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Firmware / Embedded Software Engineer (Next-Generation IoT Wearable Devices) Location: Cambridge (Hybrid) Salary: £50,000 – £60,000 + Excellent Benefits Contact: Adam Mayne – – Embedded Software Engineer OpportunityAn exciting opportunity has arisen for an experienced Firmware / Embedded Software Engineer to join a rapidly growing technology company developing next-generation IoT, Bluetooth-enabled, low-power wearable devices.You’ll be part of a talented, supportive R&D team working on real products with real users, contributing to both current-generation firmware and new product development from concept through to mass production.This is an environment known for innovation, employee development, and a genuinely collaborative culture, offering excellent training, career growth and the chance to work with cutting-edge embedded technologies. Responsibilities of Firmware Engineer • Designing and developing embedded firmware for IoT wearable products, • Working across the full product lifecycle — prototyping, implementation, optimisation, validation and release, • Creating efficient, reliable firmware for battery-powered, resource-constrained devices, • Developing and maintaining low-level drivers, communication interfaces and wireless protocol stacks, • Collaboration with hardware, electronics and software teams to deliver high-quality, production-ready systemsWhat we are looking for, as much as possible from below.Education & Core Skills, • Degree/Masters/PhD in Computer Science, Electronics, Embedded Systems or similar, • Strong commercial experience in embedded C development (ideally 5+ years), • Experience with RTOS environments such as FreeRTOS, Zephyr, ThreadX or similar, • Confident working in Unix/Linux development environments, • Strong grounding in software testing (unit, regression, system)Embedded & Firmware Expertise, • Experience writing device drivers directly from datasheets, • Knowledge of low-power design techniques and firmware optimisation for constrained MCUs, • Experience working with BLE/Bluetooth, WiFi, Cellular or other wireless protocols, • Experience with battery-powered, low-energy devices is highly beneficial, • Familiarity with Git, Jira, Bitbucket, or similar toolingNice to Have, • Prior experience with wearable technologies, • Cellular expertise (e.g., LTE-M, NB-IoT), • Exposure to embedded Linux environments

Optical EngineerCambridge, UKFull Time | OnsiteOur client is an advanced nanophotonics company developing next generation optical technologies for immersive XR and automotive applications.They specialise in proprietary optical stack architectures designed to enhance visual comfort, image clarity and long duration usability across head mounted and embedded display systems.Due to continued growth, they are now looking to appoint an Optical Engineer to join their R&D team in Cambridge.This is an opportunity to work at the forefront of applied optics within a fast scaling deep tech environment, contributing directly to product innovation and IP development.The RoleYou will play a key role in the design, development and experimental validation of novel optical systems.Responsibilities include: • Designing and optimising advanced optical architectures for emerging display applications, • Developing and executing free space optical experiments, • Building and validating prototypes through hands on laboratory testing, • Collaborating with internal engineering teams, suppliers and external partners, • Contributing to patent development and technical documentationEssential Experience, • Strong grounding in geometrical and ray optics, • Experience developing free space optical experiments, • Degree in Optical Engineering, Physics or a related discipline, • Practical laboratory and experimental validation experienceDesirable Experience, • Experience with HMD, HUD or XR display systems, • Experience using optical design tools such as Ansys Speos, Lumerical, Zemax or similar, • Postgraduate qualification, MSc or PhD in a relevant field, • Ability to present complex technical concepts clearly

Machine Learning Researcher (PhD Statistics Python AI R&D) Cambridge / WFH to £85k Are you a tech savvy, PhD educated, Machine Learning Researcher looking for an opportunity to work on complex and interesting systems at the cutting edge of AI technology? You could be progressing your career working on real-world problems within a high successful SaaS tech company that provides AI and ML products fo... ZIPC1_UKTJ

GPU Compiler Engineer European Tech Recruit are working closely with a leading semicon company, based in Cambridge, who are looking for a talented GPU Compiler Engineer to join their team. In this role you will architect, design, implement, verify, and/or optimize the performance and power of GPU cores. Responsibilities as GPU Compiler Engineer: • Apply GPU knowledge and experience to architect, design, implement, verify, and/or optimize the performance and power of GPU cores., • Build functional model simulations, develops software, and tests for various graphics to verify correctness and ensures performance and power goals are met., • Program and run graphics tests using tools and methods to assess functionality, performance, and power and identify issues., • Collaborate with teams, third-party vendors, and external users to guide implementation and ensure alignment with needs and goals., • Develop driver and compiler software to support GPU products., • Write detailed technical documentation and feature descriptions for GPU projects to guide users and/or customers to use or implement software. Requirements: • Master's degree or PhD in Computer Engineering, Computer Science, Electrical Engineering, or related field., • 5+ years of relevant GPU experience. If this role is of any interest please apply directly on LinkedIn or send a copy of your CV to . By applying to this role you understand that we may collect your personal data and store and process it on our systems. For more information please see our Privacy Notice ()

