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Founded in 2024, Lab Thread creates all-in-one lab management SaaS (ELN, LIMS, molecular biology suite, project management) for academic research to enterprise pharma. Consultative Sales: Lead value-driven sales conversations tailored to labs transitioning from paper systems or legacy platforms, cre

OverviewAt QIAGEN, we are driven by a simple but powerful vision: making improvements in life possible. We’re dedicated to revolutionizing science and healthcare for the better. From our entrepreneurial roots to our current global presence, we've grown into a force for positive change. With thousands of employees across six continents, collaboration is our greatest strength. We’re always striving to identify talented individuals to join our exceptional teams. We have played a pivotal role in shaping modern science and healthcare, and we're just getting started. If you're someone who thrives on new challenges, values diversity and wants to make a tangible difference in people's lives, then QIAGEN is the place for you. At QIAGEN, every day is an opportunity to make a real-life impact. Join us, grow with us, and together, let's shape the future of biological discovery. ‎ About the opportunityJoin our Molecular Assay Development team in Manchester (on-site) and use bioinformatics to help turn complex biological data into insights that support the development of molecular diagnostic products and platforms. Working alongside experienced bioinformaticians and scientists from around the world, you will analyse digital PCR, next-generation sequencing (NGS) and image-based datasets, develop computational tools and contribute to multidisciplinary assay-development projects.Your tasksDevelop and document bioinformatics tools and workflows to improve data analysis and support molecular assay and product development.Analyse genomic, transcriptomic and other biological datasets, ranging from focused studies to larger-scale datasets, using appropriate computational and bioinformatics approaches.Visualise and interpret digital PCR, NGS and image-based data, translating complex results into clear, actionable scientific insights.Plan and coordinate bioinformatics studies, including preparing protocols, documenting analyses and communicating findings to relevant stakeholders.Apply current bioinformatics methods and technologies to ongoing projects and sharing knowledge and good practice across the team.Support reproducible bioinformatics workflows, maintaining data integrity and clear analysis documentation.Work within applicable design-control, quality and regulatory requirements throughout assay and product development.Your profileA Bachelor’s, Master’s or PhD in Bioinformatics, Computational Biology, Computer Science or a related discipline, with relevant practical bioinformatics experience.Hands-on experience analysing biological data, ideally including genomics, NGS datasets.Experience using data analysis, data visualisation and bioinformatics tools to investigate complex datasets and communicate findings.Knowledge of human genetics, genomics and/or infectious disease would be advantageous.Familiarity with relevant bioinformatics databases, such as dbSNP or COSMIC, would be beneficial.Experience developing, documenting or improving computational workflows or analysis tools, with an understanding of reproducibility and data integrity.Able to communicate complex analytical findings clearly to scientific and multidisciplinary colleagues.What we offer Attractive pension Private Healthcare and Dentalcare Gym membership contribution A range of retail discounts and offers Enhanced maternity package Flexible working options Bonus/commission 25 days annual leave (potential to increase linked to service) Employee Assistance Program and internal QIAGEN communities Hybrid work (conditional to your role) Our people are the heartbeat of everything we do. Passion drives us as we push boundaries to innovate and evolve. We inspire with our leadership and make an impact with our actions. We cultivate a collaborative, supportive environment where each individual and team can flourish. We champion accountability and encourage entrepreneurial thinking. QIAGEN is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, or disability. SummaryLocation: ManchesterType: Full time

