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Job Description Summary#LI-Hybrid Location: Cambridge, Massachusetts, USAThis position is located in Cambridge, Massachusetts, and will not have the ability to be located remotely.We are seeking an enthusiastic and motivated PK Sciences representative to lead the development and use of artificial intelligence (AI) enabled strategies to transform the clinical pharmacology support of transformative new medicines. The successful candidate will offer insight into the development of AI-based applications to support strategic, scientific and operational leadership. They would focus on developing AI-based solutions to enhance the automation, innovation and acceleration of PKS/clinical pharmacology deliverables across the organization. Our unique organizational structure enables colleagues to work seamlessly in the translational and/or clinical space, offering opportunities for development and bench-to-bedside-to-bench translation. Experience in late discovery into clinical development is preferred. The scope of the role potentially includes small molecules, biologics/therapeutic proteins, antibody drug-conjugates, radioligand therapies and/or cell therapies across major therapeutic areas in Novartis, including oncology, immunology, cardiovascular renal metabolism, neuroscience, and global health. This position drives close interdisciplinary collaboration among the PK Science disciplines, Drug Disposition (ADME, BA), Modeling & Simulation (M&S), and Operations through PK science sub-teams to achieve a holistic and integrative perspective of the ADME/clinical pharmacology properties of candidates and drugs. Collaborates effectively with broader, cross disciplinary project teams to ensure PKS strategies are well integrated into project plans and scientific discussions.Job Description Key ResponsibilitiesLead the development and oversee implementation of AI strategy for clinical pharmacology within PKS.Brings strong AI and digital fluency, using enterprise tools to further strategic, scientific and operational leadership in clinical pharmacologyIdentifies, develops and implements high-value use cases where AI can materially improve clinical pharmacology planning, analyses and decision quality.Represent the PK Sciences function in project teams, interactions with stakeholders within the organization and interactions with regulatory agencies, as appropriateProactively contributes to developing drug candidates across Research Development and Commercial continuum, providing expert pharmacokinetic / drug metabolism and clinical pharmacology inputWork with teams to use AI to accelerate and enhance the understanding of nonclinical and clinical PK/PD relationships and development dosing strategies and predictionsChampion the use of AI to accelerate and enhance the provision of , dosage, and PK/PD components of study protocols, reports, project summaries and development plans, and author pharmacokinetic/clinical pharmacology/biopharmaceutics sections of IND/IMPDs and NDA/BLAs as well as prepare appropriate responses to Health Authority questionsDrives close interdisciplinary collaboration among the PK Science disciplines, Drug Disposition (ADME, BA), Modeling & Simulation (M&S), through PK science sub-teams.Works in close collaboration with clinicians and clinical development colleagues to integrate PKS insights into study design, data interpretation, and project decision‑makingModels the use of Artificial intelligence (AI) / Machine Learning (ML) approaches to enable model guided molecular design, preclinical and clinical data automation, and authoring regulatory documents.This role reports to a Therapeutic Area Unit head within PK Sciences within Translational Medicine (TM) in Biomedical Research. PKS is a global organization situated within Translational Medicine (TM), the clinical research arm of Biomedical Research within Novartis. PK Sciences plays a pivotal role in bringing innovative medicines to patients, by building on research advances to develop new therapies, bridging drug discovery and clinical application. PK Science is an enterprise-wide organization, working across both Biomedical Research and the Development organizations to advance the scientific knowledge of pharmacokinetics, metabolism and clinical pharmacology.Essential RequirementsPh.D. / Pharm.D. with relevant experience in clinical pharmacology, drug metabolism and pharmacokinetics or a related background.A minimum of 8-10 years of experience in drug discovery and/or development in a relevant environment (academia, CRO, biotech or Pharma). 6+ years of experience preferably in a lead role overseeing ADME/DMPK project strategy in translational/clinical development, or in AI strategy.Extensive and in-depth knowledge of pharmacokinetics including, drug metabolism and PK/PD evaluation, experience in working in project teams (preferably global) as well as sound awareness of recent developments in drug development and regulatory sciences.Exposure to working in a cross-functional, matrixed, project-team environment.Strong oral and written communication skills.Desirable RequirementsHands-on project experience with Artificial intelligence (AI) approaches and examples of applying AI to clinical pharmacology topics is a plusLeadership / Novartis Behaviors in ActionDelivers results through disciplined execution, continuous improvement, and a strong focus on value and outcomes.Demonstrates an enterprise mindset and strong ownership by prioritizing resources and decisions for maximum Novartis and patient impact.Role models Novartis leadership behaviors through visible actions, continuous self reflection, and openness to feedbackBuilds trust through transparent communication, clear accountability, and consistent delivery against commitments.Novartis Compensation SummaryThe salary for this position is expected to range between $185,500 and $344,500 per year.The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.U.S.-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time-off package including vacation, personal days, holidays and other leaves.EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.Salary Range$185,500.00 - $344,500.00Skills DesiredAccountability, Biopharmaceutics, Chemistry, Clinical Pharmacology, Clinical Research, Clinical Trials, Drug Development, Due Diligence, Electronic Components, Mentorship, Non-Disclosure Agreements, Patient Care, Physics, Translational Medicine, Waterfall ModelSummaryLocation: Cambridge (USA)Type: Full time

Arm is seeking a Staff Information Developer in Cambridge to lead silicon content projects and develop scalable information architectures. You will drive content strategy, collaborate with architecture, engineering and product teams, and mentor colleagues to raise the overall capability of the information group. You will shape an engaging information experience, author using modern docs-as-code workflows, and influence content decisions across programs while enjoying a hybrid working model with #J-18808-Ljbffr

