187 jobs found in Cambridge

Business Applications Lead £60,000 - £70,000 Cambridge Fully-Flexible Remote Working Post-Covid* TEC Partners are working with a market leading Remote Access development business in central Cambridge, who are looking for an experienced Lead Developer with a background in Applications Development. Naturally, with the changes in our working habits over the last year, this business has become e...... click apply for full job details

Are you an experienced nurse looking for a rewarding career? As a Registered Nurse in Cambridge, Huntingdon, Ely, Chatteris and the surrounds, you'll love the fast-pace and variety that comes with supporting healthcare teams in a range of establishments in your area. You'll ensure that our service users receive dedicated nursing care at all times. You'll always have the desire to strive for the best possible outcome for the people in your care. This role provides you with a unique chance to forge your own career path and feel valued and respected everywhere you work. Employee advantages An hourly rate of up to £28.13, including holiday pay A facility to instantly withdraw your pay Select shifts to suit your lifestyle through our app, with part-time, full-time, night and day shifts available Free, ongoing clinical training to further your career Access to NHS registered GPs via a Virtual GP app and mental health support Exclusive access to RCNi decision making tools and support with revalidation Flexi Pay! Flexi Pay is an exciting app feature that enables you to choose when you get paid! Simply submit your timesheets through our app, and you'll gain instant access to up to 50% of the value of your existing shifts, even on weekends and bank holidays. What you'll need to join You'll have current NMC registration and strive to stay up-to-date with clinical best practices, working toward excellence in everything you do. You will have over 6 months of post-qualification experience behind you and the confidence to handle complex crisis situations with ease. You'll feel comfortable being the clinical lead in a team, offering advice to care assistants to ensure the best possible outcomes. With an excellent bedside manner, you'll demonstrate our core values of trust, empathy and expertise on every shift. You will need access to a smart device with an internet connection to pick up shifts and submit timesheets through our app, HealthForceGo. Access to your own vehicle would be beneficial but is not a requirement. Apply now, and you can start within a week!

Regulatory Affairs Specialist/Senior Regulatory Affairs Specialist - Publishing/Submissions - Home Based EMEA We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD - thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients. If you're a strategic thinker, planner and multitasker as comfortable working independently as you are on a team in delivering compliant deliverables based on solid judgment, PPD is the place to be. Our global regulatory experts contribute the regulatory strategy and knowledge to help our clients navigate the challenging regulatory environment - and help get life-changing therapies to patients faster. As a Regulatory Affairs Specialist/Senior Regulatory Affairs Specialist, you will electronically publish regulatory documents and submissions via electronic gateways using submission publishing tools. Seeking candidates with experience using Adobe Acrobat, Adobe Acrobat Plug Ins and other submission publishing tools. Summarized Purpose: Provides strategic, expedient and efficient preparation of client electronic submission deliverables and dossiers that meet current local, regional and ICH regulatory and technical requirements. Ensures successful regulatory review outcomes for product milestones. Serves in a technical quality review role and is responsible for the thorough review of published documents and submissions created within or outside of PPD to ensure quality of standards meet regulatory compliance requirements and meet or exceed client expectations. Essential Functions: Provides client electronic submission deliverables supporting regulatory compliance Prepares components of electronic regulatory submissions that meet the electronic document requirements set by regulatory guidance, publishing documents and submissions that work with sponsor and/or regulatory agency software programs, and meeting consistency and data security issues Maintains document lifecycle for submissions Supports development and implementation of project-specific processes for sponsors with unique technology requirements and may act as the PPD liaison for regulatory submission with the sponsor and assist PPD project teams in executing regulatory submission strategies Provides mentoring of other regulatory publishing personnel, as needed Uses professional judgment to evaluate the regulatory publishing needs in relationship to the overall project timelines, quality and delivery Engages other project team members, functional units or publishing management as necessary to deliver final product and resolve/mitigate identified issues or risk to delivery Acts independently within a project team or as the project team lead to evaluate and deliver publishing tasks *LI-SH1 *Qualifications:* Education and Experience: Bachelor's degree or equivalent and relevant formal academic / vocational qualificationPrevious experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years). Knowledge, Skills and Abilities: Working knowledge of global regulatory requirements and guidances for submission requirements, document management, document publishing and electronic submissions Advanced knowledge of Microsoft (MS) Word, MS Excel, Adobe Acrobat, electronic document management systems, document publishing tools, publishing systems, eCTD validation and viewing tools Advanced knowledge of electronic templates and skilled in formatting and troubleshooting templates Ability to manage several complex projects in parallel and adapt to changing priorities Ability to exercise independent judgment in developing methods, techniques and evaluation of criteria using defined procedures and practices Ability to independently assess sponsor needs and work with project team members in producing compliant deliverables Ability to independently learn new technologies Excellent organizational skills and effective interpersonal skills Excellent analytical ability and problem-solving capabilities Good working knowledge of medical terminology, statistical concepts, and guidelines and requirements of the FDA and other international regulatory agencies Excellent editorial/proofreading skills Detail-oriented, thorough, and methodical Ability to create and follow timelines and conduct long-range planning Ability to multi task performing numerous single or complex tasks without ignoring overall objectives Ability to judge when to initiate changes and make final determinations in the presentation of data in accordance with regulatory guidelines and reviewers' comments Ability to concentrate on the detail in a document without losing sight of the document as a whole At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team. We offer continued career advancement opportunities, award winning training and benefits focused on the health and wellbeing of our employees. Working Environment: PPD values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role: Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner. Able to work upright and stationary for typical working hours. Ability to use and learn standard office equipment and technology with proficiency. Able to perform successfully under pressure while prioritizing and handling multiple projects or activities. May require travel. (Recruiter will provide more details.) PPD Defining Principles: - We have a strong will to win - We earn our customer's trust - We are game changers - We do the right thing - We are one PPD If you resonate with our five principles above, and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the world's most urgent health needs, then please submit your application - we'd love to hear from you.

