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Junior Software Developer, C++, Python, Scientific Software, COR7471An exciting opportunity has arisen for a motivated Junior / Graduate Software Developer to join a world-leading scientific R&D company based in Cambridge, specialising in the design and development of hardware and software tools for pioneering research.The RoleThe Junior Software Developer will support the development and maintenance of Windows-based scientific applications used by researchers globally. Working as part of a small, collaborative development team, you’ll contribute to implementing new features, fixing bugs, testing software, and supporting integration with third-party hardware and data formats.This is an excellent opportunity for a graduate or early-career developer looking to build hands-on experience in scientific software development while learning from experienced engineers in a cutting-edge research environment.The CompanyThe Software Developer will be joining a long-established and highly respected scientific technology company, renowned for its contributions to scientific research. The organisation develops both hardware and software solutions used by researchers worldwide to advance scientific discovery. With a supportive and collaborative culture, the company offers strong mentoring and career development opportunities, making it an ideal environment for someone looking to grow their technical skills.Benefits • Gym membership, • 23 days’ holiday + Bank Holidays, • A degree in Computer Science, Software Engineering, Physics, Engineering, Mathematics, or a related field, • Commercial, internship, placement, or strong academic project experience in C++, • Experience with Python (e.g., scripting, data processing, testing, or automation), • Understanding of object-oriented programming principles, • Familiarity with Windows development or Visual Studio would be beneficial

Embedded Software Engineer – £50k - £60k – semi remote - Cambridge Hexwired Recruitment is recruiting for an expanding Electronics Manufacturer based in Cambridge now seeking an Embedded Software Engineer to help deliver key projects utilising Signal processing algorithms! The company are expanding to meet the demands of their clients and are seeking an Embedded Software Engineer ideally with experience working on Firmware RTOS. You will be working with customers internationally utilising the latest technology in Signal Processing. This is an Embedded Software Engineer job focusing on RF products. Key Skills: • 3+ commercial Embedded software experience, • Good commercial RTOS experience, • Experience or knowledge of SPI, I2C or UDP, • Experience working on RF or SDR products is highly desirable but not essential For more information on this role, or any other jobs across; Embedded, C++ programming, Electronics, FPGA, Javascript, C#, Python, LLM, Data Science, Embedded Linux, Golang Development, Machine Learning, Data Science or Simulation contact us today.

Software Engineer – Python / RF Algorithms Cambridge | Permanent | Full Time We’re recruiting a Software Engineer for a venture-backed RF semiconductor company in Cambridge building advanced RF hardware for connected devices. This is not a generic backend role. You’ll be working at the intersection of algorithms, software, and RF hardware — turning mathematical models and optimisation concepts into production-grade software that runs against real systems. The Role You will: • Design and build Python software that implements RF measurement and optimisation algorithms., • Translate algorithm specs and mathematical models into clean, maintainable code., • Work closely with RF and systems engineers to ensure software reflects real-world hardware behaviour., • Integrate and validate algorithms on hardware prototypes and production platforms., • Develop unit tests, validation frameworks and regression tools., • Troubleshoot performance issues across software and hardware boundaries., • Apply proper engineering discipline: modular design, version control, documentation.This role requires someone who can move from experimentation to robust, production-ready software — not just proof-of-concept scripts. What They’re Looking For • Strong Python development experience (structuring and implementing algorithms properly)., • Proven ability to translate maths, models or system requirements into working software., • Experience implementing optimisation methods or data-driven algorithms in hardware-adjacent environments., • Strong analytical and problem-solving ability., • Degree in Software Engineering, Electrical Engineering or similar.Strong Advantage, • Understanding of RF measurements and test procedures., • Experience interfacing with lab equipment or measurement systems., • Exposure to wireless systems, RF modules or telecoms., • Real-time processing experience.Environment Engineering-led. Fast-moving. High ownership. You’ll work directly with RF and hardware teams — this isn’t a siloed software function. If you need heavily defined requirements and long release cycles, this isn’t the place. If you like solving hard technical problems with real hardware impact, it is. Package Competitive salary + pension + share options. Private medical, life assurance, income protection. 25 days holiday + bank holidays. Flexible working options.