We are looking for a Systems Integration Engineer to plan and deliver integration, verification and validation activities for advanced aerospace and defence systems. The role will focus on bringing together hardware, software and sub-systems into coherent solutions, developing robust test approaches and generating the evidence required to demonstrate performance, compliance and readiness for demonstration or deployment. • Develop integration, verification and validation strategies aligned to system requirements, architecture and programme milestones., • Author and maintain test plans, procedures, specifications and reports for laboratory, rig, ground and flight activities., • Support the integration of sub-systems, identifying, investigating and resolving technical issues and interface problems., • Execute or oversee verification and validation activities, ensuring results are captured and linked to requirements and acceptance criteria., • Support trials and demonstrations, including planning, readiness reviews, execution support and post-activity reporting., • Work closely with design, safety, requirements and project teams to ensure integration and test activities are practical, efficient and well controlled., • Contribute to continuous improvement of integration and test processes, tools and evidence management approaches., • Experience in systems integration, verification, validation or test within complex engineering programmes., • Strong understanding of requirements-based test approaches and structured evidence generation., • Ability to produce clear test documentation and to work methodically through technical problems., • Experience supporting trials, demonstrations or system acceptance activities, particularly of airborne systems, would be beneficial., • Awareness of safety-critical development and regulated engineering environments., • Degree in a relevant engineering or scientific discipline, or equivalent practical experience., • Experience in fast-paced R&D or startup environments, with rapid prototype iteration times, • Experience in delivery of airborne systems within the defence industry would be highly advantageous., • Competitive compensation and stock options, • Private Medical & Dental, • Cycle to work scheme The mission of Cambridge Aerospace is to eliminate the risk of existential war in Europe. That risk comes from the air – low-cost drones and cruise missiles now manufactured in colossal volumes by our adversaries, ballistic missiles capable of ending the world as we know it, and a new generation of hypersonic weapons that evade every existing defence. We’re building low-cost interceptors that defeat these threats, and the surveillance systems to detect and target them – at a cost taxpayers can afford, at the pace the threat demands, and with sovereign supply chains that assure delivery. We have immense backing from the world’s best venture funds. We’re one of the fastest growing defence technology companies in history. And we’re hiring the best engineers to prosecute the mission. If you are in the top 1%, willing to work harder than you ever have, build technology better than anyone else, and contribute to the defining challenge of our time, now is the time to join us. We’re committed to building a diverse and inclusive workplace. If you’re excited about this role but don’t meet every requirement, we still encourage you to apply. #J-18808-Ljbffr

Apple’s Silicon Engineering Group (SEG) is seeking a talented and motivated SoftwareEngineer to join the Documentation Tools team. Our team develops a comprehensive platform, spanning CLIs, UIs, and APIs, that empowers silicon engineers to author the critical technical specifications guiding the design of Apple's industry-leading chips. In this role, you will help build, optimize, and scale the tools that directly impact the efficiency and quality of our chip design process. This is an excellent opportunity for an early-career engineer or recent graduate to grow their skills. You will be paired with senior mentors and have the opportunity to learn complex system architecture while making a tangible impact on the chips at the core of future Apple products loved by millions of customers. Design and develop: collaborate to build and maintain scalable CLIs, UIs, and APIs that streamline and automate the creation, review, and verification of hardware specifications. Optimize performance: assist in diagnosing and troubleshooting performance bottlenecks, learning to navigate and optimize a complex, JVM-based toolchain to ensure a seamless experience for our engineering teams. Collaborate and support: partner with the documentation support team to deliver toolchain training, technical guidance, and best practices directly to silicon designers. Document: author clear, comprehensive documentation for platform architecture, toolchain workflows, and internal processes. Innovate: bring fresh perspectives and a curious mindset to help identify and implement process and codebase improvements alongside senior engineers. • Foundational understanding of domain modeling, schema design, and complex data structures., • Familiarity with designing schemas and working with PostgreSQL or other relational databases., • Exposure to or familiarity with build systems (SBT, Gradle, Maven, or Ant) and version control systems (Git, Perforce)., • Understanding of the core concepts of software test environments, release cycles, and quality assurance best practices., • Knowledge of these is a plus: familiarity with automated CI/CD pipelines (GitLab CI, Jenkins, TeamCity)., • Comfortable working and troubleshooting within macOS, Linux, and UNIX environments., • Academic, internship, or project-based experience with Scala and the JVM ecosystem (Java experience is also valued). At Apple, we’re not all the same. And that’s our greatest strength. We draw on the differences in who we are, what we’ve experienced and how we think. Because to create products that serve everyone, we believe in including everyone. Therefore, we are committed to treating all applicants fairly and equally. As a registered Disability Confident employer, we will work with applicants to make any reasonable accommodations. Apple will consider for employment all qualified applicants with criminal backgrounds in a manner consistent with applicable law. Learn more. At Apple, we believe accessibility is a fundamental human right. You’ll find that idea reflected in everything here — in our culture, our benefits and our digital tools. By welcoming as many perspectives as possible, we help you build a career where you feel like you belong. Learn about accessibility in Apple’s workplace. #J-18808-Ljbffr

LabConnect improves lives by partnering with pharmaceutical and biotech companies, and clinical research organizations (CROs) to accelerate the development of new medicines around the world. We are an independent, global, one-stop-shop focused on delivering Central Laboratory Services that are tailor-made, timely and flexible to meet the evolving study demands of traditional to increasingly complex trials. Additionally, we provide Functional Service Provider (FSP) Solutions, supporting our clients with scientific and technical expertise, acting as an extension of their team, coordinating all laboratory related needs, advising on strategies for lab data collection and providing end-to-end analytical and logistical solutions. The Bioanalytical Program Lead, supporting an Integrated Bioanalysis (IBA) Global Team, will lead the design and implementation of robust bioanalytical strategies. This role will ensure lab-based activities are aligned with context of use, working closely with other scientific and technical lab staff in a matrix environment to manage aspects such as experimental design and tech transfer in regulated bioanalysis supporting therapeutic modalities across a range of therapeutic areas. Please note: this role is best suited for candidates within proximity to Cambridge. • Responsible for interacting closely with scientists who are primarily lab-based, aiding in experimental design where required., • Serve as the bioanalytical lead on the client’s projects, using strategic thinking, scientific knowledge and expertise while working with a range of collaborators and cross-functional groups., • Act as a Subject Matter Expert in regulated bioanalysis across a range of modalities., • Contribute to and author regulatory documents to support submissions across a range of countries and geographies., • Work with regulatory agencies and Health Authorities across a range of countries and geographies to mitigate risk, submit regulatory documents, and respond to Health Authority questions., • Bachelor of Science in a relevant subject required., • At least 10 years of experience in bioanalysis (large and small molecule) required., • Proven experience as a Subject Matter Expert in regulated bioanalysis across a range of modalities PK/CK, PD, and immunogenicity assessments (cellular and humoral) required., • Required experience as a bioanalytical lead across diverse project teams – defining, leading and executing on bioanalytical strategy to advance a portfolio that may include biomarker and target engagement strategy for dose decision endpoints., • Required scientific ability to assess and discern the advantages and pitfalls of a range of analytical techniques which may include molecular assays (ddPCR, 1PCR, RT-qPCR), flow cytometry, ELISpot, viral assays, cytokine assays, ligand binding assays and mass spectrometry., • Requires deep understanding of small and large molecule bioanalysis., • Requires proven publication and presentation record., • Requires exceptional written and verbal communication skills., • Requires proficiency in speaking and writing in the English language., • Preferred knowledge of immunology and/or metabolic diseases., • Preferred experience working in a matrix environment. None • Prolonged periods of sitting at a desk and working on a computer., • Prolonged use of computer and headphones for conference calls., • Communicate effectively via phone, video, and email., • Use hands and fingers to operate a computer and other office equipment. Join our team and discover how your work can impact patients' lives around the world! • We truly live our values: People First, Quality Focused, Customer Centered, Technology Driven and Accountability Always., • The opportunity to make a meaningful impact on a passionate and growing team., • Strong communication and collaboration within a smaller sized team., • Access to tools and resources that empower you to excel in your role. In addition to great perks and challenging work assignments, we invest in our people with enriching career growth opportunities globally. We believe in a friendly and collaborative environment with open lines of communication. We are proud to be an Equal Opportunity Employer and value the diversity of our workforce. We do not discriminate on the basis of race, gender, age, disability, religion, sexual orientation, or any other protected characteristic. LabConnect also prioritizes the privacy and security of your personal data. All candidate information is handled in accordance with the General Data Protection Regulation (GDPR). For this job posting, all hiring decisions are made with meaningful human involvement and consideration. In this context, no applicant is subject to a decision based solely on automated processing within the meaning of Article 22 of the GDPR. To learn more, please review our Privacy Notice on our website, by navigating to . If you need assistance to complete your job application, search for a job opening, or submit an online application at LabConnect - please email or call . #J-18808-Ljbffr