About this position EMBO (embo.org) stands for excellence in the life sciences. We support talented researchers at all stages of their careers in Europe and beyond, stimulate the exchange of scientific information, and help build a research environment where scientists can achieve their best work. EMBO considers openness and transparency to be key values in scientific research and publishing. We are involved in shaping open science by actively working with the scientific communities and by developing technologies and standards that serve researchers. EMBO Press (embopress.org) publishes four prestigious scientific research journals, The EMBO Journal, EMBO Reports, Molecular Systems Biology and EMBO Molecular Medicine and runs the journal-independent peer review platform Review Commons. EMBO Press has implemented numerous initiatives to promote transparency, reproducibility and efficiency in publishing. SourceData (sourcedata.embo.org) is as an open platform developed by EMBO to make research data shown in published figures findable, accessible, inter-connected and reusable. SourceData implements Open Science principles at the heart of scientific publishing. To support its multiple initiatives at the interface of scientific publishing, research policy and open science, EMBO is looking for a developer in machine learning to build tools and develop resources and technologies supporting the research community. Your role As Developer in Machine Learning you will be responsible for: -Contributing to a new Wellcome Trust-funded project to extract and organize features from peer review reports in order to facilitate their exchange, display and findability. -Developing further the SmartTag engine to automatically read scientific papers and organize them into an open knowledge graph (see , and ). -Maintaining and further developing tools for the editorial team at EMBO Press to use NLP (and possibly image analysis) to assist manuscript and data quality checks and automate repetitive tasks. -In the context of responsibilities above, working on the following sites and code repositories: ; -Coordinating with the EMBO IT team for systems administration. -Additional tasks as required by the Head of SourceData, the Head of Scientific Publications or the EMBO Director. This position will occasionally require working outside of the normal working hours, in the evenings or during the weekend. You have Your strength is solving complex problems and searching for the best possible solution while facing challenges and obstacles with ease. Proactivity and ownership are your crucial values when working on projects. You are motivated by a fast-changing environment that requires you to adapt to new scenarios as they unfold. You actively seek opportunities to learn new programming languages or to learn how to use new frameworks and new technologies. We love to work as a team and would like to welcome you as one of its key players. We would like you to have a degree in computer science, computational biology, physics, maths or equivalent work experience. An MS in any related field will be strongly valued. The position requires experience in the following fields: -Demonstrated expertise in structured, object-oriented and test-oriented programming in Python. -Experience with a major deep learning framework such as PyTorch (preferred) or TensorFlow. -Experience in natural language processing and text mining, using classical or deep learning frameworks (for example: nltk, spaCy, Gensim, BERT/transformers, …). -Experience with data processing (for example: numpy, pandas, scikit-learn, …). -Experience with relational databases (for example: PostgreSQL, MySQL…) and/or or graph database (for example: neo4j). -Familiarity with version control systems such as Git. You might also have -Experience in graph data science and network analysis. -A demonstrated involvement in Open Source development. -A background in Linux system administration: bash scripting, server deployment and maintenance (e.g. systemd), cron jobs, backups, etc... Why join us EMBO is an inclusive, equal opportunity employer offering attractive conditions and benefits appropriate to an international research organisation with a very collegial and family friendly working environment. The remuneration package comprises a competitive salary, a comprehensive pension scheme, medical, educational and other social benefits. Excellent child care facility is available on campus. The work at EMBO comes with -Relocation package -English is the working language -Creative, diverse and international environment -Flat hierarchies and freedom to make decisions and grow professionally -Possibility for position extension of the position, up to 9 years -Access to learning resources, training and budget for conference visit -Broad spectrum of technological challenges -Organized sport groups and social clubs -German classes What else you need to know The Machine Learning Developer reports to the Head of SourceData. Please note that appointments on fixed term contracts can be renewed, depending on circumstances at the time of the review.

About this position EMBO (embo.org) stands for excellence in the life sciences. We support talented researchers at all stages of their careers in Europe and beyond, stimulate the exchange of scientific information, and help build a research environment where scientists can achieve their best work. EMBO considers openness and transparency to be key values in scientific research and publishing. We are involved in shaping open science by actively working with the scientific communities and by developing technologies and standards that serve researchers. EMBO Press (embopress.org) publishes four prestigious scientific research journals, The EMBO Journal, EMBO Reports, Molecular Systems Biology and EMBO Molecular Medicine and runs the journal-independent peer review platform Review Commons. EMBO Press has implemented numerous initiatives to promote transparency, reproducibility and efficiency in publishing. SourceData (sourcedata.embo.org) is as an open platform developed by EMBO to make research data shown in published figures findable, accessible, inter-connected and reusable. SourceData implements Open Science principles at the heart of scientific publishing. To support its multiple initiatives at the interface of scientific publishing, research policy and open science, EMBO is looking for a developer in machine learning to build tools and develop resources and technologies supporting the research community. Your role As Developer in Machine Learning you will be responsible for: -Contributing to a new Wellcome Trust-funded project to extract and organize features from peer review reports in order to facilitate their exchange, display and findability. -Developing further the SmartTag engine to automatically read scientific papers and organize them into an open knowledge graph (see , and ). -Maintaining and further developing tools for the editorial team at EMBO Press to use NLP (and possibly image analysis) to assist manuscript and data quality checks and automate repetitive tasks. -In the context of responsibilities above, working on the following sites and code repositories: ; -Coordinating with the EMBO IT team for systems administration. -Additional tasks as required by the Head of SourceData, the Head of Scientific Publications or the EMBO Director. This position will occasionally require working outside of the normal working hours, in the evenings or during the weekend. You have Your strength is solving complex problems and searching for the best possible solution while facing challenges and obstacles with ease. Proactivity and ownership are your crucial values when working on projects. You are motivated by a fast-changing environment that requires you to adapt to new scenarios as they unfold. You actively seek opportunities to learn new programming languages or to learn how to use new frameworks and new technologies. We love to work as a team and would like to welcome you as one of its key players. We would like you to have a degree in computer science, computational biology, physics, maths or equivalent work experience. An MS in any related field will be strongly valued. The position requires experience in the following fields: -Demonstrated expertise in structured, object-oriented and test-oriented programming in Python. -Experience with a major deep learning framework such as PyTorch (preferred) or TensorFlow. -Experience in natural language processing and text mining, using classical or deep learning frameworks (for example: nltk, spaCy, Gensim, BERT/transformers, …). -Experience with data processing (for example: numpy, pandas, scikit-learn, …). -Experience with relational databases (for example: PostgreSQL, MySQL…) and/or or graph database (for example: neo4j). -Familiarity with version control systems such as Git. You might also have -Experience in graph data science and network analysis. -A demonstrated involvement in Open Source development. -A background in Linux system administration: bash scripting, server deployment and maintenance (e.g. systemd), cron jobs, backups, etc... Why join us EMBO is an inclusive, equal opportunity employer offering attractive conditions and benefits appropriate to an international research organisation with a very collegial and family friendly working environment. The remuneration package comprises a competitive salary, a comprehensive pension scheme, medical, educational and other social benefits. Excellent child care facility is available on campus. The work at EMBO comes with -Relocation package -English is the working language -Creative, diverse and international environment -Flat hierarchies and freedom to make decisions and grow professionally -Possibility for position extension of the position, up to 9 years -Access to learning resources, training and budget for conference visit -Broad spectrum of technological challenges -Organized sport groups and social clubs -German classes What else you need to know The Machine Learning Developer reports to the Head of SourceData. Please note that appointments on fixed term contracts can be renewed, depending on circumstances at the time of the review.

