Trabajos document preparation en MaidenheadCrear alertas

DescriptionJoin us, be part of more.We're so much more than an energy company. We're a family of brands revolutionising how we power the planet. We're energisers. One team of 21,000 colleagues that's energising a greener, fairer future by creating an energy system that doesn't rely on fossil fuels, whilst living our powerful commitment to igniting positive change in our communities. Here, you can find more purpose, more passion, and more potential. That's why working here is #MoreThanACareer. We do energy differently - we do it all. We make it, store it, move it, sell it, and mend it.Main Purpose of the roleReporting to the Group Sustainability Transformation Director, the Sustainability Transformation Manager will play a critical role in the development and implementation of the organization's sustainability initiatives ensuring compliance with environmental regulations and standards including but not limited to the Corporate Sustainability Reporting Directive and the EU Sustainability Taxonomy (CSRD) and the Corporate Sustainability Due Diligence Directive (CSDDD). The successful candidate will also be responsible for planning and co-ordinating programme management, ensuring requirements are scoped, developed and translated into plans whilst ensuring delivery controls are in place (e.g. managing risks, issues, finances and timelines).This position requires a dynamic and results-oriented individual who is passionate about sustainability and has a strong understanding of environmental management, social impact, systems, regulations and driving change within business through well managed programmes.Key Accountabilities of the role Support the CSRD Programme Director in the development and execution of relevant group-wide ESG compliance and change programmes for ESG requirements such as CSRD/CSDDDSupport the development and implementation of CSRD/CSDDD processes across the group, ensuring compliance with all relevant regulations and standards in a consistent and coherent way, including alignment with other relevant programmes such as Risk & Controls Upgrade & Enterprise Risk ManagementLead the work across all functions and business units to coordinate the specification, identification, development and implementation of appropriate mechanisms for relevant data/metric capture including procuring and implementing new data systems where necessary, including for specific workstreams applicable to CSRDLead on ESG reporting system transformation seeking opportunities to drive efficiency and quality through automation, systems integration, AI etcWork across the businesses and key functions to help establish ESG policies, goals and targets required by ESG regulationsLead on project management ensuring requirements are scoped, developed and translated into plans whilst ensuring delivery controls are in place. Develop and document key milestones and cascade these through other workstreams and ensuring visibility and management against themPrepare materials for, and help run Project Boards / Working groups and Exec Steer Co including the monitoring, review and reporting on all project and programme attributesLead on benchmarking of published peer reports to collect and disseminate relevant information to enable a comparison of material impacts, risks and opportunities as well as the approach to meeting regulatory datapointsLead the development of regulatory artefacts into structured spreadsheets to be used for gap analysis, implementation tracking and subsequent xBRL taggingWorking with internal stakeholders oversee the preparation and submission of compliant annual reporting in accordance with CSRD/CSDDD requirementsSupport and facilitate internal communication and education on CSRD/CSDDD and related topicsWork with Group Finance to facilitate third party external assurance to prepare Centrica for successful limited assuranceDevelop and maintain strong relationships with key internal stakeholdersWorking with the Legal team, monitor and advise on imminent and future Environmental/Social/ESG regulatory changes, FAQs and best practicesThe position will: Routinely collaborate with peers, business and functional management teams, including GBS across the group to develop and integrate Environmental/ESG requirements into business operations and as part of delivery governanceAttend routine cross-functional CSRD/CSDD working groupsCollaborate daily across all business units and functions, spanning numerous levels working with senior leaders and subject matter expertsWork closely with the HSE, Environmental, Responsible Business, People, Legal and Finance teamsWork Experience & Functional/Technical Skills required Knowledge: In-depth knowledge of sustainability principles, environmental/social regulations, compliance standards, and best practices, including CSRD, EU Taxonomy and CSDDDProgramme Management: A minimum of 3 years' experience delivering large projects within a structured project delivery life cycleAnalytical Skills: Strong analytical and problem-solving skills, with the ability to interpret and present complex data effectivelyReporting: Experience in ESG data collection and analysis, development of metrics and key performance indicators (KPIs), reporting systems and disclosuresExperience in automation of reporting processes and disclosures, including the