Take the Lead on Multi-Million Pound Sustainable Engineering Projects! At Envirogen Group, we deliver advanced water solutions as a premier Lifecycle Performance Company. We are seeking a high-calibre Senior Engineer to join our core engineering team in the UK though for highly accomplished professionals, flexible hybrid or remote working arrangements will be fully considered. This critical role offers an exceptional opportunity to spearhead the end-to-end lifecycle of multi-million-pound industrial water and wastewater treatment systems, transitioning seamlessly from high-level conceptual design to impactful field deployment. We value entrepreneurial execution, offering a uniquely flat structure where exceptional performance translates directly into accelerated professional development. For an ambitious engineer, this represents an unparalleled launchpad to deploy your expertise, drive visible industrial outcomes, and grow exponentially alongside our expanding UK footprint.. The Role: Drive Capital Project Success As a Senior Engineer you will hold complete technical ownership over the execution and delivery of high-impact, capital engineering infrastructure ranging from c£1M to £20M. Partnering seamlessly with our Project Management team, you will translate complex challenges into operational, high-performance systems. Key Responsibilities: • Lead Advanced System Design: Spearhead the end-to-end design lifecycle of multi-million-pound treatment systems, serving as the technical anchor for major engineering deliverables from initial concept to final execution., • Mentor & Develop Talent: Coach, mentor, and elevate the capabilities of the core engineering team, fostering a culture of technical excellence, accountability, and continuous professional growth., • Engineering Governance & Review: Serve as the definitive authority for reviewing and approving critical project documentation, including complex P&IDs, fabrication drawings, electrical schematics, and comprehensive Bills of Materials (BOM)., • High-Performance Equipment Selection: Execute advanced hydraulic calculations, precise pump design and selection, and comprehensive valve and instrumentation specifications to guarantee system performance and full contractual compliance, while supporting the sales team with precise cost, labour, and subcontractor estimates for commercial proposals., • Strategic Sourcing & Vendor Governance: Author rigorous technical data sheets, initiate RFQs, collaborate closely with key vendors, and execute data-driven procurement determinations to maintain aggressive project velocity., • Cross-Functional & Commercial Leadership: Drive critical customer- and vendor-facing technical reviews, while partnering seamlessly with the sales team to deliver precise cost, labour, and subcontractor estimates for winning commercial proposals. Why Youll Thrive at Envirogen • Exceptional Total Rewards: We offer a highly competitive base salary complemented by a comprehensive health, wellness, and retirement benefits package, alongside an impactful, performance-driven Project Incentive Plan that directly rewards your engineering successes., • An Elite, Flat Culture: Work alongside leading industry experts in a collaborative, un-siloed environment that actively rejects bureaucratic layers. Here, your technical voice is empowered, and your individual contributions directly shape project outcomes., • Global Project Horizons: Expand your engineering mastery and leadership footprint by delivering on exciting, technologically diverse industrial water and wastewater systems across the UK and key international markets Requirements Professional Qualifications • Academic Foundation: A Bachelor of Science or Bachelor of Engineering degree, with a strong preference for a discipline in Mechanical, Chemical, or Civil Engineering., • Proven Track Record: A demonstrated history of engineering success and technical achievement within the industrial water, wastewater, or fluid process industries., • Professional Attributes: A highly organized, self-directed professional who thrives in a collaborative, flat organization; possesses top-tier problem-solving acumen, exceptional communication skills, and the polished presence required for high-stakes, customer-facing technical engagements Ready to Build the Future of Water? Benefits • Supportive and collaborative culture, • Opportunity for development and career progression, • Private healthcare, • Purchase extra annual leave #J-18808-Ljbffr