MEMS Characterisation Engineer Cambridge, UK | Deep-Tech Hardware | Full-Time | Confidential Client The Company (Confidential) We are representing a venture-backed, Cambridge-based deep-tech company building navigational-grade silicon MEMS sensors. Their focus: resonant accelerometers and gyroscopes that compete at the very top end of the global inertial sensing market. This is not commodity MEMS. This is physics-heavy, performance-obsessed, failure-analysis-driven engineering. They are scaling their R&D and New Product Development capability and need a MEMS Characterisation Engineer who can think experimentally, analyse rigorously, and operate in a fast-moving startup environment. The Role You will sit inside the R&D / NPD group and take ownership of characterising high-performance resonant MEMS structures during development. In blunt terms: You will break devices, measure everything, analyse deeply, and feed the data back to designers until the physics lines up with the models. If you enjoy closing the loop between simulation and reality — this is your role. What You’ll Actually Do: 1. Resonant Mode Analysis • Characterise Q-factor, frequency stability, mode coupling and parasitic effects., • Identify non-ideal behaviour and explain it quantitatively., • Work at the level of fundamental device physics — not surface-level metrics.2. Test & Packaging Development, • Develop experimental setups to support rapid NPD cycles., • Implement novel packaging approaches to enable accurate device validation., • Build instrumentation workflows that can survive iteration.3. Inertial Performance Validation, • Quantify bias stability, noise, drift and cross-axis sensitivity., • Use specialised test systems to validate true navigational-grade performance.4. Data & Automation, • Develop Python-based analysis tools for experimental datasets., • Improve instrumentation control where required (Python, LabVIEW or equivalent)., • Turn raw data into defensible technical conclusions.5. Close the Model-to-Measurement Loop, • Work directly with MEMS designers running FEA (COMSOL)., • Compare empirical data to simulation., • Diagnose mismatch., • Feed back actionable design insight.6. Environmental Characterisation, • Evaluate performance across temperature, vibration and shock regimes., • Understand failure mechanisms, not just outcomes.What They’re Looking For: Education • Master’s or PhD in:, • Mechanical Engineering, • Electrical Engineering, • Physics, • Nanotechnology or related disciplineTechnical Depth, • Strong understanding of Design of Experiments (DOE)., • Experience designing and executing structured test campaigns., • High-level programming capability (Python essential; LabVIEW useful)., • Comfortable operating precision instrumentation and interpreting complex datasets.Mindset, • Scientific rigour in documentation., • Comfortable in ambiguity — this is a startup, not a corporate lab., • Able to operate independently without hand-holding. What You’ll Gain • Exposure to the full product lifecycle: R&D → NPD → production., • Direct mentorship from senior MEMS designers., • Real influence on next-generation sensor architectures., • Conference attendance and publication opportunities., • Performance-based bonus, pension and benefits., • Cambridge-based innovation environment with strong technical culture.Who This Is Ideal For, • An early-career engineer who wants serious technical growth fast., • A PhD graduate who doesn’t want to stay in academia but still wants physics., • An experimentalist who enjoys proving or disproving simulation models., • Someone who wants to build genuinely high-performance hardware — not incremental consumer tech.Location Cambridge, UK – on-site role within a highly technical R&D team. Confidentiality This search is being conducted on a confidential basis. Full company details will be disclosed after initial discussion.

Compiler Engineer - GPU / Semiconductors We are currently partnered with an industry leading semiconductor company looking to expand their headcount with an experienced GPU Compiler Engineer to work on their next generation GPU cores. You will collaborate with cross-functional teams to ensure GPU cores exceed performance targets for next-generation mobile and data processing platforms. This is a permanent position based in Cambridge - please note this is a fully onsite role. Key responsibilities for this Compiler Engineer position: • Architect and optimize GPU cores for peak performance and power efficiency., • Develop high-performance GPU compiler software and drivers to support cutting-edge graphics products., • Build functional model simulations and develop graphics tests to verify architectural correctness., • Program and run graphics tests to identify bottlenecks and ensure power/performance (PPA) goals are met., • Create detailed feature descriptions and technical guides for internal and external stakeholders. Key requirements: • Master’s or PhD in Computer Science, Computer Engineering, or Electrical Engineering., • 5+ years of relevant GPU experience, specifically in hardware/software co-design., • Deep understanding of GPU architectures and graphics pipelines., • Experience in compiler development or graphics driver software. Keywords: GPU Engineer / Compiler Engineer / Graphics Driver / GPU Architecture / Performance Optimization / PPA / Modeling / Simulation / C++ / Semiconductor / Cambridge / Computer Graphics If you are interested in this Compiler Engineer position, please send a CV to By applying to this role you understand that we may collect your personal data and store and process it on our systems. For more information please see our Privacy Notice ___

Quality Engineer Location: Cambridge, UK Hours: 37 hours per week Contract: 12 Months Rate: £26.07 per hour Position Overview This role sits within the Biotherapeutics Pharmaceutical Research and Development – Devices Centre of Excellence (DCoE). The Quality Engineer will provide design control and risk management expertise across medical device and combination product development programmes throughout the full product lifecycle. Responsibilities include generating and reviewing Design History File (DHF) and Risk Management File (RMF) components while partnering with cross‑functional teams at all organisational levels. Key Responsibilities • Lead design control and risk management activities for combination product development programmes, ensuring deliverables are authored, approved, and maintained to support clinical trials and commercial licensure., • Facilitate effective risk management activities at external design and manufacturing partners., • Ensure all development activities comply with internal and external quality and regulatory standards., • Provide input into design validation, including human factors engineering assessments., • Support assessment of external design companies and suppliers regarding quality systems, facilities, and capabilities., • Assist with design and manufacturing investigations for devices used in clinical trials and commercial manufacturing., • Contribute to the creation of regulatory submission data for assigned device projects., • Support internal and external audits of the DCoE Quality Management System. Education, Skills & Experience Requirements Education One of the following is required: • BSc in a relevant science/engineering discipline with minimum 2 years’ experience in pharmaceutical combination product and/or device industries, • MSc in a relevant discipline with minimum 2 years’ experience Experience & Knowledge • Demonstrated experience working to ISO 13485, ISO 14971, 21 CFR 820, 21 CFR 4, and EU Medical Devices Regulation., • Proven background in design controls and risk management for combination products., • Familiarity with Human Factors Engineering / Usability Engineering., • Understanding of device assembly and manufacturing processes. Technical Skills • Working knowledge of:, • ISO 9001, • ISO 13485, • ISO 14971, • 21 CFR 820, • 21 CFR 4, • EU MDR, • Familiarity with:, • EN 62366 (Usability Engineering), • EN 60601 (Electrical Medical Equipment), • EN 62304 (Medical Device Software), • Ability to apply established procedures consistently., • Strong attention to detail and accuracy., • Able to prioritise and manage multiple tasks simultaneously., • Capable of working independently with minimal supervision., • Effective communicator with strong interpersonal skills., • Proficiency in standard office software (Word, Excel, PowerPoint)., • Understanding of Good Manufacturing Practices (GMP).

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.