implementation of new reporting systemsCommunication Skills: Excellent verbal and written communication skills, with the ability to engage and influence stakeholders at all levels, as well as simplify complex technical messagesLeadership: Demonstrated team management skills, with the ability to inspire and motivate others in a matrix organisationProject Management: Strong project management skills, with the ability to manage multiple projects simultaneously and deliver results within deadlinesAttention to Detail: High degree of accuracy and attention to detail in all aspects of workEducation and Certifications required to perform the role Bachelor's degree in Sustainability, Environmental Science, ESG or other relevant fieldAt least 3 years of experience in ESG, sustainability, or related roles, with a proven track record of successful programme development and implementationProject Management Qualifications such as Prince II, APM or Agile desirableKey Competencies required to perform the role A proactive and collaborative manager with a passion for sustainability and a commitment to driving positive changeAbility to work across a diverse set of stakeholders, motivating and influencing without direct authorityAbility to work in an agile way, comfortable with dealing with ambiguity and navigating varying levels of stakeholder successfullyMust be able to work under pressure and to constantly changing deadlinesAbility to plan effectively and to think beyond the bounds of the initiative being delivered to ensure wider change delivery successAbility to challenge when something isn't right, or when something is not clearly understood to enable successful delivery and to make early intervention possibleFunctionally IT literate with an ability to communicate effectively with both IT and non- IT professionalsTechnically competent in using appropriate functionality in Microsoft Office data, presentation and planning tools to support and execute the job requirementsWhy should you apply?We're not a perfect place - but we're a people place. Our priority is supporting all of the different realities our people face. Life is about so much more than work. We get it. That's why we've designed our total rewards to give you the flexibility to choose what you need, when you need it, making sure that you and your family are supported not only financially, but physically and emotionally too. Visit the link below to discover why we're a great place to work and what being part of more means for you.https://www.morethanacareer.energy/centricaIf you're full of energy, fired up about sustainability, and ready to craft not only a better tomorrow, but a better you, then come and find your purpose in a team where your voice matters, your growth is non-negotiable, and your ambitions are our priority.Help us, help you. We would love for you to share any information about yourself throughout our recruitment process so that we can better understand you and help shape your journey.TPBN1_UKTJ

About the Role \n Our client, a market-leading aerospace manufacturer, is seeking a PLM Engineer with experience in Data migration to join our engineering team in Slough and take ownership of a major product data migration project. \n This is not a traditional IT or cloud-based Data Engineering role. The position is focused on the management, preparation, validation and migration of engineering and product data, including 3D CAD models, technical drawings, PDFs, Word documents and Excel files, into a Product Lifecycle Management (PLM) system. \n You will play a key role in transforming and organising legacy engineering data, ensuring it is accurate, structured and ready for migration into the company's PLM environment. \n This would suit someone with a background in Mechanical Engineering, Engineering Data, CAD, PLM, Product Data Management or Data Migration, who enjoys working with technical information and solving data quality and organisation problems. \n Key Responsibilities \n\n • Take ownership of the engineering data migration work package from assessment through to completion.\n, • Review and assess existing legacy product and engineering data.\n, • Extract, sort, organise and classify engineering data ready for migration.\n, • Clean, validate and quality-check data, identifying missing, duplicated or inconsistent information.\n, • Prepare 3D CAD models, technical drawings and associated engineering documentation for migration into the PLM system.\n, • Work closely with PLM and engineering teams across Safran sites to coordinate data transfer and migration activities.\n, • Ensure migrated data meets company standards and agreed data quality requirements.\n, • Identify opportunities to improve the way engineering data is structured, managed and maintained.\n, • Develop and document improved processes, procedures and working instructions.\n, • Support the introduction and training of tools and processes associated with the data migration project.\n, • Monitor project progress against agreed milestones and timescales.\n, • Report issues, risks and opportunities to the Engineering Manager and relevant stakeholders.\n, • Maintain project plans, dashboards and KPI reporting.\n, • Work collaboratively with engineering, PLM and other cross-functional teams.\n, • Support the implementation of best practice in engineering data management.