Job DescriptionJob Description Foundation Alloy is building the most advanced metal alloy company in the world. Our mission is to unlock performance that legacy materials and processes simply cannot deliver, enabling the next of critical hardware across space, aerospace, defense, energy, and industrial applications. Our proprietary MetalsFIRST™ platform eliminates melting entirely, using mechanical alloying and rapid sintering to produce alloys with ultra-fine grain structures and exceptional properties. We are already deploying initial materials, including our Molyclast™ alloys (MC700, MC1200, and MC-X) and specialty steels. We are a Boston-area company commercializing deep materials science developed at the intersection of advanced manufacturing and frontier materials science. We move fast, operate with high technical rigor, and are scaling the infrastructure to bring these materials into production. Currently in the process of relocating from Cambridge, MA to Woburn, MA by early next year. As our Product Engineer, you will sit at the critical link that transforms novel alloy breakthroughs into manufacturable, reproducible, and market-ready products with a focus on hands‑on testing and characterization within the Product Department. • Own post‑testing failure analysis of customer tests, determining root cause and translating findings into actionable feedback for the product and R&D teams., • Design and build custom tests, rigs, and proxy methods that let us creatively and rigorously measure how our products perform under complex, real‑world operational conditions., • Work with external labs on standard and specialized testing, including high temperature properties, wear, fatigue, oxidation, corrosion, DBTT, Gleeble, and spectroscopic analysis by vetting lab partners and arranging quotations, testing conditions, and timelines., • Maintain detailed, organized documentation of test data by alloy and product for the whole organization., • Own calibration and maintenance of internal testing equipment, implement best practices in obtaining accurate measurements., • Author and maintain material datasheets, characterization procedures, and technical documentation for all alloy product lines., • Partner with other product engineers and scientists to determine testing needs and design custom tests., • MS or PhD degree in materials science, mechanical engineering or a related field., • 2+ years of industry experience in metallurgy, materials engineering, or a related discipline, with demonstrated involvement in process and product development, testing, and characterization., • Familiarity with alloy processing techniques such as powder metallurgy, heat treatment, or additive manufacturing relevant to demanding applications., • Familiarity with powder characterization and material property measurements including mechanical, electrical, magnetic and chemical characterization., • Proven ability to develop quality assurance frameworks, write material specifications, and establish characterization test procedures., • Systematic, detail‑oriented approach to problem‑solving and process development., • Collaborative team player who works effectively across R&D, manufacturing, and commercial functions., • Comfortable operating with ownership and initiative in a fast‑paced, resource‑constrained start‑up environment., • Strong technical writing skills — able to produce clear, organized documentation including datasheets, SOPs, and process specifications. We don’t look for profiles that “fit” with our culture. We look for people that add to who we are - people with the initiative, positive approach to problem solving, and passion for something (anything!) that will make them both high impact and exciting to work alongside from day one. We know that these people come from all walks of life, with all backgrounds and levels of experience. If you’re excited about the work we can do together, please reach out. We enthusiastically welcome team members of all races, colors, religions, ages, sexes, orientations, identities, origins, different abilities, genetics, veteran statuses, and former incarceration statuses. The success of this company will be grounded in the long-term productivity of our team. To provide everyone with the physical, mental and financial safety to operate at their long-term best, we provide the following: • Meaningful, challenging, impactful work, and opportunities to grow within the company at all levels, • Competitive salary, guaranteed to rise with inflation at a minimum each year, • Equity - People at every level will have an impact, and should benefit from their work, • Unlimited paid vacation, with a very strong expectation that employees take a minimum of 15 days off per year, and a full week off at least once per year, • Flexible working style. Most jobs will require people to be present in person or in office most of the time, but in general we care about what’s getting done, not when or where you’re doing it, • Top tier health, dental and vision insurance with limited employee contributions, • A voice in future benefits. This is the beginning, and we will work together to keep adding new, better ways to provide for everyone in the company PI286870351 #J-18808-Ljbffr

AVEVA is a global leader in industrial software. Our cutting‑edge solutions are used by thousands of enterprises to deliver the essentials of life – such as energy, infrastructure, chemicals and minerals – safely, efficiently and more sustainably. We’re the first software business in the world to have our sustainability targets validated by the SBTi, and we’ve been recognized for the transparency and ambition of our commitment to diversity, equity, and inclusion. We’ve also recently been named as one of the world’s most innovative companies. If you’re a curious and collaborative person who wants to make a big impact through technology, then we want to hear from you! Find out more at AVEVA Careers. For more information about our privacy policy and how to manage cookies, visit our Privacy Policy. Job Title: Senior MES Software Engineer Location: Paris, France Employment Type: full-time We are looking for a skilled and experienced MES Software Engineer (Technical Lead Engineer or Solution Architect) to join our MES Delivery team in Europe. The ideal candidate will have a strong background in Microsoft Transact-SQL, JavaScript, and RESTful Web APIs, along with hands‑on experience in implementing Manufacturing Execution Systems (MES), ideally with AVEVA Software (System Platform, MES, Work Tasks). In this role you will be fully customer facing and a member of the AVEVA MES Delivery project team responsible for the solution fit to customer requirements to deliver business value. You will work closely with cross‑functional teams to design, develop, and implement scalable MES solutions supporting manufacturing processes. • Participate in requirements gathering, system design, and code reviews, • Ensure best practices in coding, security, and system performance, • Design, develop, and maintain MES solutions built with AVEVA products, • Integrate with external systems (e.g., SAP, PLCs, SCADA) as part of MES architecture, • Author system acceptance test criteria based on formal requirements and ensure customer requirements are met 100% in a timely fashion., • Conduct unit testing and system testing as per the test plan., • Site commissioning of the MES Solutions, • Troubleshoot and resolve application issues in manufacturing environments, • Maintain detailed technical documentation, • Travel up to 25% to customer sites for requirements gathering workshops, design workshops, training workshops, implementation etc., • Experience or exposure to MES systems (e.g., AVEVA/Wonderware, Rockwell FT, Siemens Opcenter, Apriso, etc.), • Understanding of manufacturing processes, production workflows, and shop floor integration, • Fluent in English, • Bachelor or Master degree in Computer Science, Industrial Software, Production IT, or a related field, • Experience in implementing and commissioning industrial software in a manufacturing site, • 5+ years of hands‑on experience in C#, .NET, Web API development, • Proficient in creating and optimizing SQL Server queries, stored procedures, and performance tuning, • Strong experience in implementing responsive and interactive front‑end components using JavaScript, HTML, and CSS, • Solid understanding of SCADA solutions and industrial communication protocols, • Strong problem‑solving skills and attention to detail, • Excellent communication and teamwork skills, • AVEVA MES, • AVEVA System Platform, • AVEVA Work Tasks, • AVEVA Enterprise Integrator, • AVEVA InTouch OMI Our dynamic global team of 700+ engineers, developers, consultants, solution architects and project managers are at the forefront of delivering AVEVA cutting‑edge solutions to customers. The work is complex and technical, but immensely rewarding: we empower customers to harness the full transformative potential of AVEVA’s solutions. If you’re analytical, pragmatic, and driven to make a tangible impact on the sustainability of the industrial sector, our team is the perfect place for you. Come and join AVEVA to create the transformative technology that enables our customers to engineer a better world. Find out more: en/about/careers/ AVEVA requires all successful applicants to undergo and pass a comprehensive background check before they start employment. Background checks will be conducted in accordance with local laws and may, subject to those laws, include proof of educational attainment, employment history verification, proof of work authorization, criminal records, identity verification, credit check. Certain positions dealing with sensitive and/or third party personal data may involve additional background check criteria. AVEVA is an Equal Opportunity Employer. We are committed to being an exemplary employer with an inclusive culture, developing a workplace environment where all our employees are treated with dignity and respect. We value diversity and the expertise that people from different backgrounds bring to our business. #J-18808-Ljbffr

