9 of 9 Validation Jobs in Swindon

of internal and external sub-contractors with levels of delegated authority.SE expertise across the engineering life cycle V-Model or equivalent from initial concepts, requirements, design, implementation, integration, verification, validation, maintenance, and supportability. Experienced in management of technical and project risks. Qualifications for the Principal Systems Engineer Ideally you will hold a degree or equivalent within an Engineering Discipline however More ❯

and deliver tailored solutions. Guide and mentor junior engineers while contributing to the continuous improvement of internal design processes. Collaborate with suppliers to select technologies and support broader silicon validation, test, and qualification efforts. Qualifications Degree in Electronics, Physics, or related field (Master's or PhD preferred). Proven experience in analog and digital IC design, including physical design considerations More ❯

to design new and modify existing products Analyse scope and requirements, identify and solve problems Where required take responsibility for the entire product life cycle, including specification, architecture, design, validation, production release and customer support for released products Provide innovative solutions to technical problems Work with-in an agile multi-disciplined team Be a key participant of design reviews Support More ❯

Collaborate with remote teams to design and implement solutions meeting regulatory/security requirements. Perform troubleshooting and debugging of communications systems (including TETRA) to resolve issues. Conduct testing and validation of software and 3rd party hardware components of communications systems Prepare technical documentation, including user manuals, development reports, and system specifications. Stay updated with the latest advancements in communications standards More ❯

Whilst the two areas specified above will be the immediate priority work, beyond this there are lots of opportunity to be involved in other research, development, testing, analysis, and validation activities across the air platform/mission survivability modelling and simulation domain. This unparalleled access through our customer will help accelerate you as a Subject Matter Expert (SME), allowing you More ❯

that champions continuity, security, and recovery across critical infrastructure. Your new role As the IT/OT Continuity and Recovery Senior Specialist, you'll lead the development, implementation, and validation of robust continuity and disaster recovery strategies across both IT and OT environments. You'll be responsible for: Designing and maintaining a centralised IT/OT Continuity Plan and Backup More ❯

will be provided to a BI Analyst to create dashboards etc with Power BI. Integrate data from various applications such as ERP, IoT devices and external sources Implement data validation, cleansing and quality assurance protocols Support existing Jitterbit ETL/legacy applications while Microsoft fabric is implemented Ensure the correct data enables the business to make better data led decisions More ❯

of data and understand complex weapon systems and high-fidelity modelling tools will be key.You may also be required to develop bespoke analysis tools and support the verification and validation of your advice with wider stakeholders. The invaluable experience youll bring, to help us achieve more: Essential: Degree level or equivalent in a Science or Engineering discipline (e.g. Mathematics, Physics … solutions to real-world problems. Electro-Optic sensor systems, image processing or missile systems. Developing or using synthetic models of sensors, image processing techniques or air vehicle dynamics. Verification, validation and test of systems or synthetic environments. Experience using Simulink. Experience of using MATLAB or similar tools to clean, process and analyse simulation output data. Track record of independently generating More ❯

Quality Assurance (QA) Validation- Contract Role (Sterile Pharma, Swindon - Onsite) Your new company A leading pharmaceutical organisation specialising in sterile manufacturing is seeking a skilled QA Validation expert to support a high-impact project. With a strong commitment to quality and regulatory compliance, this company offers a dynamic and collaborative environment for experienced contractors. Your new role As a Quality … Assurance QA Validation Expert, you will serve as a Document Reviewer for Commissioning, Qualification, and Validation (CQV) activities. You'll be responsible for reviewing technical documentation related to equipment used in sterile pharmaceutical manufacturing, ensuring alignment with cGMP, FDA, and EMA standards. You'll collaborate with cross-functional teams to identify gaps, recommend corrective actions, and support continuous improvement efforts. … What you'll need to succeed Experience in a quality assurance validation role within sterile pharmaceutical manufacturing Strong knowledge of FDA, EMA, and cGMP regulations Exceptional attention to detail and analytical skills Proficiency in document management systems and quality management software Excellent communication skills and the ability to work independently Familiarity with risk-based validation approaches What you'll get More ❯