As part of Convatec's Applied Research organization within the Biomedical Sciences team, the Senior Biocompatibility Specialist is responsible for execution of biocompatibility projects requiring deep expertise in biocompatibility for New Product Development (NPD), Life Cycle Management (LCM) and Research projects. From a technical standpoint, the Senior Biocompatibility Specialist will apply subject matter expertise in biocompatibility to design and perform the technical approach to biological evaluations for products, analyze data, reflect on results, report out on data to project teams and complete biological evaluation documentation in line with ISO 10993 series of standards and the quality system. They will work cross-functionally with other groups such as New NPD, regulatory, Applied Research teams, Project Management and Medical/Clinical, to ensure priorities, goals, deliverables, collaborative needs, and timelines are consistently aligned. Measures of success include (a) effectively supports and delivers biocompatibility assessments for NPD and LCM. Derisks NPD and research projects at an early stage as well as (b) completion of biological evaluation plans and reports that are accepted by regulatory authorities globally including in US, UK, Europe and Rest of World. • Deliver biological evaluations of new and existing devices in close and effective collaboration with the relevant project teams, • Evaluate projects and execute biocompatibility studies, conducted by external laboratories, in support of programs dealing with our medical devices, • Leverage internal capabilities to support biocompatibility projects, • Derisk new medical devices and research projects early in the development process in order to deliver feedback and data that support device development, • Develop or revise biological evaluation protocols, reports, and regulatory summaries in collaboration with cross-functional program teams, test laboratories, and suppliers., • Understand biocompatibility strategies that are formed in consideration of product and process changes, gaps in materials, design and process to achieve optimal solutions that satisfy cost and technical requirements as they relate to biological safety., • Make positive contributions to recommend approaches to, and support updating/ developing procedures for internal and external guidance document as they relate to biocompatibility, in compliance with applicable global regulatory requirements (e.g. FDA, ISO, MHLW, and CFDA)., • Analyze, interpret, and draw conclusions from biocompatibility testing, including, but not limited to, extractable and leachable, chemical characterization and biological evaluations, • Write, edit, and/or approve technical documentation., • Communicate effectively to expert and non-expert audiences with regular project updates in meetings as well as in the form of presentations and reports., • Effectively collaborate with project management, R&D, Regulatory, manufacturing, process engineering Global Laboratory Services etc. teams, ensuring teams are aligned on key goals, deliverables, resource needs, timelines etc., • Promote teamwork within and across departments, sharing experiences and best practices. Strive for high performing teams behaviours and activities both within the biocompatibility and Applied Research teams and between project, regulatory and other cross functional teams. Authority (if applicable): Authority over the Biological evaluations. Principal Contacts Internal · New Product Development & Life Cycle Management Teams as teammates on project work. To align on test strategies and biocompatibility strategy, agree timelines and budgets, communicate progress and risks. · Scientific & Technical Labs to execute testing, as required. · Regulatory Affairs to collaborate on requirements for biological evaluations. · Project Management to estimate resource requirements, identify key milestones, manage project governance, and develop timelines. · Applied Research to leverage other scientific and engineering capabilities outside of Adhesives. · Quality to support audits on questions related to biocompatibility and to work in a compliant way within the QMS. · Medical affairs to understand clinical use cases. External · Laboratory Testing Services to contract necessary testing. · Regulatory agencies to explain and defend biological evaluations or answer questions. BS in one or more of the following disciplines: Biomedical Engineering, Bioengineering, Biology (Biological Sciences), Molecular Cell Biology, Biochemistry, Materials Science, or Toxicology; advanced degree (MS or PhD) in these fields preferred, • +5 years related to biocompatibility evaluations and/or toxicological risk assessments of medical devices., • Fundamental understanding or direct experience of the ISO 10993 standards, biomaterials, toxicological assessment, extractable and leachable analysis, medical device manufacturing processes, and biocompatibility assessment methodology, • Capable of developing and driving a detailed project plan with scheduled and defined dependencies between tasks and deliverable, • Ability to demonstrate a high level of creativity and independence in areas of assigned responsibility and has good command of the relevant scientific and technical literature., • Demonstrates excellent analytical and problem-solving skills and ability to interpret data from a variety of sources., • Excellent verbal/written communication skills and the ability to work well in cross functional teams., • Ability to collaborate effectively to troubleshoot issues, identify solutions and optimise strategies for implementation., • Demonstrate ability to time manage multiple projects effectively and efficiently and adapt to changing priorities as required., • Very strong communication and project management skills with multiple teams from different disciplines., • undefined Travel Requirements Up to 20% travel domestically and overseas including overnight travel as appropriate. Languages · Speaking: Yes English · Writing/Reading: Yes English Convatec is entering an exciting new phase of its R&D journey with plans to establish a new state-of-the art facility in Manchester. Located within the Citylabs SciTech campus, the site is intended to become a key hub within our global R&D network, bringing together advanced analytical research, global laboratory testing, quality control, engineering, science, regulatory expertise and health innovation capabilities. The facility will strengthen collaboration with Manchester's world‑class life sciences ecosystem and support our mission of pioneering trusted medical solutions to improve the lives we touch. Over time, activities currently based at our Convatec Technology Centre in Deeside are expected to transition to the new Manchester location, targeted to open in early 2028. This move will create exciting opportunities to help shape the future of healthcare innovation at Convatec. #J-18808-Ljbffr