Selection changes the language of the page/content Apple’s Silicon Engineering Group (SEG) is seeking a talented and motivated SoftwareEngineer to join the Documentation Tools team. Our team develops a comprehensive platform,spanning CLIs, UIs, and APIs, that empowers silicon engineers to author the critical technicalspecifications guiding the design of Apple's industry-leading chips.In this role, you will help build, optimize, and scale the tools that directly impact the efficiencyand quality of our chip design process. This is an excellent opportunity for an early-careerengineer or recent graduate to grow their skills. You will be paired with senior mentors andhave the opportunity to learn complex system architecture while making a tangible impact onthe chips at the core of future Apple products loved by millions of customers. Design and Develop: Collaborate to build and maintain scalable CLIs, UIs, and APIs thatstreamline and automate the creation, review, and verification of hardware specifications.Optimize Performance: Assist in diagnosing and troubleshooting performance bottlenecks,learning to navigate and optimize a complex, JVM-based toolchain to ensure a seamlessexperience for our engineering teams.Collaborate and Support: Partner with the documentation support team to deliver toolchaintraining, technical guidance, and best practices directly to silicon designers.Document: Author clear, comprehensive documentation for platform architecture, toolchainworkflows, and internal processes.Innovate: Bring fresh perspectives and a curious mindset to help identify and implementprocess and codebase improvements alongside senior engineers • Foundational understanding of domain modeling, schema design, and complex datastructures., • Familiarity with designing schemas and working with PostgreSQL or other relationaldatabases., • Exposure to or familiarity with build systems (SBT, Gradle, Maven, or Ant) and version controlsystems (Git, Perforce)., • Understanding of the core concepts of software test environments, release cycles, andquality assurance best practices.Knowledge of these is a plus:, • Familiarity with automated CI/CD pipelines (GitLab CI, Jenkins, TeamCity)., • Comfortable working and troubleshooting within macOS, Linux, and UNIX environments., • Academic, internship, or project-based experience with Scala and the JVM ecosystem (Javaexperience is also valued). At Apple, we're not all the same. And that's our greatest strength. We draw on the differences in who we are, what we've experienced and how we think. Because to create products that serve everyone, we believe in including everyone. Therefore, we are committed to treating all applicants fairly and equally. As a registered Disability Confident employer, we will work with applicants to make any reasonable accommodations. Apple will consider for employment all qualified applicants with criminal backgrounds in a manner consistent with applicable law. Learn more At Apple, we believe accessibility is a fundamental human right. You’ll find that idea reflected in everything here — in our culture, our benefits and our digital tools. By welcoming as many perspectives as possible, we help you build a career where you feel like you belong. Learn about accessibility in Apple’s workplace #J-18808-Ljbffr

In this role you will be working within the Market Development, Global Sector Support team to deliver bespoke Solutions for targeted market sectors e.g. Beverage, Food and Pharmaceutical. You will provide embedded and PC-based software development, deployment and support. The successful candidate will: • Perform site visits/surveys internationally when required for requirements capture, testing, debugging., • Create test harnesses for validating own developments., • Work flexibly and adapt to changing priorities, providinga quick response to customer technical issues., • Author technical documentation., • Utilise their electronic/electrical skills in interfacing and wiring up e.g. AppBox3/Printers to customer equipment and internal test fixtures. We recognise that flexible homeworking can be beneficial and at Domino we want people to feel able to own the way they work. The successful candidate will be required to make occasional visits to Domino Headquarters in Cambridge. This role will also involve occasional international travel to support customers. We are looking for someone with experience of working with production systems and enjoys problem solving. You must have experience with software source code and artifact management (GitHub, Fusion, Publishing, Analysis). Candidates must be able to speak English to a high technical level. Our ideal candidate will have: • Demonstrable embedded software skills (C/C++/RTOS/IO/Peripheral-control). Especially, RS232and Ethernet comms/protocols and TLS, HTTP(S), Javascript,server/client architectures., • PC software skills (IT infrastructure, C# .NET, http, JavaScript)., • Knowledge of the C&W applications and OEM’sincludingknowledge of the development environment associated with it. [Otherwise, knowledge transfer and training will be required]., • Knowledge of Domino inkjet printing especially Ax with Komax printing pack. [Otherwise, knowledge transfer and training will be required]., • Familiarity with CRA requirements for compliant products. As a valued member of the Domino team, you’ll receive a competitive salary and a comprehensive benefits package tailored to your local site. We are a highly successful company, we’re large enough to offer career development opportunities yet small enough for your contribution to be readily recognised and rewarded. At Domino Printing Sciences we do more. Our expertise isn't just in providing cutting-edge variable data printing technology; it's in revolutionising how manufacturers embrace sustainable packaging and spearhead advancements in coding automation. We’ve been a part of the global variable data printing story for a long time, and our solutions help ensure the success of the world’s leading brands. Our goal is to be the leading global variable data printing brand through applying our expertise and reliable solutions to help the world’s manufacturers be sustainable and cut waste, while attracting, informing, and protecting their consumers. But we also know that it’s not just about the work we do—it’s about fostering a collaborative, dynamic and welcoming environment where everyone can flourish, contributing to Domino not only as a pioneer in the industry but also as an exceptional place to work. Positions may be at an advanced stage of the recruitment process and can close at any time. #J-18808-Ljbffr

We are working for a Neurosymbolic Researcher (Cambridge) for a hybrid role for one of the biggest names in Tech! 3 days onsite, 2 remote for a top three brand known worldwide on their Neurosymbolic Research! • At least 1-2 first author papers in major conferences (ACL,neurip,icml,iclr,aaai,cvpr), • Better if some background in neurosymbolic AI, robotic/embedded AI or world models #J-18808-Ljbffr