\n\n About You \n We are interested in people from a variety of engineering and technical backgrounds. You may currently be working as a: \n\n • PLM Engineer\n, • PLM Administrator\n, • Product Data Engineer\n, • Product Data Specialist\n, • CAD Data Engineer\n, • CAD Administrator\n, • Data Migration Engineer\n, • Engineering Systems Engineer\n, • Configuration Engineer\n, • Document Controller / Engineering Document Controller with strong technical data experience\n\n Essential Experience \n\n • Experience working with engineering, manufacturing or product data with Strong analytical and problem-solving skills.\n, • Experience working with large volumes of structured or unstructured technical information.\n, • Experience of data cleansing, validation, organisation or migration.\n, • Good understanding of engineering documentation and technical data.\n, • Familiarity with CAD data, technical drawings or engineering documentation.\n\n Strong Excel skills and confidence working with spreadsheets and databases. \n Ability to work independently and take ownership of a defined work package. \n Good communication and documentation skills. \n Desirable Experience \n Experience with one or more of the following would be advantageous: \n PLM / PDM systems, such as 3DEXPERIENCE / ENOVIA, Siemens Teamcenter or PTC Windchill. \n CAD databases or engineering document management systems. \n CAD models and technical drawings. \n Engineering change/configuration management. \n Data migration or legacy data transformation projects. \n Power BI or other reporting tools. \n Scripting or automation to improve data management processes. \n You do not need to come from a traditional IT Data Engineering background. Candidates with strong mechanical/engineering data, CAD, PLM, PDM or product data experience are encouraged to apply. \n The Opportunity \n This is an opportunity to join a major engineering organisation and become a key part of a significant engineering data transformation and PLM migration project. \n You will have the opportunity to work across engineering and PLM teams, develop your expertise in engineering data management and contribute directly to improving how product information is structured, controlled and used across the business.

Compliance Associate \n Slough | £35k - £40k + 2.6k car allowance | Permanent Background / Overview \n An exciting opportunity has arisen for a Compliance Associate to join a growing financial services business within the luxury automotive finance sector. \n Supporting the Compliance & Risk team, this role offers exposure to a broad range of compliance, regulatory and legal activities, making it ideal for someone looking to further develop their career within financial services compliance. Working closely with experienced compliance professionals, you will play an important role in ensuring regulatory obligations are met while contributing to the continuous improvement of internal processes. \n \n Key Responsibilities \n\n • \n Supporting the preparation of regulatory submissions and compliance reporting. \n • \n Assisting with customer complaints, claims handling and FCA-related matters. \n • \n Preparing draft responses for customers and regulatory bodies where required. \n • \n Supporting contract drafting, review and document management. \n • \n Assisting with data protection and UK GDPR activities. \n • \n Monitoring regulatory developments and preparing internal summaries. \n • \n Maintaining compliance policies, procedures and documentation. \n • \n Supporting audits, risk assessments and internal compliance reviews. \n • \n Preparing reports, presentations and documentation for internal stakeholders. \n • \n Working collaboratively across Legal, Risk, Sales and wider business functions. \nAbout you\n\n • Law degree or equivalent qualification or comparable qualification\n, • \n 1-3 years' experience within a legal, regulatory or compliance environment. \n • \n Previous experience within financial services, consumer finance or a regulated industry would be advantageous. \n • \n An understanding of FCA regulations, particularly complaints handling (DISP) \n • \n Knowledge of UK GDPR and data protection principles. \n • \n Excellent written and verbal communication skills. \n • \n Strong organisational skills with excellent attention to detail. \n • \n The ability to manage multiple priorities within a fast-paced environment. \n • \n A proactive approach and willingness to learn and develop. \n What's on Offer \n\n • \n Competitive salary + car allowance \n • \n 25 days annual leave plus bank holidays, increasing with length of service. \n • \n Company pension with 6% employer contribution. \n • \n Bupa private medical cover. \n • \n Possible hybrid working available following successful probation \n • \n Additional employee benefits including holiday buy/sell scheme, employee assistance programme and wellbeing initiatives. \n • \n Excellent opportunity to develop a career within compliance, legal and regulatory affairs in a growing financial services organisation. \n\n To learn more, apply now or give us a call

