Sökresultat för "medical degree"

Länssjukhuset Ryhov, Jönköping Välkommen till Länssjukhuset Ryhov i Jönköping! Här får du goda möjligheter och förutsättningar att omvandla dina teoretiska kunskaper till praktiska färdigheter. AT-läkargruppen består av cirka 55 AT-läkare och har god sammanhållning. Vi söker Till vårt AT-gäng söker vi dig som är engagerad, ambitiös, ansvarsfull, gillar utmaningar och vill vara med och utveckla vården i vår region. Vi erbjuder dig Vi erbjuder 1 AT-block med tillträde 2026-08-17. AT-blocken omfattar 21 månader och är fördelade på sex månader kirurgi (inklusive anestesi och ortopedi), sex månader medicin (inklusive geriatrik) tre månader psykiatri och avslutningsvis sex månader allmänmedicin. Din AT inleds med en veckas introduktion och du har fyra valfria veckor under din AT. • 2-5 dagars extern kurs • 8 dagar regiongemensamma utbildningar • 1 veckas introduktion (allmän) • 1 timma undervisning per vecka • Personlig handledare på varje klinik • Betald ledighet, konferensavgift, resa och boende till AT-stämman • Forskningsintresse välkommet. Vid intresse kan regionen erbjuda upp till tre forskar-AT platser per år. Din AT-tjänstgöring förlängs då med 6 månader. Du behöver vara antagen som doktorand vid AT-ansökan. Projektet får gärna kunna förankras till regionen. Som medarbetare hos oss inom Region Jönköpings län får du tillgång till våra anställningsförmåner. En del av dem ökar din grundtrygghet, andra sätter lite guldkant på vardagen. Läs mer om våra förmåner här: http://www.rjl.se/jobb-och-karriar/Jobba-hos-oss/Formaner/ Din kompetens Du som söker har läkarexamen vid planerat tillträde av AT-block samt goda kunskaper i svenska motsvarande minst nivå C1 enligt Europarådets nivåskala. Vår målsättning är att få en kompetent grupp med skiftande karaktär, vilket vi tror gynnar såväl AT-läkarna som vårt sjukhus. Våra urvalskriterier är en sammanvägning av meriter, intervju och referenser. Vi lägger stor vikt vid personlig lämplighet. Din ansökan För att din ansökan ska bedömas som fullständig ska den innehålla: • Personligt brev • CV • Resultatutdrag från LADOK/läkarexamensbevis • Minst en klinisk referens • Foto Sökande med utländsk examen ska, förutom läkarexamensbevis, även bifoga socialstyrelsens beslut om tillstånd att göra AT i Sverige. Om du erbjuds AT-tjänst kommer vi att begära utdrag ur belastningsregistret. Vi strävar efter att ha en snabb rekryteringsprocess och intervjuer kommer att genomföras löpande. Blir du aktuell för intervju kan inbjudan komma med kort varsel. Antagningsbeslut sker i nära anslutning till sista ansökningsdagen. Så här gör du om du är intresserad Upplysningar angående ansökan och intervju lämnas av: • AT-samordnare Marina Möller, telefon 010-242 11 96 alternativt 072-24 01 747, e-post marina.moller@rjl.se • AT-chef Houman Ebrahimi, kontakt via e-post houman.ebrahimi.ardebili@rjl.se. Övriga upplysningar lämnas av AT-läkare Isabel Björnehäll Appelsved, 010-241 00 00 (växel). Fackliga frågor besvaras av SYLF:s representant Linnea Magnusson, 010-241 00 00 (växel). Sista ansökningsdag är den 26 juli 2026. Varmt välkommen med din ansökan! Vi undanber oss all kontakt med annonsförsäljare och rekryteringsföretag. Använd Generativ AI på rätt sätt i din ansökan. Om du väljer att använda generativ AI i din jobbansökan som stöd, går det bra för oss – men vi uppmuntrar att du gör det med eftertanke. Låt AI hjälpa dig att samla information och utveckla idéer, utan att ersätta din personlighet, dina värderingar och din erfarenhet. Din ansökan ska spegla den du är, något AI aldrig fullt ut kan återskapa.

Cambio is one of the Nordics' leading suppliers in e-health with a comprehensive offering for the entire health and care chain. Our e-health solutions supports health care professionals in their daily work and offer patients safer and more easily accessible care. We are proud to be an important part of Swedish healthcare. We are growing continuously and now have about 1000 employees in several countries. What is Clinical Decision Support? CDS is an area of health information technologies that combines evidence-based knowledge and different kinds of patient data in order to generate and present helpful information to clinicians as care is being delivered. We develop standards-based, EHR-independent Clinical Decision Support (CDS) applications that aim to accelerate the learning and innovations of healthcare. At Cambio CDS, we are all passionate about improving healthcare by developing software tools to facilitate clinical decision-making at point of care. After initial success in Sweden and other countries, we anticipate a steady growth of the operation in the coming years. The position Are you passionate about healthcare? Do you want to contribute to the lives of millions? If your answers to both are true, the Cambio CDS team is the right place for you. We are looking for product owners to help us reach new heights. Your main responsibilities include the following: Author and maintain functional requirements, risk analysis and end user facing documentation of our CDS apps. Conduct user interviews, design workshops with clinicians as part of UX design of the CDS apps, in physical setting or remotely. Participate in post-market surveillance and usability studies. Lead and participate in CDS app UX design, clinical modelling, testing and releasing of CDS apps. Perform demonstration of CDS apps with potential customers. Provide training of CDS apps towards our customer representatives or partners. Help the development of authoring tools and improve our app development process About you As a person, you are a humble and responsible team player who loves problem solving. You pay attention to details and follow things through. You are open-minded, curious and keen to learn new skills. Like us, you are passionate about improving healthcare and motivated by the potentials of health IT. At Cambio, we value initiative and personal growth. Our culture is built on Trust, Care, and Together—values we believe are important to both our work and our people. It’s important to us that you recognize and identify with these values. Requirements  Medical doctor degree or similar Excellent writing and oral skills in both English and Swedish Proven record in team-based product development It's a bonus if you have Working experience in Swedish/Nordic healthcare systems Experience with UX or usability studies Clinical oncology background Experience with machine learning, natural language processing and generativeAI tools in product development Place of employment: Stockholm Scope: Full-time, hybrid work model (three days per week in-office) Form of employment: Permanent employment, 6 months trial period Additional Information: The role involves access to sensitive information, therefore a background check will be conducted on the final candidate. We review applications and conduct interviews on a rolling basis, so we encourage you to apply as soon as possible via the link. We look forward to receiving your application! CAMBIO- FOR A HEALTHIER TOMORROW Welcome to a company where healthcare is improved every day. Here you will work with leading technology in a collaborative, trusting and empowering environment where your contribution will be appreciated and celebrated. In our caring culture you will have the opportunity to pursue different paths of professional growth. Seize the opportunity to do the most important work of your life. Read more about us here! A healthier tomorrow also means taking care of those who make it possible -explore our employee benefits Learn more about our recruitment process here Are you interested in Cambio but you don’t feel that this position is the perfect match? Check out our other open positions at our career site.

