Chemical jobs in CambridgeCreate job alerts

Grounds Maintenance OperativeWe are recruiting for a Grounds Maintenance Operative to join a well-established organisation in Cambridge, helping to maintain and improve a diverse range of outdoor spaces. This is a hands-on role where you'll play an important part in ensuring the grounds and gardens remain safe, presentable and maintained to a high standard throughout the year.Working as part of an experienced team, you will contribute to the ongoing maintenance, renewal and development of outdoor areas.Key responsibilities:Carry out a range of grounds maintenance duties across designated sites, ensuring all areas are maintained to a high standard.Support the day-to-day planning and delivery of grounds and garden maintenance activities.Assist with seasonal preparations, including the ordering and management of plants, materials and records such as chemical usage.Ensure the safe use, storage and maintenance of tools, equipment, vehicles and workspaces.Follow Health & Safety procedures and assist with risk assessments, reporting hazards and incidents where necessary.About you:Previous experience within grounds maintenance, landscaping or horticulture.Good working knowledge of grounds maintenance equipment, tools and environmental practices.Strong communication skills with the ability to work effectively as part of a team.A full UK driving licence, including towing capability.The ability to work outdoors in all weather conditions and undertake physically demanding work.It would be advantageous to have plant knowledge, experience using handheld and ride-on machinery, and familiarity with Microsoft Office, PDAs or computer-aided facilities management systems.The successful candidate will be educated to GCSE level or equivalent. Training or certification in the use of grounds maintenance machinery would be beneficial, although this is not essential.The role is Full-time, site-based role working approximately 34.5 hours per week. There may be occasional weekend and out-of-hours work, which will be arranged in advance.If you are looking for a varied position where you can contribute to the upkeep and ongoing development of a large and diverse outdoor environment, we'd love to hear from you.Please apply via the advert or contact Cheryl at The HireWorks for more information.We endeavour to reply to every candidate, every time, but if you haven't heard back within 10 days, please understand that you have unfortunately been unsuccessful for this position, or the position has been filled. Please call the office or send an email to discuss other potential opportunities.TPBN1_UKTJ

Job Description SummaryWe are seeking a highly motivated and experienced scientist to lead a Human Genetics laboratory. You will drive the translation of human genetic insights into actionable biological hypotheses to enable target discovery and validation across disease areas. The successful candidate will lead a small team of biologists and shape the genotype-to-phenotype translation strategy, integrating rare variant genetics, functional biology, and advanced analytical approaches to inform target prioritization.This position is part of the Human Genetics & Targets group within the Discovery Sciences (DSc) department in Biomedical Research at Novartis. The Human Genetics & Targets team is a global group of computational and experimental scientists dedicated to validating or invalidating genetics-driven target hypotheses. The team's extensive expertise in genetics analytics, biology, and translatable models is enhanced by DSc's capabilities in AI, functional genomics, chemical biology, and more. The team collaborates with disease area specialists to not only identify disease associations but fully understand the underlying disease mechanisms and advance drug discovery projects to benefit patients in need.Job DescriptionInternal Job Title: Senior Principal Scientist or Associate Director Position Location: Cambridge, MA, onsite #LI-onsiteKey responsibilities:Lead and develop a high-performing team of 2-3 wet lab scientists, establishing state-of-the-art experimental capabilities to functionally characterize human genetic variationManage resources, priorities, and execution across multiple projects, ensuring high-quality data generation, interpretation, and delivery aligned with strategic goalsApply genetics expertise to enable recall-by-genotype strategies, including participant identification from biobank resources and design of deep phenotyping protocolsServe as senior scientific leader to evolve the genotype-to-phenotype research strategy, translating rare variants into biological hypotheses and target investment decisionsRepresent genetics expertise in cross-functional teams and governance boards, contributing to portfolio prioritization alongside computational biology and disease area expertsBuild and maintain strong internal and external partnerships, communicating scientific insights effectively to diverse audiencesEssential Requirements: PhD with 8+ years of post-graduate experience in genetics, with a focus on rare variants and/or genotype-to-phenotype translationStrong background in experimental biology, including cellular models and gene perturbation technologies relevant to variant characterizationExtensive experience connecting clinical and/or biobank genetic data to biological mechanisms and therapeutic hypotheses across disease indicationsProven people leadership skills, including mentoring and developing scientists, with the ability to influence cross-functional teams in a matrix environmentCuriosity for emerging technologies and methods, including AI-based approaches for variant interpretation and prioritizationExceptional collaboration, communication, and problem-solving skills, with a strong track record of scientific innovationDesirable Requirements:Hands-on experience in designing and executing recall-by-genotype studiesTarget and/or drug discovery experience in an industry settingThe salary for this position is expected to range between $138,600 and $257,400 USD annually for Senior Principal Scientist, and $152,600 and $283,400 USD annually for Associate Director. 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$138,600.00 - $257,400.00Skills DesiredAnalytical Thinking, Chemical Biology, Chemistry, Clinical Research, Clinical Trials, Collaboration, Curious Mindset, Data Analysis, Decision Making, Detail-Oriented, Drug Development, Ethics, Machine Learning (ML), Medical Research, Mentorship, Patient Care, Science, Stakeholder Engagement, Stakeholder ManagementSummaryLocation: Cambridge (USA)Type: Full time

Controls and Instrumentation EngineerLocation: Slough, United KingdomThe actual location of this job is in Slough, United Kingdom. Relocation assistance is available for eligible candidates and their families, if needed.Join Lonza Biologics in Slough as a Controls and Instrumentation Engineer and play a key role in supporting the reliable operation and continuous improvement of our biopharmaceutical manufacturing facilities. You will use your expertise in automation, control systems, and instrumentation to help deliver safe, compliant, and high-quality processes that support the manufacture of life-changing medicines.This is a fully site-based role. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.What you will get:An agile career and dynamic working culture where you can develop your technical expertise and grow your career.The opportunity to work with advanced automation and control technologies within a leading biopharmaceutical manufacturing environment.An inclusive and ethical workplace where collaboration and innovation are encouraged.Compensation programs that recognize high performance.A variety of benefits dependent on role and location.The full list of our global benefits can be found here: .What you will do:Design, develop, implement, and maintain control systems and instrumentation solutions that support biopharmaceutical manufacturing processes.Configure, troubleshoot, and optimise automation systems including PLCs, Distributed Control Systems (DCS), and SCADA platforms.Develop and maintain engineering documentation, including control strategies, functional specifications, control narratives, wiring diagrams, and technical drawings.Maintain, calibrate, and troubleshoot process instrumentation including sensors, transmitters, valves, and analytical equipment to ensure reliable operation.Lead and support commissioning, qualification, and validation activities for control systems and instrumentation.Collaborate with manufacturing, quality, engineering, IT teams, and external suppliers to deliver effective technical solutions.Drive continuous improvement initiatives, conduct root cause investigations, and provide technical support and training to operational teams.What we are looking for:A degree in Electrical Engineering, Automation, Chemical Engineering, or a related technical discipline, or equivalent relevant experience.Significant experience in controls and instrumentation engineering, ideally gained within a biopharmaceutical, pharmaceutical, or other regulated manufacturing environment.Strong experience with PLC programming and troubleshooting, including platforms such as Rockwell Automation or Siemens.Experience working with Distributed Control Systems (DCS), particularly Emerson DeltaV, and HMI/SCADA platforms.Strong knowledge of process instrumentation principles, calibration techniques, troubleshooting methodologies, and industrial communication protocols.Experience working in a GxP/cGMP regulated environment, with knowledge of computerized system validation (CSV) principles.Ability to interpret P&IDs, electrical schematics, and technical documentation, with excellent problem-solving and communication skills.About LonzaAt Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.Ready to shape the future of life sciences? Apply now.SummaryLocation: UK - Slough; UK - CambridgeType: Full time

Job Description SummaryNovartis Biomedical Research is seeking a highly motivated and scientifically accomplished Translational Biomarker Strategy Lead to serve as the biomarker representative and strategic advisor on DAx project teams.This role will lead the development and execution of preclinical and translational biomarker strategies from target validation through development candidate nomination and early clinical planning. The Biomarker Strategy Lead will partner closely with Biology, In Vitro, In Vivo, Data Science and Biomarker Development to ensure biomarker plans are aligned with key program decisions and support target engagement, pharmacodynamic assessment, patient stratification, and translational decision-making.The successful candidate will act as the single point of contact for biomarker strategy within assigned DAx programs, integrating scientific, technical, operational, and external capabilities to deliver execution-ready biomarker plans that enable efficient progression of the portfolio.Job DescriptionMajor accountabilities: Lead development of stage-appropriate preclinical and translational biomarker strategies for DAx programs from target validation through early clinical development readiness.Serve as the biomarker representative and single point of contact on assigned DAx project teams.Define biomarker hypotheses, context of use, evidence requirements, and decision criteria aligned with program milestones.Develop integrated biomarker plans encompassing assays, models, samples, analyses, timelines, and external partnerships.Partner across Biology, In Vitro, In Vivo, Data Science, Preclinical Safety, Quantitative Sciences, Translational Medicine, and Biomarker Development to align biomarker activities and execution.Generate translational evidence linking target biology, pharmacology, and biomarkers to support key portfolio decisions.Drive external collaborations and leverage innovative technologies, datasets, and human sample resources to strengthen biomarker strategies and research-to-development transition.Minimum QualificationsPhD, MD, PharmD, or equivalent in biology, pharmacology, immunology, translational medicine, molecular biology, or related discipline.7+ years of experience in translational research, biomarker strategy, biomarker discovery, or drug development within the pharmaceutical or biotechnology industry.Demonstrated experience developing biomarker strategies supporting drug discovery and development programs.Strong understanding of biomarker applications including target engagement, pharmacodynamics, patient stratification, disease activity, and mechanism-based biomarkers.Experience leading cross-functional matrix teams and influencing scientific strategy without direct authority.Excellent communication, presentation, and stakeholder management skills.RewardsAt Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen. The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and a minimum of 14 weeks paid parental leave. Expected Annual Base Salary Range for role: USA: 114,100.00 - 211,900.00 USD AnnualThe salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. Further details will be provided during the application process. Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics. Read our brochure to learn more about our global total rewards offering: Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process.=Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: 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$114,100.00 - $211,900.00Skills 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