Company DescriptionEurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate.Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies.Eurofins PSS Insourcing Solutions is a global, award-winning insourcing solution. We place our skilled team directly at the client site, managing operations seamlessly and eliminating complexities. We ensure a strategic, long-term service commitment that delivers value directly at the client’ site, utilising their facilities, equipment, and methodologies, while maintaining the same service, expertise, and cGMP compliance available at the Eurofins facility. If you're an employee seeking an exceptional career journey, Eurofins PSS Insourcing Solutions is your gateway to a future where innovation, collaboration, and success converge. Join us in a world where excellence knows no boundaries!If you want to continue to help make our world a safer and healthier place, then apply for the role below and become a part of the extraordinary Eurofins networkJob DescriptionUnfortunately, we are unable to offer visa sponsorship for this role. This is a full time, permanent position, working a flexible 37 hour week, Monday – Friday.As a BioAssay Senior Scientist you will perform routine, non-routine and stability testing activities of drug substances (Biologics) within the client’s Analytical Service Department.Job Responsibilities that you be covering:The purpose of this post is associated with the performance of routine, non-routine and stability testing activities of drug substances (Biologics) within the client’s Analytical Service Department.You will perform routine, non-routine and stability testing of biologic drug substances using ELISA, cell-based potency assays and Biacore (SPR) methodologies, whilst coordinating assay activities, managing project priorities and timelines, and ensuring the generation of high-quality, accurate and GMP-compliant data delivered to client expectations.• You will utilise electronic laboratory systems and software, including electronic notebooks, to accurately document, analyse and report results, while tracking project progress, coordinating deliverables and ensuring all records, reports and regulatory documentation are completed in accordance with client, Eurofins and regulatory requirements.• You will support method development, validation, troubleshooting, trend analysis and OOS investigations, applying strong scientific expertise and project management skills to deliver study objectives, mitigate risks, resolve technical issues and contribute to the successful execution of client programmes.• You will act as a subject matter expert for bioanalytical techniques, providing technical guidance, mentoring and training to colleagues, supporting recruitment activities, leading assigned project workstreams and ensuring training compliance across the laboratory.• You will maintain laboratory operations through instrument maintenance, reagent and consumable management, housekeeping activities and the preparation, review and update of SOPs, protocols, reports and other controlled documentation, ensuring resources are effectively planned to support project and operational demands.• You will build strong relationships with internal and external clients by managing project communications, providing scientific updates, delivering exceptional customer service, driving continuous improvement initiatives, promoting a strong safety and quality culture, and supporting Eurofins' commitment to operational excellence and customer satisfactionQualificationsYou will hold a degree or higher qualification in a relevant scientific discipline and possess experience within a bioanalytical, biopharmaceutical or GMP-regulated laboratory environment.You will have extensive hands-on experience with biologics testing techniques, including ELISA, cell-based potency assays, Biacore (SPR), aseptic techniques and 96-well plate formats, ideally supporting pharmaceutical drug substance development and testing.You will have expert knowledge of cell-based assays, including Vi-CELL and manual cell counting, luminescence-based assays and flow cytometry, with the ability to interpret complex datasets and provide scientifically sound conclusions.You will have demonstrated experience operating within GMP and regulatory frameworks, with strong documentation skills, proficiency in electronic laboratory systems and MS Office, and a commitment to delivering accurate, high-quality results right first time.You will have the ability to troubleshoot analytical methods and instrumentation, apply statistical analysis to support investigations and continuous improvement activities, and proactively identify opportunities to enhance efficiency, quality and customer outcomes.You will have excellent communication and interpersonal skills, with experience mentoring colleagues, acting as a technical subject matter expert, building strong client relationships and working collaboratively within a flexible, customer-focused Eurofins laboratory environment.Additional InformationAt Eurofins we are growing, innovating and always learning. We celebrate the achievements of our employees through annual long service awards, recognise our colleagues special life events.As a Eurofins employee you will benefit from:We offer exceptional opportunities for career growth, within a friendly and supportive team. As well as a competitive salary, pension and associated benefits you will enjoy an unrivalled working environment, including an active social calendar and subsidised canteen, all while working in a start of the art client facility- a leading biotechnology companyFantastic developmental opportunities