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Account & Applications Manager – Industrial Wastewater Treatment Account & Applications Manager – Industrial Wastewater Treatment Cesco Solutions, a Tidal Vision Company VP of European Expansion Full time, non-exempt Home-based in the United Kingdom (regular travel required) 50% £75,000 per annum Commission programme based on gross‑margin performance, including retained‑account growth and new business • Private medical insurance. Workplace pension with employer contributions of up to 6%; life insurance; Professional‑development and tuition support; 25 days of annual leave plus applicable UK bank or public holidays; company car or car allowance and reimbursement of approved business travel expenses We believe that sustainability should not require customers to compromise on price, convenience, or performance. Our mission is to create positive and systemic environmental impact by making our biopolymer solutions cost competitive, more convenient, and better performing than the synthetic chemicals we displace. We value innovation and take pride in challenging the status-quo; we choose to view obstacles as opportunities. We value new ideas and encourage the team to apply creativity and invent new solutions to meet challenging demands. We foster open, direct communication, and a collaborative working environment through our unique approach to work culture. We value our employees and demonstrate that through our compensation and benefits programs and opportunities for growth and development. Cesco Solutions is an industrial water treatment and sanitation chemical provider specialising in high‑organics wastewater from food processing and related industries. As part of Tidal Vision, Cesco leverages chitosan‑based chemistry as a sustainable alternative to traditional metal‑based coagulants to improve clarification, reduce sludge, and enhance treatment efficiency. By combining advanced chemistry, application expertise, and operational support, Cesco helps facilities optimise wastewater performance, lower chemical consumption, and maintain regulatory compliance while advancing more sustainable treatment practices. Tidal Vision strives to build and invest in the highest performing and most innovative team. We put our people and customers above process, avoid company-wide rules as much as possible, and have the courage to take unusual approaches to advance our mission. With this approach, we believe we can create a more flexible, fun, stimulating, creative, collaborative, and innovative organisation. Our commitment to developing, practicing and promoting direct and open communication, responsibility and freedom, and leading with and seeking context is a responsibility for every role at Tidal Vision. We are seeking an experienced wastewater application specialist who can build trusted relationships with customer teams, understand treatment‑plant performance in detail, and provide the regular technical service required to keep chemical and equipment programmes operating safely, reliably and effectively. The successful candidate will take primary responsibility for customer satisfaction, account retention and continuous improvement across an assigned UK territory. The role combines scheduled account service, wastewater applications support, process troubleshooting, operator training and commercial account development. Sales remains an important element: the postholder will identify opportunities to expand successful programmes within existing accounts and will support the development of selected new customers where Cesco’s chemistry and service model can deliver measurable value. The position is home-based and requires regular travel to customer sites, including overnight stays. The successful candidate will work closely with Cesco and Tidal Vision colleagues to coordinate technical, laboratory, equipment and commercial support and to ensure consistent follow‑through on customer commitments. • Own the day-to-day relationship with assigned customer accounts and act as the principal point of contact for treatment performance, service requirements and continuous‑improvement activity., • Plan and complete regular on‑site and virtual account‑service reviews, ensuring agreed actions are documented, assigned and followed through to completion., • Work closely with plant operators, engineering teams, environmental personnel, procurement stakeholders and site leadership to understand operational priorities, compliance risks and business needs., • Assess industrial wastewater systems, operating data and discharge performance to identify root causes of poor treatment, process constraints and opportunities for improvement., • Conduct or supervise jar testing, sampling, dose optimisation, chemical trials and treatment‑performance reviews, and translate the results into practical written recommendations., • Optimise coagulation, flocculation, clarification and solids‑separation programmes to improve reliability, effluent quality, chemical efficiency, sludge generation and total treatment cost., • Provide responsive on‑site and remote technical support, resolving treatment, dosing and application problems and escalating specialist issues when required., • Ensure customer satisfaction by providing comprehensive training on Cesco products, safe chemical handling, correct dosing, routine monitoring and operational troubleshooting., • Inspect chemical storage, make‑down, feed, pumping, control and application equipment; provide first‑line troubleshooting and coordinate repairs, maintenance or specialist support as required., • Establish service plans and agreed performance measures for key accounts, monitor results over time and communicate emerging risks before they affect compliance or customer operations., • Prepare clear service reports, trial reports and account recommendations that explain findings, required actions and the operational and financial value delivered by the programme., • Protect account retention through dependable service, technically credible advice, prompt communication and consistent delivery against customer commitments., • Identify opportunities to extend or improve Cesco programmes within existing accounts, including additional treatment points, equipment, complementary