66000 - 80000 per annumCambridge, EnglandPermanentMy Client is recruiting for an Associate Director Mechanical Engineering in the Water SectorLocation: Peterborough, Cambridge, London or SurreyWe are looking for an energetic and experienced Associate Director Mechanical Engineer to join our team within the Design & Advanced Technology (D&AT) Practice. You'll be part of a talented, multi-disciplinary team delivering cutting edge, iconic projects to our Water market clients.As a key member of our team, you'll play a vital role in delivering transformational programmes for critical UK infrastructure, with opportunities to work on landmark engineering projects both domestically and internationally. We're committed to providing industry-leading solutions throughout the project lifecycle, adding value through client-side and construction-phase support.Become part of a team where every voice matters, and together we can tackle our clients' toughest challenges. We foster a diverse and inclusive environment where world-class talent thrives without boundaries. For us, collaboration isn't a buzzword. We value the different perspectives our people bring and recognise everyone for their contributions equally.We also know that different people have different priorities, which is why we're here to support you with whatever you need.Your roleThe role will offer a challenging and rewarding opportunity to apply knowledge, experience, and problem-solving skills whilst providing good opportunities for career development.As an Associate Director Mechanical Engineer in the D&AT practice, the successful candidate would have the following responsibilities:Lead a team of Mechanical engineers for delivery of technical design work on complex multi-disciplinary projects following relevant national and project specific design codes and standards, and to high-quality levels in areas such as pumping systems and water & wastewater treatment design.Lead on the development of project design deliverables for Mechanical aspects of complex multi-disciplinary projects and work with the project management team to successfully manage time and budgets to key project milestones and programmes .Responsible for managing production, reviewing, and approving technical deliverables such as design reports, drawings, calculations, and scopes of work.Provide Technical Leadership within discipline for the regional and national D&AT practice and influence D&AT Practice wide initiatives and recommend best practices to improve internal process and services.Grow, develop, and manage the Mechanical Engineering capabilities within the regional and/or nationally practice.Work independently with guidance in only the most challenging situations. Exercise personal judgement to solve difficult problems where appropriate and provide guidance to junior team members.Advise client, operational, project, or service activities within project teams and wider D&AT Practice initiatives.Manage or collaborate on technical aspects of bid proposals.Work closely with a multi-disciplinary team in the UK and overseas to deliver integrated design solutions.About youA degree in Mechanical Engineering or equivalent.Chartered Mechanical Engineer.Proven experience in leading large-scale Mechanical engineering design delivery for a design consultancy including within a multi-disciplinary environment.Takes broad perspective to identify innovative solutions, challenges the status quo.The role requires comprehensive knowledge and proven practical experience in the design integration of a wide range of mechanical equipment, including pumps, blowers, screens, and chemical dosing systems. Additionally, it demands a thorough understanding of current UK design standards, relevant legislation, and established industry practices.Demonstrates exemplary communication skills, with the ability to convey complex technical concepts clearly and effectively to diverse stakeholders.Expert knowledge of current design codes and standards as well as industry best practices including a strong understanding of legislation such as CDM and DSEAR.Proficiency in applicable analytical software and related tools.Experience in Water market is essential.A proactive, highly motivated mindset with a collaborative approach to drive teamwork and shared success across projects and the wider D&AT practice.Comfortable liaising with stakeholders at all levels both internally and externally.

Job Description Summary#LI-OnsiteInternal job title: Principal Scientist ILocation: Cambridge, United StatesWe are seeking a motivated soluble biomarker expert to lead the development, validation, and implementation of fit-for-purpose soluble biomarker assays, with a focus on immunoassay and LC-MS based methods supporting neuromuscular and muscle disease clinical programs within the Biomarker Development (BMD) Molecular & Cellular Sciences group. This role requires strong hands-on assay development and validation expertise, scientific leadership, and the ability to translate disease biology and program needs into robust biomarker assay strategies that inform clinical decision-making. As a key member of the soluble biomarker group, you will collaborate across BMD and external partner labs to ensure high-quality and timely assay delivery, clear data interpretation, rigorous documentation, and compliance with Novartis standards.Job DescriptionKey Responsibilities: Develop, validate, and implement immunoassay- and LC-MS–based methods to quantify exploratory soluble biomarkers for clinical programs across the Novartis portfolio, with a primary focus on neuromuscular and muscle disease programs.Apply hands-on assay development expertise to build robust, fit-for-purpose biomarker methods that support clinical decision-making and advance translational science objectives.Serve as the scientific and technical lead for exploratory soluble biomarker assays, including assay strategy, data quality, interpretation, documentation, and alignment to context of use and clinical study endpoints.Translate disease biology and program needs into clear biomarker assay plans in partnership with project teams, Translational Medicine, Clinical, Data Science, and external collaborators.Evaluate and implement innovative assay technologies and workflows to improve assay sensitivity, specificity, reproducibility, throughput, and biological relevance for neuromuscular indications.Analyze, interpret, and communicate biomarker and assay data to key stakeholders, project teams, and cross-functional stakeholders to support timely, evidence-based decisions.Partner with internal line functions and external vendors to deliver high-quality fit-for-purpose biomarker assays, and sample analysis activities within agreed timelines.Maintain high standards for scientific rigor, documentation, data integrity, compliance, safety, and technical excellence in accordance with applicable Novartis policies and procedures.Essential Requirements:PhD with 2+ years of experience in drug discovery, translational research, or related field; or Master’s degree with 10+ years of experience in the pharmaceutical/ biotech industry.Strong hands-on experience developing, optimizing, validating, and troubleshooting immunoassays (ELISA, MSD, Luminex, Simoa) and LC-MS methods of varying complexity for soluble biomarkers.Experience with tissue biopsies, particularly muscle tissue, and associated assays or workflows such as IHC/IF, tissue collection, processing, and sample handling best practices.Solid experience supporting neuromuscular, muscle, or related disease biology programs, with the ability to connect assay strategy with the biomarker plan.Demonstrated ability to design rigorous experiments, solve complex technical problems, assess assay performance, and communicate conclusions clearly to scientific and non-scientific stakeholders.Experience working in cross-functional project teams and managing internal or external assay development activities, timelines, deliverables, and scientific documentation.Excellent oral and written communication skills, including the ability to present scientific strategy, data, risks, and recommendations clearly.Commitment to working collaboratively in an inclusive environment and role-modeling Novartis values and behaviors.Desirable Requirements:Experience with genomic, transcriptomic, proteomic, or other multi-omics approaches, including RNA-seq or related platforms.Strong understanding of circulating muscle proteins, including structural and functional biomarkers relevant to muscle disease biology.The salary for this position is expected to range between: $108,500 and $201,500 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.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

Job Description Summary#LI-HybridLocation: CambridgeInternal Title: Senior Principal Scientist or Associate DirectorThe Biomarker Development (BMD) group at the Novartis is seeking a Senior Principal Scientist or Associate Director to join our Clinical Imaging and Analytics team and provide strategic, scientific, technical and operational leadership on the optimal use of imaging in drug development. Be part of an imaging department with deep expertise in structural, molecular, and quantitative biomarkers and their application in translation and development. The successful candidate will provide scientific leadership across Oncology (including Radioligand Imaging), Neuroscience, Cardiovascular/Renal/Metabolic, and emerging precision medicine initiatives, including xRNA programs and novel tracer development. You will partner with clinical trial teams to establish the role of imaging endpoints along novel biological mechanisms across diverse therapeutic areas. The role offers a wide view of programs across various stages as they transition from research to early development, and subsequently to PhII/III trials. As a part of building imaging endpoints, the role also provides unique exposure to variety of other critical biomarkers (soluble and genetics) for an integrated view of identifying unique patient populations, assess target engagement and generate decision-critical readouts of efficacy, safety and mechanism of action.Job DescriptionKey Responibilities:Act as an internal expert in molecular and clinical imaging, including PET, SPECT and other advanced imaging methodologies relevant to clinical and translational drug development. Partner with Oncology and General Medicine teams to develop and lead fit-for-purpose imaging strategies across research, early development and late-stage clinical development. Develop imaging biomarker, target engagement and translational imaging strategies that generate decision-critical evidence for patient selection, pharmacodynamics, efficacy, safety and mechanism of action. Collaborate with internal operational teams, imaging CROs, academic centers and external experts to design, execute and interpret imaging readouts across multisite clinical trials. Ensure quality and timely execution of imaging trials to deliver critical drug development decisions; be agile and responsive to clinical teams during the course of design, execution and interpretation of imaging trials.Evaluate and implement novel imaging techniques, quantitative methodologies, AI-enabled analytics and imaging platform capabilities, to improve portfolio decision making.Essential Requirements:PhD or MD or MD/PhD with 8+ years of experience in PET/SPECT Imaging in academia or industry, including at least 5 years supporting clinical drug development.Deep technical expertise in PET and/or SPECT as applied to clinical drug developmentStrong understanding of clinical trial design, endpoint development, biomarker strategy, statistical considerations and clinical data flow is required. Experience with clinical protocol writing across line functions is required. Experience with PET/SPECT tracer development, radioligand imaging, dosimetry, receptor occupancy or clinical Radioligand/Radiopharmaceutical Therapy (RLT/RPT) is a plus. Experience in regulatory interactions, submissions, first-in-human imaging studies, endpoint validation or qualification is a plus.Understanding of sites, budgets, imaging CROs, imaging data standards and experience with multisite trial execution is a plus.Demonstrated track record of innovative research preferably across imaging modalitiesProactive, self-motivated and independent working style; comfortable operating in a multidisciplinary and highly matrixed organization. Ability to drive for results with urgency, accountability and sound judgment while balancing scientific quality and portfolio priorities.Strong communication skills in English, with demonstrated ability to influence, mentor and act as a collaborative servant leader.This is a dual level posting. The final level & title of the offer role would be determined by the hiring team based on the skills, experience & capabilities required to perform the role at the level the role has been offered.The salary for this position is expected to range between:Senior Principal Scientist: $132,300 and $245,700 per year.Associate Director: $145,600 and $270,400 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.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$132,300.00 - $245,700.00Skills DesiredAnalytical Thinking, Chemical Biology, Chemistry, Clinical Research, Clinical Trials, Collaboration, Curious Mindset, Data Analysis, Decision Making, Detail-Oriented, Drug Development, Ethics, Machine Learning (ML), Medical Research, Mentorship, Patient Care, Science, Stakeholder Engagement, Stakeholder ManagementSummaryLocation: Cambridge (USA)Type: Full time