Vi söker kurator för arbete på ortopedens akuta- och traumaavdelning och på handkirurgimottagningen. På avdelningen vårdas som patienter efter ortopedisk kirurgi eller trauma. Många patienter med en komplex skadebild efter exempelvis olyckor vårdas på avdelningen antingen direkt efter skadan eller efter en intensivvårdsperiod eller vård inom annat specialistområde. Du blir anställd inom verksamhetsområde Hälsoprofessioner, där vi arbetar i nära samarbete med andra professioner. Vi erbjuder dig ett utvecklande och stimulerande arbete med kompetenta kollegor i ett gott arbetsklimat där vi bryr oss om varandra, samarbetar och hjälps åt i vardagen. Arbetsuppgifter Som kurator hos oss ingår du i ett tvärprofessionellt team, där målet är att erbjuda en kvalitativ och effektiv vård av våra patienter. De primära arbetsuppgifterna är att erbjuda akut psykosocialt och praktiskt stöd till ortopediska och handkirurgiska patienter. Du har ett tryggt och professionellt bemötande till patient och närstående. Kvalifikationer Socionomexamen. Vi ser gärna att du är legitimerad hälso-och sjukvårdskurator eller har tidigare erfarenheter från social arbete inom Hälso- och sjukvården. Du har god förmåga till struktur, planering och stresstålighet. Vi värderar personlig lämplighet högt och att du har en god samarbetsförmåga. Viktigt för oss är att du har lätt för att skapa goda möten både med patienter och kollegor i teamet. Att verksamhetsområdet är nytt innebär att rutiner och samverkansformer är fortsatt i förändring, och du ska trivas med att vara en del av utvecklings- och förändringsarbete. Ansökan Urval och intervjuer sker fortlöpande under ansökningstiden. Ansökan ska innehålla CV och personligt brev. Intyg, betyg, examensbevis med mera ska lämnas vid en eventuell intervju. Om du är eller tidigare varit anställd i Region Örebro län kommer vi ta interna referenser från din nuvarande eller tidigare chef, om du blir aktuell för anställning. Kontroll av registerutdrag från Polismyndigheten kan komma att ske enligt aktuell lagstiftning. Som anställd i Region Örebro län omfattas du av trygga kollektivavtal. Läs mer om villkor och förmåner. Vi sätter löner individuellt och differentierat. Läs mer om lön och lönestatistik. Vi krigsplacerar våra tillsvidareanställda och i vissa fall även visstidsanställda. Läs mer om vad det innebär. Om verksamheten Verksamhetsområde hälsoprofessioner är en nystartad länsklinik. I verksamhetsområdet arbetar logopeder, dietister, arbetsterapeuter, fysioterapeuter, kuratorer, psykologer, undersköterskor och administratörer. Tjänsten är placerad i kuratorsenheten som är en av flera enheter inom det nya verksamhetsområdet. Universitetssjukhuset Örebro (USÖ) är ett av länets tre akutsjukhus där vi bedriver avancerad sjukvård, forskning och utbildning. Både 2020 och 2019 mottog USÖ tidningen Dagens Medicins prestigefyllda utmärkelse Bästa universitetssjukhus. USÖ har ca 3500 anställda. Vi som arbetar här är mycket stolta över vårt sjukhus och bygger vårt arbete på samarbete, utveckling och professionalism. Region Örebro län är en av länets största arbetsgivare. Tillsammans med 11 000 kollegor kan du skapa ett bättre liv för de vi finns till för. Hos oss finns meningsfulla och samhällsviktiga jobb där du kan göra skillnad i invånarnas vardag, hälsa och livskvalitet. Dygnet runt, året om, ansvarar vi för hälso- och sjukvård, tandvård och länets kollektivtrafik. Vi har också det regionala utvecklingsansvaret i länet och ett uppdrag att bidra till kulturlivet. Övrig information Välkommen med din ansökan! Vi har gjort vårt medieval för denna rekrytering och undanber oss därför erbjudanden om annonserings- och rekryteringshjälp i samband med denna annonsering.