This is a Substantive Consultant Surgeon post at Papworth Hospital. The post-holder will be expected to be proficient in adult general thoracic surgery as practiced in the UK. The post-holder will work with the existing team of NHS Consultant Surgeons. This job is currently based around fixed operating sessions and flexible cover for the other thoracic surgery sessions (currently 6 operating days Mon-Fri with ad-hoc Saturday lists). Have responsibility for patients admitted under the care of the thoracic surgical service, and provide assessment, treatment and follow up for patients requiring thoracic surgery. Provide a cohesive service with the other Consultants and contribute to the smooth running of Thoracic Services. Maximise thoracic surgery operating session use through developing and providing cover for both external and internal MDTs. Contribute to the training of junior doctors in accordance with standards required by college, Postgraduate Dean and hospital. Demonstrate a commitment to continuing professional development and work with the team to build the academic activities of the thoracic surgery group. Work with the team to support thoracic surgical / oncological related research, as part of an agreed research programme, and to contribute to audit activities. The on‑call Consultant Surgeon at Papworth Hospital also provides cover for thoracic trauma at Addenbrooke's Hospital and occasional, emergency cases from the rest of the Eastern Region. The post holder will participate in an on‑call consultant rota for thoracic surgery which is on a 1 in 4 basis. Currently there are separate on‑call rotas for thoracic surgery, cardiac surgery and cardiothoracic transplant surgery, and the surgical group works effectively together. Clinical support is provided by the resident surgical team, advanced nurse practitioners who are ward based and surgical care practitioners (SCP) on a firm and rota system. Royal Papworth Hospital NHS Foundation Trust is the UK's leading heart and lung hospital, delivering care to more than 50,000 patients a year in its new state‑of‑the‑art hospital in Cambridge. We perform the most heart and/or lung transplants in the UK and carried out the UK's first successful heart transplant in 1979. It also offers emergency heart attack treatment, sleep centre care and is one of just five centres nationally for those in severe respiratory failure. Based on the Cambridge Biomedical Campus the largest centre of medical research and health science in Europe the Trust is at the heart of treatments of the future. Royal Papworth became the first hospital trust in the country to be rated outstanding in all five areas assessed by the Care Quality Commission - a rating it still holds today. The Trust holds its values of compassion, excellence & collaboration at its core, and all colleagues joining the team are expected to uphold these in their day‑to‑day roles & interactions. Royal Papworth is proud of its diverse workforce and encourages people to embrace their individuality. The Trust values difference and welcomes all applications irrespective of age, disability, gender reassignment, marriage and civil partnership, pregnancy & maternity, race, religion & belief, sex and sexual orientation. Providing they meet the minimum post criteria, applicants with disabilities will be offered an interview. For a street view tour: virtual-tour On this page you will find a Role Profile which provides information about the hospital and full details about the role. We recommend that you review this and refer to it as you complete your application. Please include how you will meet the Trust Values Compassion, Excellence and Collaboration. If you would like more information about the role or working at Royal Papworth Hospital, please get in touch with the contact for this role. • Primary medical qualification (MBBS, MBChB, or equivalent) FRCS (CTh) or equivalent Full GMC registration with licence to practise, • Entry on the GMC Specialist Register for Cardiothoracic Surgery via CCT, CESR, or European Community Rights, • Eligible for specialist registration on commencement of the post, • Higher degree (MD, PhD, or equivalent) in a relevant discipline Postgraduate qualification in medical education, • Existing substantive NHS consultant status, • Significant post‑CCT experience in adult thoracic surgery, or equivalent consultant‑level independent practice, • Demonstrable volume of lung resections, including VATS anatomical resections, • Experience in managing thoracic oncology patients within an MDT setting, • Experience in thoracic trauma management, • Evidence of excellent clinical outcomes commensurate with a world‑class thoracic surgery centre, • Independently performs VATS lobectomy and sublobar resections, • Competent in open thoracic procedures including sleeve resections, chest wall resection, and mediastinal procedures, • Capable of managing thoracic surgical emergencies independently, • Proficient in diagnostic and therapeutic bronchoscopy, • Demonstrated ability to lead a multi‑professional clinical team, • Experience in service development and contributing to departmental strategy, • Understanding of NHS structures, governance, and consultant accountability, • Ability to manage clinical resources effectively, including theatre utilisation, • Experience in organising and delivering teaching programmes to medical students, junior doctors, and allied health professionals, • Training in educational supervision and appraisal, • Commitment to training and professional development of the wider surgical team, including SCPs, • Understanding of research methodology and clinical trial design, • Active involvement in clinical research with evidence of output, • Record of initiating, completing, and presenting clinical audit projects, • Demonstrated commitment to clinical governance and patient safety, • Experience in morbidity and mortality review processes, • Excellent communication skills -- able to engage effectively and sensitively with patients, families, and colleagues, • Demonstrated ability to work collaboratively within a multi‑disciplinary team, • Leadership skills including the ability to motivate, mentor, and support colleagues, • Flexible, adaptable, and resilient under pressure, • Commitment to the Trust values of compassion, excellence, and collaboration, • Professional integrity and accountability, • Ability to participate in a 1:4 on‑call rota,, • Willingness to work flexibly across sites when clinical need requires, • Eligibility to live and work in the UK, • Occupational health clearance, • Enhanced DBS disclosure, • Experience in robotic thoracic surgery (RATS), • Subspecialty expertise in lung volume reduction surgery, hyperinflation procedures, chest wall reconstruction, or airway surgery, • Experience in lung transplantation, • Track record of delivering enhanced recovery programmes, • Robotic thoracic surgical skills (CMR Versius or equivalent platform), • Track record of delivering organisational change or service transformation, • Postgraduate certificate, diploma, or Master's in medical education, • Educational supervisor recognition by the GMC or Postgraduate Deanery, • Faculty on national or international surgical courses, • Higher research degree (MD, PhD, or MPhil by thesis), • Peer‑reviewed publications as first or senior author in thoracic surgery, • Successful grant applications or research funding track record, • Invited lectures or presentations at national or international meetings, • Quality improvement qualification (e.g. IHI, NHS QI training), • Published audit or quality improvement outcomes, • Participation in national clinical audits (e.g. SCTS, NLCA), • Mentor or coaching qualification, • Full driving licence, • Please provide evidence of your commitment to uphold the Trust's values: Compassion, Excellence, Collaboration This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions. Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab). From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab). Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window). #J-18808-Ljbffr

