Sökresultat för "medical technology"

Vi på Manpower söker nu noggranna och engagerade montörer till ett spännande konsultuppdrag i Mölnlycke. Som montör hos vår kund får du möjlighet att arbeta med montering av medicinteknisk utrustning i en högteknologisk miljö där kvalitet och precision står i fokus. Uppdraget är på heltid. Sök rollen som montör redan idag och bli en viktig del av ett team som bidrar till livsviktig vårdteknik! Ort: Mölnlycke Start: Löpande behov Arbetstider: Dagsskift, Mån-fre: 07.00-15.30 Om jobbet som montör Som montör kommer du att arbeta med montering av både stora och små komponenter inom medicinteknisk utrustning. Du följer tydliga instruktioner och säkerställer att varje steg i processen håller hög kvalitet. Du arbetar nära ditt team för att upprätthålla ett effektivt produktionsflöde. Dina arbetsuppgifter: Montering av såväl stora som små komponenter Utföra monterings- och produktionsuppgifter enligt givna riktlinjer Säkerställa hög kvalitet och precision i varje steg av processen Samarbeta med teamet för att upprätthålla ett effektivt produktionsflöde Den vi söker Vi söker dig som har ett öga för detaljer och trivs med att arbeta i en strukturerad miljö. Du har gärna tidigare erfarenhet av montering och är van vid att följa instruktioner noggrant. Du är en lagspelare som kommunicerar obehindrat på svenska och bidrar till ett gott samarbete i teamet. Kvalifikationer: Erfarenhet av monteringsarbete Goda kunskaper i svenska i både tal och skrift Information om bakgrundskontroll I enlighet med våra kunders krav genomförs i denna rekrytering en bakgrundskontroll i brotts- och belastningsregistret som en del av anställningsprocessen. Genom att ansöka till tjänsten samtycker du till att vi får använda dina personuppgifter för detta ändamål. Den information som inhämtas motsvarar uppgifter ur polisens brotts- och belastningsregister. Uppgifterna laddas inte ner, lagras inte och används endast för bedömning kopplat till aktuell tjänst. Samtycke är frivilligt och kan återkallas när som helst. Notera att giltigt samtycke krävs för att kunna slutföra rekryteringsprocessen. Vad kan Manpower erbjuda dig? Som konsult hos Manpower har du alla möjligheter att forma din framtid utifrån din kompetens, dina behov och dina önskemål. Vi samarbetar med många populära arbetsgivare och kan öppna dörrarna till nya, spännande uppdrag. Du får en anställning med allt vad det innebär i form av marknadsmässig lön, övertidsersättning, semester, tjänstepension och försäkringar enligt kollektivavtal. Friskvårdsbidrag och företagshälsovård ingår också. Om ambulerande-rollen Som konsult hos oss får du möjligheten att möta nya utmaningar, skapa nya kontakter och bredda din erfarenhet genom att arbeta på olika spännande uppdrag hos våra kunder inom ett geografiskt område. Hur söker jag jobbet? Det är väldigt enkelt! Ansök jobbet via ansökningsknappen. Vid frågor är du välkommen att kontakta ansvarig rekryterare Klara Larsson via e-post: klara.larsson@manpower.se. Vänligen notera att vi inte tar emot ansökningar via mail! Vi ser fram emot att höra från dig! Påminnelse inför ansökan För att vi ska kunna granska din ansökan på bästa sätt ber vi dig att tydligt beskriva din tidigare arbetslivserfarenhet. Ange dina tidigare arbetsplatser, din titel och tidsperioden för varje arbete. Om du även har arbetat åt ett bemanningsföretag tidigare, vill vi gärna veta det också. Om Manpower Manpower är Sveriges ledande rekryterings- och bemanningsföretag med tiotusentals attraktiva arbetsgivare över hela landet som våra kunder. Med vårt omfattande nätverk, lokalt såväl som globalt, kan vi erbjuda mängder av spännande lediga jobb som hjälper dig att bygga din karriär, både på kort och lång sikt. Hos oss kan du söka heltidsjobb eller extrajobb vid sidan av studierna. Vi erbjuder alltid en marknadsmässig lön.

Vi har fått utökat uppdrag och söker dig som är Sjuksköterska! ARBETSUPPGIFTER: På vår klinik i Nacka erbjuder vi hemodialys och bästa möjliga vård baserat på patienternas individuella medicinska behov och med stort fokus på att våra patienter skall känna sig delaktiga och involverade i sin behandling. Vi utför dialysbehandlingar på uppdrag av och i nära samarbete med våra beställare. Här kombineras omvårdnad och medicinsk teknik och vi erbjuder dig ett varierande, utvecklande och spännande arbete, med möjlighet till vidareutbildning i njurmedicin. Den ena dagen är sällan den andra lik och du arbetar i varierande tempo i nära samarbete med erfarna kollegor. Nackakliniken behandlar ca 42 patienter och är utrustade med nya Surdial X maskiner. VI SÖKER: Dig leg. sjuksköterska som vill jobba hos oss i Nacka. Det är mycket meriterande om du har tidigare erfarenhet från att arbeta på en dialysavdelning, men du kan även ha lång erfarenhet av exempelvis akutsjukvård eller intensivvård och ha ett intresse för att utveckla dig inom dialys. Stor vikt läggs vid personlig lämplighet samt förmågan att samarbeta i team. Tillträde för tjänsten enligt överenskommelse. Alla nyanställda erhåller en personligt anpassad introduktion där vi arbetar utefter Diaverums rutiner och processer tillsammans med din mentor. Om du inte har erfarenhet av dialys erbjuds ca 8 veckors introduktion. Alla nyanställda har även tillgång till vår interna utbildningsportal d.Academy som är nätbaserad. VI ERBJUDER: Spännande och mycket utvecklande tjänster till dig som vill göra skillnad i våra patienters liv. Du kommer att bli en viktig del av ett mycket professionellt och engagerat team bestående av läkare, sjuksköterskor, undersköterskor och biträde. Teamandan är stark och det är laget före jaget som genomsyrar arbetsklimatet på vår klinik. Förmåner: Heltidsarbete utgör 37 timmar/vecka Möjlighet till en årlig bonus Tjänstepension Arbetstider förmiddagspass 7-15 eller eftermiddagspass 11-30-19 Tisdagar, Torsdagar & Lördagar är kliniken öppen till 15 och kliniken är stängd på söndagar Friskvårdspeng Kontinuerlig utbildning i dAcademy Kollektivavtalsanslutna Fredagsfrukost Internationella karriärmöjligheter Värderingsstyrd företagskultur - TRUE CARE Vi arbetar med löpande urval så sök omgående. Vi tar endast emot ansökningar via vår webbportal: https://careers.diaverum.com/ Skriv in Nacka i fältet " Sök via ort" så kommer tjänsten upp.