Vill du bidra till medicinsk forskning av toppkvalitet? Forskargruppen ESSI undersöker transdiagnostiska problematiska beteenden hos ungdomar och unga vuxna, som exempelvis självskada, självmordstankar och aggressivitet. Gruppen driver i dag tre stora randomiserade kontrollerade studier, samt flera epidemiologiska och experimentella studier som undersöker mekanismer bakom självskada. Forskargruppen ESSI är en del av Centrum för psykiatriforskning – ett samarbete mellan Karolinska Institutet och Region Stockholm, med kontor nära Torsplan / KI Campus Solna. Nu söker vi en forskningsassistent för ett projekt på två till sex månader. Din roll Ett av våra intresseområden är personspecifika ”symtomnätverk”, det vill säga ett kvantitativt och systemiskt sätt att förstå psykopatologi. Publicerade studier som har använt sådana nätverk för att identifiera behandlingsmål har ofta utgått från symptom/noders centralitet (tex out-degree). Vi söker nu en forskningsassistent med intresse för andra sätt att analysera nätverk, som tar hänsyn till mer av ett nätverks struktur. Gruppen har tillgång till redan insamlad data bestående av personspecifika nätverk som skapats med PECAN (Perceived Causal Networks). Projektets syfte är att utveckla och utvärdera sådana alternativa analyser. Exempel på utvärderingskriterier är hur begripliga resultaten är för patienter, hur väl de överensstämmer med en t.ex. klinikerbedömningar, samt om de är förenliga med teoretiska principer inom nätverksanalys. Du förväntas kunna ta fram idéer till analyser och hur de ska utvärderas, diskutera dessa konstruktivt i forskargruppen samt genomföra analyser självständigt. Målsättningen är att tvåmånadersprojektet ska leda till antingen en inskickad konferenspresentation eller till en metod som kan användas i framtida publicerbara interventionsstudier, med möjlighet till medförfattarskap. Det finns även planer på att utlysa en doktorandtjänst inom projektet under hösten 2026. Rollen innefattar arbete på plats och på distans, där minst hälften av arbetstiden utförs på plats. Exakta datum kan planeras flexibelt. Vem är du? Vi söker dig som är nyfiken, analytisk, intellektuellt flexibel och kan arbeta självständigt, samtidigt som du bidrar konstruktivt i diskussioner med andra. Du arbetar strukturerat, har gott omdöme och kan kommunicera komplexa idéer på ett tydligt sätt till både forsknings- och klinisk målgrupp. Stor vikt kommer att läggas vid personlig lämplighet. Följande är krav för tjänsten: Dokumenterad akademisk utbildning, examensarbete och/eller publikationer kopplade till nätverksperspektivet inom psykopatologi, strukturerade fallkonceptualiseringar, komplexitetsteori eller datadrivna systemiska angreppssätt inom psykiatri. Masterexamen inom relevant område, till exempel psykologi, medicin, beteendevetenskap eller närliggande ämne, avlagd senast sista ansökningsdag (9 augusti 2026). Dokumenterade kunskaper i R. Mycket god förmåga att uttrycka dig på engelska i tal och skrift. Det är meriterande om du även har: Ett masterarbete som omfattar nätverksanalys eller en strukturerad metod för fallkonceptualisering, empiriskt och/eller teoretiskt. Klinisk och/eller forsknings-erfarenhet av arbete med ungdomar eller unga vuxna. Erfarenhet av att samla in personcentrerade forskningsdata, till exempel via intervjuer, ecological momentary assessment (EMA) eller single-case experimental designs (SCED). Erfarenhet av rekrytering av deltagare till forskningsstudier, till exempel via annonsering, screening eller liknande. Vad erbjuder vi? En kreativ, internationell och inspirerande miljö fylld av kompetens och nyfikenhet. Karolinska Institutet är ett av världens ledande medicinska universitet. Vår vision är att driva utvecklingen av kunskap om livet och verka för en bättre hälsa för alla. Här bedriver vi framgångsrik medicinsk forskning och har det största utbudet av medicinska utbildningar i Sverige. Som universitet är Karolinska Institutet en statlig myndighet. Det gör att du får goda förmåner genom vårt kollektivavtal. Medarbetare på KI erbjuds också möjlighet till ett flexibelt arbetssätt. Det innebär att om den verksamhet du jobbar i tillåter, så kan du arbeta en del av din arbetstid på distans. Du får även träna fritt i våra moderna friskvårdsanläggningar där utbildad personal finns på plats. Placering: Norrtull, Stockholm Läs mer om forskargruppen du kommer att ingå i Tio skäl att välja Karolinska Institutet Ansökan Ansökan ska göras via rekryteringssystemet Varbi. I denna rekrytering söker du med ditt CV utan personligt brev. I ansökningsformuläret kommer du istället att få svara på några frågor om varför du söker jobbet. Det är möjligt att uppdatera sin ansökan fram till sista ansökningsdag. Det går därför bra att skicka in din ansökan redan nu om du planerar att slutföra din masterutbildning senast vid sista ansökningsdag, och sedan uppdatera din ansökan när du har fått ditt examensbevis. Vill du göra skillnad – och bidra till en bättre hälsa för alla? Sök jobb hos oss

SHL Medical is a world-leading provider in the design, development, and manufacturing of advanced self-injection devices. With a global team of 6,000 employees, we partner with leading pharmaceutical and biotech companies to deliver innovative autoinjectors, pen injectors, and other drug delivery systems that ensure effective treatment for patients. Headquartered in Switzerland since 2018, with key operations in Sweden, Taiwan, and the US, we are united by a commitment to innovation, impact, and growth. Together, we empower our people to develop solutions that make a meaningful difference in the lives of millions of patients while fostering a supportive, inclusive, and dynamic workplace for our colleagues. Job Overview The Risk Manger is responsible for reviewing risk management related topics within Design and Development Projects and participates in the development, implementation and administration of SHL’s risk management processes. Main Responsibilities To participate in the implementation and administration of SHL’s risk management process in the Sweden office. Participate in the implementation and administration of SHL’s Risk Management process within the Sweden office. Contribute to the continuous development and improvement of SHL’s Risk Management processes in collaboration with relevant cross-functional teams. Provide training and guidance on SHL’s Risk Management processes to employees within the Sweden organization. Participate in CAPA activities in the role of Risk Manager. Perform additional tasks and responsibilities related to the position, as required. Supporting project teams in establishing Risk Management Plans. Supporting the definition of acceptance criteria for Design Input Requirements (DIRs) based on risk assessment outcomes. Participating in design reviews in the role of Risk Manager. Minimum requirements ​Bachelor’s degree in Life Science or Engineering Minimum 3 years of relevant professional experience Experience within Risk Management, Quality Assurance, and/or Regulatory Affairs in a regulated industry Experience interpreting and applying standards such as EN ISO 14971:2019 and EN ISO 13485:2016 Experience establishing, reviewing, and approving quality documentation Experience of collaborating with pharmaceutical companies and external stakeholders Fluent in written and spoken English. Preferred Qualifications Experience working within the Medical Device or Combination Product industry Experience participating in product development projects and Design Control activities Knowledge of CAPA, change control, and non-conformance management processes Fluent in written and spoken in Swedish We Offer Challenging assignments in a fast-growing and innovative industry. An exciting opportunity in a fast-growing international medical technology company. A modern working environment with multicultural and dynamic teams. A centrally located office in Zug, very close to the train station. Interested in joining SHL Medical and in supporting us with your expertise and personality? Then we look forward to receiving your application to our Talent Acquisition Department. Please note: We do not accept applications from recruitment agencies for this position.

Dignus Medical specializes in recruiting doctors, specialists and nurses for the healthcare sector across Scandinavia. We help solve staffing challenges by matching the right professionals with the right employers – at the right time. This year, we proudly celebrate our 20th anniversary. Watch our anniversary film (https://vimeo.com/1114843079?share=copy) and join us on our journey! Are you a dedicated nurse looking to take your skills to new heights while immersing yourself in the unique lifestyle of northern Europe? We’re seeking experienced general nurses to join healthcare teams across Northern Sweden – a region known for its stunning landscapes, tight-knit communities, and excellent working conditions. Why Northern Sweden? Northern Sweden offers more than just a job – it offers a lifestyle. Imagine finishing your shift and stepping out into fresh, clean air, surrounded by forests, lakes, and snow-capped mountains. This region is perfect for those who value space, calm, and a closer connection to nature. You’ll experience the beauty of the midnight sun in summer and the northern lights in winter – all while working in one of the most advanced healthcare systems in the world. About the role As a general nurse, you will play a vital role in delivering compassionate, high-quality care in settings such as: Regional hospitals, where teamwork and acute care go hand in hand Health centers and outpatient clinics focused on continuity and community care Administering treatments, supporting patient recovery, and contributing to care planning Working alongside multidisciplinary teams to improve patient outcomes and innovate care delivery What we’re looking for EU-recognized nursing license and degree Proficiency in English and readiness to learn Swedish A flexible, team-oriented approach and solid nursing experience A genuine passion for patient-centered care What you’ll get Career development in a forward-thinking healthcare environment Work-life balance that supports your well-being Support throughout the process – from licensing to relocation Free personalized Swedish language training via Teams or Skype Assistance with accommodation and family relocation, if needed Curious about life in the North? Let’s talk. We’re happy to tell you more about the region, the roles, and how we support you every step of the way. Apply today to stay in the loop about upcoming opportunities for nurses across Sweden. You can also register your CV (https://dignusmedical-en.recman.page/login) or sign up for our newsletter (https://www.dignusmedical.no/en/sign-up-for-newsletter/) to stay updated on future opportunities.