PPD's mission is to improve health. It starts as an idea to find a cure. It becomes a life saved. All in-between, it's you! We know that meaningful results not only require the right approach, but also the right people. We invite you to re-imagine health promoting protocols with us, working alongside our talented, bright and energetic teams. Our Project Delivery team directs, coordinates and manages the technical and operational aspects of projects, securing the successful completion of clinical trials. We collaborate with functional area leads to identify and evaluate fundamental issues on the project and ensure that solutions are implemented. The *Project Manager/Senior Project Manager - Consumer Health* is responsible for the overall coordination and management of consumer health clinical trials and non-interventional studies from start up through close out activities. Directs the technical and operational aspects of the projects, securing the successful completion of clinical trials At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team. We offer continued career advancement opportunities, award winning training and benefits focused on the health and well being of our employees. *Summarized Purpose: * * * Responsible for the overall coordination and management of of consumer health clinical trials and non-interventional studies from start up through close out activities. Directs the technical and operational aspects of the projects, securing the successful completion of clinical trials. Works with major functional area leads to identify and evaluate fundamental issues on the project, interpret data on complex issues, makes sound business decisions and ensure solutions are implemented. Works to ensure all project deliverables meet the customer's time/quality/cost expectations. Accountable for ensuring all project deliverables meet the customer/contract expectations, providing accurate hour forecasts, reviewing pass-through costs and ensuring timely invoicing with the support of Project Management Directors and/or Associate Directors while working in collaboration with other functional area leads. May work with Directors and/or Associate Directors, Project Management and Contracts & Proposals Development on the development of new proposals and general capabilities presentations to Customers for new business. *Essential Functions:* * Manages allocated studies according to timelines and quality standards. Coordinates activities of all functional departments and vendors involved in the project. Works with team and management to develop plans/guidelines for project implementation using PPD tools. Monitors and analyzes project status to ensure successful completion of project parameters, milestones, timetables (i.e., regulatory document, research agreement, site payments, interim monitoring, CRF retrieval, CRF data entry, etc.). Ensures teams are entering and updating internal tracking tools e.g. Project Pulse, CASCADE, etc. Works with team to identify potential risks, develop contingency plans * Acts as principal liaison between Sponsor and PPD by facilitating the flow of information between PPD and client. Provides Sponsor with timely project updates, project related fiscal information, ensures correct protocol interpretations, and obtains direction and feedback on implementing scope of work. May discuss and obtain feedback from Sponsors regarding PPD's performance to date * Plans and communicates to team members study specific tasks and priorities for projects. Delegates, as appropriate, assigned responsibilities to project team members. Liaises with managers in all functional areas within PPD to optimize performance and utilization of the project team members. Appropriately escalates any issues or potential issues to the Project Management Director or Associate Director for all project related issues * Works closely with finance and legal to manage all financial and contractual aspects of the study including establishing and recognizing financial milestones for invoice and subcontractor purposes, subcontracting with third-party service providers, approving subcontractor invoices, establishing proper accrual for investigator grants, assisting with negotiation of the investigator grants as needed and similar pass-throughs * Works with the project team to establish appropriate controls to ensure that project resources and expenses are aligned with budgets. Works closely with Project Management Director or Associate Director to provide details for the development and negotiation of contract modifications, as needed. Ensures that appropriate assessment and coordination of project/protocol specific and therapeutic area training needs and activities are occurring for the team members as needed * Provides input into hiring, performance management, training and other activities related to leading project staff members across functional areas. * Works to prepare and present at client meetings as the assigned Project Manager. Attends bid defenses as necessary. *Qualifications:* *Education and Experience: * Bachelor's degree or equivalent and relevant formal academic / vocational qualification Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8+ years' for Sr PM level) or equivalent combination of education, training, & experience. Years of experience refers to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions. *Knowledge, Skills and Abilities: * * Knowledge of the key principles of cross functional project management (Time, Quality, Cost). * Solid financial acumen. * Applies a range of negotiation techniques to achieve desired outcomes with evidence of commercial and organizational acumen. * Can effectively plan and deliver a dynamic and persuasive presentation, using effective graphics, overheads or slides. * Displays effective communication skills (listening, oral, written) and can communicate in English language (oral, written). * Sound interpersonal skills, is flexible and adapts to changing situations. * Has the ability to persuade, convince, and influence or impress others. * Is organized, proficient at multi-tasking with good attention to detail * Able to lead, motivate and coordinate teams. Coach/mentor team members as appropriate. * Able to delegate, effectively prioritizes own and workload of project team members. * Ability to effectively use automated systems and computerized applications such as Outlook, Excel, Word, etc. * Possesses cross cultural awareness and is able to adapt appropriately. * Has an in-depth understanding and appreciation of clinical research/development, including medical and therapeutic areas, phases and medical terminology. * Has experience with leading, liaising and coordinating cross-functional project teams. * Has an in-depth knowledge/understanding of clinical development guidelines and directives *PPD Defining Principles: * - We have a strong will to win - We earn our customer's trust - We are game changers - We do the right thing - We are one PPD - If you resonate with our five principles above, and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the world's most urgent health needs, then please submit your application - we'd love to hear from you.

Molecular Biology Technician Cambridge 6 Month contract £18-£21/ph Brief Molecular Biology Technician needed for a multinational Pharmaceutical organisation based in Cambridge who are looking to employ an experienced and well-rounded Molecular Biology Technician This role is lab based and the client is looking for candidates that live local to Cambridge...... click apply for full job details

About this position EMBO (embo.org) stands for excellence in the life sciences. We support talented researchers at all stages of their careers in Europe and beyond, stimulate the exchange of scientific information, and help build a research environment where scientists can achieve their best work. EMBO considers openness and transparency to be key values in scientific research and publishing. We are involved in shaping open science by actively working with the scientific communities and by developing technologies and standards that serve researchers. EMBO Press (embopress.org) publishes four prestigious scientific research journals, The EMBO Journal, EMBO Reports, Molecular Systems Biology and EMBO Molecular Medicine and runs the journal-independent peer review platform Review Commons. EMBO Press has implemented numerous initiatives to promote transparency, reproducibility and efficiency in publishing. SourceData (sourcedata.embo.org) is as an open platform developed by EMBO to make research data shown in published figures findable, accessible, inter-connected and reusable. SourceData implements Open Science principles at the heart of scientific publishing. To support its multiple initiatives at the interface of scientific publishing, research policy and open science, EMBO is looking for a developer in machine learning to build tools and develop resources and technologies supporting the research community. Your role As Developer in Machine Learning you will be responsible for: -Contributing to a new Wellcome Trust-funded project to extract and organize features from peer review reports in order to facilitate their exchange, display and findability. -Developing further the SmartTag engine to automatically read scientific papers and organize them into an open knowledge graph (see , and ). -Maintaining and further developing tools for the editorial team at EMBO Press to use NLP (and possibly image analysis) to assist manuscript and data quality checks and automate repetitive tasks. -In the context of responsibilities above, working on the following sites and code repositories: ; -Coordinating with the EMBO IT team for systems administration. -Additional tasks as required by the Head of SourceData, the Head of Scientific Publications or the EMBO Director. This position will occasionally require working outside of the normal working hours, in the evenings or during the weekend. You have Your strength is solving complex problems and searching for the best possible solution while facing challenges and obstacles with ease. Proactivity and ownership are your crucial values when working on projects. You are motivated by a fast-changing environment that requires you to adapt to new scenarios as they unfold. You actively seek opportunities to learn new programming languages or to learn how to use new frameworks and new technologies. We love to work as a team and would like to welcome you as one of its key players. We would like you to have a degree in computer science, computational biology, physics, maths or equivalent work experience. An MS in any related field will be strongly valued. The position requires experience in the following fields: -Demonstrated expertise in structured, object-oriented and test-oriented programming in Python. -Experience with a major deep learning framework such as PyTorch (preferred) or TensorFlow. -Experience in natural language processing and text mining, using classical or deep learning frameworks (for example: nltk, spaCy, Gensim, BERT/transformers, …). -Experience with data processing (for example: numpy, pandas, scikit-learn, …). -Experience with relational databases (for example: PostgreSQL, MySQL…) and/or or graph database (for example: neo4j). -Familiarity with version control systems such as Git. You might also have -Experience in graph data science and network analysis. -A demonstrated involvement in Open Source development. -A background in Linux system administration: bash scripting, server deployment and maintenance (e.g. systemd), cron jobs, backups, etc... Why join us EMBO is an inclusive, equal opportunity employer offering attractive conditions and benefits appropriate to an international research organisation with a very collegial and family friendly working environment. The remuneration package comprises a competitive salary, a comprehensive pension scheme, medical, educational and other social benefits. Excellent child care facility is available on campus. The work at EMBO comes with -Relocation package -English is the working language -Creative, diverse and international environment -Flat hierarchies and freedom to make decisions and grow professionally -Possibility for position extension of the position, up to 9 years -Access to learning resources, training and budget for conference visit -Broad spectrum of technological challenges -Organized sport groups and social clubs -German classes What else you need to know The Machine Learning Developer reports to the Head of SourceData. Please note that appointments on fixed term contracts can be renewed, depending on circumstances at the time of the review.