\n About ScionxBio\n ScionxBio is engineering the next generation of RNA medicines, combining synthetic chemistry and artificial intelligence to create xRNA — a platform for long‑acting therapeutics. By expanding RNA beyond nature's four‑letter alphabet, we engineer molecules that sustain protein expression for weeks to months rather than days, with a lower immunogenic burden and the durability that chronic disease demands. At the heart of the platform is our TERA® engine, a closed‑loop system in which deep‑learning design, proprietary combinatorial assembly, high‑throughput screening, and continuous model retraining work together to optimise each molecule for its payload. With an initial focus on cardiometabolic disease, we are working to turn transient treatments into durable therapies. A spin‑out from Eleven Therapeutics, we are an international team operating across Cambridge (UK), Tel Aviv, and Cambridge (MA), with our Cambridge (UK) site serving as our largest research and development hub. Role Overview\n The Vice President of Platform is the architect of ScionxBio's core technology engine. Reporting to the CEO and sitting within the company's senior leadership, this individual owns the entire upstream pipeline — from computational design and AI‑driven sequence optimisation through to the formulation and delivery systems that carry our molecules into the body, and onward into the evolution of our next‑generation xRNA modalities. This is a rare opportunity to lead, and continue to build, the platform that defines the company: to set its scientific direction, to shape a multidisciplinary team of exceptional scientists and engineers, and to translate a validated modality into a durable, defensible, and endlessly generative source of medicines. We are looking for a scientific leader who is equally comfortable setting long‑range strategy and engaging deeply with the technical substance of the work. Core Responsibilities\n \n • Computational Biology and AI Innovation\n Lead the development of our proprietary AI/ML models and computational biology pipelines for sequence design, structural prediction, and codon optimisation, with the goal of maximising translation, stability, and tissue specificity. This work is conducted in close collaboration with our strategic advisor. \n • Next‑Generation xRNA Evolution\n Spearhead the continued strategic evolution of our modality, guiding the platform's advance into ever more sophisticated xRNA chemistries and ensuring that it remains firmly at the state of the art. \n • Formulation and LNP Development\n Oversee the formulation engineering team in optimising lipid nanoparticles (LNPs) for targeted, safe, and efficient in vivo delivery, again working in collaboration with our strategic advisor. \n • Platform Scalability\n Ensure that platform discoveries are robust, reproducible, and engineered from the outset with manufacturing scalability in mind, so that what works at the bench translates reliably towards the clinic. \n • Strategic Leadership\n Own the resourcing, planning, and timelines for the platform team, and mentor and grow a multidisciplinary group of data scientists, biologists, and engineers into a high‑performing, collaborative whole. \n • Intellectual Property Generation\n Actively identify and protect novel sequence motifs, AI design algorithms, and proprietary LNP formulations, building and defending the intellectual property moat that underpins the company's long‑term value. \n • Platform Interfacing\n Serve as the pivotal bridge between Platform and Discovery, working closely with our chemistry and biology colleagues to transition optimised candidates smoothly from the Platform team into the Discovery team. \n Qualifications and Experience\n \n • A PhD in a relevant discipline — for example computational biology, bioinformatics, RNA biology, biochemistry, chemical or biomedical engineering, or a closely related field — together with substantial and progressive experience in RNA, oligonucleotide, or nucleic‑acid therapeutics, gained over a senior industry career.\n, • A demonstrable track record of building and leading platform or technology functions in a biotech or pharmaceutical setting, including direct leadership of multidisciplinary teams spanning computation, biology, and engineering.\n, • Deep, hands‑on familiarity with the application of AI and machine learning to molecular design, together with a genuine understanding of the experimental science the platform serves.\n, • Strong knowledge of delivery technologies, in particular LNP formulation for nucleic acids, and of the considerations that carry a discovery‑stage platform towards manufacturable, scalable processes.\n, • A record of intellectual property generation, and the strategic instinct to recognise and protect what is defensible.\n, • Outstanding leadership, communication, and collaboration skills, with the ability to operate effectively across a geographically distributed, multicultural organisation and to translate between technical and strategic audiences.\n What We Offer\n The opportunity to own and shape the defining technology platform of an ambitious, well‑founded biotech at a pivotal moment in its story; a seat within the senior leadership team, with real influence over the company's scientific direction; and the chance to build something durable alongside a talented, international community at the heart of the Cambridge life sciences ecosystem. \n #J-18808-Ljbffr

Working at the intersection of electrochemistry, operando characterisation and product development, the Application Scientist will play a key role in expanding the capabilities of a cutting-edge battery analysis platform. This role combines hands-on laboratory work with product development, supporting the creation of new experimental workflows, specialised test hardware and advanced data analysis approaches that help customers gain deeper insights into battery behaviour and performance. \n \n The Application Scientist will be responsible for: \n\n • Designing and optimising experimental workflows across a range of battery chemistries\n, • Developing and refining bespoke operando battery cell designs to improve performance, usability and manufacturability\n, • Using CAD software to design components and support rapid prototyping activities\n, • Preparing battery electrodes and assembling laboratory-scale test cells\n, • Analysing electrochemical, imaging and multidimensional datasets to support product and application development\n, • Presenting technical findings and recommendations to customers, collaborators and internal teams\n, • Supporting scientific collaborations, customer demonstrations, training activities and industry events\n\n \n The Application Scientist will have: \n\n • An MSc or PhD in Electrochemistry, Chemistry, Materials Science, Chemical Engineering, Engineering or a related discipline\n, • Hands-on experience working with lithium-ion or other advanced battery technologies\n, • Experience in battery cell assembly and electrochemical testing\n, • A strong understanding of battery chemistries and electrochemical processes\n, • Strong CAD capability and experience designing technical components\n, • Excellent data analysis and experimental problem-solving skills\n, • Strong communication skills and the ability to work effectively with customers and multidisciplinary teams\n\n \n This role is ideal for someone who enjoys developing new experimental approaches, solving practical engineering challenges and working closely with customers to advance battery technology. If you're looking for the opportunity to combine scientific research, product development and real-world application, apply with your CV and we will be in touch.

Cambridge | £55,000 to £65,000 + bonus \n \n If you want an HSE role where your COMAH experience will genuinely influence how a manufacturing site operates, this is worth exploring. \n \n We are recruiting an HSE Manager for a manufacturing business in Cambridge. You will take ownership of the site’s health, safety and environmental agenda, working closely with senior leaders while remaining visible and credible on the factory floor. \n \n This is an opportunity to improve how HSE works in practice. You will help create an environment where people understand why standards matter, managers take responsibility and compliance becomes part of everyday decision-making \n \n What you will be doing: \n\n • Leading the site’s health, safety and environmental strategy\n, • Managing the site’s COMAH responsibilities and maintaining regulatory compliance\n, • Identifying risk and turning your findings into practical improvements\n, • Supporting leaders and managers to take greater ownership of HSE\n, • Leading investigations and ensuring lessons result in meaningful action\n, • Working with employees across the site to strengthen safety awareness and behaviours\n, • Monitoring performance, reporting clearly and prioritising the areas that need attention\n, • Building effective relationships with regulators and other external stakeholders\n\n \n What makes this opportunity worth considering? \n You will have the visibility and responsibility expected of a senior site role, with the opportunity to influence both immediate safety performance and the longer-term HSE culture. \n The package includes: \n\n • £55,000 to £65,000 salary\n, • Annual bonus\n, • A senior, influential position within a chemical manufacturing environment\n, • The opportunity to make visible improvements across a live operational site\n\n \n What do you need? \n The essential requirement is genuine, hands-on COMAH experience. \n You will also need: \n \n\n • HSE management experience within manufacturing\n, • The confidence to influence senior leaders and challenge constructively\n, • A practical approach that works on the factory floor, not only on paper\n, • Strong knowledge of UK health, safety and environmental legislation\n, • The ability to translate complex requirements into clear, workable actions\n\n \n Experience within chemical or another process-led manufacturing environment would be particularly relevant. \n \n You do not need an updated CV to start a conversation. Apply through LinkedIn or send me a private message for a confidential discussion about the business, the site and what the role could offer you.

Senior Mechanical Project Engineer?? Hybrid Working Office, Home & Site-Based - Cambridge ?? Water & Wastewater ProjectsBinnies, part of the RSK Group, is looking for a Senior Mechanical Project Engineer to support the successful delivery of water and wastewater projects across the UK.Working closely with Project Managers, Quantity Surveyors, Engineering teams and the supply chain, you'll act as a key technical interface throughout the project lifecycle, from procurement and design review through to construction, commissioning and handover.Why Binnies?Hybrid and flexible working arrangementsWorking on the best and most interesting projects in the industryPrivate medical insurance9 Day fortnights - long weekend every other weekAnnual leave plus bank holidays, with the option to buy additional leaveProfessional membership support and career development opportunitiesEmployee discounts and lifestyle benefits through the RSK GroupA collaborative and supportive team culture focused on wellbeing, inclusion and growthWhat you'll be doingManaging mechanical and M&E work packages from tender through to completion.Supporting project planning, procurement and delivery activities.Coordinating with site, engineering and commissioning teams.Managing subcontractors and supply chain partners.Supporting testing, commissioning and mechanical isolation processes.Reviewing RAMS and ensuring safe delivery of works.Building strong relationships with clients and project stakeholders.What we're looking forDegree, HND or equivalent qualification in Mechanical Engineering.Extensive project engineering experience within the water and wastewater sector.Significant experience delivering M&E projects.Experience preparing, procuring and managing supply chain work packages.Knowledge of engineering contracts, ideally NEC.Strong communication and stakeholder management skills.Ability to work independently and take ownership of project outcomes.DesirableChartered Mechanical Engineer (MIMechE).Experience developing critical path programmes.Knowledge of clean water and wastewater treatment systems.Understanding of pressure systems, chemical dosing systems, testing and commissioning activities, procurement processes and CDM regulations.Ready to make an impact? Apply today and help us deliver sustainable solutions for the future of water.TPBN1_UKTJ

LI-onsiteJob descriptionIn this lab-based role, with team assistance, you will carry out multi-step organic chemistry synthesis routes preparing organic molecules that test molecular biology hypotheses and interrogate molecular pathways implicated in disease. A mechanistic understanding of organic c

Skills DesiredAlgorithms, Analytical Chemistry, Automation, Chemical Analysis, Chemical Biology, Chemical Laboratory, Chemical Synthesis, Chemistry, Collaboration, Creativity, Data Analysis, Drug Development, Innovation, Medicinal Chemistry, Organic Chemistry, Pharmaceutical Industry, Physics, Team

Skills DesiredAnalytical Thinking, Chemical Biology, Chemistry, Clinical Research, Clinical Trials, Collaboration, Curious Mindset, Data Analysis, Detail-Oriented, Ethics, Gene Therapy, Immunology, Machine Learning (ML), Mammalian Cell Culture, Medical Research, Molecular Biology, Patient Care, Scie

Skills DesiredAlgorithms, Analytical Chemistry, Automation, Chemical Analysis, Chemical Biology, Chemical Laboratory, Chemical Synthesis, Chemistry, Collaboration, Creativity, Data Analysis, Drug Development, Innovation, Medicinal Chemistry, Organic Chemistry, Pharmaceutical Industry, Physics, Team

