Cardiff, Wales, United Kingdom Hybrid / WFH Options
BJSS
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 »
Swansea, Wales, United Kingdom Hybrid / WFH Options
BJSS
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 »
Processing Work Stream Leader for cross-functional Projects, working closely with Sales/Marketing, Production & Engineering, Quality & Occupational Health/Safety Manage the required Validation works (Stability Tests and all required external User trials, Challenge tests and Product Assessments (e.g. CPSR)). Support the product transfer of new products from more »
Responsibilities Preparing standards for calibration and quality purposes Conducting analysis and reporting of results to company methods and procedures Control of instrument and method validation Ensuring all analytical procedures comply with accreditation quality standards Ensuring adherence to good lab practice and housekeeping at all times Instrument calibration, routine maintenance and more »
control. Thorough knowledge of cGMP (MHRA, EMEA, FDA, MHLW, ANVISA, Health Canada, etc.) and regulatory expertise in those related to analytical method development and validation (ICH, USP, EP, JP, etc.) Excellent verbal and written communication skills, experience with scientific technical writing including authoring and revising SOP's and technical reports. more »
Immunoassay techniques • Document procedures undertaken and apply QC procedures to ensure their accuracy • Produce and review/approve relevant documentation such as protocols, procedures, validation/study reports, SOP’s, CAPA’s, file notes. • Provide technical advice to business development and participate in laboratory-related discussions with auditors, Sponsors and more »
test solutions primarily in C and C#. Creation of design documentation. Practical hands-on experience working with and debugging embedded systems. Overseeing the team. Validation of tuning production firmware Experience with the following will be needed: Has strong knowledge of C language programming for embedded platforms. Has experience in conducting more »
supporting documentation is clear, relevant, organised and centrally available. Lead and organise technical reviews with the supplier, assessing supplier control processes and ensuring correct validation of all PPAP/quality documentation. Working with the supplier, providing technical leadership to ensure samples and pre-production parts are delivered appropriately and on more »
with internal and external suppliers and customers Work simultaneously across a variety of different projects & activities Champion innovative and efficient methods of test and validation Completion of design activities including CAD, FMEA, calculations & tolerance layouts Participate in technical design reviews & support of IPR activities Knowledge, Skills & Experience: Mechanical Engineering Degree more »
and coordinate system development tasks to include design, integration, formal testing, and transitions into production. Undertake meticulous functional, non-functional and interface verification and validation of systems. Prepare verification and validation requirements compliance matrices and reports. Create and maintain programmatic and technical documentation. Manage and document system configurations. Support user more »
implement new best practices and processes within the company. Manage system development tasks including design, integration, testing, and production transitions. Conduct rigorous verification and validation of systems, both functional and non-functional. Prepare compliance matrices and reports to ensure verification and validation requirements are met. Generate and maintain technical documentation more »
Newport, Shropshire, West Midlands, United Kingdom
Omega Leeds
with the Engineering Project Manager, in all aspects of managing project engineering services to support manufacturing operations. To include the specification, installation, commission and validation of equipment within liquid-based manufacturing. Key Responsibilities: Senior Projects Engineering Lead– Process Engineering Lead Process Understanding and Project Engineering Capability and Engineering Projects in … and processing Assist process improvement projects on site, ensuring appropriate technical change control to deliver robust, sustainable solutions Leading CAPEX and improvement projects, RCAs, validation activities etc Investigate new technologies for plant/equipment efficiency improvements Ensure compliance with site standard operation procedures Role Qualifications & Requirements: Senior Projects Engineering Lead more »
made permanent) A global company at the forefront of its tech sector are looking for an Engineering Technician to join their hardware test and validation team in Cardiff. The successful candidate will be responsible for test operations, which validate products developed by the engineering teams prior to production/industrialisation. … manual test operations and use automated test processes including, but not limited to, jigs and fixtures, interfaces and graphical user interfaces to support product validation processes and to improve tests. This contract would be suitable for an apprentice trained, or experienced, electronics technician, a recent electronics graduate, or an individual more »