Are you interested in medical images, image analysis and leading projects? Would you like to work in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A company, where you would contribute and be a part of a collaborative team? If this ticks your boxes, you should continue reading. At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI), Positron Emission Tomography (PET), and Dual-energy X-ray (DXA) to design and deliver clinical studies for decision making and differentiation in drug development. We value competence and development as well as ideas and solutions. Relations and trust are keys to success, and it is equally important for us to have fun while doing a meaningful job. We have currently around 140 employees working at our offices in Mölndal, Uppsala, and Lund, and we are continuously growing and developing. As a part of our growth journey, we are looking for a quality-focused and communicative Project Lead Corelab with good organisational skills to join our Corelab Team in Mölndal. As a Project Lead Corelab, you will be part of a project team where you are responsible for the analysis and delivery of data according to the project’s timeline, as well as to our quality requirements and ICH-GCP. You will also to some extent work with quality control and analysis of images from MR, PET and DXA investigations and communicate with national and international imaging centres. As part of your on-boarding you will receive a mentor and undergo an extensive training programme. Your main responsibilities will be: Ensure that systems for data handling in the project are set up and configured Development and maintenance of documentation for data handling in project Planning and follow-up of analysis and delivery of data to customer according to the project’s timeline Delivery of data and reports to customer Quality control of the images and documentation from the MR, PET and DXA investigations in the clinical trials Segmentation and analysis of images from the MR, PET and DXA investigations including documentation of this Communication with national and international imaging centres on image quality   Who are we looking for? We emphasize personal suitability and believe that you are a structured and thorough person with attention to quality. We further believe that you are a positive and service-oriented person with good communication skills who enjoys collaborating with others. We are happy to see that you have an interest in images, technology, and medicine. You also enjoy working on multiple tasks simultaneously and to plan, coordinate, and follow-up on work in projects. We are also happy to see that you like to work with systems. Desired qualifications and skills: University degree or relevant higher education, such as in engineering, biomedicine, pharmacy, biomedical laboratory science or similar Good computer proficiency Good knowledge of spoken and written English Experience from project management and programming are an advantage, however not a requirement. Are you interested? Great to hear! Please submit your application via this link with a short personal letter and your CV included, no later than July 31st 2026. Interviews can take place during the advertisement period. For more information about the position, please contact Anna Ringheim Cadete, Head of Corelab, at anna.ringheim@antarosmedical.com The recruitment refers to permanent full-time employment. We only handle applications via our recruitment system Teamtailor. The recruitment if managed by Antaros Medical. We kindly decline any contact from recruitment- or staffing firms.   About Antaros Medical At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialized in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotechs, and several European collaboration initiatives such as Innovative Medicine Initiative (IMI) and COST. Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. If you want to find out more about our company, go to our website: www.antarosmedical.com. Our culture is our people, and our values makes us everything that we are. Please feel free to have a look upon our Culture Handbook to get to know us even more: Our culture - Antaros Medical.

At Neoventa, we develop fetal monitoring solutions that help clinicians make critical decisions during childbirth. We are looking for a Technical Product Manager to take lifecycle responsibility for our fetal/maternal monitoring platform. About the role You will own our fetal/maternal monitoring platform, including CTG and fetal ECG/ST analysis, and guide it throughout its lifecycle—from requirements to development, release, and continuous improvements. Working closely with R&D, Clinical, Regulatory, Quality, Commercial teams, and external partners, you will turn user needs into safe, compliant, and meaningful products. The role is based at our HQ in Mölndal, reporting to the Chief Technology Officer. What you will do Own the products' roadmap and technical backlog Translate clinical and user needs into product and system requirements Drive technical decisions together with the rest of the R&D team Ensure solutions meet safety, regulatory, and commercial requirements Contribute to verification, validation, and product release Analyze field performance and drive continuous improvement Act as the technical expert internally and externally Your profile Engineering degree (Biomedical, Electrical, Software, Systems or similar) 8+ years of experience in technical product management, systems engineering or similar Experience from active medical devices (or other regulated industries) Strong understanding of embedded systems, signal processing, and HW/SW integration Fluent in professional English Who you are You combine deep technical curiosity with a strong sense of ownership You are comfortable navigating complexity and making sound decisions with incomplete information You are a collaborative problemsolver with a can-do attitude You communicate with clarity and adapt your message to your audience You focus on what creates real value - balancing technical possibilities with clinical and business needs Why join us? This is a unique opportunity to become the techincal product manager for a complex medical device and help shape the future of fetal monitoring. You'll work at the intersection of technology, clinical practice, and innovation - where your professionallism will have a direct impact on healthcare professionals, mothers, and babies worldwide. To apply  Neoventa is committed to sustainability and diversity and encourages applicants from all backgrounds.  The application deadline is August 9th, 2026. Due to the summer vacation candidate selection and interviews will be done after the application period. We do not accept applications via email or phone; instead, we kindly ask you to apply directly through our career website.  If you have any questions regarding the recruitment process or the position, you are welcome to contact Thomas Börstell, Chief Technology Officer, thomas.borstell@neoventa.com or Frida Svenningsson, Chief People & Culture Officer, frida.svenningsson@neoventa.com.  We look forward to receiving your application!