Description Nuclera is a venture-backed biotech company headquartered in Cambridge, UK with significant operations in Boston, USA. Nuclera’s mission is to accelerate discovery by enabling rapid, easy access to functional proteins essential for drug discovery research. Our eProtein Discovery™ benchtop system accelerates protein expression and purification optimization in research labs. Nuclera is seeking a strategic, hands-on Product Manager - Antibody Applications to own the antibody applications roadmap on our eProtein Discovery system. This high-impact role will drive adoption among antibody discovery and reagent developers by translating market needs into differentiated product strategy, offerings, and go-to-market plans. Serving as the antibody domain expert within the product organization, you will partner closely with R&D, commercial, and customer‑facing teams to accelerate growth in this core application area. You will own end‑to‑end success for the antibody applications segment, including roadmap definition, commercial performance, and lifecycle strategy. The ideal candidate will be a seasoned antibody scientist with proven commercial experience—deeply familiar with the pain points, challenges, and opportunities in antibody discovery workflows. They will be skilled at translating deep domain knowledge and voice-of-customer insights into compelling product strategies that drive adoption and success of Nuclera’s eProtein Discovery System. This role requires approximately 20% travel, including domestic and international trips, to attend customer meetings, industry events, and visits to Nuclera offices as needed. About the role Product Strategy & Roadmap • Define and drive the antibody application strategy, identifying key workflows and unmet customer needs, • Develop and defend business cases for investments supported by market analysis, competitive positioning, and ROI modeling., • Develop a sequenced roadmap to guide productization of antibody-relevant workflows, • Champion market-fit, pricing models, and routes to scale adoption Go-to-Market & Commercialization • Collaborate with commercial and marketing teams to launch and scale antibody-focused solutions, • Support market messaging, product positioning, and customer segmentation, • Lead rigorous, ongoing market research and VOC programs (surveys, in-depth interviews, advisory boards) to surface unmet needs in protein science. Translate these insights into prioritized feature investments and clear business cases that inform the product roadmap., • Spend significant time in the field with customers to understand pain points and validate fit, • Distill voice-of-customer insights into clear product needs and roadmap clarity, • Track competitive landscape to ensure differentiation and sharpen value proposition Cross-Functional Leadership & Stakeholder Management: • Serve as the senior liaison between external stakeholders (customers, KOLs, sales, marketing) and internal teams (R&D, operations, quality, finance)., • Champion product requirements, secure executive buy-in, and ensure transparent communication on priorities, timelines, and metrics., • Support onboarding, training, and internal enablement for antibody use cases, • Contribute to strategic planning and resource prioritization for antibody and adjacent applications Cultivate Strategic Partnerships with Thought Leaders: • Build and steer high-impact relationships with Key Opinion Leaders (KOLs), academic and industry collaborators, and channel partners—co-developing new applications and pioneering use cases that expand and differentiate our eProtein Discovery platform Requirements • 5-10+ years of experience in product strategy or product management with increasing scope and responsibility, • Advanced degree (PhD, MS) in related field required and/or or application development in the antibody discovery or life sciences tools space, • Extensive knowledge of recombinant antibodies and downstream uses, • Proven track record building roadmaps, aligning cross-functional teams, and launching successful solutions, • Significant experience with customer engagement, market validation, and commercial translation, • Ability to think both strategically and tactically in a fast-paced, startup environment UK Benefits What we offer: In addition to competitive salaries, we offer a range of benefits including: • Company bonus scheme of 5%, • Life insurance, • Private medical insurance and cash plan, • 25 days' annual leave + Bank Holidays, • Enhanced employer's pension contributions, • Enhanced maternity and paternity Leave, • Investment in professional development and learning, • Access to amenities on Vision Park and in Histon, • Fresh fruit, tea, coffee, and snacks in the office, • Organised team events

Firmware / Embedded Software Engineer (Next‑Generation IoT Wearable Devices) Location: Cambridge (Hybrid) Salary: £50,000 – £60,000 + Excellent Benefits Contact: Adam Mayne – – 01234 823373 Embedded Software Engineer Opportunity An exciting opportunity has arisen for an experienced Firmware / Embedded Software Engineer to join a rapidly growing technology company developing next‑generation IoT, Bluetooth‑enabled, low‑power wearable devices. You’ll be part of a talented, supportive R&D team working on real products with real users, contributing to both current‑generation firmware and new product development from concept through to mass production. This is an environment known for innovation, employee development, and a genuinely collaborative culture, offering excellent training, career growth and the chance to work with cutting‑edge embedded technologies. Responsibilities of Firmware Engineer • Designing and developing embedded firmware for IoT wearable products, • Working across the full product lifecycle - prototyping, implementation, optimisation, validation and release, • Creating efficient, reliable firmware for battery‑powered, resource‑constrained devices, • Developing and maintaining low‑level drivers, communication interfaces and wireless protocol stacks, • Collaboration with hardware, electronics and software teams to deliver high‑quality, production‑ready systems What we are looking for, as much as possible from below. Education & Core Skills • Degree/Masters/PhD in Computer Science, Electronics, Embedded Systems or similar, • Strong commercial experience in embedded C development (ideally 5+ years), • Experience with RTOS environments such as FreeRTOS, Zephyr, ThreadX or similar, • Confident working in Unix/Linux development environments, • Experience writing device drivers directly from datasheets, • Knowledge of low‑power design techniques and firmware optimisation for constrained MCUs, • Experience working with BLE/Bluetooth, WiFi, Cellular or other wireless protocols, • Experience with battery-powered, low-energy devices is highly beneficial, • Prior experience with wearable technologies, • Cellular expertise (e.g., LTE‑M, NB‑IoT), • Exposure to embedded Linux environments

