battery management software and development of functions to meet application requirements. Ensuring compliance with relevant regulatory requirements Conducting function and performance tests, including regulatory validation Developing processes and equipment for battery pack build and commissioning Providing post-delivery support and investigating faults Required Skills: Degree in an engineering discipline Proficiency … ECE Regulation No. 100 Understanding of battery thermal management systems Experience with battery pack test equipment Ability to analyze battery system data for performance validation Desirable Skills: Proficiency in CAN analysis tools such as Vector CANalyzer, Kvaser CANKing, and Peak-Systems PCAN-View Experience with functional safety management (e.g., ISO more »
Acceptance testing with the business users to ensure a high-quality delivery. Research, design, configure, test, document, and manage implementation of system changes. Develop validation test plans, user and system procedures and training materials for customizations, upgrades, and patches. more »
Acceptance testing with the business users to ensure a high-quality delivery. Research, design, configure, test, document, and manage implementation of system changes. Develop validation test plans, user and system procedures and training materials for customizations, upgrades, and patches. Provide expertise for IT projects and Oracle implementation support across the more »
across the organization. Data Management and Reporting: Manage data integrity and accuracy within the ERP system by performing regular audits, data cleansing activities, and validation checks. Generate ad-hoc and scheduled reports to provide insights into key performance indicators (KPIs), operational metrics, and business trends for informed decision-making. Collaboration more »
Electronics Engineering, Computer Science, or related field. Key Skills: Experience in analyzing, designing, constructing, and testing electronic circuits. Proficiency with electronic test equipment and validation methodologies. Strong understanding of analogue and digital circuit design. Proficiency in schematic and PCB design tools. Excellent analytical and problem-solving skills. Knowledge of communication more »
of project activities as directed. Responsible for the development and creation of regular reports on workflow, error reporting and resolution. Undertake detailed analysis and validation of various types of data to inform assessment of organizational performance and help identify opportunities for improvement. This involves analysis of a range of facts more »
subsequent generation of a range of trials documentation/material. About You; You’ll have experience in firing trials and/or system integration & validation You’ll ideally have experience of external trials preparation and conduct You’ll be an excellent communicator possessing the ability to communicate with stakeholders at more »
of the most sophisticated, innovative, and successful Life Sciences companies. Our 750 consultants are working on innovative activities in engineering, production, quality (QA, QC, validation), R&D, and regulatory affairs across Belgium, Switzerland, Germany, Denmark France, and Canada. Thanks to our excellent team, we support manufacturers in all stages of more »
of the most sophisticated, innovative, and successful Life Sciences companies. Our 750 consultants are working on innovative activities in engineering, production, quality (QA, QC, validation), R&D, and regulatory affairs across Belgium, Switzerland, Germany, Denmark France, and Canada. Thanks to our excellent team, we support manufacturers in all stages of more »
Stevenage, England, United Kingdom Hybrid / WFH Options
Omega
Use Case analysis Carry out concept assessments, and design trade studies System architecture design and functional modelling Performance assessment and systems behaviour analysis Verification, Validation, and Certification Model-based engineering techniques Work across the product lifecycle If applicable, lead a team of engineers or assist in mentorship Qualifications & Requirements – Systems more »
NHS Bedfordshire, Luton and Milton Keynes Integrated Care Board
MiDoS related aspects of patient/public/healthcare professional feedback. 11. Ensuring services populated directly on MiDoS are maintained in line with DoS validation process. 12. Championing innovation and improvements to MiDoS to support user community 13. Work closely with NHS 111/IUC and 999 providers to improve more »
the perfect opportunity for you to join our Planning and Environment Support Team. We need you to support the Planning service including for; receipt, validation and recording of a variety of planning and other applications; general enquiries and advice; preparation of planning committee agendas; assisting in the processing of land more »
onto the QMS as necessary. Working alongside CMO’s and in-house specialists to support the production scaling activities. Create and implement QC and validation protocols, ensuring that regulatory processes are followed meticulously. Report any QC pass and fails, monitoring any non-conformance closely and taking corrective action. Strictly adhere more »
of the most sophisticated, innovative, and successful Life Sciences companies. Our 750 consultants are working on innovative activities in engineering, production, quality (QA, QC, validation), R&D, and regulatory affairs across Belgium, Switzerland, Germany, Denmark France, and Canada. Thanks to our excellent team, we support manufacturers in all stages of more »
of the most sophisticated, innovative, and successful Life Sciences companies. Our 750 consultants are working on innovative activities in engineering, production, quality (QA, QC, validation), R&D, and regulatory affairs across Belgium, Switzerland, Germany, Denmark France, and Canada. Thanks to our excellent team, we support manufacturers in all stages of more »
of the most sophisticated, innovative, and successful Life Sciences companies. Our 750 consultants are working on innovative activities in engineering, production, quality (QA, QC, validation), R&D, and regulatory affairs across Belgium, Switzerland, Germany, Denmark France, and Canada. Thanks to our excellent team, we support manufacturers in all stages of … a stimulating environment, with a lot of opportunities for your professional and personal development. Job Summary We are seeking an experienced Commissioning, Qualification, and Validation (CQV) Engineer to join our team. The CQV Engineer will play a crucial role in ensuring that all systems and equipment are properly commissioned, qualified … and validated according to industry standards and regulatory requirements. Responsibilities Lead CQV activities for pharmaceutical manufacturing projects. Develop and execute commissioning, qualification, and validation protocols. Ensure compliance with industry regulations and standards, such as cGMP and FDA guidelines. Collaborate with cross-functional teams to ensure the successful implementation of CQV more »