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 Sr Quality Engineer is responsible for acting as Workstream Lead Quality (QE Lead) in the Design & Development projects as responsible for design assurance activities across all project phases ensuring quality and robustness of the product design and manufacturing processes (including product care projects, design changes and design reviews). Furthermore, the Quality representative is responsible to assure compliance with applicable regulations and SHL Medical AB’s Quality Management System (QMS) in both Design & Development Projects and other Quality element tasks such as CAPAs and Change Control handling. Main Responsibilities Maintain and calibrate laboratory equipment and instruments to ensure operational reliability and compliance. To act as Workstream Lead Quality applying Quality Engineering principles in a dynamic way in development and production projects. To represent Workstream Lead Quality in all Design Controls and Product Development related aspects. To ensure that all design control and production/process control projects meet applicable (local and international) regulations, Corporate, Customer, and Local QMS requirements. To utilize Quality Engineering best practices, ensuring internal and external customers’ needs and requirements are built into new products and future product changes. To support SMEs in the identification and traceability of Critical to Quality attributes by applying Advanced Product Quality Planning/DFSS/Risk tools and techniques across all product development phases. To promote the use of statistics in testing and control of quality. To support and guide Risk Management activities (FMEAs). To assess and approve the risk mitigation techniques implemented and whether these are consistent with the product classification, potential defect types, defect frequency, severity, patient risk, process capability, product and process controls. To support Device product/process development and production activities, including the following: Develop or review product/process specifications and requirements. Develop or review product reliability specifications/predictions, and reliability test activities. To develop quality plans and work further with Manufacturing on the transfer of quality requirements. To contribute to compilation and maintenance of Design History Files (DHF). Minimum requirements Minimum 5+ years' work experience in relevant roles such as Quality Assurance, Quality Engineering Fluent in written and spoken English. Experience from working with interpretation of ISO Standards, e.g EN ISO 14971:2019 and EN ISO 13485:2016 Experience in establishing, reviewing and approving quality documentation Experience with model development, test method validation and statistical analysis. Green Belt practitioner, or demonstrated experience in application of Quality Methodologies such as DFSS, DMAIC, Lean Hands-on experience in product development from ideation to launch in the Medical Device Industry Preferred Qualifications Fluent in written and spoken Swedish. Experience with Design Controls and Design Transfer activities within the Medical Device industry Experience with injection molding and automated assembly manufacturing processes. Familiarity with validation activities including IQ/OQ/PQ and Test Method Validation (TMV). Experience working in cross-functional and international environments. 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

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.

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. We are looking for a Business Development Manager – Medical Oncology to help define and drive RaySearch's expansion into the Medical Oncology market.  This is a unique opportunity to join RaySearch at an early stage of a new strategic growth initiative. As we explore opportunities beyond our traditional radiation oncology business, you will play a key role in helping shape our strategy, evaluate market opportunities, define commercialization approaches, and support the successful introduction of future solutions into the Medical Oncology landscape.  About the job  You will translate strategic direction into concrete market activities, ensuring strong alignment between product positioning, customer needs, and commercial execution.  Your main tasks  Lead market intelligence activities to develop a comprehensive understanding of the Medical Oncology landscape, including market dynamics, customer needs, competitive positioning, treatment pathways, reimbursement models, and emerging trends  Identify and evaluate growth opportunities, unmet needs, and strategic market segments within Medical Oncology  Develop and execute market development and commercialization strategies for future Medical Oncology solutions  Build and maintain relationships with key stakeholders including Medical Oncologists, Oncology Nurses, Hospital Administrators, Cancer Centers, Professional Societies, and Industry Partners  Assess emerging clinical evidence, technology trends, and evolving standards of care to identify opportunities for innovation and growth in alignment with the overall RaySearch ecosystem.   Support customer discovery activities to ensure future solutions address meaningful clinical and operational challenges  Conduct market assessments, competitive analysis, and business case development to support strategic decision-making  Support the development and execution of go-to-market strategies for future product launches  Identify and assess strategic partnership opportunities that support growth objectives  Monitor competitive developments, market access considerations, and industry trends relevant to Medical Oncology  Your Profile  You are commercially minded, strategically driven, and passionate about improving cancer care.  You bring a strong understanding of the Medical Oncology environment and are motivated by the opportunity to help shape a completely new business area for RaySearch. You enjoy working in situations where there is ambiguity, and you are comfortable helping define strategy, build relationships, and create new opportunities from the ground up.  You are equally comfortable engaging with clinicians, healthcare leaders, and business stakeholders, and you have the ability to translate market insights into actionable business recommendations.  Experience & Skills  BSc or MSc in Life Sciences, Healthcare, Nursing, Pharmacy, Medicine, Business, Medical Technology A minimum of 5 years of clinical experience within Medical Oncology, Oncology Nursing, Oncology Pharmacy, Hematology/Oncology, or a related oncology specialty  A minimum of 2 years of experience in business development, strategic marketing, product management, commercial strategy, market development, or a related function  Strong understanding of Medical Oncology treatment pathways, clinical workflows, and healthcare systems  Experience engaging with clinical stakeholders and key opinion leaders  Strong analytical, communication, and stakeholder management skills  Experience working in international and cross-functional environments  Excellent command of English, spoken and written  It is considered a strong advantage if you have experience within:  Medical Oncology  Oncology Drug Development  Precision Medicine  Biomarker-Driven Therapies  Clinical Decision Support Solutions  Oncology Informatics  Healthcare Software  Market Access and Reimbursement  Exposure to pharmaceutical, biotechnology, healthcare software, oncology informatics, or medical technology companies is highly desirable.