We are urgently looking for Yoga Instructors to take on clients from our website. Are you passionate about helping your clients change their lives for the better and improve their mental and physical health? Are you looking for new clients? If this sounds like you, we'd love to hear from you. Who are we looking for? We want friendly and professional Yoga Instructors who know how to bring out the best in their clients to achieve lasting lifestyle changes. Tasks may include teaching one to one lessons for Vinyasa, Hatha, Ashtanga, Power, pre- or post-natal Yoga or more, but we encourage our Yoga Instructors to work within their speciality. If you are happy to liaise and work directly with clients and you have availability to take on more clients, please get in touch.

We are urgently looking for Yoga Instructors to take on clients from our website. Are you passionate about helping your clients change their lives for the better and improve their mental and physical health? Are you looking for new clients? If this sounds like you, we'd love to hear from you. Who are we looking for? We want friendly and professional Yoga Instructors who know how to bring out the best in their clients to achieve lasting lifestyle changes. Tasks may include teaching one to one lessons for Vinyasa, Hatha, Ashtanga, Power, pre- or post-natal Yoga or more, but we encourage our Yoga Instructors to work within their speciality. If you are happy to liaise and work directly with clients and you have availability to take on more clients, please get in touch.

We are urgently looking for Yoga Instructors to take on clients from our website. Are you passionate about helping your clients change their lives for the better and improve their mental and physical health? Are you looking for new clients? If this sounds like you, we'd love to hear from you. Who are we looking for? We want friendly and professional Yoga Instructors who know how to bring out the best in their clients to achieve lasting lifestyle changes. Tasks may include teaching one to one lessons for Vinyasa, Hatha, Ashtanga, Power, pre- or post-natal Yoga or more, but we encourage our Yoga Instructors to work within their speciality. If you are happy to liaise and work directly with clients and you have availability to take on more clients, please get in touch.

We are urgently looking for Yoga Instructors to take on clients from our website. Are you passionate about helping your clients change their lives for the better and improve their mental and physical health? Are you looking for new clients? If this sounds like you, we'd love to hear from you. Who are we looking for? We want friendly and professional Yoga Instructors who know how to bring out the best in their clients to achieve lasting lifestyle changes. Tasks may include teaching one to one lessons for Vinyasa, Hatha, Ashtanga, Power, pre- or post-natal Yoga or more, but we encourage our Yoga Instructors to work within their speciality. If you are happy to liaise and work directly with clients and you have availability to take on more clients, please get in touch.

Senior Bioinformatician - crop science company Cambridge. Python, R programming, statistics & NGS experience Your new company My client is an innovative and very well funded company, based in Cambridge, looking to add several talented bioinformaticians to their team to focus on cutting edge genetic experiments to provide food security and help solve the global food crisis...... click apply for full job details

Kymab is a clinical-stage biopharmaceutical company developing a deep pipeline of novel antibody-based therapies in a broad range of indications. The Company generates its product candidates using its proprietary, integrated platforms collectively called IntelliSelect®. Kymab's platforms have been designed to maximize the diversity of human antibodies produced in response to immunization with antigens. Selecting from a broad diversity of fully human antibodies allows for the identification of antibodies with optimal drug-like properties. To work as part of the Facilities Team, primarily responsible for overseeing Goods In, Inventory Control, Purchasing, as well as providing a range of support activities in conjunction with the Director, Operations, Facilities Manager, Laboratory Manager and the Facilities Support Team Key Responsibilities: Manage the Goods In department: receive deliveries, unpack and store in appropriate storage location, check goods in on the Amici procurement system, communicate to staff they can pick up goods, file all paperwork and liaise with finance re any disputed invoices for goods received. Implement and develop new Inventory management system to control and monitor all goods received by Kymab and their location Sample management: overhaul current LN2 storage system and manage all samples in and out of the system thereafter, set up a service for staff to receive samples Procurement of all stock items for general use Maintain and manage all asset and goods storage areas Job Requirements: Education and Experience: General science education, to 'A' /BTEC level standard or equivalent Previous relevant inventory systems and stores experience Skills and Knowledge: Thorough understanding of inventory policies and procedures, data analysis skills Strong IT skills, Word, Excel, web-based databases Solid written and oral communication skills A high level of organisation & problem solving skills, with ability to multi-task and prioritise work to meet deadlines Excellent attention to detail Experience of liaising with suppliers Competencies: Can work well in a team and has the ability to work independently Great customer service attitude, confident and polite Dependable and efficient Flexible attitude, with a 'can-do' approach Can maintain confidentiality and show discretion Kymab embraces diversity and equality of opportunity and are committed to building inclusive and diverse teams representing all backgrounds. We welcome and consider applications to join from all qualified candidates, regardless of their characteristics.

Clear Glass are a bespoke glass works company based in Cottenham. We require a bespoke glass installer or trainee. The candidate would be installing bespoke glass splashbacks, showers, balustrades and balconies as well as single and double glazing, glass cutting and glass spraying. The ideal candidate must have: Full UK Driving License It would be a benefit if the candidate had the following: Some experience of glass or carpentry (not essential but would be ideal) CSCS card or training Full training and PPE will be provided upon induction to the company. Along with completing the application, the candidate must also indicate their earliest start date. Hours: Monday to Friday 7:30 - 16:30 Some occasional weekend work may be required. Job Type: Full-time Benefits: On-site parking Job Types: Full-time, Permanent Salary: £18,000.00-£25,000.00 per year COVID-19 considerations:To keep our employees safe we have installed a glass safety screen at reception along with a hand santising station. Our employees have been supplied with masks, gloves and sanitising equipment and advised to keep to social distancing measures. #Jora

About The Role A first-class shopping experience starts with our in-store Style Advisors. Natural promoters of customer service excellence, they go out of their way to provide an outstanding in-store experience to ensure that our customers return time and time again. Hardworking and dedicated, our Style Advisors treat our customer as their primary focus, actively listening to their needs and provid...... click apply for full job details