We are looking for a Head of Marketing & Communications to strengthen our product marketing and drive commercial impact globally. The role is based at our HQ in Mölndal, reporting to the Chief Commercial Officer, with responsibility for a marketing team of two. Your impact You will play a key role in strengthening our commercial impact, by shaping how we position our products, how we communicate their value, and how we support our sales teams and distributors globally. You are comfortable switching between thinking long-term and getting things done yourself – whether that means shaping a message, creating material, or supporting a launch together with sales. You will play a key role in strengthening our global presence, supporting sales, and positioning Neoventa as a trusted partner in obstetric care. What you will do Strengthen how we position our product offer and ensure our messaging is clear and consistent across markets and distributors Own and drive Neoventa’s global marketing and communications strategy Partner and contribute closely with Sales/distributors, R&D and Clinical teams to translate customer and market insights into impactful communication Develop marketing campaigns and sales materials to support distributors and sales teams Contribute to the development of Neoventa Academy for education and engagement together with KOL’s and the Clinical team. Develop our digital channels and content, including growing our e-learning offering Own and drive product launches and portfolio communication together with sales Define budget, team goals and KPIs, measure performance and continuously improve marketing effectiveness Lead and develop the marketing team, create clear priorities, a positive work environment, and strong execution across global marketing and communications activities. Your profile We believe you are commercially minded, collaborative, and comfortable working close to both products and sales. You likely bring: Degree within Marketing or a related field Minimum 5 years experience from marketing within MedTech or other Life Science business Experience from international marketing in a commercial and product-focused environment Experience working closely with sales teams and distributors Track record of translating strategy into execution and results Experience leading projects and teams Experience in service selling is considered an advantage Who you are A strategic thinker with a hands-on approach and a strong sense of ownership Collaborative and proactive, with ease in working across teams and functions Driven and structured, able to create clarity in dynamic environments You can take complex clinical and product information and turn it into clear, simple messaging Curious about customers and markets, with a focus on creating real impact Unpretentious, warm, and considerate in how you engage with others Why Join Neoventa?  This is an opportunity to join a purpose-driven company where your work truly matters. You will shape the future of a growing global brand while contributing to better healthcare outcomes for families around the world.  To apply  Neoventa is committed to sustainability and diversity and encourages applicants from all backgrounds.  The application deadline is July 26th, 2026. Selection will be done during the application period, and interviews will start after the summer period in August, so please do not wait to submit your application.  We do not accept applications via email or phone; instead, we kindly ask you to apply directly through our career website.  If you have any questions regarding the recruitment process or the position, you are welcome to contact Josefine Wihlborg, Chief Commercial Officer, josefine.wihlborg@neoventa.com or Frida Svenningsson, Chief People & Culture Officer, frida.svenningsson@neoventa.com.  We look forward to receiving your application!

Role Purpose Be part of the medical technology revolution – Neko Health is expanding and looking for talented assistant nurses to join our team. Are you ready for an exciting career where you can make a real difference? This is your chance to become part of our dynamic team and help shape the exciting journey ahead! In this role you will be at the center of our mission. Based at one of our futuristic Neko Health clinics in Central Stockholm, your main tasks will be to carry out examinations, collect clinical research data, take blood samples, analyse blood samples, and handle administrative documentation. You will be a key person in ensuring the smooth operation and high quality of our activities. You will work closely in teams with other skilled medical operators and experienced professionals, but you will also have the opportunity to take initiative and work independently. We are looking for an assistant nurse who can work 80-100% in shifts (days, evenings, and Saturdays). Minimum Qualifications Relevant healthcare education as an assistant nurse. Clinical skills: Confident in performing ECGs and blood sampling. Minimum of one year of clinical experience. Excellent customer service skills: Warm, friendly, and professional approach. You are solution-oriented, flexible, and committed to delivering high-quality patient care. Start-up mindset: Comfortable working in a fast-paced, evolving environment. Adaptable to change and digitally proficient with good technical skills. Strong communication skills: Clear, structured, and pedagogical in your communication. Language skills: Fluent in Swedish and highly proficient in English. We offer a dynamic work environment with a high degree of autonomy that fosters growth and development. If you are passionate about building a better healthcare system for everyone and you thrive in a fast-paced environment, we would love to hear from you. Interviews are ongoing, so don’t hesitate to send in your application today!

Site Director Medical Who We Are Essity is a global leader in health and hygiene headquartered in Stockholm, Sweden. We are a multi-billion-dollar company with a purpose to break barriers to well-being for the benefit of consumers, patients, care givers, and customers across the globe. We do this through innovations in our Professional Hygiene, Personal Care, and Health & Medical business units that provide hygiene and health solutions to over a billion people every day worldwide. Working at Essity is more than a career, it is where you will play your part in a better future, to improve well-being for people and have opportunities to drive positive change for society and the environment. As an employee at Essity, you will belong to a team where you feel valued, are safe, supported to grow and challenged to generate business results in a friendly and open atmosphere. About the Role As Site Director, you will lead a manufacturing site with approximately 75 employees, overseeing all aspects of production, quality, safety, supply chain, and operational performance. You will drive our manufacturing strategy in line with the site’s Compelling Business Need (CBN) and global objectives. We’re looking for people who embody our values, aren’t afraid to challenge, innovate, experiment, and move at a fast pace. If this sounds like you, we’d love to talk. What You Will Do Lead day‑to‑day operations with a strong focus on Safety, Quality, Cost, Delivery, and Motivation (SQCDM). Own the site’s full P&L, define operational targets, and drive competitiveness and productivity. Strengthen a proactive, compliance‑driven safety culture and ensure audit‑readiness at all times. Build, mentor, and empower a high‑performing leadership team that fosters accountability and continuous improvement. Champion Lean Manufacturing and TPM to accelerate efficiency, automation, and digitalization. Collaborate closely with global commercial and functional teams to ensure product availability and exceptional customer satisfaction. Represent the site in global initiatives, steering committees, and cross‑functional forums. Maintain strong, constructive union relationships in partnership with HR. Drive a culture of ownership, learning, and performance excellence at all levels. Drive innovation, implement capital investments, and enhance the site’s long‑term strategic capabilities. Who You Are University degree or equivalent education. Minimum 6 years of experience in site or plant leadership within FMCG or MedTech environments. Strong background in TPM, Lean, automation/digitalization, and continuous improvement. Demonstrated P&L ownership and experience driving measurable operational improvements. Skilled collaborator with experience in matrixed, multinational organizations. Excellent communication and leadership capabilities, able to inspire teams and influence stakeholders. Entrepreneurial, resilient, and energized by transformation and fast‑paced global environments. What We Can Offer You Our purpose, Breaking Barriers to Well-Being, provides meaning to everything we do. Join us to improve well-being for people and drive positive change for society and the environment. At Essity, you'll feel valued, empowered to grow, and challenged to achieve business results in a collaborative and open atmosphere. Innovate for Good | Excel Together | Be You With Us