Job Description SummaryAs a Principal Scientist, you will lead and execute formulation development and characterization strategies for complex biologics—including monoclonal antibodies (mab’s), multispecifics, antibody-drug conjugates (ADCs), and other modalities. You will work closely with a team of more than 10 associates, driving scientific excellence while fostering a culture of collaboration, integrity, and innovation aligned with Novartis values.You will play a key role in shaping formulation strategies during early-stage development and supporting candidate selection by identifying developability risks. This position offers broad exposure to diverse biologics modalities and opportunities to contribute both experimentally and strategically.Job DescriptionInternal Job Title: Principal Scientist I/IIPosition Location: Cambridge, MA, onsiteJob descriptionThe Biologics Center at Novartis Biomedical Research (BRC) is seeking a highly motivated leader and experienced scientist in biologics formulation to join the Analytics, Bioanalytic, and Formulation (ABF) unit. In this role, you will contribute to the development of a diverse portfolio of biotherapeutic modalities.The ABF unit supports the characterization and formulation of therapeutic protein candidates across multiple formats, spanning discovery through transition to development. Our multidisciplinary team brings deep expertise in physicochemical characterization, mass spectrometry, and formulation sciences within a collaborative, global environment.Role OverviewAs a Principal Scientist, you will lead and execute formulation development and characterization strategies for complex biologics—including monoclonal antibodies (mAbs), multispecifics, antibody-drug conjugates (ADCs), and other modalities. You will work closely with a team of more than 10 associates, driving scientific excellence while fostering a culture of collaboration, integrity, and innovation aligned with Novartis values.You will play a key role in shaping formulation strategies during early-stage development and supporting candidate selection by identifying developability risks. This position offers broad exposure to diverse biologics modalities and opportunities to contribute both experimentally and strategically.Key responsibilities:Design and execute formulation screening strategies for large-molecule therapeutics, with emphasis on mAbs and related biologic modalitiesLead studies to identify stable formulations and communicate results to cross-functional R&D teamsManage team resources, timelines, and deliverables with a strong customer-focused mindsetProvide leadership, mentorship, and direction to team members as the functional managerPromote a safe, inclusive, and collaborative environment while engaging stakeholders across biologics discovery and technical developmentPartner with CMC teams to advance clinical candidates, finalize clinical formulations, and support drug product process developmentDevelop stabilization strategies for liquid, frozen, and lyophilized drug product formats for clinical developmentApply and interpret biophysical and analytical methods, including DSC, DLS, UV-Vis, turbidity, subvisible particle analysis, viscosity, SEC, and HICWork with automation teams to implement high-throughput formulation screening and physicochemical characterization across discovery, optimization, and early developmentOperate analytical instrumentation, analyze data, maintain ELN documentation, and author technical reportsContribute to data interpretation, scientific presentations, and cross-functional discussions within the global BRC communityEssential Requirements: PhD in biochemistry, biotechnology, chemistry, or a related field with 2+ years of relevant industry experienceProven experience leading, coaching, and developing scientific teamsHands-on expertise in protein formulations and assessment of biophysical properties of the molecule (e.g., DLS, Viscosity, Thermal and colloidal stability)Strong background in developing strategies for formulations for large-molecule therapeutics, with understanding of early-stage development workflowsExperience designing and executing preformulation studies and interpreting stability-indicating assays (e.g., SEC, CE, charge variants, MS)Demonstrated problem-solving skills, scientific curiosity, and ability to work independentlyExcellent communication, organizational, and multitasking skillsDesirable Requirements: Knowledge of viral vector-based gene therapy (AAV, LVV) formulation and characterizationFamiliarity with DoE tools (e.g., JMP) for high-throughput experimental designExperience working with automated liquid handling systemsCompensation and Benefits:The salary for this position is expected to range between $108,500 and $201,500 per year for Principal Scientist I, and between $119,700 and $222,300 per year for Principal Scientist II. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.To learn more about the culture, rewards and benefits we offer our people click here. EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.Salary Range$108,500.00 - $201,500.00Skills DesiredAnalytical Thinking, Chemical Biology, Chemistry, Clinical Trials, Collaboration, Curious Mindset, Data Analysis, Detail-Oriented, Drug Development, Ethics, Gene Therapy, Immunology, Inventory Management, Machine Learning (ML), Medical Research, Molecular Biology, Python (Programming Language), ScienceSummaryLocation: Cambridge (USA)Type: Full time

Apple’s Silicon Engineering Group (SEG) is seeking a talented and motivated Software Engineer to join the Documentation Tools team. Our team develops a comprehensive platform, spanning CLIs, UIs, and APIs, that empowers silicon engineers to author the critical technical specifications guiding the design of Apple's industry‑leading chips. In this role, you will build, optimize, and scale the tools that directly impact the efficiency and quality of our chip design process. You will support the engineers designing the chips at the core of future Apple products loved by millions of customers. • Design and Develop: Build and maintain scalable CLIs, UIs, and APIs that streamline and automate the creation, review, and verification of hardware specifications., • Optimize Performance: Proactively diagnose, troubleshoot, and resolve performance bottlenecks across a complex, JVM‑based toolchain to ensure a seamless experience for our engineering teams., • Collaborate and Train: Partner with the documentation support team to deliver toolchain training, technical guidance, and best practices directly to silicon designers., • Document: Author clear, comprehensive documentation for platform architecture, toolchain workflows, and internal processes., • Innovate: Bring experience and sound judgment to continuously drive architectural and process improvements across multiple simultaneous projects and systems., • Strong software engineering background with deep expertise in Scala and the JVM ecosystem (Java experience is also valued)., • Solid understanding of domain modeling, schema design, and complex data structures., • Working knowledge of XML and related document technologies (e.g., XSLT, XPath)., • Experience designing schemas and working with PostgreSQL or other relational databases., • Proficiency with build systems (SBT, Gradle, Maven, or Ant) and version control systems (Git, Perforce)., • Experience building and maintaining automated CI/CD pipelines (GitLab CI, Jenkins, TeamCity)., • Strong understanding of software test environments, release cycles, and quality assurance best practices., • Advanced expertise in the XML stack: XSLT 2.0/3.0, XPath 2.0/3.1, XQuery 3.1, XSD 1.0/1.1, and XProc., • Experience developing custom plugins for build systems., • Hands‑on frontend or app development experience (HTML/JavaScript/CSS, iOS, or macOS)., • Comfortable working and troubleshooting within macOS, Linux, and UNIX environments. At Apple, we are committed to treating all applicants fairly and equally. We draw on the differences in who we are, what we've experienced, and how we think, to create products that serve everyone. As a registered Disability Confident employer, we will work with applicants to make any reasonable accommodations. Apple will consider for employment all qualified applicants with criminal backgrounds in a manner consistent with applicable law. Our accessibility policy reflects our belief that accessibility is a fundamental human right, and we welcome a wide range of perspectives. #J-18808-Ljbffr

Author and maintain Safety Data Sheets (SDS) in line with regulatory requirements.

We are looking for an experienced Technical Author to work within a highly technical environment, partnering closely with SMEs at the Met Office. Proven experience as a Technical Author / Technical Writer.

OEM Client in Gaydon seeks a Technical Author for Homologation to translate customer needs and regulations into vehicle efficiency requirements.

The Document Author shall be responsible for assisting in the production of operational documenta.

Technical Author needed for a manufacturing business specializing in luxury vehicles. Responsibilities include setting vehicle efficiency requirements and authoring technical requirements for a team.