An established international pharmaceutical organisation is expanding its Biologics R&D capability in Cambridge and is seeking an experienced Project Manager to support the advancement of Antibody Drug Conjugate (ADC) programmes from candidate nomination through IND/CTA and into early clinical development. This is a delivery-focused role within a growing biologics function, ideal for a project leader with experience in complex biologics programmes and a strong understanding of early development. The Role You will be responsible for driving cross-functional coordination of ADC early development programmes, ensuring alignment, delivery and risk management across key functions. Key responsibilities include: • Leading cross-functional project teams across CMC, non-clinical, regulatory and clinical functions, • Building and maintaining integrated development plans, • Managing timelines, milestones, risks and mitigation strategies, • Supporting the preparation and submission of IND/CTA documentation, • Ensuring clear communication and alignment between scientific and operational stakeholders What We’re Looking For You will likely bring: • A PhD or equivalent experience in life sciences (biochemistry, immunology, chemistry, pharmacy or related field), • 6–10+ years’ experience within biotech or pharma, • Proven project management experience within biologics or oncology programmes, • Exposure to ADC or complex biologics modalities, • Experience supporting preclinical development and IND/CTA submissions, • Strong project planning, risk management and cross-functional leadership skills Why Consider This Role? • Opportunity to join a growing biologics platform in Cambridge, • Exposure to next-generation oncology modalities, • High visibility within a strategically expanding R&D function, • Collaborative, values-driven culture

An established international pharmaceutical organisation is expanding its Biologics R&D capability in Cambridge and is seeking an experienced Project Manager to support the advancement of Antibody Drug Conjugate (ADC) programmes from candidate nomination through IND/CTA and into early clinical development. This is a delivery-focused role within a growing biologics function, ideal for a project leader with experience in complex biologics programmes and a strong understanding of early development. The Role You will be responsible for driving cross-functional coordination of ADC early development programmes, ensuring alignment, delivery and risk management across key functions. Key responsibilities include: • Leading cross-functional project teams across CMC, non-clinical, regulatory and clinical functions, • Building and maintaining integrated development plans, • Managing timelines, milestones, risks and mitigation strategies, • Supporting the preparation and submission of IND/CTA documentation, • Ensuring clear communication and alignment between scientific and operational stakeholders What We’re Looking For You will likely bring: • A PhD or equivalent experience in life sciences (biochemistry, immunology, chemistry, pharmacy or related field), • 6–10+ years’ experience within biotech or pharma, • Proven project management experience within biologics or oncology programmes, • Exposure to ADC or complex biologics modalities, • Experience supporting preclinical development and IND/CTA submissions, • Strong project planning, risk management and cross-functional leadership skills Why Consider This Role? • Opportunity to join a growing biologics platform in Cambridge, • Exposure to next-generation oncology modalities, • High visibility within a strategically expanding R&D function, • Collaborative, values-driven culture

Our Organization IONTAS is part of the FairJourney Biologics family, which operates across four global sites (Porto – Portugal, Cambridge – UK, San Francisco and San Diego – USA). FairJourney Biologics is dedicated to discovering high-quality biologics drug candidates for our partners, providing solutions to their technical challenges, and helping bring life-changing medicines to patients. Our antibody discovery and engineering services have benefitted over 200 biotech and pharma partners worldwide. With more than 1,000 completed projects using a range of molecular formats and 20 clinical-stage molecules, we are internationally recognized for tackling novel and challenging discovery programs. Our expertise in Phage and Mammalian Display platforms enables us to push the boundaries of antibody discovery, driving innovation for next-generation therapeutics. The Role We are seeking a highly capable and enthusiastic Scientist to join the expanding Discovery & Engineering Unit at our South Cambridgeshire site (DEU III). The ideal candidate will bring significant expertise in SPR and Protein Sciences with a good understanding of Biologics drug discovery and display technologies. Teamwork is a key skill for this role - Scientists are lab-based staff with significant experience in antibody discovery & engineering and assay development, providing lab-based leadership and collaborating with internal experts in antibody discovery & display technologies. The role will include execution of labwork, training and mentoring other team members. Work will not be limited to SPR – there will be involvement in other methods of selecting and screening novel antibody-based therapeutics. You will use your keen interest and expertise in Biologics drug discovery to shape and deliver projects involving identification, optimisation, and screening of novel antibody-based therapeutics, applying, and refining our (phage and mammalian) display technologies and engineering methods and working closely with our structural & bioinformatics team when considering client projects. This will be an onsite and predominantly lab-based role. Your responsibilities will include the independent design and execution of experiments, data analysis and interpretation and communication of the findings to the team and clients. Your will provide technical training to other team members. This role will suit an experienced scientist seeking to gain or expand their Biologics drug discovery experience. A positive and solution-focused mindset is required to deliver on a wide range of innovative and intellectually challenging projects. Key responsibilities • Plan, execute and train other team members in kinetic assessments of standard and complex antibody formats., • Lead aspects of antibody discovery programs using phage and/or mammalian display, ensuring timely delivery and high-quality outcomes., • Manage and strengthen client and stakeholder relationships to drive project success., • Plan and execute biochemical assays to generate and evaluate project hit panels., • Apply your knowledge of antibody drug discovery to shape and guide project decisions in collaboration with team leaders and clients., • Contribute to novel research directions and strategies to advance business objectives., • Work with the Technology Unit to evaluate and integrate novel platforms to the drug discovery process., • Collect, analyse, and interpret scientific data to inform decision-making., • Present findings and progress updates to senior management, partners and at scientific conferences. Your Profile • PhD (or equivalent industry experience) in Antibody Discovery, Molecular Biology, Biotechnology, Immunology or a related field., • Significant experience of independently performing SPR assessments of biologics, including complex formats., • Additional 3+ years post-PhD hands-on experience in antibody drug discovery, preferably within industry, with a demonstrable understanding of therapeutic antibody formats, structures, and sequences., • In-depth understanding and practical research experience of using protein structure insights to guide protein engineering campaigns., • Practical experience in antibody display technologies (e.g. phage/mammalian display), • Experience in additional biochemical assays., • Molecular biology and cell culture experience., • Excellent data analysis, interpretation and problem-solving skills., • Influencing skills to shape project decisions and direction., • Ability to plan time and prioritise work., • Maintain clear written records in a timely manner., • Ability to present and communicate effectively to internal and external stakeholders., • Strong interpersonal skills with the ability and desire to build strong collaborative working relationships. The following are desirable, but not required: • Experience in antibody display library construction., • Experience of antibody isolation and engineering for optimisation., • Hands-on experience with flow cytometry & FACS. We Offer Be Part of a Global Team By being part of the FairJourney Biologics family, you will be collaborating with teams in Porto, Cambridge, San Francisco and San Diego. You will have the opportunity to work alongside world-class scientists, share insights and contribute to ground breaking antibody projects. Innovating the Future of Therapeutic Antibodies IONTAS was co-founded in 2012 by John McCafferty, a pioneer of antibody phage display technology, which contributed to the 2018 Nobel Prize in Chemistry, and became part of the FairJourney Biologics family in 2020. By integrating phage and mammalian display expertise, we deliver high-affinity, developable antibodies that are shaping the future of drug discovery. Career Development & Growth As the biopharmaceutical industry continues to evolve, there is a growing reliance on specialized CROs to drive innovation in antibody discovery. With an increasing number of biotech and pharmaceutical companies outsourcing their research, FairJourney Biologics is well positioned for long-term growth and expanding opportunities. • Be part of a dynamic, motivated team at our expanding Cambridge site., • Contribute to projects that impact partners, patients and the broader scientific community. Competitive Benefits • Attractive salary & life insurance., • Generous parental leave policies., • Located on Unity Campus, a growing science park offering good transport links, an on-site gym with personal training, a cafe and a vibrant social community. A Culture That Empowers We foster an inclusive, collaborative environment where diverse perspectives are valued. At FairJourney Biologics, your ideas and contributions matter – helping us transform antibody discovery and deliver next-generation therapeutics.