Skills DesiredAnalytical Skill, Analytical Skill, Analytical Thinking, Chemical Biology, Chemistry, Clinical Research, Clinical Trials, Collaboration, Communication Skills, Curious Mindset, Data, Data Analysis, Decision Making, Design Of Experiments, Detail-Oriented, Drug Development, Drug Discovery

Skills DesiredAlgorithms, Analytical Thinking, Chemical Biology, Clinical Research, Clinical Trials, Collaboration, Curious Mindset, Data Analysis, Detail-Oriented, Ethics, Hypothesis Testing, Immunology, Mammalian Cell Culture, Medical Research, Molecular Biology, ScienceSummaryLocation: Cambridge

ScientistMelbournAre you an experienced laboratory scientist ready to take the next step in your career?Intertek is looking for a Scientist to join our growing laboratories in Melbourn, Cambridgeshire. This is an excellent opportunity for someone with industry experience who is ready to take greater ownership of analytical work.Working within an experienced team, you'll perform laboratory testing, interpret data and contribute to investigations, method activities and client projects across the pharmaceutical and chemical industries.If you're confident in the laboratory, committed to quality and ready to continue developing your scientific career, we'd love to hear from you.ABOUT YOUWe're looking for someone with practical experience who can work accurately and apply scientific judgement and contribute positively within a collaborative team.Required skills and experience:A degree (BSc or MSc) in Chemistry, Pharmaceutical Sciences, Biochemistry, Biology or another relevant scientific disciplineIndustry experience within an analytical or scientific laboratoryHands-on experience of relevant analytical techniquesExperience of GMP, GLP or equivalent quality standards in a regulated environmentThe ability to interpret data and communicate scientific findings clearlyA methodical approach with excellent attention to detail and a commitment to data integrityThe ability to plan and manage multiple priorities effectivelyConfidence working independently and collaborating with project teamsExcellent communication and IT skills, including Microsoft OfficeExperience of method development, validation or transfer, laboratory investigations or laboratory data systems would be advantageous.ABOUT THE OPPORTUNITYAs a Scientist, you'll take responsibility for preparing and analysing samples using a range of analytical techniques.You'll deliver accurate results, interpret scientific data and contribute to investigations and technical problem-solving, ensuring work is completed safely and in line with quality requirements.You'll broaden your technical expertise, contribute to varied client projects and progress your career within one of the world's leading testing, inspection and certification companies.Key activities:Preparing and analysing samples using relevant analytical techniquesFollowing validated methods, SOPs and data integrity requirementsRecording, interpreting, reviewing and reporting analytical dataContributing to investigations, troubleshooting and technical problem-solvingSupporting method development, validation and transfer activitiesMaintaining equipment and a safe, organised and compliant laboratoryWorking with project teams to deliver high-quality results on timeSharing technical knowledge and supporting less-experienced colleaguesWHAT WE OFFERJoin Intertek and become part of our global network of inspiring and entrepreneurial colleagues. We are a global family that values diversity and we thrive working together with precision, pace, and passion. We are working to make the world Ever Better, ensuring the quality, safety and sustainability of products and services used by millions of people around the world.Competitive salary/benefits Development and career opportunities around the Globe Working in a highly motivated team and dynamic working environmentWe are an Equal Opportunity Employer and are committed to creating an inclusive workplace. We do not discriminate against applicants, and all qualified individuals will receive consideration for employment regardless of age, disability, gender reassignment, marriage or civil partnership, pregnancy or maternity, race, colour, nationality, ethnic or national origin, religion or belief, sex, or sexual orientation. We are committed to fair and equitable pay and are proud to be a Real Living Wage employer, ensuring our colleagues are compensated in line with independently assessed living standards. We are also committed to providing reasonable adjustments throughout the recruitment process and employment to support candidates and employees with disabilities or special needs. Intertek operates a preferred supplier arrangement, and we do not accept unsolicited approaches from agencies..Full timePosting Date: 2026-08-10

Job Description Summary#LI-OnsiteLocation: Cambridge, MA, USAAbout the RoleWe are seeking an accomplished Associate Director to join our discovery organization and lead scientific strategy across ADC payloads, linker technologies, and conjugation approaches. This role is central to advancing differentiated antibody-drug conjugates (ADCs) and related targeted therapeutics by integrating deep payload expertise, linker/conjugation knowledge, and biology-driven mechanism-of-action insights.The ideal candidate brings strong industry experience in ADC discovery or development, with a proven track record of applying payload, linker, and conjugation expertise to therapeutic program strategy. You will collaborate closely with cross-functional teams to design, evaluate, and advance next-generation ADC concepts with the goal of delivering transformative therapies to patients.Job DescriptionKey ResponsibilitiesLead scientific strategy for ADC payload selection, linker design, conjugation approaches, and related platform innovationsApply deep expertise across payload classes, mechanisms of action, potency, resistance biology, bystander activity, and tolerability to guide program designPartner with chemistry, biology, protein engineering, pharmacology, translational sciences, and CMC teams to advance next-generation ADCsEvaluate and prioritize novel payloads, linker technologies, and conjugation approaches for internal programs and external opportunitiesProvide biology-driven insights into payload mechanism of action, tumor context, therapeutic index, and combination strategiesDesign and guide experimental strategies to assess ADC activity, selectivity, resistance mechanisms, linker stability, and payload-related pharmacologyContribute to next-generation ADC platform strategy, including differentiated payload-linker concepts and biology-aligned ADC designRepresent payload/linker expertise in cross-functional project teams, governance discussions, and external collaborationsMonitor scientific, clinical, competitive, and IP landscapes related to ADC payloads, linkers, and emerging targeted modalitiesMentor scientists and contribute to a collaborative, high-performing research environmentEssential RequirementsPh.D. in cancer biology, pharmacology, chemical biology, biochemistry, medicinal chemistry, bioengineering, or related discipline5–10 years of relevant industry experience in ADC discovery, targeted therapeutics, or oncology drug discoveryExtensive expertise in ADC payloads, including mechanism of action, potency, resistance biology, and therapeutic index considerationsStrong knowledge of linker and conjugation technologies, including stability, release mechanisms, site-specific conjugation, and developabilityDeep understanding of ADC biology including tumor targeting, internalization, trafficking, payload release, bystander effects, and pharmacologyDemonstrated ability to integrate biology, chemistry, and translational data into actionable program strategiesProven experience leading cross-functional scientific discussions and influencing program directionStrong communication, collaboration, and leadership skillsNovartis Compensation and Benefit Summary: The salary for this position is expected to range between $152,600-$283,400 USD Annual 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.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.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$152,600.00 - $283,400.00Skills DesiredAnalytical Skill (Inactive), Analytical Skill (Inactive), Analytical Thinking, Chemical Biology, Chemistry, Clinical Research, Clinical Trials, Collaboration, Communication Skills (Inactive), Curious Mindset, Data (Inactive), Data Analysis, Decision Making, Design of Experiments (DOE), Detail-Oriented, Drug Development, Drug Discovery Process, Ethics, Gene Therapy- Leadership (Inactive), Influence (Inactive), Laboratory (Inactive), Leading Project Teams, Lifesciences (Inactive), Machine Learning (ML), Medical Research {+ 11 more}SummaryLocation: Cambridge (USA)Type: Full time

A growing scientific instrumentation company, based in Cambridgeshire, are currently keen to recruit a hand on experimental physicist. When we say hands on we mean we are looking for people who have built experimental bits of scientific equipment from scratch rather then used computer programs to see if it works first.This is the type of role that will really appeal to engineering focused physicists who enjoy the challenge of creating new pieces of scientific equipment from scratch. You will focus on instrumentation systems that are used in the engineering and life sciences sectors. If you have a few years’ experience working on any of the following types of technologies we would be keen to hear from you; Microfluidics, electrophoretic, colloids, inkjet and other complex fluidic based technologies.We are looking for people who have a real passion for engineering and really want to push the boundaries of technologies. The type of people who do well in this type of role will be people who have had technical hobbies for years. Some of the people at this organisation have hobbies where they build engines from scratch, built a glider and other complex technical projects.You will have a strong understanding of the fundamentals as well as the complex engineering processes as you will have full responsibility of the invention and the improvement of complex systems and will be expected to be hands on at every stage of the projects. This is not the type of role where you delegate sections of the projects, this is something where you will get your fingerprints on every part of the technology and hopefully you will be proud to do this.It is expected that you will hold a 1st or 2:1 degree from a leading engineering or physics university. If you also hold a PhD this will be advantageous but not essential.We are open minded to your background so if you were originally working within a chemistry or biology field and transferred over to engineering and physics we will still be interested as the fluidics part of these projects transfer well across all the scientific fields.This is an already successful growing company that is developing into new areas, the growth potential of this organisation is unlimited meaning your career will develop with it. They like people from within the business to develop their skills and knowledge so continual training and development is on offer. Apart from the career growth and skills training you will be rewarded with an excellent salary, benefits package and relocation assistance (when needed).So, if as a physicist you want to be challenged and tested you need to apply now as I do not expect this role to be open for long.For more information please feel free to call Andrew Welsh, Director of Scientific Engineering recruitment specialists Newton Colmore, on 0121 268 2240 or make an application and one of our team at Newton Colmore will contact you.Newton Colmore is a specialist recruitment company within the Medical Devices, Scientific Engineering, Scientific Software, Robotics, Science, Electronics Design, New Product Design, Human Factors, Regulatory Affairs, Quality Assurance and Field Service Engineering sectors.Physicist, Microfluidics, Electrophoretic, Colloids, Inkjet, Fluidics, Physical Engineering, Chemical Engineering, Bioengineering, Experimental Physicist, Prototype Engineering, Scientific EngineeringHiring organizationEmployment TypeFull-timeDuration of employmentPermanentIndustryMedical DevicesJob Location Cambridge, CambridgeshireDate posted 16th July 2026Valid through 31st October 2026PDF Export Export as PDFApply below or email directly: andrew.welsh@newtoncolmore.com