of the most sophisticated, innovative, and successful Life Sciences companies. Our 750 consultants are working on innovative activities in engineering, production, quality (QA, QC, validation), R&D, and regulatory affairs across Belgium, Switzerland, Germany, Denmark France, and Canada. Thanks to our excellent team, we support manufacturers in all stages of … a stimulating environment, with a lot of opportunities for your professional and personal development. Job Summary We are seeking an experienced Commissioning, Qualification, and Validation (CQV) Engineer to join our team. The CQV Engineer will play a crucial role in ensuring that all systems and equipment are properly commissioned, qualified … and validated according to industry standards and regulatory requirements. Responsibilities Lead CQV activities for pharmaceutical manufacturing projects. Develop and execute commissioning, qualification, and validation protocols. Ensure compliance with industry regulations and standards, such as cGMP and FDA guidelines. Collaborate with cross-functional teams to ensure the successful implementation of CQV more »
Great opportunity for a Validation Engineer to join a leading UK technology manufacturing company that offers excellent training, support, and career development. This new role will suit a ‘hands-on’ Validation Engineer who will enjoy a broad role in a small specialist team working on complex printing equipment (electrical elements … . The role will involve setting up, running, fault finding/problem solving and interpreting the results of a broad variety of hardware product validation projects. The Opportunity Linx Printing Technologies designs and manufactures innovative industrial printing and laser coding equipment used to mark batch info and consumption dates on … packaging within food & beverage, pharmaceutical and related sectors. Based 3-4 days a week at the Linx HQ in PE27 5JL, the Validation Engineer will be part of a small, newly created ‘Value Analysis & Value Engineering’ team looking to drive product cost reduction without sacrificing performance and quality. The specialist more »
Lead Validation Engineer position Working hours are Monday to Friday 40 hours per week Day shift Based close to Stowmarket, Suffolk Permanent position Paying up to £45,000 per annum Our client is recruiting for a Validation engineer to join their team within a permanent basis. Candidates will need to … have exceptional communication skills to fulfil this role. Main duties include ? Leading validation ac... more »
of software operating/automation systems, including, but not limited to, utility, development, and diagnostic software. They perform technical planning, system integration, verification and validation, cost, risk, supportability and effectiveness analyses for total systems. The Embedded Software Engineer will report to the Electronic and Sensor Integration Manager, Energy and will … MV & HV applications. Responsibilities: All aspects of the software development life cycle: Requirements capture Feasibility study and architecture definition Software design & implementation Integration and validation test Firmware development Design and implement embedded software Implementing hardware drivers, interfaces, abstractions, state machines, advanced signal processing algorithms, application modules and unit tests What more »
LEX is currently seeking a Verification and Validation Engineer who will actively engage in hands-on testing of the LEX diagnostic system. You will be working closely with the head of Quality and Engineering team and will be responsible for defining, designing, and executing verification and validation activities for the … read more about LEX here. You’ll develop testing strategies and methodologies with the wider LEX team to complete testing and draft verification and validation protocols. Your contributions will be crucial in ensuring the successful execution of validation and verification activities required ahead of regulatory approval and product launch. Responsibilities … include: Supporting with verification & validation to prepare the LEX System for clinical study and FDA approval. Implement verification and validation test plans and protocols for the system/product, documenting all activities within the Quality Management System (eQMS). Contribute to the development of Work Instructions and Standard Operating Procedures more »
from engine installation into test cells, along with fitting work and component changes, to running test programmes to engineering requirements in certification, performance and validation areas Duties and Responsibilities include, but may not be limited to: Fitting/Assemble of parts and components Using various hand, power tools and lifting … machines. Work on breakdowns and getting test cell to run again. Diagnose and fix a range of faults Run tests via software packages/Validation testing Work from engineering drawings (electrical, mechanical and hydraulic) Keep the work area clean, tidy and safe in line with 5S and total preventative maintenance more »
of the most sophisticated, innovative, and successful Life Sciences companies. Our 750 consultants are working on innovative activities in engineering, production, quality (QA, QC, validation), R&D, and regulatory affairs across Belgium, Switzerland, Germany, Denmark France, and Canada. Thanks to our excellent team, we support manufacturers in all stages of … the System/Business Owner and SME for all compliance platforms, responsible for training users and leading continuous improvement efforts. Lead and represent in validation efforts, ensuring consistency with QMS and corporate policies. Qualifications Bachelor's or Master's degree in Occupational Health and Safety, Construction Management, Engineering, or a more »
of the most sophisticated, innovative, and successful Life Sciences companies. Our 750 consultants are working on innovative activities in engineering, production, quality (QA, QC, validation), R&D, and regulatory affairs across Belgium, Switzerland, Germany, Denmark France, and Canada. Thanks to our excellent team, we support manufacturers in all stages of … the System/Business Owner and SME for all compliance platforms, responsible for training users and leading continuous improvement efforts. Lead and represent in validation efforts, ensuring consistency with QMS and corporate policies. Qualifications Bachelor's or Master's degree in Occupational Health and Safety, Construction Management, Engineering, or a more »
on validating the onboarding of new computerised systems to meet the needs of a rapidly growing customer base, as well as supporting the ongoing validation of expanding software systems. The position involves close collaboration with IT to establish data integrity requirements and evaluate the effectiveness of implemented solutions. Responsibilities: Support … the implementation of a risk-based approach to the validation of computerised systems to ensure compliance with Annex 11, 15 and GAMP 5. Preparing and execution of protocols for configuration, functional, end-to-end and user acceptance testing. Preparing and maintaining validation plans, assisting system owners with impact assessments, risk … assessments and identifying validation requirements for computerised systems projects. Assist in the authoring of User Requirement Specifications. Experience: Sufficient prior experience of validating computer systems in a Biopharmaceutical setting. A Degree (or equivalent experience) in a Science or related discipline . Experience in the validation of GxP software and Laboratory more »