PhD‑Level Ultrasound Technology Consultant - Cambridge A prominent medical technology innovator in Cambridge is seeking a PhD‑level ultrasound specialist to help drive the development of next‑generation surgical and interventional devices. The organisation has a long-standing reputation for transforming complex scientific challenges into commercially successful products and works extensively across healthcare, life sciences and the wider physical sciences. You would be joining a culture that values curiosity, open collaboration and entrepreneurial thinking. It is an environment where scientific creativity is encouraged, ideas are shared freely and individuals are given the space to shape projects and influence technical direction. This position is ideal for someone who wants to play a central role in advancing surgical technology. The work spans the development of sophisticated medical systems, including robotic surgical platforms and intelligent instruments with integrated sensing, all designed to support clinicians in delivering safer and more effective procedures. You will take responsibility for high‑impact technical programmes, combining scientific depth with commercial awareness, and you will apply your ultrasound expertise across the full innovation pathway, from early feasibility studies through to preparing products for market. A key part of the role involves working closely with partner organisations...

Job Title: PhD Graduate/Science Writer – Photonics / Optics (Technical Marketing).

This is a four-year (1+3 MRes/PhD) studentship funded through the Cambridge EPSRC Centre for Doctoral Training in Future Infrastructure and Built Environment: Unlocking Net Zero (FIBE3 CDT).

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PhD‑Level Ultrasound Technology Consultant - Cambridge. A prominent medical technology innovator in Cambridge is seeking a PhD‑level ultrasound specialist to help drive the development of next‑generation surgical and interventional devices. This position is ideal for someone who wants to play

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MSc/PhD in a relevant scientific discipline (Pharmaceutical Sciences, Chemistry, Computational Chemistry) with a solid foundation in molecular modelling built in a pharma/biotech/CRO setting. We are looking for dynamic, creative, and talented computational chemist to join our expanding Discovery & M

Work closely with collaborators to develop 2D/3D nano‑percolation modelling for molecular transport, thin film integration, and advanced characterisation processes for solid‑state structures. Relevant experience in numerical modelling and semiconductor and thin‑film processes at PhD, postdoc o

Degree in biochemistry or similar, and ideally a PhD holder. Strong understanding of protein chemistry and ideally antibody‑based drugs. This Cambridge based life science start-up is seeking an experienced Protein Chemist to join them.

With the continued growth in AI for fully automated detection from medical data, research into novel, problem-focused visualisation has received less attention. Successful applicants will hold a PhD in information engineering, biomedical imaging, computer graphics or a related area; have strong tech

The Cambridge Sustainable Design Group within the Department of Architecture invites applications for a Research Assistant or Research Associate to work on the Health-driven Design for Cities (HD4) programme. If the candidate is yet to receive their PhD award, they will be appointed at Research Assi

You will have a PhD in a relevant subject such as computer science or engineering, together with essential experience in advanced analysis of medical images, particularly machine-learning analysis of musculoskeletal MR. This is a collaborative translational research post focussing on the development

Job Title: PhD Graduate/Science Writer – Photonics / Optics (Technical Marketing). Are you a PhD graduate with a passion for Photonics, Optics, and Lasers? Step into a role where innovation meets expertise, and where your skills will be valued and nurtured. Join a well-established company renowned

Electronics Engineer - Programme Manager - Medical Devices - Cambridge Due to a growth in company output, there is a need for a new Programme Manager who has an Electronics Engineering pedigree. Based in Cambridge, you will be leading several projects. Some projects will involve you offering support and mentorship to junior members of staff, while other projects will involve you taking on the Electronics design aspects yourself. We are looking for someone who has been working hands on developing new Medical Devices technologies in their current role, while mentoring other members of staff. Most projects will be on electro-mechanical Medical Devices, so you will need to have worked on these types of technologies. They could be implantable medical devices, wearable tech or another medical technology that abide by EN60601 standards. Alongside past work experience, it is expected that you hold a relevant degree within a suitable subject that led you into a Medical Devices Electronics Engineering role. It would also be advantageous if you hold a master's or PhD, but not essential as the active work experience in industry is more important. The types of technologies you will be developing are lifesaving and life improving medical devices, truly industry disrupting technologies that will save and improve thousands of people's lives. This role will involve working with external and internal entities, involving a lot of communications both virtual and in real life, due to this it would be advantageous if you have worked in a role that involved communicating updates and project changes continuously. I mentioned knowing about EN60601, but it would also be essential to have a strong understanding of ISO 13485. People who have been successful in this role previously tend to have a highly technical hobby, this could be building drones, tinkering with engines, computer programming or another hobby that involves problem solving. If you do have such a hobby, make sure you highlight it on your CV to give you the best chance of gaining an interview. Apart from working on industry changing technologies, you will be offered a proven career development plan, continuous training to keep you at the forefront of the medical devices sector, excellent salary, bonus, enhanced pension, medical insurance, free meals and other excellent benefits you'd expect from a multinational blue-chip organisation. I expect a lot of interest in this role, so apply now or ensure consideration. For more information, please contact Andrew Welsh, Director of Medical Devices, Biotech and Drug Discovery Recruitment at Newton Colmore, on (phone number removed). Alternatively, submit your application and a member of our team will be in touch. Please note that without a CV, we can only provide limited information