Job Description Summary#LI-Onsite Location: Cambridge, MAThis position is located in Cambridge, MA and does not have the ability to be located remotely. Please only apply if this area is accessible to you.Over 40 therapies in the clinic! NIBR Oncology strives to reimagine medicines for cancer patients through a combination of treatment approaches including targeted therapies, immunotherapies, CAR-T, and radioligand therapy. NIBR is seeking an in vivo scientist to join our Oncology Pharmacology team in Cambridge, MA. The successful candidate will join a dynamic, multi-disciplinary team and play a key role in the development and application of in vivo models for evaluating novel cancer therapies and advancing the early-stage drug discovery pipeline. This is a labhead-based position, where the ideal candidate is expected to lead efforts in the design and execution of in vivo anti-tumor efficacy and PK/PD studies aimed at evaluating drug candidates in CDX, PDX, and syngeneic models. Applicants are expected to develop novel in vivo assays to interrogate key scientific questions and deliver high-value translationally relevant data that can inform clinical development. Qualified candidates will have extensive experience in a variety of molecular biology skills. A strong background and expertise in antibody drug conjugates is preferred. We are looking for highly motivated, inquisitive, and creative individuals, who thrive in a highly matrixed work environment, and can effectively communicate within multidisciplinary project teams.Job DescriptionResponsibilities:Design pre-clinical in vivo studies to explore novel hypotheses, screen candidate molecules, and establish proof-of-concept of new modalitiesDevelop in vivo CDX, PDX, and syngeneic models to evaluate anti-tumor activity, PK/PD relationships, relevant biomarkers, and key translational questionsManage associate-level scientistsCollaborate with cross-functional project teamsCritically analyze and present results within a multidisciplinary team environmentCareful adherence to animal protocols and proper documentation of data and methods in electronic laboratory notebookQualifications:PhD with 5-8 years of research experience as a postdoc or in the pharmaceutical/biotech industryDeep knowledge of antibody drug conjugatesExtensive experience working with CDX and PDX xenograft tumor models and/or syngeneic modelsExpertise in cell culture, PCR, ELISA, western blot, and flow cytometryStrong analytical, communication (written and verbal), and organizational skills, including a proficiency with PowerPoint and commonly used data analysis programs, such as Prism and ExcelNovartis Compensation and Benefit Summary: The salary for this position is expected to range between $126,000 and $234,000 per year.The final salary offered is determined based on factors like, but not limited to, relevant skills andexperience, and upon joining Novartis will be reviewed periodically. Novartis may change the publishedsalary range based on company and market factors.Your compensation will include a performance-based cash incentive and, depending on the level of therole, eligibility to be considered for annual equity awards.US-based eligible employees will receive a comprehensive benefits package that includes health, life anddisability 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$126,000.00 - $234,000.00Skills DesiredAnalytical Skill (Inactive), Analytical Skill (Inactive), Analytical Thinking, Chemical Biology, Chemistry, Clinical Trials, Collaboration, Communication Skills (Inactive), Curious Mindset, Data (Inactive), Data Analysis, Design of Experiments (DOE), Detail-Oriented, Drug Development, Drug Discovery Process, Ethics, Gene Therapy, Immunology, Inventory Management, Laboratory (Inactive), Leading Project Teams, Lifesciences (Inactive), Machine Learning (ML), Management (Inactive), Medical Research {+ 10 more}SummaryLocation: Cambridge (USA)Type: Full time

Job Description Summary#LI-OnsiteLocation: Cambridge, USARelocation Support: YesImagine advancing the next generation of RNA therapeutics that have the potential to transform patients’ lives around the world. As a Principal Scientist I or II, Oligonucleotide Chemistry and Innovation, you will play a critical role in building and advancing Novartis’ xRNA therapeutic platform, bringing scientific creativity, technical expertise, and innovation to the forefront of drug discovery. Working alongside a collaborative team of world-class scientists, you will lead the development of novel oligonucleotide chemistries, drive therapeutic innovation, and help shape the future of RNA medicines in a dynamic and fast-paced research environment. This is an exciting opportunity to make a meaningful scientific impact while mentoring others and contributing to breakthrough therapies that could redefine what is possible for patients.Job DescriptionKey ResponsibilitiesLead synthesis, purification, characterization, and analysis of chemically modified oligonucleotides and conjugates.Design and optimize novel oligonucleotide chemistries through structure-activity relationship studies.Develop and implement robust synthetic routes for preclinical RNA therapeutic candidates.Drive cross-functional collaboration to advance oligonucleotide therapeutic programs from discovery through preclinical stages.Mentor scientists and enhance laboratory workflows to improve efficiency, quality, and innovation.Establish and maintain standard operating procedures supporting reproducible oligonucleotide manufacturing processes.Operate, troubleshoot, and maintain critical analytical and synthesis instrumentation, including high performance liquid chromatography and liquid chromatography mass spectrometry.Essential RequirementsDoctor of Philosophy in Chemistry or a related scientific discipline.At least five years of experience synthesizing therapeutic oligonucleotides in an industry or research setting.Deep expertise in solid-phase oligonucleotide synthesis, deprotection, purification, and characterization.Proven experience developing and optimizing novel oligonucleotide chemistries and conjugates.Strong knowledge of phosphoramidite chemistry and modern synthetic chemistry techniques.Hands-on experience operating automated oligonucleotide synthesizers and analytical instrumentation.Demonstrated understanding of RNA therapeutics, including small interfering ribonucleic acid and antisense oligonucleotides.Excellent collaboration and communication skills with the ability to work across multidisciplinary teams.At Novartis, our purpose is to reimagine medicine to improve and extend people's lives. If you are passionate about scientific innovation, thrive in a collaborative environment, and are excited by the opportunity to help shape the future of RNA therapeutics, we encourage you to apply and make a lasting impact on patients worldwide.Rewards At Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen. The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and a minimum of 14 weeks paid parental leave. Expected Annual Base Salary Range for role: US: 108,500.00 - 201,500.00 USD AnnualThe salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. Further details will be provided during the application process. Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics. Read our brochure to learn more about our global total rewards offering: Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process. 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 DesiredAlgorithms, Analytical Chemistry, Chemical Analysis, Chemical Biology, Chemical Laboratory, Chemical Synthesis, Chemistry, Computational Chemistry, Creativity, Data Analysis, Drug Development, Employee Development, Innovation, Medical Research, Medicinal Chemistry, Mentorship, Organic Chemistry, Pharmaceutical Industry, Physics, Project Team Management, Results-Oriented, ScienceSummaryLocation: Cambridge (USA)Type: Full time

A fantastic opportunity has arisen for a Business Development Executive to join a growing highly specialised chemical manufacturing company with a presence across the UK and Ireland, responsible for generating new business opportunities through outbound sales activity. Monitor sales activity against

Publishing Assistant - Journals - Cambridge Circa: Salary - Salary Plan, 26,000.00 GBP AnnualWe are currently look for a Publishing Assistant, Journals on a full time temporary basis, expected to be up to 12 months. About the RSC The Royal Society of Chemistry is a not-for-profit organisation whose mission is to advance chemical sciences. As a not-for-profit publisher, we reinvest surplus funds back into the global scientific community, supporting our purpose to help the chemical science community make the world a better place. The RSC strives to continuously innovate its product and services to adapt to market and customer needs, maintain relevancy and diversify revenues from print journals. This requires a market-led and outside-in thinking approach to product and service innovation. Benefits At the Royal Society of Chemistry, we promote a healthy work/life balance and flexible working options across the organisation. We offer a comprehensive benefits package to all employees including: 26 days paid holiday per annum 35-hour working week with flexible options Enhanced maternity and paternity leave Paid volunteering days Pension plan with up to 12% employer contributions (depending upon your contribution) Life assurance at three times basic annual salary The role The main purpose of this role is to provide excellent customer service through the provision of key administrative support for our journals, in accordance with editorial and production procedures and deadlines. Working within a large team, this role involves dealing with queries from scientists around the world, and helping them to submit their manuscripts to the large portfolio of journals published by the Royal Society of Chemistry. The Publishing Assistant role plays a key role enabling the Journals publishing team to achieve its aim of being a digital-first publisher focused on delivering high-quality, accessible, impactful content and an excellent customer experience. Your responsibilities will focus on: administrative duties associated with the processing of articles submitted and published in our journals; daily correspondence with authors, reviewers and publishing staff; accurate record keeping of article workflow using management systems; prepare invoices for payments using financial systems; collaboration with other Publishing Assistants and journals teams to ensure the smooth running of the department. We are looking for: previous administration experience is required; efficient and competent in the use of software packages associated with PCs. Ability to use other software packages associated with opening and manipulating of file attachments of varying types of software. good organisational and time-management skills are required together with the ability to work under pressure and to meet deadlines; good attention to detail; good communication skills in interacting with internal and external contacts are essential; ability to work well in a team; experience of a database tracking system is desirable. If you are interested in this opportunity, please apply before the end of our closing date. Visit our Work For Us website to learn more about us, our benefits, equal opportunities statement and inclusive culture pledge. At the RSC, we recognise the benefits of a diverse workforce and welcome applicants from a range of backgrounds to apply. We particularly encourage applications from disabled and ethnic minority candidates. As a part of the Disability Confident Scheme, we endeavour, where possible, to offer an interview to candidates meeting the essential criteria of the role, who has a substantial physical/mental impairment which impacts their ability to carry out day-to-day tasks. We are committed to making our recruitment processes accessible to all and as part of this, we are flexible in the ways we give and receive information. If you would like to apply using a different format, please contact the Recruitment Team at or on +44 (0) and we will do our best to put any reasonable adjustments in place. If you have any questions, please contact us at

Job Description:Role Overview: Join Huntsman’s Supply Chain team in Duxford, UK, and play a pivotal role in keeping our global business moving. We are looking for an experienced and proactive Transport Planner to coordinate the worldwide transportation of chemical products, ensuring deliveries reach customers safely, efficiently, and on time. This is an exciting opportunity to join a fast-paced logistics environment where no two days are the same. Working across international markets including China, North America, Japan, India, Brazil, and Europe, you will collaborate with colleagues, freight partners, and operational teams to manage complex shipments, solve challenges, and continuously improve logistics performance. We are looking for someone who thrives under pressure, enjoys problem-solving, and can confidently manage competing priorities while maintaining exceptional attention to detail. Do you think you’re the right fit for this opportunity? Apply today! Role Responsibilities: As a Transport Planner, you will be responsible for: Planning, scheduling, and coordinating the transportation of chemical products worldwide. Managing air and sea freight shipments while ensuring customer delivery commitments are achieved. Selecting the most effective transportation routes and shipping methods based on cost, service, and operational requirements. Ensuring all shipments comply with relevant safety, environmental, customs, and transport regulations. Preparing and maintaining shipping documentation, labels, customs paperwork, and shipment records. Monitoring transportation performance and proactively resolving logistics issues and delays. Acting as a key liaison between logistics providers, freight forwarders, warehouses, customer service teams, and supply chain stakeholders. Supporting continuous improvement initiatives to enhance efficiency, reduce costs, and improve customer experience. Preparing logistics performance and cost-analysis reports for management. Identifying opportunities to optimize transportation processes and improve operational effectiveness Experience and Competencies: What we are looking for: Previous experience in logistics, transportation, shipping, or supply chain operations. Experience coordinating international shipments, ideally including air and sea freight. SAP experience, preferably within Warehouse Management (WM) or logistics-related processes. Strong organizational skills with the ability to manage multiple priorities and deadlines. Excellent communication skills and the ability to build effective working relationships with internal and external stakeholders. Strong problem-solving skills and attention to detail. Ability to work effectively under pressure and respond to changing customer and business demands. A proactive, resilient team player who enjoys working in a fast-paced environment. What next? If you would like to join an innovative, collaborative and multicultural team, please apply now. Your application will be forwarded to a Talent Acquisition Partner, who will strive to get back to you as soon as they can. We understand that applying for a new job is a big decision and we will work hard to keep you updated and support you along the way. About Us: At Huntsman, we pride ourselves on being a people-oriented organization. Our family-like atmosphere is cultivated by our diverse groups of team members around the world. We welcome the talent, experience and fresh ideas that employees at all stages of their careers, from interns to seasoned professionals, bring to Huntsman. In return, we offer you the opportunity to become an integral part of a dynamic, industry-leading company, where safety and ethics always come first. Additional Locations:SummaryLocation: UK - DuxfordType: Full time