Gör skillnad. Varje dag. Är du specialistsjuksköterska eller allmänsjuksköterska med flerårig arbetslivserfarenhet som vill arbeta på en mottagning som präglas av laganda, god kommunikation och hög kompetens? Trivs du med att arbeta såväl självständigt som i team, och alltid med patienten i fokus? Då kan du vara den vi söker! Vi välkomnar nu två sjuksköterskor till vår mottagning på neurokirurgen för arbete med ryggmärgsstimulering. Område neurokirurgi i Lund ingår i Verksamhetsområde (VO) neurokirurgi och smärtrehabilitering vid Skånes universitetssjukhus (Sus). Vi är en av sju neurokirurgiska verksamheter i Sverige och tillgodoser Södra sjukvårdsregionen med högspecialiserad vård. Vi bedriver vård av patienter med skador och sjukdomar i det centrala nervsystemet. Inom verksamhetsområdet finns intensiv-, intermediär pre- och postoperativ vård samt operationssjukvård och mottagningsverksamhet. Neurokirurgen ansvarar tillsammans med smärtrehabiliteringen för ryggmärgsstimulering Spinal Cord Stimulation (SCS) inom Södra Regionen. I dagsläget ingår sjuksköterskemottagningen kring ryggmärgsstimuleringen i smärtrehabiliteringens verksamhet. Den överflyttas nu till neurokirurgen. Med SCS behandling kan verksamheten erbjuda en smärtreduktion till patienter med perifer neuropatisk smärta. En reducerad smärta innebär ett minskad lidande och medför ökad livskvalité för patienter. Behandlingen är ofta livslång och uppföljning görs fortlöpande samt med årliga kontroller. Detta innebär kontinuerlig och återkommande kontakt med patienter i form av operativa åtgärder som inläggning av system, batteribyten, byte av elektroder, programmering, rådgivning, uppföljning med tekniska kontroller, omprogrammering och stöd till patient, samt andra vårdgivare vad gäller hantering av utrustning och behandling. 2 plats(er). ARBETSUPPGIFTER Vi välkomnar nu två sjuksköterskor till vårt ryggmärgsstimuleringsteam! Du är en av två sjuksköterskor i vår ryggmärgstimuleringsverksamhet på Skånes universitetssjukhus (Sus). Du har ett nära samarbete med teamet som består av smärtläkare, neurokirurg och sekreterare. Därtill kommer teamet ha samarbete med en fysioterapeut och en psykolog från smärtrehabiliteringen som är knutna till teamet. I uppdraget ingår att medverka vid SCS:s konferens med remisshantering och vid bedömning/selektion. Du förbereder patienten inför operation på mottagningen med information och teknisk undervisning, deltar vid inläggning av utrustning på operation och gör programmeringsinställningar för en individuellt anpassad behandlingsterapi. Detta görs i samråd med ansvarig läkare. Arbetet på mottagningen innebär hantering av tekniskt system och sedvanligt mottagningsarbete i samarbete med ansvarig läkare. Därtill består arbetet av telefonrådgivning, patientuppföljningar och årliga kontroller, samt kontakt med företagsrepresentanter. Förhållningssättet till patienterna är holistiskt och utifrån ett biomedicinskt psykosocialt perspektiv. Det ingår också att arbeta med hälsorådgivning kring levnadsvanor gällande kost, tobak och alkohol. Uppdraget i SCS-teamet är planerat till 75 procent per sjuksköterska, övrig arbetstid är du i neurokirurgens verksamhet. Tjänsten är främst dagtid på vardagar, den innebär även två helgpass i månaden inom vår slutenvårdsverksamhet. Du får en strukturerad introduktion med bredvid gång och stöd av erfarna kollegor. Dina arbetsuppgifter som sjuksköterska inom Neurokirurgensverksamheten på 25 procent utformas efter verksamhetens behov och din kompetens. KVALIFIKATIONER Vi söker dig som är legitimerad sjuksköterska med behörighet att verka inom svensk sjukvård. Du är allmänsjuksköterska eller har specialistutbildning inom anestesi eller intensivvård eller annan lämplig inriktning. Därtill har du flerårig arbetslivserfarenhet i sjuksköterskeyrket. Vidare är språkkunskaper i svenska motsvarande lägst nivå C1 enligt Europarådets nivåskala ett krav. Vi ser det som meriterande med något av följande: • Erfarenhet av operationsverksamhet • Arbetslivserfarenhet inom ditt specialområde som specialistutbildad • Erfarenhet av arbete med patienter med akut och långvarig smärta, postoperativ vård eller neurokirurgi. • Specialiserad kunskap med vidareutbildning inom smärta • Erfarenhet av arbete med ACT och/eller motiverande förhållningssätt såsom MI • Erfarenhet av rådgivning inom levnadsvanor Vi söker dig som har ett intresse av att arbeta med patienter med långvarig smärta och teknisk utrustning, tycka om att arbeta i team och uppskatta ett omväxlande tempo. Vidare tycker du att det är roligt att utveckla och driva processer framåt, arbeta i komplexa team och är ansvarstagande. Därtill värdesätter vi att du är strukturerad och har förmåga att prioritera i det självständiga arbetet. Du har även ett omsorgsfullt och personcentrerat bemötande. För oss är det en självklarhet att du har förmågan att bemöta såväl patienter som anhöriga, medarbetare och studenter med omtanke och respekt. Vi lägger stor vikt vid personlig lämplighet. I denna rekrytering arbetar vi med löpande urval. Varmt välkommen med din ansökan redan idag! Anställningsform: Tillsvidareanställning. Region Skåne ansvarar för hälso- och sjukvård, kollektivtrafik och en hållbar utveckling i hela Skåne. Vårt högsta beslutande organ är regionfullmäktige, som väljs direkt av invånarna i Skåne. Region Skåne är en värderingsstyrd organisation som arbetar med värderingarna välkomnande, drivande, omtanke och respekt i allt vi gör. Skånes universitetssjukhus (Sus) finns i Lund och Malmö och är landets tredje största sjukhus. På https://www.skane.se/ledigajobb kan du se i vilket skede Region Skånes rekryteringar befinner sig och hur många som har sökt tjänsterna. Om du har skyddade personuppgifter ska du kontakta den kontaktperson som finns angiven i annonsen så att din ansökan blir hanterad enligt särskilda rutiner. När du söker ett jobb hos Region Skåne blir din ansökan en allmän handling enligt offentlighetsprincipen. Uppgifterna behandlas och sparas enligt dataskyddsförordningen (GDPR). Till bemannings- och rekryteringsföretag och till dig som är försäljare: Vi undanber oss vänligen men bestämt direktkontakt med bemannings- och rekryteringsföretag samt försäljare av ytterligare jobbannonser.