Physicist - Defence Sector Engineering - Cambridge A growing Defence company, based in Cambridge, offers an exciting opportunity for a Physicist to work on a wide range of cutting-edge technologies that will enhance the UK's defence against external threats, with a focus on defensive technologies rather than offensive ones. You will be involved in a variety of physics projects, including (but not limited to) thermal, optics, electromagnetics, acoustics, fluidics, chemical, and other scientific technologies. If you have experience with complex projects in these fields, I recommend providing as much detail as possible on your CV. We are open to candidates from various sectors; however, it will be highly advantageous if you already have experience in the Defence sector. As you will be working in the Defence sector, you will need to be able to obtain security clearance or already hold security clearance. Given the increasing importance of Artificial Intelligence and Machine Learning in various sectors, a keen interest in these areas would be welcomed, as many of your projects will involve work in this field. In addition to working on complex and cutting-edge technologies, you will also be rewarded with an excellent starting salary, dependant on experience. The compensation package includes a bonus, enhanced pension, dental care, gym access, free lunch, and other excellent benefits. The level of experience sought can range from a PhD holder who has worked in a post-doc role to someone with years of industry experience. We are looking to recruit several individuals for this team, so if you are in the early stages of your career, you will receive development opportunities, and if you are further along in your career, you will have the chance to mentor junior team members. This company places a strong emphasis on collaboration, both within the team, with other teams, and with external parties. Given the anticipated high level of interest in this role, and the company's desire to recruit quickly, I recommend applying immediately if you are interested in this position to avoid missing out. Please note we will not be able to discuss the role specifics until we have a copy of your CV.

Quality Engineer, Compliance Location: Cambridge, UK Hours: 37 hours per week Contract: 12 Months Maximum Supplier Bill Rate: £26.07 per hour Position Overview This role sits within the Biotherapeutics Pharmaceutical Research and Development - Devices Centre of Excellence (DCoE). The Quality Engineer will provide design control and risk management expertise across medical device and combination product development programmes throughout the full product lifecycle. Responsibilities include generating and reviewing Design History File (DHF) and Risk Management File (RMF) components while partnering with cross‑functional teams at all organisational levels. Key Responsibilities Lead design control and risk management activities for combination product development programmes, ensuring deliverables are authored, approved, and maintained to support clinical trials and commercial licensure. Facilitate effective risk management activities at external design and manufacturing partners. Ensure all development activities comply with internal and external quality and regulatory standards. Provide input into design validation, including human factors engineering assessments. Support assessment of external design companies and suppliers regarding quality systems, facilities, and capabilities. Assist with design and manufacturing investigations for devices used in clinical trials and commercial manufacturing. Contribute to the creation of regulatory submission data for assigned device projects. Support internal and external audits of the DCoE Quality Management System. Education, Skills & Experience Requirements Education One of the following is required: BSc in a relevant science/engineering discipline with minimum 2 years' experience in pharmaceutical combination product and/or device industries MSc in a relevant discipline with minimum 2 years' experience PhD in a relevant science/engineering disciplineRelevant fields include: chemistry, biology, biomedical sciences, mechanical engineering, materials sciences, chemical engineering, or related areas. Experience & Knowledge Demonstrated experience working to ISO 13485, ISO 14971, 21 CFR 820, 21 CFR 4, and EU Medical Devices Regulation. Proven background in design controls and risk management for combination products. Familiarity with Human Factors Engineering / Usability Engineering. Understanding of device assembly and manufacturing processes. Technical Skills Working knowledge of: ISO 9001 ISO 13485 ISO 14971 21 CFR 820 21 CFR 4 EU MDR Familiarity with: EN 62366 (Usability Engineering) EN 60601 (Electrical Medical Equipment) EN 62304 (Medical Device Software) Ability to apply established procedures consistently. Strong attention to detail and accuracy. Able to prioritise and manage multiple tasks simultaneously. Capable of working independently with minimal supervision. Effective communicator with strong interpersonal skills. Proficiency in standard office software (Word, Excel, PowerPoint). Understanding of Good Manufacturing Practices (GMP). Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy

Technology development, proof of concept and prototyping with diverse applications Cambridge (south); to £80k DoE plus good benefits This small and multi-disciplinary group within a larger company develop diverse, groundbreaking electronics technologies. Explore new challenges, collaborate, and see your work come to fruition in months rather than years – and then onto the next challenge. You’ll get to co-develop systems which combine advanced sensors, imaging, EM, acoustics, fluidics and AI, with applications in edge computing, instrumentation and special projects. You may apply skills in digital electronics, FPGA, DSP, embedded code, analogue electronics and RF. Along with the innate perks of such work, the company offer a generous salary, strong pension contribution, catered lunches, social and leisure facilities, and family-friendly leave policies. Your CV will show your strong relevant degree and supporting qualifications, and additional experience, likely commercial, or through a master’s degree and/or PhD. In addition, your experience will include several of: • Digital electronics design, schematics capture and PCB layout, • FPGA design, RTL development in VHDL / Verilog / SystemVerilog, • DSP, signal processing and/or related algorithms, • Analogue electronics, which may include work with sensors, RF or microwave EM, • Network protocols design and communications generally, • Embedded software in C, C++ and/or Rust It is likely you will have collaborated with other engineers and scientists on past projects. Any additional experience in Python, C#, MATLAB or other software systems is a plus. Some projects may involve security clearance, hence you will need to be a British citizen with 5+ years’ UK residence. Another top job from ECM, the high-tech recruitment experts. Even if this job's not quite right, do contact us now - we may well have the ideal job for you. To discuss your requirements call (phone number removed) or email your CV. We will always ask before forwarding your CV. Please apply (quoting ref: CV27582) only if you are eligible to live and work in the UK. By submitting your details you certify that the information you provide is accurate