Water Treatment Engineer Leicester / Midlands | £30,000£40,000 + Benefits Build your expertise. Work with major commercial and industrial clients. Develop your career within a leading water treatment business. Are you an experienced Water Treatment Engineer looking for a role offering variety, autonomy and the opportunity to work across some of the UK's most important commercial and industrial sites? Were working with a leading specialist in water treatment and water hygiene, who are looking to appoint a Water Treatment Engineer to cover clients across Leicester and the wider Midlands region. This is a hands-on field-based role covering cooling towers, steam boilers and domestic water systems, with a strong focus on water treatment, monitoring and compliance. The Role As a Water Treatment Engineer, youll visit a range of commercial and industrial sites, carrying out routine water treatment and water hygiene services while ensuring systems remain compliant, safe and operating effectively. Your responsibilities will include: • Carrying out routine water treatment services on cooling towers and evaporative cooling systems, • Monitoring and testing steam boiler water systems, • Conducting water quality testing and analysing results, • Taking domestic water hygiene samples from client sites, • Carrying out temperature monitoring and other routine water hygiene checks, • Collecting samples for laboratory analysis, • Dosing and monitoring chemical treatment programmes, • Identifying issues with water systems and recommending appropriate remedial action, • Completing accurate service reports and maintaining site records, • Liaising with customers and site contacts regularly, • Ensuring all work is carried out in line with relevant legislation, standards and company procedures, • Travelling to customer sites throughout Leicester, the Midlands and surrounding areas About You Were looking for someone with experience within water treatment, water hygiene or a related technical environment. You might already be working as a Water Treatment Engineer, Water Hygiene Engineer or Service Engineer, or have relevant experience within a commercial or industrial water treatment environment. Youll ideally have: • Experience working with cooling towers and/or steam boiler systems, • Knowledge of water treatment and chemical dosing, • Experience carrying out water sampling and testing, • An understanding of domestic water hygiene and Legionella control, • Strong attention to detail and accurate record keeping, • Good mechanical and practical ability, • Excellent customer-facing and communication skills, • The ability to work independently and manage your own schedule, • A full UK driving licence Whats On Offer? • £30,000£40,000 basic salary, depending on experience, • Benefits package, • Company vehicle, • Ongoing technical training and development, • The opportunity to work with a respected name within the water treatment sector, • A varied field-based role with plenty of autonomy, • Long-term career progression Water Treatment Engineer Leicester / Midlands | £30,000£40,000 + Benefits Build your expertise. Work with major commercial and industrial clients. Develop your career within a leading water treatment business. Are you an experienced Water Treatment Engineer looking for a role offering variety, autonomy and the opportunity to work across some of the UK's most important commercial and industrial sites? Were working with a leading specialist in water treatment and water hygiene, who are looking to appoint a Water Treatment Engineer to cover clients across Leicester and the wider Midlands region. This is a hands-on field-based role covering cooling towers, steam boilers and domestic water systems, with a strong focus on water treatment, monitoring and compliance. The Role As a Water Treatment Engineer, youll visit a range of commercial and industrial sites, carrying out routine water treatment and water hygiene services while ensuring systems remain compliant, safe and operating effectively. Your responsibilities will include: • Carrying out routine water treatment services on cooling towers and evaporative cooling systems, • Monitoring and testing steam boiler water systems, • Conducting water quality testing and analysing results, • Taking domestic water hygiene samples from client sites, • Carrying out temperature monitoring and other routine water hygiene checks, • Collecting samples for laboratory analysis, • Dosing and monitoring chemical treatment programmes, • Identifying issues with water systems and recommending appropriate remedial action, • Completing accurate service reports and maintaining site records, • Liaising with customers and site contacts on a regular basis, • Ensuring all work is carried out in line with relevant legislation, standards and company procedures, • Travelling to customer sites throughout Leicester, the Midlands and surrounding areas About You Were looking for someone with experience within water treatment, water hygiene or a related technical environment. You might already be working as a Water Treatment Engineer, Water Hygiene Engineer or Service Engineer, or have relevant experience within a commercial or industrial water treatment environment. Youll ideally have: • Experience working with cooling towers and/or steam boiler systems, • Knowledge of water treatment and chemical dosing, • Experience carrying out water sampling and testing, • An understanding of domestic water hygiene and Legionella control, • Strong attention to detail and accurate record keeping, • Good mechanical and practical ability, • Excellent customer-facing and communication skills, • The ability to work independently and manage your own schedule, • A full UK driving licence Whats On Offer? • £30,000£40,000 basic salary, depending on experience, • Benefits package, • Company vehicle, • Ongoing technical training and development, • The opportunity to work with a respected name within the water treatment sector, • A varied field-based role with plenty of autonomy, • Long-term career progression Interested? If you're an experienced Water Treatment Engineer, Water Hygiene Engineer or Service Engineer looking for your next opportunity, we'd be keen to hear from you. Apply now for a confidential conversation about the role. JS Selection specialises in recruitment across the UK water treatment and environmental sectors. If you're an experienced Water Treatment Engineer, Water Hygiene Engineer or Service Engineer looking for your next opportunity, we'd be keen to hear from you. Apply now for a confidential conversation about the role. JS Selection specialises in recruitment across the UK water treatment and environmental sectors. JBRP1_UKTJ

?LOCATION: UK Home Office Based ?Exciting commercial role with a successful, established and growing chemical distributor to develop new business and manage existing accounts within manufacturing industries that are producing composites (including polyester and epoxy fibre reinforced products), thermosets and masterbatch. You will promote a specialist portfolio of products and work with a sourcing ... JBRN1_UKTJ

52000 - 72000 per annumCambridge, England Permanent My Client is recruiting for a Senior and Principal Mechanical Engineer in the Water Sector.Locations: Cambridge, Peterborough, London or Surrey - HybridAre you a Mechanical Engineer who is passionate about making the world a better place? Are you ready to take up a vital role in some of the UK's most exciting and innovative projects? We are looking for experienced Senior/Principal Mechanical Engineers to join our team within the Design & Advanced Technology (D&AT) Team. You'll be part of a talented, multi-disciplinary team delivering cutting edge, iconic projects to our Water market clients. As a key member of our team, you'll play a vital role in delivering transformational programmes for critical UK infrastructure, with opportunities to work on landmark engineering projects both domestically and internationally. We're committed to providing industry-leading solutions throughout the project lifecycle, adding value through client-side and construction-phase support. Become part of a team where every voice matters, and together we can tackle our clients' toughest challenges. We foster a diverse and inclusive environment where world-class talent thrives without boundaries. For us, collaboration isn't a buzzword. We value the different perspectives our people bring and recognise everyone for their contributions equally. We also know that different people have different priorities, which is why we're here to support you with whatever you need.Your role The role will offer a challenging and rewarding opportunity to apply knowledge, experience, and problem-solving skills whilst providing good opportunities for career development. As Senior/Principal Mechanical Engineer in the D&AT practice, the successful candidate would have the following responsibilities: Coordinate or manage a team of Mechanical engineers for delivery of technical design work on complex multi-disciplinary projects following relevant national and project specific design codes and standards, and to high-quality levels in areas such as pumping systems and water & wastewater treatment design. Responsible for producing and reviewing technical deliverables such as design reports, drawings, calculations, and scopes of work with defined scope. Provide technical input into project design deliverables for Mechanical aspects of complex multi-disciplinary projects and work with the project management team to successfully manage time and budgets to key project milestones and programmes.Collaborate with client, operational, project, or service activities within your immediate team and other related teams.Provide mentorship to less experienced colleagues and help to grow the Mechanical Engineering capabilities within the local team.Work independently with minimal technical guidance. Exercise personal judgement to solve difficult problems where appropriate and provide guidance to junior team members.Provide technical support for bid proposals. Work closely with a multi-disciplinary team in the UK and overseas to deliver integrated design solutions.Adhere to quality assurance standards in design including check and review of own work as well as others.About youA degree in Mechanical Engineering or equivalent.Chartered or Incorporated Mechanical Engineer.Water/Wastewater Sector experienceProven experience in coordinating or managing a Mechanical engineering design delivery team for a design consultancy including within a multi-disciplinary environment.Takes broad perspective to identify innovative solutions to design problems.The role requires comprehensive knowledge and proven practical experience in the design integration of a wide range of mechanical equipment, including pumps, blowers, screens, and chemical dosing systems. Additionally, it demands a thorough understanding of current UK design standards, relevant legislation, and established industry practices.Practical knowledge of current design codes and standards as well as industry best practices, including a strong understanding of legislation such as CDM and DSEAR.Ability to work independently with minimal technical guidance.Proficiency in applicable analytical software and related tools.Experience in Water market is preferable.Demonstrates strong communication skills, with the ability to convey technical concepts clearly and effectively within diverse multi-disciplinary teams.A proactive, highly motivated mindset with a collaborative approach to drive teamwork and shared success across projects.

Chemical & Engineering News (C&EN) is the award-winning, editorially independent news organization of the American Chemical Society. Contribute content across a variety of platforms, including articles, newsletters, podcasts, videos, webinars, and social media. Strong news judgment and enthusiasm fo

A strong background in chemical reaction engineering and chemical reactor operations would be essential. Applications are invited for a two-year Postdoctoral Research Associate (PDRA) position in Chemical Process Engineering under the supervision of Prof Erwin Reisner within the Yusuf Hamied Departm

A PhD or equivalent experience in chemical engineering, energy systems, environmental engineering, applied mathematics, computer science or another relevant science or engineering discipline (essential).