An exciting opportunity has become available for a Senior Medical Writer EMEA to join an innovative global pharmaceutical contract research organization at their site in the UK. *As a Senior Medical Writer, you will:* * Provide high-quality medical and scientific writing from planning and coordination of literature search through to the delivery of final drafts to internal and external clients * Effectively manage medical writing projects to deliver quality products to agreed timelines * Independently research, write and edit clinical study reports, study protocols and standard response documents * Have excellent data interpretation and medical writing skills, including grammatical, editorial, and proofreading skills, plus strong project management skills * Produce complex clinical or scientific documents, such as IBs, and sections of INDs, NDAs, CTDs, as well as dossiers * Provide a senior review of documents and training/mentoring for other writers *Basic Qualifications and Experience:* * Bachelor's degree in a scientific discipline * Previous experience that provides the knowledge, skills, and abilities to perform the job equivalent combination of education, training, & experience * Experience working in the pharmaceutical/CRO industry * Additional qualifications in medical writing a bonus (AMWA; EMWA; RAC) * Strong negotiation skills * Significant knowledge of Global, Regional, and National document development guidelines-In-depth knowledge in a speciality area such as preclinical, therapeutic, regulatory submissions, and communications * Great judgment and decision-making skills * Excellent computer skills and skilled with client templates; Good knowledge of document management systems and other relevant applications (e.g. Excel, Outlook) *In Return You Will Receive:* * Competitive remuneration package * A truly inspiring working environment in a highly prestigious, global company If you have the correct skill-set or you know of any professionals who may be suitable, please do get in touch [](mailto:) or (0). Fleur is a Search Consultant at Haybury Search covering Europe, UK, North America and Asia.

Company Description Mundipharma is a global (ex-US) network of independent associated companies that research, develop and manufacture innovative pharmaceutical medicines and consumer healthcare products. We are an agile and fast-paced company seeking to increase access to health care through programmes and effective partnerships...... click apply for full job details

Self Employed - Mortgage Advisor - CeMap Qualified or working towards CeMap qualifications as a trainee Have you ever wondered, what would it be like to be the "Boss", but not sure where to start? We are currently working with a national client, who is looking to offer Mortgage Advisers the opportunity to run their own business whilst being part of a national growing brand!! You will receive ongoing ...... click apply for full job details

Regular Officer Be the one others turn to. Be responsible. Be trusted with the safety of the nation. Become a British Army Officer, and you'll be doing something that really matters. Leading a team. Making a difference to the world. You don't need a degree for many Officer roles, and specific entry requirements vary from role to role...... click apply for full job details

Job Purpose : · To safely operate, maintain, repair and improve clients' assets within the Energy sector with inlet pressure up to 85 bar Location: · Cambridgeshire, Northamptonshire, Essex, Nottinghamshire Responsibilities: · Monitor condition of client/company equipment - ensure reports are completed as applicable · Ensure comprehensive records of vehicle stock and calibration of tools and equipment on vehicles are maintained and kept up to date · Carry out assigned activities on all equipment associated with Gas transportation. (planned; defect; and projects activities) · Complete maintenance on a variety of gas process equipment, i.e., commission, overhaul, functional checks · Ensure full and detailed records are maintained on all plant and operations completed (both manual and computerized) · Ensure availability of all safety critical systems · Contribute to projects, investigations and audits (internal and external to the site) · Site supervision of direct and contract labour as and when required · Carry out assigned duties and work without direct supervision and in potentially remote/hazardous locations. · The Technician will be required to participate in a standby rota for emergency call out · Provide training, advice, guidance and support to other teams or individuals when applicable · Responsible for operating and using mobile plant, mechanical lifting handling equipment, tools and other equipment properly and safely, ensuring they are correctly maintained and stored.

Is building meaningful and lasting relationships with the people you care for important to you? As a Care Assistant in Cambridge, Saffron Walden and the surrounds, you'll be the person that brings smiles to the faces of the people in our care. This role is a chance to make a real difference to people's lives - without your support, they may live a life constrained to specialist units or hospitals...... click apply for full job details

Company Description Mundipharma is a global (ex-US) network of independent associated companies that research, develop and manufacture innovative pharmaceutical medicines and consumer healthcare products. We are an agile and fast-paced company seeking to increase access to health care through programmes and effective partnerships...... click apply for full job details

Are you a strategically focussed Regulatory professional and would like to play an integral part in bringing life changing Oncology medicines to patients? If you are please read on... At AstraZeneca work with diverse minds, all united by a shared passion to learn, grow and discover. Within *Oncology Regulatory Science and Strategy (ORSS)* we bring hope and solutions to patients with unmet needs across the globe. As Regulatory professionals working on Oncology products, we work in areas of unmet need and take innovative regulatory approaches to bring life-changing treatments to patients. We work across our pipeline and the business to get medicines to patients as efficiently and effectively as possible. *The Regulatory Affairs Director (RAD)* provides *strategic and operational regulatory leadership to the development, commercialisation and life cycle management of assigned product(s)*. You will serve as the *global regulatory lead (GRL) on early stage projects or specific indications of larger programs, or as regional regulatory lead*. You'll contribute significantly to overall product and clinical strategy. The role plays a key role *influencing regulatory authorities* through regular contacts to improve regulatory outcomes. The RAD *leads cross-functional teams in major regulatory submissions (NDA, IND/CTA)*, *health authority interactions, label discussions, and securing NDA/BLA approvals.* As a GRL, the RAD leads the Global Regulatory Strategy Team (GRST) in formulating Global Regulatory strategy and delivering on NDA Filings and Approvals. Alternatively, as a regional regulatory lead, the RAD is a member of the GRST and is accountable for providing the region-specific Regulatory strategy and advice. The RAD serves as the face of the company with health authorities. *Typical Accountabilities, what you will be doing:* * Accountable for leading the development and implementation of the regional or global regulatory strategy for a product/group of products. Ensures that the strategy is designed to deliver rapid approval with competitive labeling in keeping with the properties of the product(s) and the needs identified by the business, markets and patients. This includes health authority engagement strategy and considerations of expedited regulatory programs. * Lead cross-functional Teams in major health authority interactions. This includes setting the strategy and planning for the interaction, driving the formulation of the briefing document focused on strategy and scientific content, leading the team through meetings rehearsals, and moderating the meeting itself. * Lead a Global Regulatory Strategy Team (GRST) of key contributing members from the regions, emerging markets, RA CMC, Labelling and members of the submission and execution team. Participate in coaching, and performance feedback to members of your GRST. * May (depending on role and project) represent Regulatory Affairs on Global Product Teams (GPTs) providing strategic Regulatory advice and be accountable for all Regulatory activities * Accountable for the delivery of all regulatory milestones on your team including assessment of the probability of regulatory success based on a thorough assessment of regulatory risks and mitigations. Lead preparation of the regulatory strategy document and target product labeling. * Demonstrate strategic leadership skills contributing to effective product development. Provide team leadership and participate in coaching, and performance feedback to members of the GRST. * Accountable for initiating and delivering key regulatory documents and plans and leading the negotiations with health authorities. * Lead the objective assessment of emerging data against aspirations and update senior management on project risks/mitigation activities. * Ensures appropriate planning and construction of the global dossier and core prescribing information led by the respective teams. Accountable for product maintenance, supply and compliance activities associated with marketed brands. * Partner with marketing companies (countries) and regional regulatory affairs staff to influence developing views/guidance. *Education, Qualifications, Skills and Experience:* *Essential:* * An advanced degree in a science related field and/or other appropriate knowledge/experience. * Previous demonstrated experience of regulatory drug development or equivalent, and experience with major Health Authority interactions. Prior experience with phase 3 design including end of phase 2 health authority interactions is desired. Contribution to a regulatory approval including leading response team and labelling negotiations would be a plus. * A solid knowledge of regulatory affairs within at least one therapeutic area in early and late development. * Demonstrated competencies of strategic thinking, strategic influencing, innovation, initiative, leadership and excellent oral and written communication skills. * The ability to think strategically and critically and evaluate risks to regulatory activities. *Desirable:* * A good understanding of guiding principles in drug development such as benefit/risk profile, dose selection or statistical design. * Broad background of experience working in pharmaceutical business and prior experience in several areas within regulatory affairs. Experience in relevant therapy area (small molecules & biologics) is preferred. * Ability to work strategically within a complex, business critical and high-profile development program. * Critical thinking on current global regulatory science questions and good understanding of the corresponding scientific and clinical components *Location:* Cambridge, UK *Salary:* Competitive + Excellent Benefits *Closing Date:* 30th April 2021 Next steps, if the role looks suitable to you please apply! *Where can I find out more?* Our Social Media, Follow AstraZeneca on LinkedIn []() Follow AstraZeneca on Facebook []() Follow AstraZeneca on Instagram []()