Are you a highly capable finance professional who wants to build and manage the financial backbone of a rapidly growing deep-tech and medical technology company? Ascilion is now recruiting a Financial Controller to the company. The position is full-time and based at our headquarters in Kista. At Ascilion we are singularly focused on solving one of medicine’s big challenges: providing real-time access to molecular biomarkers. Ascilion’s proprietary, industry-leading microneedle technology enables quick, reliable, and painless access to molecular biomarkers. Ascilion is entering a phase of significant international growth with substantial investor involvement, increasing reporting requirements, expanding operations, and likely future subsidiaries and / or international sales entities. We already work with strong external partners in bookkeeping and audits, but we now need an internal financial leader who owns the full picture and ensures the company operates at a world-class level financially and operationally. The Financial Controller is a key leadership position responsible for the overall financial management of the company, ensuring the accuracy, integrity, and compliance of our financial reporting. Depending on profile and experience, the role may develop into a CFO position and become part of the senior management team with responsibility for strategic financial planning and board-level reporting. This is an excellent opportunity for you to join a dedicated and highly competent team and a growing company with an exciting journey ahead. If this sounds interesting to you, please contact us using the details below! We will interview candidates continuously for the position and welcome your application today. Responsibilities As our Financial Controller, you will drive the company’s financial success by ensuring reporting accuracy, robust compliance, and strategic control over day-to-day financial operations. You will report directly to the CEO. Your main responsibilities will be to: Own and manage the company’s financial operations and reporting structure Ensure high-quality financial reporting towards investors, board, auditors, and authorities Prepare board material, financial presentations, forecasts, and KPI reporting Coordinate and manage relationships with bookkeeping firms, auditors, banks, investors, and external financial partners Develop and improve internal financial processes, controls, and reporting systems Support international expansion including subsidiaries, sales offices, and cross-border financial structures Drive budgeting, liquidity planning, cash flow management, and long-term financial planning Ensure audit readiness, regulatory compliance, and professional financial governance Support operational scaling of the company together with management and technical leadership Potentially take responsibility for HR administration, contracts, insurance, and internal operational processes depending on profile and interest Your Profile Key qualifications for the position include: Degree in Accounting, Finance, Business Administration, or Economics. Several years of experience in accounting, with a strong focus on financial reporting, accounting, controlling, and compliance Experience working with investors, boards, auditors, and external financial stakeholders Strong understanding of financial reporting, budgeting, forecasting, and corporate governance A deep understanding of Swedish GAAP. Direct experience with US GAAP or IFRS is a competitive advantage Experience from scaling companies, international operations, startups, medtech, deep-tech, or manufacturing environments is highly valuable Experience with subsidiaries, international reporting structures, or US operations is a strong plus Fluency in Swedish and English We are looking for a structured, reliable, and highly detailed-oriented professional who enjoys taking ownership and creating order and clarity in a dynamic and fast-paced environment. As a person, you are analytical, strategic, pragmatic and execution-focused, with a strong ability to work with both details and the bigger picture. You have strong communication and collaboration skills, and you are comfortable operating close to both management and technical teams and presenting financial information clearly to both investors and engineers. Importantly, you thrive in an ambitious, high-performance environment and want to help build a globally significant company, not just manage spreadsheets At Ascilion, you will have the opportunity to make an impact not only in your own area of responsibility, but also on the development of the company as a whole. About Ascilion Ascilion was founded in 2012 with a mission to solve the problem of sampling dermal interstitial fluid in an efficient and pain-free way. A team of engineers with deep experience in MEMS technology and microfluidics took on the challenge of solving what turned out to be a very complex problem. We exist to bridge the worlds of precision engineering and biomarker science, creating innovative microneedle technologies that make dISF accessible, reliable, and painless; empowering researchers, clinicians, and companies to unlock the full potential of health monitoring and diagnostics. We are currently in a very exciting expansion phase where we grow all aspects of the organization from R&D to sales. Our customer base is increasing with numerous close collaborations in Europe, the US, and Asia. Come, join our journey! To learn more about us please visit www.ascilion.com For more information about this position, please contact: Krishan Johansson Haque, PhD Sr Recruitment Consultant, QRIOS Life Science & Engineering T: 0720701653 E: krishan.johansson-haque@qrios.se

About Powerbox PRBX is a leading manufacturer of high-performance power conversion products. We deliver innovative and reliable custom solutions across diverse industries, from medical technology and railway applications to defense and industrial automation. With a commitment to constant development and a focus on building strong client partnerships, Powerbox offers a dynamic and rewarding work environment. Job description We are searching for a highly motivated and driven Key Account Manager to join our team in Stockholm. You will be responsible for developing and managing long term business relationships with our key clients in the Nordics, focusing on power conversion systems and custom solutions. Responsibility and tasks Develop and maintain strong relationships with key clients in the assigned territory. Identify and pursue sales opportunities, driving revenue growth. Lead the entire sales process, from prospecting to closing deals. Collaborate closely with internal teams to ensure timely delivery and customer satisfaction. Provide technical guidance and tailor solutions to meet client requirements. Conduct negotiations and finalize contracts with clients. Manage customer forecast, prepare sales reports and territory updates. Stay abreast of industry trends and competitor activities to inform sales strategies. Qualifications You have: Proven experience as a high-performing Key Account Manager or similar sales role, preferably within the power electronics industry. A deep understanding of power conversion and its applications. Strong negotiation and communication skills, with the ability to build trust and rapport with clients at all levels. Experience successfully managing complex sales cycles (ideally 6 months or longer). Fluency in Swedish and English, both written and spoken. Self-motivated and capable of working independently, yet also a collaborative team player. Excellent organizational and time management skills, with the ability to thrive in a fast-paced environment. Proficiency in CRM software a plus. Willingness to travel within the Nordics for client meetings and industry events. Personality To be successful in