with global IT teams to leverage existing platforms and capabilities Engineering & Operational Leadership Support engineering strategy, CAD oversight, and design reviews Lead … laboratories Skills & Attributes Excellent stakeholder engagement and communication Ability to bridge functional business needs with IT/engineering solutions Skilled in system validation and change control processes Strong leadership capability in matrix organisations Able to influence, motivate and guide teams through change Strong documentation, analytical and problem-solving skills ...

countries. We’re expanding our Integrations team and looking for an Integration Solutions Specialist who will lead customers through the setup, configuration, and validation of their integrations with Papaya. This role is a blend of data analysis, workflow design, technical onboarding, and customer-facing guidance - not a software development … Guide customers through Papaya’s self-service integration tools, enabling them to manage routine changes independently. Diagnose and resolve data inconsistencies, transformation issues, and validation errors. Collaborate with Product, Support, and Engineering to resolve complex integration cases and prevent recurring issues. Provide product feedback based on customer experience to improve ...

countries. We’re expanding our Integrations team and looking for an Integration Solutions Specialist who will lead customers through the setup, configuration, and validation of their integrations with Papaya. This role is a blend of data analysis, workflow design, technical onboarding, and customer-facing guidance - not a software development … Guide customers through Papaya’s self-service integration tools, enabling them to manage routine changes independently. Diagnose and resolve data inconsistencies, transformation issues, and validation errors. Collaborate with Product, Support, and Engineering to resolve complex integration cases and prevent recurring issues. Provide product feedback based on customer experience to improve ...