We are now seeking to make an appointment at a more senior level who will either bring a new area of chemical biology to the Department or who will have significant synergies with existing researchers. Candidates must demonstrate a firm commitment to teaching at both undergraduate and postgraduate l

This is an exciting opportunity for an ambitious graduate or early‑career candidate with a background in materials science, chemistry, polymer science, chemical engineering or a related field. Conduct exploratory research to identify suitable chemical and material solutions based on performance cr

The Head of Sales will build partnerships with chemical and pharma organizations, develop sales strategies, and manage a team.

Working at the intersection of electrochemistry, operando characterisation and product development, the Application Scientist will play a key role in expanding the capabilities of a cutting-edge battery analysis platform. This role combines hands-on laboratory work with product development, supporting the creation of new experimental workflows, specialised test hardware and advanced data analysis approaches that help customers gain deeper insights into battery behaviour and performance. The Application Scientist will be responsible for: Designing and optimising experimental workflows across a range of battery chemistries Developing and refining bespoke operando battery cell designs to improve performance, usability and manufacturability Using CAD software to design components and support rapid prototyping activities Preparing battery electrodes and assembling laboratory-scale test cells Analysing electrochemical, imaging and multidimensional datasets to support product and application development Presenting technical findings and recommendations to customers, collaborators and internal teams Supporting scientific collaborations, customer demonstrations, training activities and industry events The Application Scientist will have: An MSc or PhD in Electrochemistry, Chemistry, Materials Science, Chemical Engineering, Engineering or a related discipline Hands-on experience working with lithium-ion or other advanced battery technologies Experience in battery cell assembly and electrochemical testing A strong understanding of battery chemistries and electrochemical processes Strong CAD capability and experience designing technical components Excellent data analysis and experimental problem-solving skills Strong communication skills and the ability to work effectively with customers and multidisciplinary teams This role is ideal for someone who enjoys developing new experimental approaches, solving practical engineering challenges and working closely with customers to advance battery technology. If you're looking for the opportunity to combine scientific research, product development and real-world application, apply with your CV and we will be in touch

Head of Quality As Head of Quality, you'll lead quality strategy across a highly regulated pharmaceutical and medical manufacturing operation, ensuring patient safety remains at the heart of everything whilst driving continuous improvement, operational excellence and business growth. BASIC SALARY: £90,000 - £100,000 BENEFITS: Bonus 25 days holiday pension Car allowance Healthcare LOCATION: North West COMMUTABLE LOCATIONS: Liverpool, Manchester, RELOCATION: We are fully prepared to relocate the right candidate, this role therefore as also been posted in Leeds, Cambridge, Oxford, Derby, Birmingham, Bristol and London Why read on: In this critical leadership role, you'll: ·Set the direction - shaping and delivering the quality strategy across multiple manufacturing and technical locations (2x UK, US and Far East). ·Lead from the front, be visible and present - developing and inspiring established quality teams whilst creating a culture of quality beyond compliance (4 direct c30 indirect reports). ·Influence the business - acting as a key member of the senior leadership team, helping shape operational and strategic decisions. ·Drive improvement - championing continuous improvement, modern quality systems and best practice across highly regulated environments. ·Protect what matters most - ensuring patient safety, regulatory compliance and world-class customer service remain central to every decision. Job Description Reporting to the UK Operations Director with a dotted line to the Business Unit Head, you'll have overall responsibility for the quality function across a complex manufacturing business supplying products into highly regulated pharmaceutical and medical markets. This is a genuine leadership role where you'll balance strategic planning with operational execution, working closely with manufacturing, engineering, technical, commercial and external regulatory stakeholders. You'll be responsible for developing quality capability, ensuring regulatory compliance, supporting commercial growth and creating a collaborative culture focused on excellence. Key Responsibilities: ·Lead all aspects of Quality across pharmaceutical, medical and industrial operations. ·Develop and implement quality strategies aligned to wider business objectives. ·Provide leadership to multi-site quality teams, developing talent and succession plans. ·Ensure GMP, regulatory (MHRA/EudraLex/FDA) and customer quality requirements are met or exceeded. ·Lead customer, regulatory and third-party audits and inspections. ·Maintain oversight of quality systems, change management, deviations, non-conformances and compliance activities. ·Drive a culture centred around quality, collaboration, accountability and continuous improvement. PERSON SPECIFICATION: You'll be joining a business at an exciting point in its growth journey. To be successful in your application, you'll be able to demonstrate: ·A degree qualification in Chemistry, Pharmaceutical Sciences, Life Sciences or a related scientific discipline. ·Significant experience within pharmaceutical, excipient, API, medical device, specialty chemical or similarly regulated manufacturing environments. ·A strong understanding of GMP and pharmaceutical quality systems. ·Proven experience leading, developing and mentoring Quality professionals. ·Experience operating within complex manufacturing environments where safety, quality and compliance are critical. ·A track record of building high-performing teams and driving continuous improvement initiatives. ·Exposure to COMAH, process manufacturing, auditing and regulatory inspections would be highly advantageous. THE COMPANY: We are a globally recognised manufacturing business supplying products into critical healthcare and industrial markets. Our operation combines advanced manufacturing, technical innovation and regulatory excellence to support customers around the world. This is an opportunity to join the senior leadership team of a business investing heavily in growth, technology and people. You'll have the platform to influence strategy, develop capability and leave a lasting impact on both operational performance and patient outcomes. PROSPECTS: It is highly likely you will have worked in any of the following roles and/or markets, and worked with the following products and/or services: INTERESTED? Please click apply. You will receive an acknowledgement of your application. Wallace Hind Selection, alongside our client embrace diversity, champion equality, and foster inclusion to create a work environment where everyone belongs and thrives. Please Note: Wallace Hind Selection have been chosen as the recruitment partner of our client. REF: MH18633

A leading UK water sector capital delivery organisation is seeking a Process Engineer to work on a diverse programme of water treatment and supply projects. This is a hands-on role designing treatment plants and distribution systems that meet environmental, efficiency, and customer requirements. You'll collaborate with multi-disciplinary teams, applying innovative approaches to reduce carbon, protect natural capital, and use digital tools. What were looking for: BEng/MEng/MSc in Chemical/Water Process Engineering or related discipline Process design experience, including technology selection, sizing, detailed design - within the water sector Knowledge of water treatment (ground or surface water) or pumped distribution systems Strong communication and collaborative skillsDesirable: Working towards Chartered Engineer status Onsite experience of water treatment or distribution assets The role offers professional development, exposure to innovative projects, and a collaborative, award-winning environment

Are you a Business Development Manager with experience selling engineered or industrial solutions into manufacturing or process industries? This is an opportunity to combine technical sales with genuine long-term career progression within a specialist water treatment business. BASIC SALARY: Up to £55,000 BENEFITS: · Annual Bonus linked to business growth · Pension · 23 Days Holiday LOCATION: This is a hybrid role, you must be commutable to our office in Hertfordshire. COMMUTABLE LOCATIONS: Luton, Stevenage, Bedford, Cambridge, St Albans, Milton Keynes, Hemel Hempstead, Northampton JOB DESCRIPTION: Technical Sales Manager, Business Development Manager - Water Treatment, Process Equipment As our Business Development Manager, you'll be responsible for driving new business growth whilst developing an established customer base across the UK. Working with Engineering Managers, procurement professionals and business owners, you'll provide technically engineered water treatment solutions into industrial and process markets. Initially, your focus will be approximately 70% account management and 30% new business development, building long-term customer relationships and identifying opportunities to grow revenue. As your knowledge of the business develops, you'll gain increasing exposure to commercial strategy, operations and business management as part of a planned succession programme. You will: · Sell technically engineered water treatment and process equipment solutions into industrial markets. · Prepare quotations, negotiate commercial agreements and manage opportunities through to completion. · Work closely with technical colleagues and manufacturing partners to deliver the right solution for every customer. · Contribute towards future business growth through market development, commercial strategy and long-term planning. PERSON SPECIFICATION: Technical Sales Manager, Business Development Manager - Water Treatment, Process Equipment You'll enjoy building long-term customer relationships and be motivated by winning new business. You're commercially aware, naturally curious and keen to develop your career beyond sales, with an interest in understanding how a successful engineering business operates. Previous experience within water treatment would be beneficial, but we're equally interested in candidates from other technical or industrial sales backgrounds who can demonstrate a consultative approach and the ambition to progress. You'll also have: · A successful track record of generating new business whilst developing existing customer relationships. · Experience selling engineered products, capital equipment or technical solutions into industrial markets. · The ability to understand technically complex products and recommend the right solution for each customer. THE COMPANY: For over 20 years we've been designing and manufacturing high-quality engineered water treatment systems for customers across a range of industrial sectors. Our reputation has been built on technical expertise, high-quality engineered solutions and exceptional customer service. PROSPECTS: This role has been created as part of our long-term succession planning strategy. You'll begin by developing your commercial expertise before gaining exposure to wider business functions including operations, finance, production and strategic planning, creating genuine opportunities to progress into senior leadership within approximately five years. It is highly likely you will have worked in any of the following roles and/or markets, and worked with the following products and/or services: Technical Sales Manager, Business Development Manager, Area Sales Manager, Sales Engineer, Key Account Manager, Technical Sales Engineer - Process Engineering, Water Treatment, Water Purification, Filtration, Pumps, Valves, Process Equipment, Industrial Automation, Process Control, Manufacturing Equipment, Industrial Machinery, Utilities, Chemical Processing, OEM, Engineering, Industrial Manufacturing. INTERESTED? Please click apply. You will receive an acknowledgement of your application. Wallace Hind Selection, alongside our client embrace diversity, champion equality, and foster inclusion to create a work environment where everyone belongs and thrives. Please Note: Wallace Hind Selection have been chosen as the retained recruitment partner of our client and therefore any direct applications to our client from candidates or agencies will be forwarded on to us direct. REF: SM18608, Wallace Hind Selection