chemistry and service support., • Develop and execute account plans that combine customer‑service objectives, retention priorities and realistic sales‑growth opportunities., • Support selected new‑business opportunities through technical discovery, site surveys, water testing, trials, proposals and the transition from successful trial to a stable serviced account., • Build relationships with key stakeholders, including plant and facility executives, to support long‑term partnerships and appropriate commercial development., • Actively promote and support Cesco and Tidal Vision innovations within assigned accounts where they address a verified customer need and strengthen the overall treatment programme., • Maintain accurate CRM records, account plans, service activity, forecasts, opportunities and gross‑margin information., • Work collaboratively with operations, laboratory, technical, equipment and commercial colleagues, communicating customer context, priorities, risks and support requirements clearly., • Be willing to travel regularly throughout the assigned UK territory, normally around 50% of working time and potentially more during trials, start‑ups or periods of intensive account support., • 10+ years of experience in industrial wastewater treatment, with substantial hands‑on responsibility for customer applications, process diagnosis and treatment optimisation., • Practical technical knowledge of wastewater‑treatment plants, preferably involving high‑organics effluent from food and beverage processing or a closely related industrial sector., • Demonstrable experience managing customer accounts or providing ongoing field technical service in water treatment, process chemicals or a related industry., • Experience of coagulation, flocculation, clarification and solids separation, including DAF or comparable primary‑treatment processes., • Experience conducting or supervising jar tests, chemical trials, sampling, dose optimisation and treatment‑performance reviews., • Experience working with chemical storage, dosing pumps, controls and application equipment, including first‑line troubleshooting., • Ability to interpret operational and laboratory data and produce clear, practical written recommendations., • A record of building strong customer relationships, maintaining account satisfaction and identifying appropriate opportunities for account growth., • Working knowledge of UK trade‑effluent consents, discharge compliance, COSHH requirements and safe chemical‑handling practices, or the ability to develop this knowledge rapidly., • A full UK driving licence, the right to work in the UK and willingness to travel regularly, including overnight stays., • 5-10 years of experience in industrial water‑treatment chemicals, wastewater applications, technical account management or a combination of these areas., • Direct experience supporting food, beverage, seafood, meat, poultry, dairy, brewing, distilling, rendering or other high‑COD industrial wastewater accounts., • Experience with chitosan, biopolymers, metal‑salt coagulants, organic coagulants, polymers or related treatment chemistries., • A demonstrable record of retaining and growing technically complex customer accounts and converting successful applications into long‑term commercial programmes., • Experience introducing new chemistry or treatment approaches into operating industrial sites through structured trials and close customer support., • Bachelor’s degree, HNC, HND or equivalent professional experience in chemistry, biology, environmental science, chemical engineering, water treatment or a related field., • Strong competence in Microsoft Excel, Word and PowerPoint and experience using customer‑relationship‑management systems., • Travel is expected to account for approximately 50% of working time and may increase during trials, start‑ups or periods of intensive customer support., • The role involves working in operational industrial environments, walking around treatment plants, using stairs and access platforms and wearing appropriate personal protective equipment., • While performing the duties of this job, the employee will regularly use hands and fingers to handle testing equipment, tools, controls and samples and may occasionally be required to lift or move equipment or materials of a reasonable weight., • Reasonable adjustments will be considered to enable disabled applicants and employees to perform the essential functions of the role., • Any offer will be conditional on satisfactory references and verification of the applicant’s right to work in the UK., • A valid UK driving licence is required by the time of appointment. Where a personal vehicle is used for business travel, appropriate business‑use insurance will be required., • Employment may be subject to proportionate background, qualification and driving‑record checks relevant to the role. Tidal Vision and Cesco Solutions provide equal employment opportunities to all employees and applicants and prohibit unlawful discrimination or harassment on the basis of age, disability, gender reassignment, marriage or civil partnership, pregnancy or maternity, race, religion or belief, sex, sexual orientation, or any other characteristic protected by applicable UK law. We welcome requests for reasonable adjustments at any stage of the recruitment process. This policy applies to all terms and conditions of employment, including recruitment, hiring, placement, promotion, termination, redundancy, recall, transfer, leave, compensation and training. The statements contained herein reflect the general details necessary to describe the principal functions of this role, the level of knowledge and skill typically required and the scope of responsibility but should not be considered an all-inclusive listing of work requirements. The employee may perform other reasonable duties consistent with the nature and seniority of the role, including work in other functional areas to cover absences, respond to peak workloads or otherwise balance business requirements. This job description does not itself establish a contract of employment. The applicable terms and conditions will be set out in the employee’s written employment contract and may be amended in accordance with that contract and applicable law. #J-18808-Ljbffr

