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        2 Permanent API jobs in Suffolk + 30 miles

        Approved Premises Residential Worker - Ipswich Lightfoot House - Fixed Term Contract

        THE HOME OFFICE
        Ipswich, Suffolk
        £20,001 - £40,000 a year
        Overview of the job - The job holder will work as part of a team providing 24 hour cover at an Approved Premises (AP) including security and monitoring services. The job holder will undertake a full range of work with the offender whilst resident at the Approved Premises. This will include; providing support in contributing to the risk management and sentence plan objectives and reporting any significant changes relating to risk and/or re-offending to any non-compliance within agreed enforcement procedures to ensure that offenders resident at an AP and the fabric of it are kept safe and secure throughout their shift. Summary - The job holder will assist in the well-being and supervision of residents, maintaining discipline, adnce to AP rules, licence conditions, sentence plan objectives specific to residency in the Approved Premises and court orders.
        Overview of the job - The job holder will work as part of a team providing 24 hour cover at an Approved Premises (AP) including security and monitoring services. The job holder will undertake a full range of work with the offender whilst resident at the Approved Premises. This will include; providing support in contributing to the risk management and sentence plan objectives and reporting any significant changes relating to risk and/or re-offending to any non-compliance within agreed enforcement procedures to ensure that offenders resident at an AP and the fabric of it are kept safe and secure throughout their shift. Summary - The job holder will assist in the well-being and supervision of residents, maintaining discipline, adnce to AP rules, licence conditions, sentence plan objectives specific to residency in the Approved Premises and court orders.
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        Overview of the job - The job holder will work as part of a team providing 24 hour cover at an Approved Premises (AP) including security and monitoring services. The job holder will undertake a full range of work with the offender whilst resident at the Approved Premises. This will include; providing support in contributing to the risk management and sentence plan objectives and reporting any significant changes relating to risk and/or re-offending to any non-compliance within agreed enforcement procedures to ensure that offenders resident at an AP and the fabric of it are kept safe and secure throughout their shift. Summary - The job holder will assist in the well-being and supervision of residents, maintaining discipline, adnce to AP rules, licence conditions, sentence plan objectives specific to residency in the Approved Premises and court orders.
        Overview of the job - The job holder will work as part of a team providing 24 hour cover at an Approved Premises (AP) including security and monitoring services. The job holder will undertake a full range of work with the offender whilst resident at the Approved Premises. This will include; providing support in contributing to the risk management and sentence plan objectives and reporting any significant changes relating to risk and/or re-offending to any non-compliance within agreed enforcement procedures to ensure that offenders resident at an AP and the fabric of it are kept safe and secure throughout their shift. Summary - The job holder will assist in the well-being and supervision of residents, maintaining discipline, adnce to AP rules, licence conditions, sentence plan objectives specific to residency in the Approved Premises and court orders.
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        3 exact matches jobs are outside your preferred location

        Broad and expert knowledge of analytical methodologies supporting API development. The site includes state-of-the-art GMP facilities for API development, oral solid dose manufacture, formulation development, and process chemistry.
        Broad and expert knowledge of analytical methodologies supporting API development. The site includes state-of-the-art GMP facilities for API development, oral solid dose manufacture, formulation development, and process chemistry.
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        Data Scientist