Proposals Engineer/Technical Support Engineer (Monday to Friday: 08:00 – 16:30) High Speed Food Manufacturing Equipment (Processing, Packaging, Inspection & Materials Handling Solutions) Previous Relevant Experience is Essential OR Transferable Skills from a Relevant Technical Industry - SolidWorks/AutoCAD experience is non-negotiable!! ----- Our Client is a Market Leading Company in the sector with an excellent reputation and over 40 years of experience providing high-performance automation solutions to various sectors including food & beverage, meat, poultry and seafood, dairy and bakery, ready meals, snacks and convenience foods, fresh produce, health & beauty, home care, pet food and other industrial sectors. Due to substantial growth we are looking for a Proposals Engineer/Technical Support Engineer: Overview The Proposals Engineer is a technically skilled and commercially aware individual who sits at the intersection of engineering and sales. The purpose of the role is to produce high-quality, accurate, and compelling technical and commercial proposals that convert client opportunities into awarded projects. Working closely with the Sales, Engineering, Project Management, and Procurement teams, the Proposals Engineer will take ownership of the full bid life cycle — from initial enquiry and cost estimation through to submission, client negotiation support, and internal handover. This role is central to revenue generation and its ability to grow into new markets and client relationships across the UK and Ireland market sectors. With 3 main areas of responsibility: Proposals and Bid Management Technical Sales Support Internal Collaboration and Handover Essential Experience Ideally experience in a Proposals Engineer, Applications Engineer, Technical Sales Engineer, or similar technically focused commercial role Qualifications: Bachelor's degree in Engineering — Mechanical, Electrical, Food, Chemical or a related discipline Cost Estimation: Strong, demonstrable experience in cost estimation methods and best practice for engineering projects CAD: Ability to read, interpret, and produce technical drawings using SolidWorks and/or AutoCAD IT Skills: Proficient in Microsoft Office 365, particularly Excel (for costings and modelling), Word (for proposal writing), and PowerPoint (for client presentations) Communication: Strong written and verbal communication skills, with the proven ability to produce high-quality technical specifications, quotations, and proposal documents Commercial Acumen: Demonstrated ability to identify, develop, and convert sales opportunities in a technically complex environment Organisation: Highly organised, methodical, and detail-oriented for accuracy in proposals is non-negotiable in this role Desirable Background in the FMCG, food processing, beverage, or wider process industries Exposure to turnkey project environments where proposals span design, fabrication, installation, and commissioning Familiarity with contract forms and commercial terms relevant to capital equipment supply * Experience presenting proposals and technical solutions directly to clients at senior level This is an exciting opportunity to join a talented team of individuals with an exceptional company culture that is fun, friendly, fast paced and ambitious with a focus on growth! For further details and a full Job Description please forward your up to date CV. We look forward to hearing from you

Quality Assurance Manager – Industrial Food Manufacturing (FMCG) Monday - Friday 09:00 - 17:30 About the Role Experienced and proactive Quality Assurance Manager to lead the Quality function within a large-scale, multi-level industrial food manufacturing facility. Operating within a high-volume FMCG environment, you will be responsible for maintaining an effective Quality Management System (QMS) while ensuring the highest standards of food safety, product quality, legality and authenticity across all manufacturing operations. Reporting to the Technical Manager, you will lead the Quality Assurance and Hygiene teams, driving a culture of continuous improvement, operational excellence and compliance throughout the site. This role requires strong leadership, technical expertise and the ability to work collaboratively with Production, Engineering, Supply Chain and Technical teams to ensure products consistently meet customer, retailer and regulatory requirements. Key Responsibilities • Lead, develop and motivate the Quality Assurance and Hygiene teams, creating a high-performance culture focused on food safety, quality and continuous improvement., • Champion a positive Food Safety and Quality Culture across the entire manufacturing facility, ensuring standards are embedded at every level of the organisation., • Maintain and continuously improve the site's Quality Management System, ensuring ongoing compliance with BRCGS Food Safety Standards, customer codes of practice and all relevant legal and regulatory requirements., • Ensure robust implementation, verification and continuous review of HACCP and TACCP/VACCP programmes across all manufacturing operations., • Drive compliance with GMP, hygiene, environmental monitoring and allergen management programmes throughout the production facility., • Manage site hygiene standards and pest control programmes, ensuring all planned activities are completed, verified and any corrective actions closed effectively., • Oversee raw material, in-process and finished product quality verification programmes, including microbiological, chemical and physical testing through accredited laboratories., • Ensure all quality monitoring, inspections and verification activities are completed accurately and on schedule., • Lead investigations into customer complaints, non-conformances and quality incidents using structured root cause analysis, implementing effective corrective and preventive actions (CAPA)., • Monitor quality KPIs, trend performance data and identify opportunities to improve product quality, process capability and operational performance., • Ensure full product traceability is maintained across the manufacturing operation and lead mock recalls to verify system effectiveness., • Plan and conduct internal audits while supporting external customer, retailer and certification audits., • Deliver food safety, GMP and quality training to colleagues, ensuring competency across all operational teams., • Collaborate with Production, Engineering and Continuous Improvement teams to deliver sustainable improvements in manufacturing processes and quality performance., • Support the implementation, validation and maintenance of product specifications, quality standards and manufacturing controls., • Ensure compliance with all customer specifications, retailer requirements and internal quality standards., • Provide technical support during new product introductions, process changes and capital investment projects., • Deputise for the Technical Manager where required and provide technical leadership across the wider site., • Promote a proactive quality-first mindset, ensuring quality is built into every stage of the manufacturing process rather than inspected at the end. About You You are an experienced Quality professional with a passion for food manufacturing and operational excellence. You are comfortable working in a fast-paced, complex FMCG environment and have proven experience leading technical teams within large manufacturing operations. Experience & Skills • Minimum of 3 years' experience in a Quality Assurance leadership role within food manufacturing or FMCG., • Experience managing Quality Assurance teams within a high-volume industrial manufacturing environment., • Strong working knowledge of BRCGS Food Safety Standard and retailer standards., • Proven experience managing internal and external audits., • Thorough understanding of HACCP, TACCP, VACCP, GMP, hygiene and allergen management., • Experience managing environmental monitoring, pest control and sanitation programmes., • Excellent root cause analysis and problem-solving skills using structured continuous improvement methodologies., • Strong communication and stakeholder management skills with the ability to influence at all levels., • Experience working within complex manufacturing sites, including multi-floor or vertically integrated production facilities, is highly desirable., • Experience within milling, cereals, grains or dry ingredient manufacturing would be advantageous., • Strong analytical skills with experience using quality KPIs and data to drive performance improvements. Qualifications Degree in Food Science, Food Technology or a related discipline, or equivalent industry experience. HACCP Level 3 (minimum). Food Safety Level 3 (minimum; Level 4 desirable). Internal Auditor qualification (BRCGS or equivalent preferred). Full UK Driving Licence

If you're an experienced technical salesperson who enjoys building long-term customer relationships and solving engineering challenges, this is an opportunity to grow an established customer base whilst developing new business across UK manufacturing and industrial markets. BASIC SALARY: Up to £55,000 BENEFITS: · Company Car or Car Allowance · Annual bonus based on business growth and personal growth (circa £10,000) · Pension Contributions · Private Healthcare · Death in Service (4x Salary) · 24 Days Holiday plus Birthday Off · Free EV Charging at the Office LOCATION: Home based with travel to customers nationwide and occasional visits to the office in Bedfordshire. COMMUTABLE LOCATIONS: Milton Keynes, High Wycombe, Oxford, Reading, Slough, Aylesbury, Luton, Watford, Hemel Hempstead, Northampton, Bedford. JOB DESCRIPTION: Business Development Manager, Account Manager, Technical Sales - Water Treatment, Industrial Engineering Reporting to the General Manager, as our Account Manager, you'll manage a healthy mix of existing accounts and new business opportunities (approximately 70% account management and 30% new business). Working with engineers and manufacturing customers, you'll recommend specialist UV disinfection solutions that improve efficiency and protect critical assets. Supported by the Business Manager and an experienced technical team, you'll represent a portfolio of market-leading UV technologies, building long-term customer relationships across UK manufacturing and industrial markets. KEY RESPONSIBILITIES: Business Development Manager, Account Manager, Technical Sales - Water Treatment, Industrial Engineering As our Account Manager, you will: · Develop new business opportunities whilst increasing revenue within an established portfolio of industrial customers. · Build strong relationships with engineers, production managers, maintenance teams and procurement professionals across UK manufacturing businesses. · Recommend technical solutions that improve efficiency, productivity and operational performance. · Manage the full sales process from enquiry and quotation through to negotiation, order and ongoing account development. · Maintain an active sales pipeline and CRM whilst identifying future growth opportunities. · Work closely with internal technical specialists and supplier partners to deliver exceptional customer support. PERSON SPECIFICATION: Business Development Manager, Account Manager, Technical Sales - Water Treatment, Industrial Engineering You will be someone who enjoys building long-term customer relationships whilst growing existing accounts and winning new business. You'll be comfortable working with engineers and taking a consultative approach to technical sales. Experience within water treatment or UV technology would be preferred, although we'll also consider candidates from a wider technical or industrial sales background. You'll also have: · Experience selling technical products, engineered solutions or industrial equipment into manufacturing, industrial or process-led environments. · The ability to build credibility with engineers, production managers, maintenance teams and procurement professionals. · Experience managing your own sales pipeline and forecasting activity through a CRM system. · Strong commercial awareness with the ability to identify opportunities, negotiate effectively and convert enquiries into orders. THE COMPANY: We're a well-established engineering business supplying specialist technical solutions into manufacturing and industrial markets across the UK. Our reputation has been built on technical expertise, quality products and long-term customer relationships. As we continue to grow, we're looking to strengthen our commercial team with an experienced Business Development Manager to help drive the next phase of our success. It is highly likely you will have worked in any of the following roles and/or markets, and worked with the following products and/or services: Business Development Manager, Technical Sales Engineer, Area Sales Manager, Regional Sales Manager, Account Manager, Applications Engineer or Technical Sales - water treatment systems, pumps, filtration, valves, instrumentation, UV, industrial automation, process equipment, process control, manufacturing equipment, engineering consumables, industrial machinery - food & beverage, pharmaceutical, chemical, utilities, manufacturing, industrial processing, energy or OEM markets. INTERESTED? Please click apply. You will receive an acknowledgement of your application. Wallace Hind Selection, alongside our client embrace diversity, champion equality, and foster inclusion to create a work environment where everyone belongs and thrives. Please Note: Wallace Hind Selection have been chosen as the retained recruitment partner of our client and therefore any direct applications to our client from candidates or agencies will be forwarded on to us direct. REF: SM18606, Wallace Hind Selection

Job Description Faststream is recruiting for oil/chemical experienced 2nd Engineers to join a highly reputable Shipping Giant. The role offers:Permanent employmentX 12 monthly paid salary3 month toursPerformance bonusCompany share scheme The desired candidate will have the following:Valid license +

Chemical Manufacturing Operations Manager.

As a chemicals regulatory / compliance specialist with REACH experience you will be is responsible for ensuring products and consumables meet applicable chemical regulations, industry standards, and internal compliance requirements across international markets. An exciting opportunity has arisen for

This role offers a unique opportunity to combine synthetic chemistry expertise with cutting-edge automation and AI technologies, helping shape the future of intelligent chemical research and development. Work closely with Computational Chemistry and AI R&D teams to optimize chemical experimental pla

Our client is a well established, growing manufacturing company and an extremely valued customer of ours who is currently recruiting a R&D Manager (Chemical Engineering, Product Design, Technical) in Burnley. R&D Manager (Chemical Engineering, Design, Technical).