PhD‑Level Ultrasound Technology Consultant - Cambridge A prominent medical technology innovator in Cambridge is seeking a PhD‑level ultrasound specialist to help drive the development of next‑generation surgical and interventional devices. The organisation has a long-standing reputation for transforming complex scientific challenges into commercially successful products and works extensively across healthcare, life sciences and the wider physical sciences. You would be joining a culture that values curiosity, open collaboration and entrepreneurial thinking. It is an environment where scientific creativity is encouraged, ideas are shared freely and individuals are given the space to shape projects and influence technical direction. This position is ideal for someone who wants to play a central role in advancing surgical technology. The work spans the development of sophisticated medical systems, including robotic surgical platforms and intelligent instruments with integrated sensing, all designed to support clinicians in delivering safer and more effective procedures. You will take responsibility for high‑impact technical programmes, combining scientific depth with commercial awareness, and you will apply your ultrasound expertise across the full innovation pathway, from early feasibility studies through to preparing products for market. A key part of the role involves working closely with partner organisations to define technical strategy, strengthen long‑term relationships and deliver meaningful outcomes. As you progress, you will have opportunities to build your profile within the surgical technology community and contribute to shaping future industry direction. Each project offers the chance to broaden your scientific knowledge, develop leadership capability and see your work translate into real clinical benefit. Candidates previously placed with this organisation have consistently advanced their careers and expanded their responsibilities. You will thrive in this role if you enjoy working within multidisciplinary teams and value an environment where rigorous thinking and open discussion are central to the way problems are solved. A strong foundation in ultrasound is essential, gained through a PhD, postdoctoral research or relevant industrial experience. The organisation welcomes applications from recent PhD graduates as well as individuals with early‑career industry experience. Knowledge in areas such as transducer design, ultrasound signal processing, high‑speed electronics, image segmentation, regulatory standards like EN 60601 and metrology techniques including scanning hydrophones will be particularly valuable. The company operates from a purpose‑built, award‑winning campus surrounded by green space and designed to support creative and collaborative work. Employees benefit from a comprehensive package that includes an annual bonus, enhanced pension contributions, private medical cover, free meals, life assurance and a range of additional perks typically associated with a leading technology employer. Interest in this opportunity is expected to be high. If the role aligns with your experience and ambitions, early application is strongly recommended. You may also submit your CV, and a member of the team will be in touch to guide you through the next steps.

An established international pharmaceutical organisation is expanding its Biologics R&D capability in Cambridge and is seeking an experienced Project Manager to support the advancement of Antibody Drug Conjugate (ADC) programmes from candidate nomination through IND/CTA and into early clinical development. This is a delivery-focused role within a growing biologics function, ideal for a project leader with experience in complex biologics programmes and a strong understanding of early development. The Role You will be responsible for driving cross-functional coordination of ADC early development programmes, ensuring alignment, delivery and risk management across key functions. Key responsibilities include: • Leading cross-functional project teams across CMC, non-clinical, regulatory and clinical functions, • Building and maintaining integrated development plans, • Managing timelines, milestones, risks and mitigation strategies, • Supporting the preparation and submission of IND/CTA documentation, • Ensuring clear communication and alignment between scientific and operational stakeholders, • Providing modality awareness in ADC technologies to enable informed programme decision-making This role reports into senior leadership within Project Management & Operations. What We’re Looking For You will likely bring: • A PhD or equivalent experience in life sciences (biochemistry, immunology, chemistry, pharmacy or related field), • Experience within biotech or pharma, • Proven project management experience within biologics or oncology programmes, • Exposure to ADC or complex biologics modalities, • Experience supporting preclinical development and IND/CTA submissions, • Strong project planning, risk management and cross-functional leadership skills, • The ability to operate confidently within a dynamic R&D environment You do not need to be the scientific architect of the molecule — but you must be comfortable working within technically complex biologics programmes. Why Consider This Role? • Opportunity to join a growing biologics platform in Cambridge, • Exposure to next-generation oncology modalities, • High visibility within a strategically expanding R&D function, • Collaborative, values-driven culture, • Genuine opportunity to shape early development execution This is an excellent opportunity for a biologics Project Manager seeking greater programme ownership within a well-funded and expanding R&D organisation