and career progression pathways such as leadership, training, compliance and Subject Media Expert.Full Benefits Package including:-PensionPrivate Medical InsuranceIncome protection and life assuranceAnnual discretionary bonusBirthday Holiday entitlementExciting Eurofins Incentives: Employee Activity Committee (EAC), Equality Driving Excellence (EDE), significant Reward and Recognition programme Opportunity to benefit from Eurofins Operational Development training platform, plus potential support for part-time training (relevant to the position)Full use of the canteen facilities and barista on the client siteFree parking onsite and onsite electric chargingAdditional annual leave days with continued serviceThe opportunity to work on life saving productsSummaryType: Full-timeFunction: General BusinessExperience level: ExecutiveIndustry: Biotechnology

Associate Director, Clinical Trial Disclosure & Transparency応募locations: EMEA, GB, Berkshire, Maidenhead, CSL Behring: Americas, US-PA, King of Prussia, CSL Behringtime type: 正社員posted on: 募集開始 - 今日job requisition id: R-284815The Associate Director Clinical Trial Disclosure and Transparency is a global subject matter expert responsible for ensuring timely, accurate, and compliant clinical trial disclosures across all regions and study types (interventional and observational). This role guides global strategy, drives process excellence, and oversees the delivery of clinical trial disclosure activities including registration, results disclosure and layperson summaries while providing support for transparency activities including anonymization and redaction of commercially confidential information (CCI) as required for business continuity and operational needs. All activities and deliverables must be conducted in alignment with international regulations, CSL policies, industry standards and transparency requirements.Key ResponsibilitiesStrategic Oversight & ComplianceLead enterprise clinical trial disclosure and transparency strategy and advise therapeutic areas and Medical Affairs on global requirements (e.g., FDAAA 801 and the Final Rule, clinicaltrials.gov, CTIS, EU CTR 536/2014, UK Clinical Trials Regulations 2025 (MHRA), EMA Policy 70, Health Canada PRCI)Monitor emerging regulatory and industry trends and influence CSL's disclosure and transparency strategy accordingly. Develop and implement scalable, efficient processes that meet evolving regulatory and industry standardsServe as the primary liaison to public registries (e.g., ClinicalTrials.gov, CTIS, EU PAS).Disclosure ExecutionOversee and deliver high-quality, compliant disclosures including study registration, protocol amendments, summary results, and lay-person summariesEnsure timely communication of disclosure obligations to clinical teams, affiliates, and stakeholdersSupport CROs and local teams with regional disclosure needsTransparency ExecutionSupport transparency activities, including the preparation and delivery of compliant redacted document packages for public release by global Health Authorities, ensuring appropriate business continuity across the disclosure and transparency function.Provide input on transparency obligations and best practices, including promotion of Smart Authoring practices, to clinical teams and functionsCross Functional EngagementPartner with Clinical Development, Biostats, Medical Writing, Regulatory, IP, Legal, Data Privacy and CMO staff to embed disclosure and transparency requirements across the development lifecycleCollaborate closely with other CMO Office team members to ensure effective knowledge sharing, operational continuity and seamless execution of interconnected activitiesRepresent CSL’s disclosure and transparency practices internally and externally, ensuring alignment with global standards and expectationsVendor ManagementSelect, manage, and oversee disclosure and transparency vendors to ensure high-quality deliverables and on-time executionDrive process improvement, innovation and operational excellence in disclosure activitiesOptimize resourcing and technology to support cost-effective deliveryMetrics & MonitoringTrack, analyse and report key metrics to demonstrate compliance, identify risks and drive continuous improvementEducation Requirements 10+ years in pharmaceutical/biotech environment with deep knowledge of the drug development process Strong judgement, initiative and ability to operate independently as the global subject matter expert responsible for clinical trial disclosure activities Demonstrated ability to independently interpret emerging regulations, assess business impact, identify compliance risks and develop practical, business-focused recommendations. Proven track record in managing global disclosure and transparency deliverables. Demonstrated ability to lead through influence in a matrix environment without direct reporting authority Excellent written and verbal communication skills, with the ability to translate complex regulatory requirements into clear guidance for stakeholders at all levels. Strong influencing skills and ability to communicate confidently with senior stakeholders, study teams and external vendors. Ability to constructively challenge stakeholders and vendors, provide evidence-based recommendations and maintain professional credibility in complex discussions Strong critical thinking skills, with the ability to make decisions and recommendations in ambiguous situations, escalating appropriately when required. Strong understanding of ICH-GCP, ICMJE, GDPR and industry best practices Demonstrated experience providing strategic oversight of vendors, critically reviewing recommendations and maintaining accountability for final decisions* Hands on experience with the use and administration of the Trialscope Disclose system (or equivalent)Education RequirementBachelor’s degree in a scientific, medical, or pharmaceutical discipline requiredThis role requires working in office 3 days per week. #LI-Hybrid #J-18808-Ljbffr