MediCarrier är Region Stockholms centrallager och bolag för logistik och transporter till hälso- och sjukvården. Vårt uppdrag har betydelse för vardagen för nästan en fjärdedel av Sveriges befolkning. Varje dag, året runt, skapar vi förutsättningar för våra kollegor i vården att utföra sitt arbete. Genom att till exempel säkerställa att viktiga blodprov transporteras till analys och att produkter som provrör, operationsmaterial och skyddsutrustning alltid finns på plats, bidrar vi till Region Stockholms hälso- och sjukvård. Det är ett ansvar som inte alltid märks, men som är avgörande för att vården ska fungera tryggt och säkert. Utan rätt förutsättningar i rätt tid stannar vården. Hos MediCarrier är du en del av ett samhällsviktigt uppdrag, mitt i vårdens vardag. Om verksamheten  I en tid med ett snabbt föränderligt omvärldsläge, nya krav i lagstiftning, nationella uppdrag och ett tydligare ansvar inom det civila försvaret, ökar kraven på att hälso- och sjukvården ska kunna fungera även under fredstida kriser och höjd beredskap. Förändrade regelkrav avseende lagerhållning av sjukvårdsprodukter ställer krav på en sammanhållen och integrerad IT-miljö för varuförsörjning som möjliggör transparens, spårbarhet, analys och styrning av försörjningsflöden för hälso- och sjukvården. Målet är att skapa en samlad, säker och effektiv systemmiljö som stödjer hela försörjningskedjan – från beställning och lagerhantering till distribution, uppföljning och analys och som stöttar en gemensam logistikdesign, möjliggör effektiva flöden och ökad automation samt skapar förutsättningar för en datadriven verksamhet. Vill du vara med och framtidssäkra Region Stockholms varuförsörjning? Om tjänsten Som Domänarkitekt varuförsörjning har du det strategiska ansvaret för att utveckla målarkitekturen för området och säkerställa att verksamhetsförmågor, processer, information och IT utvecklas som en sammanhållen helhet. Du har en nyckelroll i ett långsiktigt utvecklingsprogram där målet är att skapa en sammanhållen, robust och framtidssäker IT-miljö för Region Stockholms varuförsörjning. Du kommer att arbeta tvärfunktionellt över hela försörjningskedjan och bidra till att skapa en hållbar arkitektur som stödjer framtida utveckling, innovation och förändring. Dina arbetsuppgifter i huvudsak  Ansvara för och utveckla målarkitektur och arkitekturbeskrivningar för domänen varuförsörjning Leda och coacha arkitekturarbetet inom domänen Granska och kvalitetssäkra lösningsförslag tillsammans med arkitekter inom domänen Delta i program och transformationsledning för att inför nya processer, förmågor, plattformar och system inom domänen Säkerställa att processer, verksamhetsförmågor, information och integrationer bildar en långsiktig och sammanhållen helhet Integrera arkitekturperspektivet i verksamhetsutveckling i samverkan med vårdgivare, logistikfunktioner, och övriga IT- funktioner i regionen Omvärldsbevaka trender inom domänen, digitalisering och IT i stort  Vem är du?  Rollen kräver en mycket god förmåga att omsätta verksamhetsbehov och teknikutveckling till långsiktigt hållbara lösningar och strategier. Som person har du ett strategiskt och analytiskt tankesätt samt förmågan att kommunicera, förankra och skapa samsyn mellan olika intressenter. Du har lätt för att skapa goda relationer, trivs med att samarbeta och är van vid att leda andra genom påverkan snarare än via ett formellt personalansvar. För att lyckas i rollen ser vi att du har:  Akademisk examen inom IT, teknik, systemvetenskap, industriell ekonomi eller annat som arbetsgivaren bedömer relevant för rollen Minst fem års erfarenhet av arbete i en ledande roll som enterprise eller domänarkitekt Akademisk utbildning som arbetsgivaren bedömer som relevant Har god förståelse för och lång erfarenhet av ERP-plattformar eller andra verksamhetskritiska plattformar och hur de stödjer verksamhetsprocesser Har arbetat med komplexa verksamheter där processer, information och IT behöver utvecklas tillsammans God förståelse för arkitekturprinciper, processer, standarder, metoder och ramverk Flytande svenska, både muntligt och skriftligt Det är meriterande om du har:  Erfarenhet från större offentlig verksamhet Erfarenhet av verksamhetskritiska plattformar inom logistik- och varuförsörjning Erfarenhet av infrastruktur och säkerhetsarkitektur, molnplattformar och informationssäkerhet  Villkor Tillsvidareanställning. Provanställning kan komma att tillämpas. Heltidsanställning, 39,30 timmar/v. Placering på både MediCarrier i Spånga och Region Stockholms kontor på Kungsholmen. Möjlighet till distansarbete utifrån verksamhetens behov. Intresserad av att ansöka eller veta mer? I denna rekrytering samarbetar MediCarrier med Computer Sweden Recruitment. Vid intresse eller frågor är du varmt välkommen att kontakta Maria Widegren, rekryteringskonsult: Telefon: 0734-231550, E-post: maria.widegren@csrecruitment.se. För att ansöka, vänligen skicka in ditt CV eller ansök med LinkedIn. Att söka jobb i Region Stockholm Vi eftersträvar jämställdhet och jämlikhet på vår arbetsplats och ser gärna sökande med olika bakgrund och förutsättningar. Vi tar endast emot ansökningar via detta system. Ansökningar per brev eller e-post beaktas inte. Vi undanber oss direktkontakt med bemannings- och rekryteringsföretag samt säljare av ytterligare jobbannonser. Vårt rekryteringssystem kan inte hantera anonyma ansökningar eller sökande med skyddade personuppgifter. Om du har skyddade personuppgifter ber vi dig att kontakta den kontaktpersonen som finns angiven i annonsen. Din ansökan kommer då att hanteras utanför rekryteringssystemet. Du bör även vara försiktig med vilken information du lämnar i din ansökan och endast ta med information som är relevant för den aktuella befattningen. Region Stockholm ansvarar för hälso- och sjukvård, kollektivtrafik, regional utveckling och bidrar till kulturlivet. Varje dag, dygnet runt. I landets snabbaste växande region. Tillsammans skapar vi Europas attraktivaste storstadsregion.

Surgical Science is a global organisation and leading provider of medical training simulations and software solutions. Surgical Science is listed on Nasdaq First North Growth Market.   Together with healthcare partners and customers in more than 90 countries, we enhance patient safety and healthcare outcomes through evidence-based, state-of-the-art simulation technology that improves clinical proficiency and performance - enabling safe and effective training without putting patients at risk.   Our solutions are used by medical training centres, universities, hospitals, and the medical device industry for practice, assessment, and certification.   With offices in Gothenburg (HQ), Stockholm, Tel Aviv, Cleveland, Cardiff, and Shenzhen, we are a fast-growing and stable organisation in a rapidly evolving world. We foster a hybrid work culture that supports onsite and remote collaboration across teams and time zones.   Job Summary You will work with our Stockholm-based team to develop state-of-the-art surgical simulations for teaching surgeons. Your responsibilities will include:  Developing and refining advanced surgical simulations with realistic 3D graphics and rigid/soft body dynamics. Using the latest simulation technologies to create immersive surgical training. Collaborating with a global team, both on-site and remote. Together with the team, you will help shape the future of surgical training.   Your profile To succeed in this role, we are seeking not only technical competence but a person who can fit in our diverse team culture.   Must have requirements: Minimum 2 years of professional work experience with C++. Experience working with low-level graphics or compute APIs such as Vulkan, CUDA and/or experience with low-level physics simulation such as constraint-based solvers. Up to date with modern development tools and workflows, including AI-assisted coding. Generalist mindset, comfortable combining multiple skills and technologies to solve problems. You enjoy working in a project-oriented, multicultural environment within a global team. You work well independently while also enjoying being part of a collaborative team. You are not afraid to reach out to others when facing complex challenges and are open to sharing your knowledge generously. A degree in Computer Science, Software Engineering, or an equivalent field. Professional-level English and strong communication skills.   Nice to have: Experience using Git and Jira. Experience with agile methodologies.   Career path: Exposure to international collaborations Grow into a senior developer role or team leader in the future Work in a dynamic environment with unique projects   Benefits: 🌍 Global environment (English as primary language) 💻 Hybrid work ⌚️ Flexible working hours 🏩 Optional Private healthcare 💚 Wellness allowance (Friskvårdsbidrag) 🚲 Optional bicycle lease   Surgical Science as an employer Surgical Science is a global and continuously expanding organisation. You will be part of a dynamic, creative environment where we make sure to allow all employees to influence and contribute with their own unique experiences and knowledge.   Guided by our core values -  curiosity, respect, and perseverance - we strive to empower our people by recognising their strengths, supporting their growth, and creating opportunities to make a real impact.   We invite you to join us on this exciting and meaningful journey - to shape the future of medical training and improve care for patients around the world.   Apply today! If you think you would fit our fantastic team and enjoy our work environment, apply as soon as possible as recruitment is ongoing. Let us meet and work out together whether we are a match!We kindly request that you apply with a CV in English.