If you are a current Jazz employee please apply via the Internal Career site. Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit for more information. The Director of Drug Product Development is responsible for providing scientific and technical leadership for Jazz Pharmaceuticals’ Pharmaceutical Development programs at various stages of the development life-cycle including preformulation, formulation and process development, technical transfer and validation. The Director of Drug Product Development will oversee drug product aspects of development and manufacturing projects from pre-formulation and product feasibility through to clinical trial supply and technology transfer/commercialization. In addition, the Director of Drug Product Development will be expected to provide leadership of cross-functional CMC development teams. The Director of Drug Product Development will have extensive experience in pharmaceutical product development, demonstrated problem solving ability, module 3 authorship, development of robust manufacturing processes through designed experiments and data analysis, and excellent project management, teamwork and leadership skills. Essential Functions Leads the development of small molecule drug product formulations, appropriate to the phase of pharmaceutical development, with sufficient stability and robustness for clinical and/or commercial manufacturing. Responsible for specifying product and process requirements, including manufacturing equipment and methods, performance criteria, materials, test protocols, required analytical methodology, packaging (clinical and commercial); and in developing robust processes for pharmaceutical production. Directs projects and leads cross-functional teams with technical proficiency, scientific creativity, collaboration with others to achieve project goals on time and within budget. Create intellectual property covering Jazz Pharmaceuticals products and ensure freedom to operate in the development of new drug products Support the identification and selection of suitable drug product development and commercial manufacturing vendors (CMOs). Direct technical projects (internally and at CDMOs) including developing detailed technical work plans and managing performance of vendors. Work cooperatively with, or lead, internal and external teams as required. Author CMC sections of regulatory dossiers for products at all stages to enable acceptance by global regulators. Supports asset due diligence and new product introduction and integrations Apply current knowledge of cGMP and industry standards for process design and validation to manage vendors and contract development organizations. Assist other department team members in providing guidance / mentoring / reviewing documents / data in support of product development (e.g. clinical protocols, PK study results). Enhance and improve ways of working in Drug Product development, utilising knowledge of industry best practice Required Knowledge, Skills, and Abilities 10 – 15 years’ experience in drug product development in the pharmaceutical industry required. Direct experience with formulation development, process development, technical transfer and/or process validation. Demonstrated technical proficiency, engineering, collaboration with others, and independent thought. Strong track record in delivering achievements with meaningful impact in Pharmaceutical Development projects Demonstrated ability to lead cross-functional CMC Development teams Demonstrated troubleshooting and problem-solving skills including the use of designed experiments, statistical process control, Development/authorship of CMC regulatory filings for pharmaceutical products. Experience in defending processes, procedures and investigation during Regulatory Agency inspections desirable. Track record in generating intellectual property development. Broad exposure to multiple drug delivery technologies and knowledge of standard dosage forms. Excellent written and verbal communication skills, with demonstrated ability to communicate at executive leader level Current knowledge of quality systems and FDA and EU regulations as they relate to pharmaceutical development and validation. Proven project management skills for technical programs. Flexibility to travel on company business when required Required/Preferred Education and Licenses Master’s degree, PhD, or equivalent combination of education and work-related experience required. Description of Physical Demands Occasional mobility within office environment. Routinely sitting for extended periods of time. Constantly operating a computer, printer, telephone and other similar office machinery. Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law. FOR US BASED CANDIDATES ONLY Jazz Pharmaceuticals, Inc. is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. For this role, the full and complete base pay range is: $(phone number removed) - $(phone number removed) Individual compensation paid within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, and other pertinent factors. The goal is to ensure fair and competitive compensation aligned with the candidate's expertise and contributions, within the established pay framework and our Total Compensation philosophy. Internal equity considerations will also influence individual base pay decisions. This range will be reviewed on a regular basis. At Jazz, your base pay is only one part of your total compensation package. The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan. The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, 401k retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here

If you are a current Jazz employee please apply via the Internal Career site. Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit for more information. The Breast Cancer / Pan Tumor Medical Director (MD) will, in partnership with the Global Medical Affairs Lead, co lead the development and execution of strategic medical plans for this molecule across breast cancer and broader pan tumor indications. The role will drive the implementation of global and regional medical affairs activities aligned with the overarching strategy. Deep medical affairs expertise and strong clinical knowledge in oncology are essential, with a preference for experience in breast cancer, HER2 expressing tumors, or targeted therapies. As a key member of the Global Medical and Scientific Affairs (GMSA) organization, the MD will report directly to the Therapy Area Head, Oncology. The successful candidate will co create and lead annual and long range Global Medical Plans, including integrated evidence generation strategies, ensuring alignment with Franchise and Global Product Team (GPT) objectives. This individual will demonstrate leadership within a fast paced, high performing medical team, foster cross functional collaboration, and communicate effectively across global and regional stakeholders. The role requires strong partnerships with Medical Affairs, Clinical Development, Commercial, Regulatory, and Market Access teams, as well as influential engagement with external experts in breast cancer and other relevant tumour types. Key Responsibilities Co‑lead the development and execution of annual and long‑range Global Medical Plans and evidence generation strategies for the assigned molecule in breast cancer and pan‑tumour settings. Drive global and regional medical affairs strategies, ensuring actionable insights inform robust, cross‑functional plans. Actively influence the Medical Functional Matrix Team (FMT) for the molecule and lead team meetings when delegated. In collaboration with the GMAL, oversee protocol and study design development, ensuring scientific rigor and strategic alignment across tumour types. Build impactful scientific platforms and narratives that shape disease‑area and product positioning in breast cancer and broader HER2‑expressing malignancies. Co‑direct global medical communications strategy and publication planning, ensuring timely, high‑quality scientific deliverables. Provide strategic guidance for core materials (e.g., training decks, scientific platforms, study summaries) for global and regional dissemination. Partner with Commercial to co‑lead launch readiness and lifecycle management initiatives across multiple tumour indications. Represent Global Medical Affairs at cross‑functional team meetings and external scientific or medical engagements. Maintain deep subject‑matter expertise in breast cancer and pan‑tumour HER2 biology, anticipating disease‑area evolution through competitive intelligence and insights generation. Build and maintain external stakeholder engagement plans, including expert mapping, advisory boards, and collaborative opportunities with key opinion leaders. Champion patient advocacy initiatives in partnership with Global Advocacy teams, ensuring patient perspectives inform strategy. Contribute to the Investigator‑Sponsored Trial (IST) and collaborative research strategy across tumour types. Required Knowledge, Skills & Abilities Strong background in solid tumours, preferably breast cancer and/or HER2‑targeted therapies. Minimum of 5 years’ experience in Medical Affairs with demonstrated leadership in strategic planning and execution. Proven ability to shape medical strategies that drive clinical impact and business success. Experience leading Phase IV studies, ISTs, and Real‑World Evidence initiatives. Expertise across marketed and pipeline products with strong strategic and operational leadership capabilities. Ability to influence and operate effectively within complex matrix environments. Strong understanding of regulatory, commercialization, market access, and reimbursement frameworks. Exceptional communication skills and leadership presence in high‑growth, fast‑paced settings. Willingness to travel as required. Education & Qualifications Doctoral degree required (MD, PharmD, PhD); MD (or equivalent) strongly preferred. #LI-Remote #LI-DM1 Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law. FOR US BASED CANDIDATES ONLY Jazz Pharmaceuticals, Inc. is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. For this role, the full and complete base pay range is: $(phone number removed) - $(phone number removed) Individual compensation paid within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, and other pertinent factors. The goal is to ensure fair and competitive compensation aligned with the candidate's expertise and contributions, within the established pay framework and our Total Compensation philosophy. Internal equity considerations will also influence individual base pay decisions. This range will be reviewed on a regular basis. At Jazz, your base pay is only one part of your total compensation package. The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan. The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, 401k retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here