This 18-month, full-time role focuses on infection biology and translational research, with a strong emphasis on cell culture, microbiology and translational workflows.

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Seeking a passionate Science Teacher (Biology) for a full-time, long-term to permanent role at a secondary school in Stockport, starting April 2026.

European Molecular Biology Laboratory (EMBL-EBI) is launching a Digital Transformation Specialist role to drive EMBL-wide change programmes, with an initial focus on HR and expanding to Finance and Procurement.

A leading biotechnology recruitment firm seeks a Synthetic Biology/Fermentation R&D Scientist for an innovative company near Shanghai, China.

A leading life sciences organisation in Cambridge is looking to appoint an experienced Head of Computational Biology to lead and develop its computational biology capability. This is an exciting opportunity for an established computational biology leader to take a strategic role in a highly collabor

This tenure-track Group Leader post sits in the Cell Biology Division of the Laboratory of Molecular Biology, part of the Medical Research Council. Develop and lead a research programme on fundamental cell or tissue biology, or on methods for studying them. Studying fundamental processes in molecula

Familiarity with modern lab equipment and digital tools relevant to synthetic biology and fermentation; English is the working language; additional languages are a plus. Synthetic Biology/Fermentation R&D Scientist (m/f/d). The teams collaborate across disciplines to turn cutting‑edge synthetic bi

The Laboratory of Molecular Biology (LMB), part of the Medical Research Council, invites applications for a tenure-track Group Leader to build and run an independent research programme in cell biology.

EMBL-EBI, part of the European Molecular Biology Laboratory, is a worldwide leader in the storage, analysis and dissemination of large biological datasets.

Durham University invites applications for a Laboratory Technician to support Dr Jeongmin Choi's laboratory.The post is full-time, fixed-term for 2 years with an option to extend for 1 year.The role supports a friendly and vibrant team in a brand-new laboratory that prioritises wellbeing and a posit

You hold a PhD (or equivalent experience) in machine learning, computational biology, or structural biology, with a proven track record of applying machine learning to real-world protein structure or drug discovery challenges. Principal Machine Learning Engineer, Structural Biology | Pharma/BioTech

Seeking a Head of Biology with KS5 experience for a secondary school in Kingston. Responsibilities include teaching KS5 Biology and guiding the curriculum alongside the Director of Science.