Experienced Technical Author needed for a manufacturing business to create high-level documentation for machinery.

Seeking a Technical Author for a hybrid role at Westlakes Science Park/Sellafield Site.

Are you looking to benefit from a new career in Project Management?.If you are organised, competent, dependable and can communicate well and motivate those around you; you could have a truly rewarding future as a Project Manager.We do this using our specialised programme looking at placing candidate

Residential Support Worker – Children’s Services - Glenrothes, Fife (KY7).Be the reason a child feels safe, supported, and heard.At Newcross Healthcare, we’re on a mission to help children and young people thrive.We’re looking for compassionate.If you’ve got experience working with childre

Work within the Councils estate of buildings undertaking cleaning duties as directed by line manager in accordance with the practices and procedures of the service.We are keen to employ a diverse workforce that reflects the people of Scotland.We welcome applications from all backgrounds and particul

Early Learning Support Worker (Supply).Renfrewshire Council are looking to recruit enthusiastic and caring early learning support workers for our general supply pool.Appointable candidates will be required to work on a temporary basis covering short or long-term requirements within early learning an

Fixed Term until 31 December 2027.Work within the Councils estate of buildings undertaking cleaning duties as directed by line manager in accordance with the practices and procedures of the service.We are keen to employ a diverse workforce that reflects the people of Scotland.We welcome applications

The salary advertised is full time (35 hours per week, 52 weeks per year).Part-time hours / sessional posts will be pro-rated accordingly.This is a 40-week sessional post i.Monday - Thursday, 15:00-18:00.To assist in the provision of a high quality cleaning service within Council buildings.Please do

Applicants who have been resident outside the UK within the last 5 years, if offered a position, in addition to a Disclosure Scotland Check, will be required to provide a completed police record check from the police authority in the country or countries in which they were resident.

General Assistant / Cleaner - Netherfield.Help Create an Exceptional Fitness Environment.At Everlast Gyms, we're committed to delivering outstanding fitness experiences for our members.Our clubs are built on high-quality facilities, exceptional service and an environment where people can train with

Holidays Cottage Cleaner - Veryan.We are looking for 2 Holidays Cottage Cleaners to clean and prepare our stunning holiday cottages in Veryan and Porth (just outside Portscatho).This role is based on annualised hours, where the amount of hours you work each month may vary, however your salary will b

The National Autistic Society is committed to safeguarding and promoting the welfare of all children and adults who use our services.Successful applicants will be required to complete the relevant safeguarding checks.Join Us as a Bank Support Worker.The National Autistic Society helps create a world

Job Title: Associate Project Manager.Location: Cambridge (Projects in Norfolk & Cambridgeshire + Flexible working).Salary: c£75k-£80k plus competitive package inc car allowance, pension, health etc.A innovative project management consultancy are looking for a client focused Associate level Project

The National Autistic Society is committed to safeguarding and promoting the welfare of all children and adults who use our services.Successful applicants will be required to complete the relevant safeguarding checks.Join Us as a Senior Support Worker.The National Autistic Society helps create a wor

Alternating weekly early and late shifts.Early shift (45 hours) Monday 8am-4pm, Tuesday 7am-5pm, Wednesday - Friday 7am-4pm.Late shift (32 hours) Mon-Thurs 2:30pm-10:30pm.Gretton School welcomes autistic children and young people aged from 5-19 years old, as weekly boarders or as day learners.Every

The National Autistic Society is committed to safeguarding and promoting the welfare of all children and adults who use our services.Successful applicants will be required to complete the relevant safeguarding checks.The National Autistic Society helps create a world that works for autistic people,

We are looking for passionate Childrens Support Workers who are available to work on a flexible basis.As a Childrens Support Worker you will work as part of a team to deliver a high standard of care at all times and support the Young Persons emotional wellbeing.You recognise that the role is to help

Cameo is recruiting for a Project Manager to join an established and innovative technology business based in Banbury on a full time, permanent basis.This is a great opportunity for someone looking to develop their project management career within a software and technology environment, working on int

Barker Ross are currently recruiting for Warehouse Operatives to join a busy logistics operation based in Banbury, OX16.We are looking for reliable and hardworking people who are comfortable working in a fast paced warehouse environment.Previous warehouse experience is useful, but not essential,

Maintenance Manager Ellesmere Port Monday to Friday Up to £50,000 *Additional Hours If Required* We are looking for a motivated Maintenance Manager to join a market leading company within their field.Reporting directly to the Group Engineering Manager you will be a key member in ensuring the pr

Childrens Residential Support Worker Temp to Perm 39 hours per week | £12.Immediate starts available We are currently recruiting for a Childrens Residential Support Worker to join a residential home supporting children aged 513 years with emotional and behavioural difficulties (EBD).This is a

Self-Employed Cleaner GBP £13 - 16 per hour Your role Provide cleaning services in clients' homes near you, in the area you choose to cover.Typical tasks may include c leaning living areas, kitchens, bedrooms and bathrooms , as well as general home upkeep based on each client's needs.Jobs can be on

Technical Manager Duration: 4 months Outside IR35 Rate: £60 ph Location: Batley, Hybrid working Role Overview We are seeking an experienced Technical Manager with a Systems Engineering background to lead and coordinate technical activities across projects and programmes.The successful candidate wil

Vacancy Summary Job Title: Project Manager Job Type: Permanent Job Ref: #1438 Location: Cambridge Start Date: ASAP Salary: c£70k-£80k basic plus competitive package inc car allowance, pension, bonus, market leading holiday allowance etc.Company & Project: A successful and privately ow

Sector: EnergyReference: BBBH273436_1792057352Technical Manager (Renewable Energy)Field and Office-based - 1-hour radius of Cambridge55,000-60,000 + Growth + Healthcare + Enhanced Pension + Enhanced Parental Pay + Life Assurance + 25 Days Holiday!Are you an experienced engineer who is looking to tak

Are you a Project Manager looking for your next opportunity?Thanks to our growing client relationships across the country, our teams are tackling an exciting range of projects across the regulated water industry.These opportunities are enabling us to continue our growth, and we are looking to appoin

Sector: EngineeringReference: BBBH280741_1791472827Regional Business Development Manager50,000 - 55,000 (OTE 65,000) + Car Allowance + Progression + Full AutonomyHome Based (Ideally located: Cambridge, Bedford, Luton, Oxford and Surrounding Areas)Are you from a technical sales, or business developme

Ensure de-escalation is the primary response and that restrictive interventions are only used as a last resort where lawful, necessary, proportionate and authorised.