the role we believe you: A highly motivated and results-driven individual with a strong work ethic. You possess excellent communication skills and can effectively convey technical information to clients. Are a strategic thinker with the ability to identify opportunities and develop innovative solutions. Thrive in a dynamic and fast-paced environment, adapting quickly to changing circumstances. You are resilient and persistent, able to navigate and persevere through long and complex sales cycles. Are customer-focused, dedicated to providing exceptional service and building long-term relationships. What we offer At Powerbox, we offer a stimulating environment where you'll embark on a journey of professional growth and development. As a Key Account Manager, you'll lead sales efforts in the Swedish market, engage in challenging projects that drive our company's success. We provide competitive compensation packages, including salary, benefits, and incentives, to attract and retain top talent in the industry. With a strong emphasis on work-life balance, we offer flexible arrangements to ensure your well-being both inside and outside of work. Our culture is rooted in excellence, empowering you to excel in your role and contribute to our continuous growth and success. Take this chance to be part of a team dedicated to innovation, collaboration, and excellence. We look forward to hearing from you! Application process Addilon is our partner in this recruitment. Please apply (CV and personal letter in English) via the link. We will fill the position immediately after finding the right candidate. Questions about the position are answered on weekdays between 09.00 am -10.00 am, +46 10 207 43 20.

Are you a reliable, hands-on and driven person who wants to work with manufacturing activities at a rapidly growing medical technology company? Ascilion is now recruiting a Production Operator to the company. The position is full-time and based in our headquartered office in Kista and we are looking for a new colleague to join the Operations group at Ascilion. At Ascilion we are singularly focused on solving one of medicine’s big challenges: providing real-time access to molecular biomarkers. Ascilion’s proprietary and industry leading microneedle technology enables quick, reliable, and painless access to molecular biomarkers. Our dermal interstitial fluid (dISF) sampling platform can be tailored towards virtually any analytical or sensor technology used within products intended for spot measurement or wearables. The Production Operator is a practical role in a fast-moving startup environment where you will participate in purchasing, logistics, manufacturing, testing, and day-to-day operational work connected to advanced medical technology products. The role is well suited for someone early in their career with a strong work ethic and willingness to learn. This is an excellent opportunity for you to join a dedicated, competent and friendly team and a growing company with an exciting journey ahead. If this sounds interesting to you, please contact us using the details below! We will interview candidates continuously for the position and welcome your application today. Responsibilities As a Production Operator, your main responsibilities will be to: Support daily operations including purchasing, goods receiving, incoming inspection, inventory handling, manufacturing, testing, packing, and shipping Manufacture company disposables according to written procedures Perform incoming inspection and microscope-based inspection of microneedle structures Operate semi-automated manufacturing and inspection systems Pack and coordinate shipments to customers worldwide Assemble and test development products Support inventory management, sterilization logistics, and material handling Participate in quality and continuous improvement work, including process flows, routines, and production documentation Your Profile Key qualifications for the position include: Engineering technician, junior engineer, or equivalent practical technical background Previous industry experience is a plus but not required Experience from manufacturing, laboratory work, logistics, electronics, or technical assembly is beneficial Comfortable working with written procedures and documentation in both Swedish and English We are looking for a positive and driven junior professional who is eager to learn and develop. As a person, you are trustworthy, diligent, and practical and appreciate structure, quality, and attention to detail. You enjoy hands-on and experimental work and have strong communication and collaboration skills. You are able to work independently, take responsibility and want to work in a high-ambition and dynamic startup environment. Importantly, you are someone who wants to contribute, improve, and get things done. At Ascilion, you will have the opportunity to make an impact not only in your own area of responsibility, but also on the development of the company as a whole. About Ascilion Ascilion was founded in 2012 with a mission to solve the problem of sampling dermal interstitial fluid in an efficient and pain-free way. A team of engineers with deep experience in MEMS technology and microfluidics took on the challenge of solving what turned out to be a very complex problem. We exist to bridge the worlds of precision engineering and biomarker science, creating innovative microneedle technologies that make dISF accessible, reliable, and painless; empowering researchers, clinicians, and companies to unlock the full potential of health monitoring and diagnostics. We are currently in a very exciting expansion phase where we grow all aspects of the organization from R&D to sales. Our customer base is increasing with numerous close collaborations in Europe, the US and Asia. Come, join our journey! To learn more about us please visit, www.ascilion.com For more information about this position, please contact: Krishan Johansson Haque, PhD Sr Recruitment Consultant, QRIOS Life Science & Engineering T: 0720701653 E: krishan.johansson-haque@qrios.se

CellaVision AB – Lund, Sweden About us CellaVision is a global leader in digital cell morphology within hematology, and our analyzers are trusted in healthcare services around the world. We focus on innovation, working with the latest in programming, digital imaging, and machine learning to provide value to our customers. By joining us, you’ll be part of a creative, skilled team shaping the future of medical technology www.cellavision.com Lead the future of AI-driven diagnostics What if your next role was not only about building advanced AI systems, but also about improving healthcare diagnostics worldwide? At CellaVision, machine learning has been an important part of our technology for more than 30 years. We are now consolidating our expertise into a dedicated machine learning organization, further strengthening capabilities built over decades. We are now looking for a Director Machine Learning to lead this journey. Why this role matters CellaVision is a global leader in digital microscopy for hematology, helping laboratories deliver faster and more accurate diagnoses. Our solutions combine advanced imaging, robotics, and AI-powered analysis to improve patient outcomes worldwide. As Director Machine Learning, you will: Lead and develop a strategically important machine learning organization Work alongside some of the most experienced experts in machine learning and medical image analysis Help shape the future of AI-powered diagnostics in a company where machine learning is already proven, deployed, and used at scale Drive the development of advanced algorithms used in laboratories around the world This is a unique opportunity to combine technical leadership, organizational influence, and meaningful impact on healthcare. Your mission You will lead and develop CellaVision’s machine