Job Title: Quality Engineer II Location: Cambridge, UK Duration: 12 Months WorkType : Hybrid Overview: TekWissen is a global workforce management provider throughout the UK, Europe and many other countries in the world. The below client is an American multinational pharmaceutical and biotechnology corporation. Job Description: • This position is in the Biotherapeutics Pharmaceutical Research and Development Devices Centre of Excellence located in client location., • The incumbent will provide design control and risk management subject matter expertise to medical device and combination product development programmes throughout the product lifecycle., • This will involve generation and review of design history file and risk management file components whilst interacting with cross functional development teams at all levels of the organisation. POSITION RESPONSIBILITIES • Lead design control and risk management activities for combination product development programs, ensuring deliverables are appropriately authored, approved, and maintained to support clinical trials and commercial licensures., • Support and facilitation of effective risk management activities at external design companies and manufacturing facilities related to assigned projects., • Ensure combination product development activities are compliant with quality and regulatory standards, both internal and external., • Provide input and support to design validation including, but not limited to, human factors engineering assessments., • Support the assessment of external design companies and suppliers for capability of quality systems, facilities, and procedures to support device development and supply., • Support device design and manufacturing investigations from devices used in clinical trials and commercial manufacture., • Support the generation of all regulatory submission data and content for assigned device projects., • Support internal and external audits of the DCoE Quality Management System. EDUCATION, SKILLS AND EXPERIENCE • BSc in appropriate science & engineering discipline (chemistry, biology, biomedical sciences, mechanical engineering, materials sciences, chemical engineering; or other related discipline) with a minimum of 2 years of relevant experience in the pharmaceutical combination product and/or device industries, • OR MSc in appropriate science & engineering discipline (chemistry, biology, biomedical sciences, mechanical engineering, materials sciences, chemical engineering; or other related discipline) with a minimum of 2 years of relevant experience in the pharmaceutical combination product and/or device industries OR PhD in appropriate science & engineering discipline (chemistry, biology, biomedical sciences, mechanical engineering, materials sciences, chemical engineering; or other related discipline)., • History of working in accordance with the requirements of ISO 13485, ISO 14971, 21 CFR 820, 21 CFR 4, and the EU Medical Devices Regulation., • Experience in design controls and risk management for combination products., • Familiar with Human Factors Engineering - Usability Engineering., • Familiar with device assembling manufacturing processes. TECHNICAL SKILLS REQUIREMENTS. • Working knowledge of ISO 9001, ISO 13485, ISO 14971, 21 CFR 820, 21 CFR 4, and the EU Medical Devices Regulation., • Familiarity with EN 62366, EN 60601, and EN 62304., • Able to learn and apply established procedures in a reliable and consistent manner., • Capable of working independently with minimal supervision., • High level of attention to technical details and accuracy., • Able to prioritize multiple responsibilities and to work on multiple tasks simultaneously., • Able to work collaboratively in cross functional teams., • Excellent communication (e.g., oral, written, presentation) and interpersonal relationship skills., • Proficiency in general computer software such as word processing, spreadsheets, presentations., • Understand Good Manufacturing Practices (GMP). PHYSICAL POSITION REQUIREMENTS • Sitting, ability to travel TekWissen® Group is an equal opportunity employer supporting workforce diversity.

Wealth Planning Assistant Cambridge Job Purpose Provide administrative and operational support to Wealth Planners to ensure effective client service delivery and compliant business processes. Serve as the primary contact between Wealth Planners, the Client Services team, and third-party providers, ensuring all client data and applications are accurately maintained within company systems. Key Responsibilities Administrative Support • Meet documentation standards with exceptional accuracy., • Support Wealth Planners with case submissions to the paraplanning team., • Handle finance queries (invoices, billing, WIP, commissions)., • Produce accurate Service Agreements when relevant., • Coordinate central services (paraplanning, valuations, business processing) to ensure smooth workflow., • Manage client onboarding, including CDD and new account paperwork, in line with AML requirements., • Organize client meetings, manage diaries, and prepare meeting packs., • Complete post-meeting actions and record minutes., • Act as first client contact for queries, escalating where appropriate and adapting communication for vulnerable clients., • Greet clients, manage correspondence, and prepare letters of authority., • Prepare accurate application forms as per suitability reports and process them within agreed timeframes., • Maintain up-to-date client records in XPlan and associated systems., • Support efficiency initiatives and share best practices., • Undertake additional duties as directed by management., • Engage in ongoing technical and professional training (including CPD)., • Keep up to date with market trends and industry developments. Competencies & Skills Technical Knowledge • Full understanding of the end-to-end Wealth Planning process., • Strong Microsoft Office and Outlook skills (Word, Excel)., • Experience with XPlan (desired)., • Strong understanding of regulatory and compliance requirements relevant to Wealth Planning., • Ability to identify, follow, and escalate issues in line with company policy.

The role involves developing bioinformatics solutions for their Enspyre platform, focusing on NGS data processing and cloud-based tools.

The successful candidate will work closely with a dedicated team, collecting and processing biological samples, ensuring compliance with data regulations, and maintaining essential research documentation.

A global music company is seeking a Revenue Processing Analyst for a 12-month FTC. The role involves ingesting and validating various revenue files and supporting the review of financial data.