Data Migration Engineer \n \n Working onsite in Slough \n Fixed Term Contract for 18 months \n Salary is £38K per annum \n \n Working on the migration of existing Engineering Product Data, to a new PLM tool. \n \n Engineering Product Data contains 3D CAD data, drawings, PDF, Word and Excel documents. \n \n \n Essential Duties and Responsibilities \n \n\n • Takes ownership and delivers the Data Migration work package.\n, • Responsible for Data Migration of Legacy and In-Production Product Data to PLM (Product Lifecycle Management)\n, • Key activities involve Data Assessment and Planning, Data Extraction and Data Sorting, Data Cleaning and Data Validation, and preparing the data to Migrate to PLM.\n, • Work along with PLM team from other sites for transfer activity.\n, • Data Preparation – adhering to company guidelines.\n, • Harmonize and improve methods for Data Modelling.\n, • Document these improvements through procedures and instructions.\n, • Responsible for organizing tool associated training.\n\n \n \n Requirements \n \n Background in Data Engineering, Mechanical Engineering or General Engineering. \n \n Awareness with PLM Systems: Knowledge with PLM platforms. e.g. Siemens Teamcenter, PTC Windchill or similar PLM tool. \n \n Knowledge of CAD database: Awareness of CAD and drawing data contents. \n \n Data Management / Database Management: Key activities involve Data Assessment and Planning, Data Extraction and Data Sorting, Data Cleaning and Data Validation, and preparing the data to migrate to PLM. \n \n Programming: Familiarity with scripting for automation and tool integration. Excel & Power BI. \n \n \n Additional Desirable Skills: \n \n\n • Familiarity with digital twin concepts and IoT Data Integration.\n, • Exposure to Data Analytics, reporting tools (e.g., Power BI, Tableau) for engineering KPIs.\n\n

Job Role:- Automotive Service Advisor Salary:- £42,000 OTE Location:- Maidenhead Falling short on career development? Missing monthly bonus targets? We have taken on an Automotive Service Advisor role in the Maidenhead Area for a very successful Premium Dealership Group. The lifespan of this dealership goes well over 50 years; a household name brand, with a very loyal / repeat customer base. This is a very active site, which means high upsell potential and strong team bonuses too. Here are a few pointers: - Bonus up to £1000 extra per month + quarterly CSI bonuses totalling over £42,000 Very quick accreditation - one fact about the Group is the majority of their managers progress frequently from within, so you will be given training for growth through their training academy. Multi-faceted team and personalities – great working environment at a high pace, if you enjoy the activity this is worth a look. Key role and responsibilities for this Service Advisor role Ensure customers are aware of service and repair work required to their vehicles in a professional manner Advise on estimated costs of repairs and work to be undertaken Sell additional products as appropriate to customer's needs Advise on timescales and collection arrangements / Produce job cards on in-house computer system Update customer and vehicle records / Document all warranty work in accordance with manufacturer policy Preparation and completion of invoices Minimum requirements for this Service Advisor role Experience as a Service Admin / Service Advisor in the Motor Trade The ability to sell additional products and services to customer Driving license Excellent communication skills and the ability to deliver outstanding customer service The ability to manage multiple tasks If you are interested in finding out more get in contact with Eric Duxbury on (phone number removed), email (url removed) or send us your CV by Clicking Apply Now

About the Role Our client, a market-leading aerospace manufacturer, is seeking a PLM Engineer with experience in Data migration to join our engineering team in Slough and take ownership of a major product data migration project. This is not a traditional IT or cloud-based Data Engineering role. The position is focused on the management, preparation, validation and migration of engineering and product data, including 3D CAD models, technical drawings, PDFs, Word documents and Excel files, into a Product Lifecycle Management (PLM) system. You will play a key role in transforming and organising legacy engineering data, ensuring it is accurate, structured and ready for migration into the company's PLM environment. This would suit someone with a background in Mechanical Engineering, Engineering Data, CAD, PLM, Product Data Management or Data Migration, who enjoys working with technical information and solving data quality and organisation problems. Key Responsibilities Take ownership of the engineering data