Surgical Science is a global organisation and leading provider of medical training simulations and software solutions. Surgical Science is listed on Nasdaq First North Growth Market.   Together with healthcare partners and customers in more than 90 countries, we enhance patient safety and healthcare outcomes through evidence-based, state-of-the-art simulation technology that improves clinical proficiency and performance - enabling safe and effective training without putting patients at risk.   Our solutions are used by medical training centres, universities, hospitals, and the medical device industry for practice, assessment, and certification.   With offices in Gothenburg (HQ), Stockholm, Tel Aviv, Cleveland, Cardiff, and Shenzhen, we are a fast-growing and stable organisation in a rapidly evolving world. We foster a hybrid work culture that supports onsite and remote collaboration across teams and time zones.   The role As a Software Developer in our team, you’ll dive into a large C++ codebase and work with our proprietary 3D engine and physics engine to build lifelike simulators for healthcare professionals. Collaborating with team members across different locations, you’ll refine and develop advanced medical simulations with realistic 3D graphics, soft-body dynamics, VR integration, and custom hardware integration, including robotics.   Your profile We think you are a self-driven, results-oriented professional with a curious mindset. You take a holistic approach to coding and persevere in solving problems. You enjoy working independently, are comfortable working with complex code bases, and like building solutions together with brilliant colleagues. You are generous in sharing your knowledge with others and reaching out when needed.   To succeed in this role, we think you have: 2+ years of experience in C++ and a solid foundation in linear algebra and 3D mathematics. Worked with Git/GitHub & agile methodologies. Experience developing real-time or performance-critical applications. Experience with Windows development environments and Visual Studio. A degree in computer science, software engineering, or equivalent. A professional level of English.   It is beneficial if you also have any of the following: Prior knowledge of graphics rendering APIs such as Vulkan or DirectX. Experience with game and physics engines or related frameworks (e.g. Unreal, Unity, PhysX, Cuda, or similar). Experience in Dev tools such as JIRA, Jenkins, CMake, TeamCity, etc. Experience in VR Development, haptics & shader programming. Experience in additional programming languages, preferably C# & Python. A passion for programming and crafting robust, maintainable, and high-performance code. Experience with AI-assisted coding tools and workflow.   Why choose us? Be part of a team developing the next-gen medical simulators with life-like graphics, world-leading haptics feedback and cutting-edge physics simulations Collaborate with a multidisciplinary team of highly experienced developers, UX designers, medical experts, and product specialists to push the boundaries of realism and interactivity in simulation-based learning. Work in an environment where your creativity, passion and ideas truly matter, and help shape products that train healthcare professionals and ultimately contribute to better patient outcomes. Take ownership of meaningful technical challenges, from architecture and performance optimization to user experience and device integration, with a high degree of influence over technical decisions, product direction, and engineering practices.   Benefits: 🌍 Global environment (English as primary language) 💻 Hybrid work ⌚️ Flexible working hours 🏩 Optional Private healthcare 💚 Wellness allowance (Friskvårdsbidrag) 🚲 Optional bicycle lease   Surgical Science as an employer Surgical Science is a global and continuously expanding organisation. You will be part of a dynamic, creative environment where we make sure to allow all employees to influence and contribute with their own unique experiences and knowledge.   Guided by our core values -  curiosity, respect, and perseverance - we strive to empower our people by recognising their strengths, supporting their growth, and creating opportunities to make a real impact.   We invite you to join us on this exciting and meaningful journey - to shape the future of medical training and improve care for patients around the world.   Apply today! If you think you would fit our fantastic team and enjoy our work environment, apply as soon as possible as recruitment is ongoing. Let us meet and work out together whether we are a match! We kindly request that you apply with a CV in English.