LCMS Senior Scientist Cambridge £35,000 - £45,000 As an LCMS Senior Scientist, would you want the next step in your career to be within a fast-growing, dynamic, successful team? Do you aspire to work for a company that appreciate and even reward their team members based on their performance? Are you an LCMS Senior Scientist looking for your next exciting position as an LCMS Senior Scientist? This LCM...... click apply for full job details

Deliver great technology that matters. About Simprints Simprints is a nonprofit tech company from the University of Cambridge. Our mission is to transform the way the world fights poverty. We build technology to radically increase transparency and effectiveness in global development, making sure that every vaccine, every dollar, every public good reaches the people who need them most. Simprints' biometric technology helps verify coverage and increase impact on the frontlines. We have already reached over 850,000 individuals and are contracted to reach more than 1.4m people by the end of 2021 through flagship projects like our work with BRAC in Bangladesh and the Ministry of Health in Ethiopia. Role Overview We are looking for a full-time Technical Project Manager who is passionate about building and implementing technology-based solutions in service delivery and research projects around the globe. You will work closely with Simprints' partners to gather requirements and oversee the delivery of robust solutions. This role is unique in its breadth, offering the opportunity to collaborate with almost every team at Simprints. You'll have the chance to collaborate with partnership managers to build relationships with external stakeholders, work with engineers to build custom technical solutions, coordinate on-the-ground activities with our in-country teams; and analyse data with monitoring & evaluation (M&E) specialists. This post is based in Cambridge, UK, with remote working in the near term. RESPONSIBILITIES Oversee successful delivery of our projects from start to finish, coordinating activities with both internal and external stakeholders Create multi-disciplinary project teams and collaboratively define detailed requirements, prioritise deliverables and feature requests, align behind implementation plans, and oversee execution (including sprint planning) Actively manage the technical implementation and work closely with engineers to optimise timelines, resolve bottlenecks and understand limitations Build relationships with external partners to promote understanding and use of Simprints' biometric solutions. Provide troubleshooting and remote supervision support Proactively identify and mitigate project risks Collaborate with M&E to establish theories of change, define project metrics, monitor and analyse data, and close the feedback loop with partners to support successful implementation on the ground Prepare and submit financial and narrative reports to partners and/or funders Travel to project sites to conduct or support trainings of trainers and monitor field activities, if needed and pending a travel risk assessment MUST HAVE REQUIREMENTS Significant project management and/or product management experience, ideally in the ICT4D space. You've deployed projects in developing country contexts. Familiarity with data collection platforms, such as DHIS2, CommCare, ODK, OpenSRP, and/or other technology platforms commonly used in global development. You are knowledgeable about, have designed, or implemented workflows common among frontline workers in development programs (e.g. health care, aid distribution, research, education). Excellent written and verbal communications. You are empathetic and seek to understand different perspectives, bring clarity to ambiguous or ill-defined needs, can negotiate diplomatically when there are competing interests, and secure buy-in and alignment across stakeholder groups. Attention to detail. Global development work is complex and unpredictable. To proactively anticipate risks, assess implicit requirements on top of contractual deliverables, and successfully meet ever-changing needs, you need to be able to translate a high-level idea into concrete, detailed action steps and documentation. Strong training skills. We work across multiple sectors with a variety of stakeholders. Being able to tailor trainings to audiences of varying technical literacy levels, for a number of different use cases and workflows, is crucial. You are comfortable hosting virtual trainings as well as conducting in-person trainings in resource-limited settings. Time management. You are organised, process-oriented, and attentive to following through on planned tasks and activities. You know how to allocate and shift resources to provide support to team members as needed, ensuring that project deliverables are met on time and on budget. Permission to work in the UK. NICE-TO-HAVE REQUIREMENTS Grit and an appreciation of a challenging, fast-paced environment Working proficiency in French, Arabic, Spanish, or other common language Experience with agile development methods and processes (e.g. scrum) An engineering mindset and passion for building technology solutions Interest in and/or experience in M&E or data analysis WE OFFER Life is short. We believe work should be awesome, meaningful, and fun. At Simprints we're taking on global development's biggest challenges, powered by an amazing culture and incredible people. Work with us, and you will grow faster, learn more, and take on great responsibilities with potential to make lasting change. Social impact. Work directly with our partners and users to deliver technology that has the potential to impact millions of lives. Incredible, diverse team. Ask any "Simprintster" what their favourite thing about working at Simprints is, and the answer is likely to be "the people." Our work is at the intersection of technology and global development, and we've managed to build an amazing team drawn from the best technology companies, iNGOs, UN agencies, and universities around the world. Flexible hours. More efficient late at night? Better before the sun rises? That's fine by us. We are looking for people who get the job done, not for people who work between 9am and 5pm. Unlimited paid time off. We set high standards and goals, but give people the freedom to choose when and how to recharge. Join a team that trusts you with the job. Professional development and wellbeing. We promote continual learning with self-directed learning objectives, external mentors, and regular one-on-one feedback. We also put our money where our mouth is with a dedicated 'Learning & Wellness' budget, managed by our Talent and Operations team. Simprints is an equal opportunity employer. We pride ourselves in our firm commitment to improving diversity, equity, and inclusion in our workplace. We aim to attract, hire, grow, and retain the most qualified candidates regardless of race, gender, ability, religion, nationality, age, sexuality, and other differences. We encourage interested and suitable candidates who are part of underrepresented groups to apply for this position. #Jora

CK Group are recruiting for a Statistical Programmer to join a company in the Pharmaceutical industry at their site based in Cambridge on a contract basis for 12 months. * Company:* Our client is a global pharmaceutical company with a major presence in the UK. Their purpose is to deliver life-changing medicines and to do this they are completely science-led and like to share this with the scientific, healthcare and business communities within the UK. *Location:* This Statistical Programmer role will be home based with occasional travel to our clients site in Cambridge. *Salary:* £65 per hour Ltd or £50 per hour PAYE. *Statistical Programmer Role:* * Focused on late stage clinical trials within Respiratory and Immunology. * Implements statistical programming aspects of the protocol or clinical development program. * Programs independently with high efficiency and quality. *Your Background:* * Degree in Mathematics (i.e., Applied Math, Engineering, etc), Statistics, Computer Science, Life Science or equivalent. * Excellent programming skills including macro language. * Proficient knowledge of the clinical development process. * Experience in late stage clinical trials within Respiratory and Immunology. *Apply:* For more information or to apply for this Statistical Programmer position, please contact Julie on or email , quoting job ref 50354. It is essential that applicants hold entitlement to work in the UK.