migration work package from assessment through to completion. Review and assess existing legacy product and engineering data. Extract, sort, organise and classify engineering data ready for migration. Clean, validate and quality-check data, identifying missing, duplicated or inconsistent information. Prepare 3D CAD models, technical drawings and associated engineering documentation for migration into the PLM system. Work closely with PLM and engineering teams across Safran sites to coordinate data transfer and migration activities. Ensure migrated data meets company standards and agreed data quality requirements. Identify opportunities to improve the way engineering data is structured, managed and maintained. Develop and document improved processes, procedures and working instructions. Support the introduction and training of tools and processes associated with the data migration project. Monitor project progress against agreed milestones and timescales. Report issues, risks and opportunities to the Engineering Manager and relevant stakeholders. Maintain project plans, dashboards and KPI reporting. Work collaboratively with engineering, PLM and other cross-functional teams. Support the implementation of best practice in engineering data management. About You We are interested in people from a variety of engineering and technical backgrounds. You may currently be working as a: PLM Engineer PLM Administrator Product Data Engineer Product Data Specialist CAD Data Engineer CAD Administrator Data Migration Engineer Engineering Systems Engineer Configuration Engineer Document Controller / Engineering Document Controller with strong technical data experience Essential Experience Experience working with engineering, manufacturing or product data with Strong analytical and problem-solving skills. Experience working with large volumes of structured or unstructured technical information. Experience of data cleansing, validation, organisation or migration. Good understanding of engineering documentation and technical data. Familiarity with CAD data, technical drawings or engineering documentation. Strong Excel skills and confidence working with spreadsheets and databases. Ability to work independently and take ownership of a defined work package. Good communication and documentation skills. Desirable Experience Experience with one or more of the following would be advantageous: PLM / PDM systems, such as 3DEXPERIENCE / ENOVIA, Siemens Teamcenter or PTC Windchill. CAD databases or engineering document management systems. CAD models and technical drawings. Engineering change/configuration management. Data migration or legacy data transformation projects. Power BI or other reporting tools. Scripting or automation to improve data management processes. You do not need to come from a traditional IT Data Engineering background. Candidates with strong mechanical/engineering data, CAD, PLM, PDM or product data experience are encouraged to apply. The Opportunity This is an opportunity to join a major engineering organisation and become a key part of a significant engineering data transformation and PLM migration project. You will have the opportunity to work across engineering and PLM teams, develop your expertise in engineering data management and contribute directly to improving how product information is structured, controlled and used across the business

Quality Inspector Slough Salary = £35K Duties Inspect, measure, and test all incoming goods, materials and components to verify conformity to specifications and industry standards Highlight and document any non-conformities or issues identified during inspection. Support Root Cause Analysis for both supplier and internal rejects, and help determine corrective actions as needed. Monitor and record the effectiveness of implemented corrective actions. Ensure a smooth workflow of inspected goods through to the next stage of production or storage. Liaise with suppliers to resolve non-conformance issues relating to delivered goods. Produce timely, clear, accurate, and comprehensive inspection reports as required (for customers, suppliers, regulatory bodies, etc.). Generate and communicate statistical data and inspection summaries as needed. Maintain and complete all inspection documentation to required standards.This includes accurate records for traceability and audit purposes. Ensure safe handling and proper care of QA tools and inspection equipment, maintaining them in good condition. Requirements Previous Quality Inspection experience is essential. Goods In Inspector / Goods Inwards Inspector QC Inspector / Quality Control Inspector QA Inspector / Quality Assurance Inspector QA Technician / Quality Assurance Technician / Quality Technician Experience of using various digital and analogue measurement equipment to determine conformance to specification. For example: gauges, verniers, micrometers, or other inspection equipment. Technical background essential with knowledge of inspection and control methods, techniques and documentation including preparation of First Article Inspection reports. Experience of reading engineering specifications. e.g. Engineering drawings, tolerances, surface finishes etc. Familiar with Continuous Improvement methodologies, tools and concepts Familiar with Quality concepts and practices. IT experience including the use of Microsoft Word and Excel