RaySearch develops innovative software solutions to improve cancer care. About 1000 clinics in more than 40 countries use RaySearch software to improve treatments and quality of life for patients. RaySearch was founded in 2000 and is listed on Nasdaq Stockholm. The headquarters is located in Stockholm, with subsidiaries in the US, Europe and Asia - Pacific. Today we are more than 400 employees with a common vision of improving cancer care with innovative software. Our great staff is crucial for our success and we offer a fantastic working environment in modern offices, flexibility and good opportunities for development. We believe in equal opportunities, value diversity and work actively to prevent discrimination. Are you a driven regulatory professional who enjoys ownership, collaboration and working close to product development? This could be the role for you. Apply and help shape the future of medical device software at RaySearch.About the role  We are looking for an experienced and driven Regulatory Lead to own the regulatory strategy and lifecycle oversight for one of RaySearch's products. In this role, you will be the regulatory point of contact for the product, working closely with key stakeholders in the Development, Corporate Strategy and Sales teams. You will help shape product strategy, guide development activities, drive market access, and ensure compliance throughout the product lifecycle.  This is a highly visible role for someone who enjoys combining deep regulatory expertise with strategic thinking, project coordination, and collaboration across the organization.  What you'll do  Own and drive the global regulatory strategy for your product throughout its lifecycle.  Lead the preparation, review, and maintenance of Technical Documentation and regulatory submissions, including EU MDR.  Act as the regulatory expert within development projects and ensure regulatory requirements are integrated throughout the design and development process.  Coordinate and oversee multiple projects, priorities, and submission timelines while maintaining a long-term view of the product roadmap.  Partner closely with Development, Corporate Strategy, Sales and other key stakeholders to support product development and market access.  Support inspections, audits, post-market activities, and continuous improvements.  Your profile  You are a proactive and pragmatic regulatory professional who enjoys taking ownership and driving things forward. You are technically strong, comfortable working with development teams, and able to translate complex regulatory requirements into practical solutions.  You like having oversight of the full product picture—from early development and regulatory strategy to submission and post-market activities—and you thrive in a collaborative, fast-paced environment where you can make a real impact.  Requirements  Bachelor's or Master's degree in Engineering, Life Sciences, Biomedical Engineering, Regulatory Affairs, or a related field.  Several years of Regulatory Affairs experience within the medical device industry.  Strong experience preparing and reviewing Technical Documentation under EU MDR.  Experience working with medical device product development and design control processes.  Experience with medical device software  Strong knowledge of IEC 62304, IEC 60601 and ISO 14971  Strong project management and stakeholder management skills.  Ability to manage multiple activities and timelines while maintaining the bigger picture.  Proficiency in English.  Meriting experience  US regulatory experience, Experience with FDA submissions, including eSTAR/510(k).  Experience with IEC 62366 and ISO 14155  Experience with Cybersecurity requirements for medical devices.  Experience with AI/ML-enabled medical devices.  Our Culture Culture at RaySearch is the driving force behind our organization, where everything we do is driven by a shared passion for innovation and the fight against cancer. Our dedication is reflected in our ability to deliver exceptional results, pay close attention to detail, and consistently go the extra mile. Our employees stand out as experts in their field, driven by a relentless focus on solving problems - no matter how complex. At RaySearch, we take pride in leading the way in cancer treatment, leveraging cutting-edge technology to develop innovative solutions that make a real difference in patient care. Our Offer At RaySearch, we offer a diverse and inclusive work environment, fostering openness, sincerity, and collaboration. Located in Hagastaden, Stockholm's Life Science Hub, our modern and creative workspace includes an in-house gym, yoga, and social activities like ping pong, table football, and regular after-work events. Our bistro serves a fantastic lunch buffet, and we offer morning- and afternoon-fika every day. Our rooftop terrace also provides a stunning 360-degree view of Stockholm, enhancing the work experience. All of this comes attached with a competitive compensation and benefits package. Application Please apply to the position through the application form below. Selection and interviews will be ongoing. We do not accept applications by e-mail.

RaySearch develops innovative software solutions to improve cancer care. About 1000 clinics in more than 40 countries use RaySearch software to improve treatments and quality of life for patients. RaySearch was founded in 2000 and is listed on Nasdaq Stockholm. The headquarters is located in Stockholm, with subsidiaries in the US, Europe and Asia - Pacific. Today we are more than 400 employees with a common vision of improving cancer care with innovative software. Our great staff is crucial for our success and we offer a fantastic working environment in modern offices, flexibility and good opportunities for development. We believe in equal opportunities, value diversity and work actively to prevent discrimination. Are you an experienced regulatory leader who enjoys developing people, improving processes, and driving regulatory excellence in a global medical device environment? Then this could be the right role for you.About the role We are looking for an experienced Regulatory Affairs Manager to lead a team of 5 Regulatory Affairs Specialists supporting our global medical device portfolio. This is a key leadership role for someone who combines deep global regulatory expertise with proven people leadership. You will lead and develop a team responsible for global regulatory submissions and registrations, regulatory compliance, vigilance, post-market regulatory activities, and regulatory intelligence. Success in this role requires a leader who is strategic, pragmatic, hands-on, and passionate about developing people while driving operational excellence.   What you'll do   Manage a team of 5 Regulatory Affairs Specialists.   Manage resource planning and allocation across global regulatory activities.   Ensure high-quality execution of global regulatory submissions, product registrations, and other regulatory operational activities.   Own and continuously improve core regulatory processes and ways of working.   Support global post-market regulatory activities, including vigilance, Post-Market Surveillance (PMS), Periodic Safety Update Reports (PSURs), regulatory compliance, and regulatory intelligence.   Provide technical guidance and hands-on support to the team on complex regulatory matters.   Foster a collaborative, engaged, and high-performing team focused on delivering regulatory excellence.  Your profile  You are an experienced regulatory leader with a passion for developing people, improving processes, and supporting a global medical device organization. You are a pragmatic and collaborative leader who translates regulatory requirements into practical, efficient processes that ensure compliance while supporting the business. You thrive in dynamic environments, focus on what matters most, build strong cross-functional relationships, and are motivated by developing talent and driving the continued success of the organization. Experience & skills  Extensive Regulatory Affairs experience within the medical device industry,   Proven people management experience, with the ability to lead, coach, and develop regulatory professionals.  Expert knowledge of the European Medical Device Regulation (EU MDR).   Demonstrated experience leading global regulatory submissions and product registrations, experience with at least one of the following regulatory authorities is required: China (NMPA), Japan (PMDA), India (CDSCO), US (FDA)   Experience with medical device software and IEC 62304.   Experience with medical device standards such as ISO 13485 and ISO 14971.  Strong understanding of global medical device regulations throughout the product lifecycle, including medical device product development and design control processes.  Demonstrated ability to optimize regulatory operations, improve processes, and lead teams through organizational change.   Excellent planning, prioritization, and stakeholder management skills.   A pragmatic, positive, and solution-oriented leader who leads by example, takes ownership, and thrives in a dynamic environment.   Proficiency in English.  Meriting experience  US regulatory experience, Experience with FDA submissions, including eSTAR/510(k).  Experience with IEC 62366 and ISO 14155  Experience with regulatory intelligence, regulatory signal monitoring, and evolving global regulatory requirements.   Experience with Cybersecurity requirements for medical devices.  Experience with AI/ML-enabled medical devices.  Our Culture Culture at RaySearch is the driving force behind our organization, where everything we do is driven by a shared passion for innovation and the fight against cancer. Our dedication is reflected in our ability to deliver exceptional results, pay close attention to detail, and consistently go the extra mile. Our employees stand out as experts in their field, driven by a relentless focus on solving problems - no matter how complex. At RaySearch, we take pride in leading the way in cancer treatment, leveraging cutting-edge technology to develop innovative solutions that make a real difference in patient care. Our Offer At RaySearch, we offer a diverse and inclusive work environment, fostering openness, sincerity, and collaboration. Located in Hagastaden, Stockholm's Life Science Hub, our modern and creative workspace includes an in-house gym, yoga, and social activities like ping pong, table football, and regular after-work events. Our bistro serves a fantastic lunch buffet, and we offer morning- and afternoon-fika every day. Our rooftop terrace also provides a stunning 360-degree view of Stockholm, enhancing the work experience. All of this comes attached with a competitive compensation and benefits package. Application Please apply to the position through the application form below. Selection and interviews will be ongoing. We do not accept applications by e-mail.