Fundraising Manager We have an exciting opportunity for an experienced Fundraising Manager, to help a Cambridge based charity increase income from trusts and foundations, major donors and legacies. Our client is a local charity that cares about Cambridge and its green landscapes, they protect the green setting of Cambridge and its most valuable landscapes and work to enhance and connect them for people and nature. Position: Fundraising Manager Salary: circa £35,000 pro-rata, dependent on experience. Location: Wandlebury Country Park, Cambridge - This role is suitable for home working combined with team working at the office and site-based activity. Duration Full-time (37.5 hrs per week) preferred but will consider flexible working arrangements to accommodate work-life balance. Benefits: 33 days annual holiday entitlement pro rata, includes allowance for Public/Bank Holidays, a pension contribution of up to 5% of gross pay. Closing date: 10:00am, Monday 17 May 2021 About the role: As Fundraising Manager you will be a key member of the Management Team, you will co-ordinate and deliver fundraising activity and own the charity's fundraising targets. This role potentially covers the full range of fundraising opportunities, the main focus will be fundraising from mid-level donors, legacies, membership and trusts/foundations. The charity's ambition is to develop a small team who can work to broaden the scope of the fundraising work, there will be opportunities for line management responsibilities if desired. Some of your key responsibilities will include: Increase charitable giving from current supporters. Research and identify fundraising opportunities from trusts and foundations as well a major donors and corporate fundraising. Develop and promote appealing memorial and legacy giving opportunities. Responsible for membership recruitment and retention to achieve annual targets for membership subscriptions. Develop and maintain effective systems to support the fundraising functions of the charity. With the CEO, discuss and agree an annual budget for fundraising. Prepare accurate, succinct and easy to understand reports on the charity's fundraising work. Ensure that the charity adheres to relevant fundraising legislation, including compliance with the Fundraising Regulators guidelines. About you: To be successful in the role of Fundraising Manager you will be supportive of the charity's cause; you will use your relationship management skills to strengthen existing funding relationships and use your research and networking skills to identify and cultivate new opportunities. You will bring with you the following key skills and experience: Demonstrable evidence of successful fundraising from individual donors, trusts & foundations and legacies. Excellent written and visual communication skills, with evidence of producing effective fundraising content. Excellent interpersonal skills, with the ability to encourage support for the charity and build long-term relationships. Knowledge of UK fundraising and data protection regulations. An excellent eye for detail. Good IT skills (spreadsheets, Microsoft Office suite, database management) and experience of fundraising support systems. Experience of administering grants and donations. Experience of organising donor cultivation and solicitation events. This is a fantastic opportunity to join a small, friendly and committed management team where you can make a real difference and your work will have an impact, so apply today! Please ensure that, along with your CV, you submit a covering letter telling us how you feel you would be a good fit for the role. Other roles you may have experience of could include: Fundraiser, Corporate Fundraising Manager, Community Fundraising Manager, Donor Manager, Major Donor Fundraising, Individual Giving, Philanthropy, Community Fundraising Manager, Trust Fundraising, Partnerships Fundraising, Development Manager, Regional Fundraising Manager, Area Fundraising Manager etc

Simprints aims to contribute to transformative change in the international development sector. We recognise this can only be achieved through close collaboration with our partners, clients and supporters. We currently deliver diverse projects with different clients in a variety of country contexts. The Solutions Architect is a new role at Simprints and will help us to increasingly meet the needs of our clients with the most appropriate technology and service solution. This is an exciting opportunity for a candidate with relevant experience in Engineering Pre-Sales, Solutions Architecture, and/or Customer Solutions Design. About Simprints Simprints is a nonprofit tech company spun out of the University of Cambridge. Our mission is to transform the way the world fights poverty. We build technology to radically increase transparency and effectiveness in global development, making sure that every vaccine, every dollar, every public good reaches the people who need them most. We use biometric technology to help verify coverage and increase impact on the frontlines. Our goal is to enable our partners in the international development sector to better track and deliver progress towards the Sustainable Development Goals, contributing to a world where every person counts in the fight against poverty. We work with organisations such as Children's Investment Fund Foundation, the Gates Foundation, USAID, DFID, and Gavi, and partner with organisations such as the Ethiopian Federal Ministry of Health, BRAC, Mercy Corps, Dimagi and D-Tree to achieve our mission. Simprints has already reached over 1 million individuals through our flagship projects in Ethiopia and Bangladesh. We are in a unique situation: a nonprofit, impact driven company that is processing millions of highly sensitive biometric records in some challenging settings. The Solutions Architect Role gets to play a pivotal role in shaping and defining these exciting solutions for challenging problems! About the role The Solutions Architect role helps bridge the needs of our partners with the exciting potential of Simprints' technology. It is a key position within the company that involves close interaction with our prospective partners as well as involvement in the evolution of our product and services. You will oversee the gathering, design and negotiation of requirements on exciting and complex international development opportunities. Working next to your peers in Sales, Project Delivery, Engineering and Product you will be helping chart a clear solution to best optimise social impact for our partners. Simprints wants someone who is passionate about designing technology-based solutions in service delivery and research projects around the globe. There is an opportunity to expand and grow within the organization, whilst having an exciting role scope and the ability to contribute to social impact objectives. This post is based in Cambridge, UK, with remote working in the near term. RESPONSIBILITIES This role will report to the Director of Delivery, whilst maintaining close working relationships with the Director of Partnerships and with the Chief Product and Engineering Officer. Your responsibilities will include: Serve as the technical solution lead across several Simprints engagements, carefully weighing the balance between introducing new feature design and platform complexity to maximize partner impact realization Demonstrate mastery of our platform feature flexibility and limitations Understand common integration points (Commcare, ODK, DHIS2, etc..) and recommend technology pairings for complete use cases Helping to qualify and close opportunities (alongside the partnerships team) through developing a deep understanding of client needs. Demonstrating excellent stakeholder management and attention to detail whilst designing bespoke custom solutions and providing technical input into donor (funding) proposals. Maintaining strict control over new project sign-off to ensure all project commitments are ethical and have undergone appropriate feasibility and impact assessments. Collating and analysing technical market intelligence to contribute to the continual refinement and improvement of Simprints' value proposition and understanding of the market. Supporting project start-up phases until project teams are recruited. MUST HAVE REQUIREMENTS Significant Solutions Architecture experience (or other relevant experience in product/project design and development), ideally in the tech for development space where you've designed projects with clients in developing country contexts. Leadership skills, ownership and self-starting drive. An ability to articulate a clear vision for Solutions Architecture, the skill to implement a comprehensive change plan, the experience to collaborate positively to make the change happen, and the grit to deliver on all the detailed work requirements. Excellent written and verbal communications. You are empathetic and seek to understand different perspectives, bring clarity to ambiguous or ill-defined needs, can negotiate diplomatically when there are competing interests, and secure buy-in and alignment across stakeholder groups. Attention to detail & troubleshooting skills. Global development work is complex and unpredictable. To proactively anticipate risks, assess implicit requirements on top of contractual deliverables, and successfully meet ever-changing needs, you need to be able to translate a high-level idea into concrete, detailed design and funding proposal. Strong presentation and demo skills. We work across multiple sectors with a variety of stakeholders. Being able to tailor presentations to audiences of varying technical literacy levels, for a number of different use cases and workflows, is crucial. You are comfortable hosting virtual presentations as well as conducting in-person. Permission to work in the UK. NICE-TO-HAVE REQUIREMENTS Familiarity with data collection platforms, such as DHIS2, CommCare, ODK, OpenSRP, and/or other technology platforms commonly used in global development. Ideally you have designed workflows common among frontline workers in development programs (e.g. health care, aid distribution, research, education). Working proficiency in French, Arabic, Spanish, or other common language A technical mindset and passion for designing technology solutions The Solutions Architect will interact directly with stakeholders from a variety of backgrounds (both cultural and organisational). Being familiar with developing country contexts and prior experience interfacing with donors and/or government officials will be quite important. WE OFFER Life is short. We believe work should be awesome, meaningful, and fun. At Simprints we're taking on global development's biggest challenges, powered by an amazing culture and incredible people. Work with us, and you will grow faster, learn more, and take on great responsibilities with potential to make lasting change. Genuine Impact. The opportunity to be part of our delivery of frontline projects around the world that impact millions of lives. Global Leadership. Be part of a global team of country directors, project managers, engineers, and delivery partners dedicated to making a difference. In the process, working with exhilarating people from around the world representing over 20 different nationalities with a wide range of cultures, experiences, and viewpoints, with diverse backgrounds spanning tech companies like Google, businesses like BCG, and NGOs like Save the Children. Career Advancement. Join the leadership team of a fast-growing social enterprise that is breaking onto the global stage. Four years since we were founded, we are already working directly with the most influential and exciting partners in development-from ministries of health, to top donors like Gavi & USAID, to leading NGOs like JSI & BRAC. Unlimited Paid Time Off & Flexible Hours. We set high goals and give people the freedom to choose when and how to achieve them. Work when, where, and how suits you best. Join a team that trusts you with the job. Real Professional Development. Beyond on-the-job learning, Simprints will support you with a professional development budget and access to global experts across our Board of Directors & Advisers Simprints is an equal opportunity employer. We pride ourselves in our firm commitment to improving diversity, equity, and inclusion in our workplace. We aim to attract, hire, grow, and retain the most qualified candidates regardless of race, gender, ability, religion, nationality, age, sexuality, and other differences. We encourage interested and suitable candidates who are part of underrepresented groups to apply for this position. #Jora