        Pro Contract Jobs Ltd
        UK
        £500 per day 500 per day Outside IR35
        Location: United Kingdom (Remote) Type: 12 months Contract - Rate/Salary: 500 per day - IR35 Status: Outside IR35 - Role Summary - Join a major UK public sector organisation to help expand data science and analytics capability across a high-impact portfolio of services. Deliver advanced analytical models and practical AI/ML solutions that support better decision-making and improved outcomes for the public. Work end-to-end across discovery, data acquisition, modelling, deployment, reporting and continuous improvement. Operate within a controlled and governed environment, producing clear, audit-friendly artefacts and defensible analytical outputs. Remote-first engagement with occasional site visits (as required for workshops, stakeholder sessions, or delivery milestones). What Youll Be Doing - Lead the design and build of data science solutions from problem definition to production-ready ...
        Location: United Kingdom (Remote) Type: 12 months Contract - Rate/Salary: 500 per day - IR35 Status: Outside IR35 - Role Summary - Join a major UK public sector organisation to help expand data science and analytics capability across a high-impact portfolio of services. Deliver advanced analytical models and practical AI/ML solutions that support better decision-making and improved outcomes for the public. Work end-to-end across discovery, data acquisition, modelling, deployment, reporting and continuous improvement. Operate within a controlled and governed environment, producing clear, audit-friendly artefacts and defensible analytical outputs. Remote-first engagement with occasional site visits (as required for workshops, stakeholder sessions, or delivery milestones). What Youll Be Doing - Lead the design and build of data science solutions from problem definition to production-ready ...
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        Senior Data Scientist - Location: UK Remote - Salary: £60,000 - £70,000 - Employment Type: Full-Time - Please note: Sponsorship is not available for this position. Overview - A growing organisation is looking for a Senior Data Scientist to help develop advanced AI and analytics capabilities that power large-scale intelligence and data-driven products. This is an opportunity to work within a research-focused environment, building scalable machine learning models and AI systems across areas such as NLP, recommendation systems, predictive analytics, and workforce intelligence. The Role - As a Senior Data Scientist, you will contribute to the development and optimisation of advanced machine learning and AI models while maintaining high standards of experimentation, validation, and responsible AI practices. You'll work closely with AI Engineers, Product teams, and cross-functional stakeholders ...
        Senior Data Scientist - Location: UK Remote - Salary: £60,000 - £70,000 - Employment Type: Full-Time - Please note: Sponsorship is not available for this position. Overview - A growing organisation is looking for a Senior Data Scientist to help develop advanced AI and analytics capabilities that power large-scale intelligence and data-driven products. This is an opportunity to work within a research-focused environment, building scalable machine learning models and AI systems across areas such as NLP, recommendation systems, predictive analytics, and workforce intelligence. The Role - As a Senior Data Scientist, you will contribute to the development and optimisation of advanced machine learning and AI models while maintaining high standards of experimentation, validation, and responsible AI practices. You'll work closely with AI Engineers, Product teams, and cross-functional stakeholders ...
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        EMBL-EBI
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        From £43,015 to £60,957 per annum
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        As a Senior Scientist in Protein and Cell Sciences, you will design, express, purify and characterize recombinant proteins that underpin antibody discovery and other biologics programs. Are you ready to turn recombinant protein design into therapies that change the way cancer is treated? You will use modern computational tools alongside rigorous experimental methods to ensure the proteins you produce behave as intended. * Recombinant Antigen Design: Apply computational structural biology (including AlphaFold and ProteinMPNN) to design target proteins that are fit-for-purpose for discovery and development. * Protein Production: Express and purify recombinant proteins using bacterial and transient mammalian systems (E.coli, HEK, CHO), building robust, scalable methods and standard operating procedures that improve throughput and reproducibility.
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        MASS Consultants
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        From £45,000 to £65,000 per annum DOE plus company benefits
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        Peterborough (PE2)
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        Medpace is expanding a new Clinical Informatics team and is looking for qualified individuals to support this initiative. Our analysts work directly with Clinical Operation teams to identify needs and establish solutions spanning data analytics, visualization, and accessibility. Analysts will be trained to evaluate study protocols and work collaboratively with Clinical Trial Managers to develop and validate data products that increase operational efficiency. Analysts will support both custom- and enterprise-wide solutions as they work hand-in-hand with our software engineering team. * Innovate algorithms to describe, classify, and predict operational outcomes of clinical trials; and * Bachelors in informatics, computer science/engineering, biomedical engineering, health information, statistics, or related field; * Clinical research experience is preferred;
        Medpace is expanding a new Clinical Informatics team and is looking for qualified individuals to support this initiative. Our analysts work directly with Clinical Operation teams to identify needs and establish solutions spanning data analytics, visualization, and accessibility. Analysts will be trained to evaluate study protocols and work collaboratively with Clinical Trial Managers to develop and validate data products that increase operational efficiency. Analysts will support both custom- and enterprise-wide solutions as they work hand-in-hand with our software engineering team. * Innovate algorithms to describe, classify, and predict operational outcomes of clinical trials; and * Bachelors in informatics, computer science/engineering, biomedical engineering, health information, statistics, or related field; * Clinical research experience is preferred;
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        Avantor is looking for a Sample Dispatch Technician to support the global shipment of R&D samples from our Cambridge site. This is a hands-on, operational role focused on logistics, dispatch coordination, and shipment documentation. The position does not involve scientific research or experimentation, but plays a critical role in ensuring that samples are shipped safely, on time, and in full compliance with international regulations. • Receive, prepare, and package samples (biological, chemical, and dangerous goods) • Manage dispatch materials and inventory - Cambridge, UK | The Discovery Centre - Bio-Medical Campus - Monday-Friday | 9:00-17:00 - Permanent | Full-time - About the Role - Key Responsibilities • Coordinate domestic and international shipments via air, road, and sea • Prepare shipping documentation, labels, and customs paperwork in line with IATA / ADR / IMDG, CLP (GHS), and REACH requirements
        Avantor is looking for a Sample Dispatch Technician to support the global shipment of R&D samples from our Cambridge site. This is a hands-on, operational role focused on logistics, dispatch coordination, and shipment documentation. The position does not involve scientific research or experimentation, but plays a critical role in ensuring that samples are shipped safely, on time, and in full compliance with international regulations. • Receive, prepare, and package samples (biological, chemical, and dangerous goods) • Manage dispatch materials and inventory - Cambridge, UK | The Discovery Centre - Bio-Medical Campus - Monday-Friday | 9:00-17:00 - Permanent | Full-time - About the Role - Key Responsibilities • Coordinate domestic and international shipments via air, road, and sea • Prepare shipping documentation, labels, and customs paperwork in line with IATA / ADR / IMDG, CLP (GHS), and REACH requirements
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        FEATURED
        Clinical Trial Managers with expertise in Oncology or other therapy areas are welcome to continue to work in their area of expertise or to expand to a new therapeutic area. Medpace is the leading CRO for Biotech companies and is continuing to add a Director of Clinical Trial Management (Operational role) to join our Clinical Trial Management Group in London, UK. * Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables * Minimum of 5 years of Clinical Trial Management experience, CRO experience preferred; We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates. Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Job Summary
        Clinical Trial Managers with expertise in Oncology or other therapy areas are welcome to continue to work in their area of expertise or to expand to a new therapeutic area. Medpace is the leading CRO for Biotech companies and is continuing to add a Director of Clinical Trial Management (Operational role) to join our Clinical Trial Management Group in London, UK. * Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables * Minimum of 5 years of Clinical Trial Management experience, CRO experience preferred; We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates. Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Job Summary
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