learning function, with responsibility for both technical excellence and organizational growth. Your responsibilities include: Building, leading, and developing a highly skilled machine learning organization, including a dedicated validation team Driving the design, development, and deployment of advanced machine learning models for medical image analysis Ensuring robustness, performance, and regulatory-grade quality of algorithms Establishing efficient processes, workflows, and ways of working Collaborating cross-functionally to translate clinical and business needs into technical solutions Engaging with universities and research partners to stay up to date with the latest developments in machine learning and AI Ensuring CellaVision remains at the forefront of developments in machine learning and AI As Director Machine Learning, you will play an important role in shaping CellaVision’s long-term machine learning capabilities. You will report to the VP Devices & Software and be part of the Devices & Software division’s management team. Who you are You are an experienced technical leader with deep expertise in machine learning. You enjoy going deep into complex problems while also enabling others to perform at their best. You likely bring: More than 10 years of experience in R&D, including several years in leadership roles Strong expertise in machine learning and AI, ideally within medical imaging Experience delivering machine learning solutions from research to production A track record of building and leading high-performing teams, including senior talent The ability to bridge technical and non-technical stakeholders A structured mindset, with experience working in quality- and regulation-driven environments Experience working in regulated or other quality-critical environments is considered an advantage A strong academic background in applied mathematics, computer science, or a related field A genuine interest in developments within machine learning research and modern AI methods Most importantly, you are motivated by solving meaningful and technically challenging problems together with highly skilled colleagues. Why CellaVision More than three decades of machine learning innovation Technology that contributes directly to faster diagnoses and improved patient care A global company with products used in laboratories in more than 40 countries An engineering-focused environment built on quality, collaboration, and long-term thinking The opportunity to shape and develop a new organizational unit with strong existing expertise and technology Practical details Location: Lund, Sweden Reporting to: VP Devices & Software Travel: Limited Join us At CellaVision, you will combine advanced machine learning, technical leadership, and real-world healthcare impact. If you are ready to help shape the next generation of healthcare diagnostics, we would love to hear from you. In this recruitment process, we are partnering with Radeptus. For any questions regarding the position, please contact Jenny Månsson at +46 703 318 506 or via email at jenny@adeptus.se. Please submit your application here

Do you have deep expertise in fluidics and flow-cell design for analytical instrumentation? Are you excited by the opportunity to drive development from early concepts to production and product care? Join Moleculent and play a key role in developing a cutting-edge life science instrumentation! Moleculent is on a mission to build products that yield new insights into the molecular foundation of human biology. This is a chance to join a focused and dedicated team with extensive experience building successful life-science companies and products. This is a permanent position based in Solna, Stockholm. The position is full-time and based at Moleculent’s headquarters in Solna, Stockholm. Please don’t wait to submit your application. We review candidates on an ongoing basis, and the position may be filled before the final application deadline. Applicants must be eligible to work in Sweden without sponsorship. JOB DESCRIPTION As a Senior Systems Engineer – Fluidics at Moleculent, you will be responsible for flow cells and fluidics design throughout the entire product development life cycle – from concept development and prototyping to design transfer and product care. You will work closely with cross-functional teams and external partners to develop robust and scalable solutions for advanced analytical instrumentation. You will combine hands-on laboratory work with system-level thinking and project leadership responsibilities. Key responsibilities include: Lead flow cell and fluidics design activities, including design, testing, troubleshooting, and verification Drive development of new flow cell concepts and consumable designs Support flow cell production engineering and production troubleshooting Ensure production equipment is maintained, supported, and qualified Participate in and drive instrument-level testing and verification activities Lead or contribute to throughput improvement initiatives Manage system-related project activities and integration work Contribute to early-stage conceptual development for future instrument generations Collaborate closely with R&D, Operations, Product Management, Biochemistry teams, suppliers, and contract manufacturers QUALIFICATIONS To fit the role, you most likely hold an MSc in Technical Biology, Molecular Biotechnology, Material Science, Mechanical Engineering, or a related field. A PhD within a relevant discipline is considered a strong advantage. Fluent written and spoken English is required. You have several years of experience working with fluidics and flow cell development in analytical or life science instrumentation environments. You are comfortable moving between development, testing, production support, and cross-functional collaboration. We believe you have: Experience with fluidics design in analytical systems Experience with consumable prototyping, product development, and transfer to manufacturing Knowledge of plastics and adhesives commonly used in life science or medical technology products Experience from product development of instrumentation within Life Science Hands-on laboratory experience and practical troubleshooting skills Project management or project leadership experience Experience with testing, verification, and troubleshooting activities Good understanding of integrated hardware/software instrumentation systems Nice to have: Experience with flow simulations Experience with requirements engineering and formal verification methodologies Experience working with analytical instruments, in vitro diagnostics systems, or medical devices Experience writing test specifications and verification documentation Swedish language skills You are hands-on, analytical, and solution-oriented, with a strong ability to navigate complex technical challenges. You enjoy working closely with both development and production teams and thrive in collaborative environments where innovation and quality are central. You are structured in your approach while remaining pragmatic and adaptable in a fast-moving environment. You take ownership of your work and enjoy driving projects forward together with others. MOLECULENT We believe innovative biotechnology has enabled massive leaps forward in understanding the composition of tissues and organs. However, the functional understanding of how cells communicate in their native context and form these complex systems has just begun. We develop technology designed to uncover radical new insights into the cellular level of human biology by mapping the communication between cells in human tissue and providing meaningful data. https://www.moleculent.com/ Please note that Moleculent manages the recruitment process for this position. External recruitment agencies are requested to refrain from direct contact with us in this regard.