Infrastructure Engineer Salary up to £34472 pa 37 hours per week This is an exciting opportunity to join our IT team providing a vital role in the management of College I.T. The Infrastructure Engineer will monitor and guide every task that IT department employees engage in, from performing routine system updates to installing entirely new elements. You will also be expected to provide security and functionality of the entire IT infrastructure as well as plan and perform the design, installation, and connectivity of information systems and network infrastructure to ensure the continual operation of the College IT resources. You will also provide input into and support the College's IT strategy and supervise and train more junior members of the IT team in both day-to-day operations and project work. You should have experience of supporting IT infrastructure in a large user-base environment and an excellent understanding of IT networking concepts. Together with an excellent knowledge of networking protocols and services such as TCP/IP, DNS and DHCP you will also have the ability to communicate effectively orally and in writing. Please visit our website for a full job description and application details All applications should be sent to the HR Manager, Homerton College, Hills Road, Cambridge, CB2 8PH or click apply now. The closing date is midday on Friday 30 April 2021. The College pursues a policy of Equal Opportunities.

Build great technology that improves millions of lives. Overview Simprints builds innovative technology aimed to help some of the world's most vulnerable and marginalised populations access essential services. We work to radically increase transparency and effectiveness in global development, making sure that every vaccine, every dollar, every public good reaches the people who need them most. We design and develop both hardware and software by applying modern tools and pioneering technology in new, challenging contexts where there is little to no internet connectivity. Simprints is currently on track to help over 1.4 million people access critical services by 2021. We are looking for a Senior Android Engineer to join our growing tech team, working on our core Simprints ID platform. You will be responsible for the design, development, and maintenance of Simprints applications and their integrations, both with our internal back-end services and with external data collection applications. You will work on an agile, collaborative team with a commitment to clean code and robust design, along with a strong culture of continuous learning and improvement. If building technology for global health sounds exciting, we want to meet you! This is a remote job, with a possibility to work in our Cambridge based office for UK permit holders. RESPONSIBILITIES Design technical infrastructure to help Simprints scale to support projects all over the world Team with other Android engineers to write robust code that is easy to test and maintain, and runs reliably in challenging settings Work on cross-functional projects by collaborating with back-end engineers, data analysts and project managers Mentor junior engineers by guiding them through code reviews and making design decisions Create specification documents that outline designed solutions and a plan of action to achieve them MUST HAVE REQUIREMENTS Deep understanding of the Android SDK with at least 5 years of experience building, integrating, testing, and supporting Android applications for mobile and tablet devices Solid understanding of the full software development lifecycle including application architecture design Experience working within a team with a focus on code quality, where testing, code reviews, and continuous integration are the norm Working knowledge of Kotlin (our codebase is written entirely in Kotlin) Experience with Coroutines, Koin and Android Jetpack, especially Architecture Components (ViewModel, LiveData, Room, WorkManager) NICE-TO-HAVE REQUIREMENTS BS/MS/PhD in Computer Science or a related field Familiarity in working within a culture that incorporates radical candour, 360 feedback, and other techniques to build a high-trust team Experience building applications for offline or low-connectivity settings WE OFFER Work with the latest technologies: Languages: Kotlin Libraries: Jetpack, Coroutines, Koin, WorkManager Testing: Mockk, Firebase Test Lab Cloud: Firebase, BigQuery, Cloud Functions Other tools: Bitbucket Pipelines, Jira Make a positive impact on millions of the most vulnerable people in the world Work in a team of dedicated and talented engineers committed to writing high quality code Opportunities to see our tech in action by joining our deployments around the world: Bangladesh, Ethiopia, or Zimbabwe just to name a few Unlimited paid time off. Last year, the average Simprints employee took a total of 31 days off (annual leave plus UK bank holidays), an increase from 26 days two years ago Truly flexible working hours. More efficient late at night? That's fine by us, start after lunch. We are looking for people who get the job done, not for people who get the job done between 9am and 5pm A generous Eduprints budget to spend on individual learning. In the past, Simprints engineers have spent this on attending tech conferences, enrolling in a Udacity nanodegree, and all the books you could possibly read Two 'LEGO Days' each quarter where you can work on any project you want. Past projects have ranged from exploring image processing techniques to building a LEGO train to deliver beer around the office How to apply Go to and check out our open positions, or follow the link below: #Jora