Vill du bli en viktig del av ett engagerat serviceteam? Vi söker en vårdadministratör som vill vara med och utveckla en verksamhet där kvalitet, patientsäkerhet och samarbete står i centrum! Om oss Aleris Rehab Station har sedan 1987 bedrivit högspecialiserad neurologisk rehabilitering för personer med ryggmärgsskada, MS, stroke och Parkinson, samt rehabilitering av patienter med ortopediska skador, multitrauma och avancerad sårproblematik. Aleris Rehab Station ligger vackert belägen vid Hagaparken i Frösundavik, Solna. Vi är över 200 medarbetare som tillsammans arbetar med att skapa ett bättre, tryggare och friskare liv för våra patienter. Här möts du av ett varmt arbetsklimat där teamkänsla, innovation och respekt för individen genomsyrar allt vi gör. Rollen Tjänsten omfattar sedvanliga arbetsuppgifter för vårdadministratör med fokus på patientnära administration och kvalitetssäkrade vårdprocesser. På Aleris Rehab Station arbetar vi med automatiserad journalföring med stöd av AI, där du som vårdadministratör har en viktig roll i att säkerställa korrekta registreringar samt introducera nya kollegor i arbetssättet. Arbetsuppgifter Vårdregistreringar, kontroller och annan patientnära administration Hantering av inkommande och utgående dokument samt rekvirering av journaler Kvalitetssäkring av automatiserad journalföring och stöd vid introduktion av nya kollegor Stöd i reception vid behov och professionellt mottagande av besökare Deltagande i APT, personalmöten och handledning Aktiv medverkan i förbättringsarbete, verksamhetsutveckling samt intern och extern samverkan Rollen innebär även samarbete med flera professioner och ett aktivt deltagande i verksamhetens utveckling. Vårt erbjudande Som medarbetare på Aleris får du tillgång till en rad olika förmåner som stödjer dig både i arbetsliv och privat. Vi strävar efter att skapa de bästa möjliga förutsättningarna för dig att trivas och utvecklas. Läs mer om våra förmåner här. Utöver detta erbjuder vi: En tydlig och anpassad introduktion Självständigt arbete med eget ansvar Möjlighet till flexibilitet En arbetsplats där engagemang och nya idéer uppmuntras En god arbetsmiljö med korta beslutsvägar och möjlighet att påverka Om dig Du är utbildad medicinsk sekreterare/vårdadministratör och har erfarenhet av arbete inom hälso- och sjukvård. Du har ett professionellt och serviceinriktat förhållningssätt och trivs i en roll med många kontaktytor, där samarbete, struktur och noggrannhet är viktiga delar av vardagen. På Aleris Rehab Station värdesätter vi ett gott bemötande högt – både gentemot patienter och kollegor. Krav Examen som medicinsk sekreterare/vårdadministratör Erfarenhet av vårdregistreringar och patientadministration inom hälso- och sjukvård Goda kunskaper i vårdadministrativa system och journalhantering Mycket god kompetens i journalsystemet Take Care Mycket goda kunskaper i svenska i tal och skrift samt god förståelse för engelska Meriterande Erfarenhet av eller intresse för förbättringsarbete och utveckling av administrativa processer Vana av arbete i verksamheter med många kontaktytor Intresse för verksamhetsutveckling och kvalitetsarbete Vi lägger stor vikt vid dina personliga egenskaper och söker dig som är engagerad, flexibel och ansvarstagande. Du tycker om att samarbeta, bidra med idéer och vill vara en del av en utvecklingsorienterad verksamhet. Anställningsvillkor  Anställningsform: Tillsvidare med 6 månaders provanställning Omfattning: Heltid (på plats) Tillträde: Enligt överenskommelse Lön: Individuell lönesättning Kollektivavtal finns Ansökan Välkommen med din ansökan. Vi rekryterar löpande så vänta inte med att skicka in din ansökan. Vid frågor om tjänsten kan du kontakta rekryterande chef Valeria Rossetti Jakobsson (valeria.jakobsson@aleris.se)

BUILD SOMETHING MONUMENTAL FOR HEALTHCARE! At Tandem Health we’re reimagining healthcare by putting clinicians first. Our platform - designed by clinicians, for clinicians - is built on deep insight into real-world pain points, with intuitive medical notes and workflows that truly support patient care. We’re a fast-scaling health-tech company backed by top investors and expanding globally. We move fast, stay curious, and believe building something that matters starts with an extraordinary team. If you're passionate about impact and innovation, we'd love to meet you! ABOUT THE ROLE At Tandem Health, we're building the clinical co-pilot of the future - one that empowers clinicians, enhances care delivery, and scales impact. As part of our Medical Operations team, you’ll play a pivotal role in ensuring that Tandem is successfully adopted across Norway. You’ll work at the intersection of medicine and technology, bringing clinical insight into how our tools are implemented in real-world clinical settings. From onboarding new users to refining workflows and sharing feedback with the product team, you’ll help ensure Tandem fits seamlessly into the daily realities of patient care. This is a unique opportunity to be part of a mission-driven team transforming healthcare at scale - and to shape how clinicians across Sweden experience and benefit from next-generation tools.   WHAT YOU WILL DO * Guide clinicians through onboarding, training, and day-to-day support via tools like Intercom. * Ensure clinicians are getting the most out of Tandem, solving problems and gathering feedback for continuous improvement. * Build templates and prompts, and contribute to ongoing refinement of Tandem’s AI assistant. * Run live product demos for prospective clients and support commercial efforts. * Log and manage clinical safety incidents and optimise internal operations to scale safely. * Work closely with product, engineering, and commercial teams to ensure smooth rollout and workflow integration. * Represent Tandem at conferences, events, and workshops, sharing our vision with clinicians and stakeholders. WHAT YOU BRING * Clinical experience in a healthcare setting (e.g. general practice, private practice, hospital roles). * Some experience in consulting, corporate, or startup environments. * A passion for technology, AI, and its potential to transform healthcare. * Excellent communication and collaboration skills - comfortable working with clinicians, engineers, and commercial teams. * Strong organisational skills and a process-driven mindset. * A strong sense of ownership and initiative coupled with a proactive and curious approach * Willingness to work flexibly, travel as needed, and step up during critical moments. * Fluency in Norwegian, with the ability to engage confidently with local stakeholders   BONUS POINTS * Familiarity with prompting and large language models (LLMs). * Experience working in a healthtech or SaaS company. * Exposure to regulatory standards in the EU (e.g. clinical safety, digital health compliance). * Experience running implementation projects or customer-facing rollouts. LOCATION We believe great ideas thrive when we connect in person. This is a full-time role based in either Norway or Stockholm in our vibrant HQ in the heart of Stockholm where you will work primarily from our office to collaborate, connect, and build our culture. There will be occasional travel to meet the core team in Stockholm and clinicians across the country as needed. HOW TO APPLY We adopt a continuous selection process, so please make sure to apply with your CV in English. Our interview process consists of 4 stages: 1. Screening interview with Talent Acquisition 2. First interview with our Country Director 3. Follow up interview with some of our Medical Operations team members 4. Working Day - Join us in the Stockholm office for a day to experience our culture firsthand, collaborate with our team, and see how you work in action. BENEFITS * Competitive salary * 30 days per year of paid vacation * Social and team-building activities (off-sites, after works, winter/summer parties) * An opportunity to make a real positive impact in the world of healthcare * Work with some of the best minds in AI, healthcare, and engineering. We review our benefits packages on a regular basis and might modify our benefits from time to time. CULTURE AT TANDEM At Tandem, we move fast, think big, and take ownership. We're a high-performing, diverse team with a shared drive to change the future of healthcare - and we’re just getting started. Our culture is built on action, ambition, and learning. You'll be trusted to take the lead, challenge yourself, and make an impact from day one. We believe real growth happens when you're stretched, supported, and surrounded by smart, passionate teammates who want to win together. Even though we’re spread across countries, we come together often in Sweden for team meetings, social events, and offsites - blending global reach with real human connection. We hire for talent, potential, and attitude - valuing different backgrounds and fresh perspectives. Great ideas come from everywhere, and we’re building a team that reflects the world we want to change. Tandem handles sensitive patient data and will conduct a background check before hiring any candidate.

Gör skillnad. Varje dag. Vi välkomnar dig som söker ett jobb där ingen dag är den andra lik och där just ditt bidrag gör stor skillnad för våra patienter. Tycker du, liksom vi, att det är viktigt med ett gott bemötande och ett professionellt samarbete, kommer du att trivas hos oss. Här får du arbeta i en varierad och utvecklande miljö där engagemang, ansvarstagande och vilja att hjälpa andra står i centrum. Dialys är ett spännande område som är under ständig utveckling, där samspelet mellan medicinsk teknik samt omvårdnad har en stor betydelse. Hos oss får kroniskt njursjuka patienter regelbundet sin bloddialysbehandling. Vi tar även emot patienter med akut njursvikt. För att kunna erbjuda bästa möjliga vård till våra patienter har vi ett nära samarbete mellan sjuksköterskor, undersköterskor, läkare, paramedicinare och medicintekniska ingenjörer. Vår verksamhet är fysiskt uppdelad på två dialysmottagningar och en medicinteknisk ingenjör är placerad på vardera dialysmottagning, med samarbete mellan er. 1 plats(er). ARBETSUPPGIFTER Som medicinteknisk ingenjör hos oss är du ett viktigt stöd till vården. Du utför service och möjliggör insatser som påverkar många. Vi söker dig som ser en glädje i att arbeta med intressant teknik som göra direkt nytta i vården. Du ansvarar för drift och underhåll av våra dialysmaskiner och vattenreningsanläggningar. Arbetet är varierande och innebär allt ifrån handgripligt tekniskt ingenjörsarbete, till förebyggande och akut underhåll. I arbetet ingår också att vara delaktig vid upphandlingar och installation av medicinteknisk utrustning samt ansvara för kvalitetsarbete. Verksamheten ökar sin digitalisering vilket medför att du även arbetar mycket med IT i denna roll. Tjänsten ger dig stora möjligheter till utveckling inom dialysområdet. Hos oss erbjuds du ett omväxlande arbete och en arbetsplats med positiv stämning. Vi arbetar kontinuerligt med att utveckla vår verksamhet och vi erbjuder goda utvecklingsmöjligheter för dig och ditt engagemang. KVALIFIKATIONER Vi söker dig som är utbildad högskoleingenjör inom medicinteknik eller utbildad gymnasieingenjör alternativt annan utbildning/yrkeserfarenhet vi bedömer lämplig för tjänsten. Du som söker har goda kunskaper i svenska och engelska, i såväl tal som skrift. Vidare ser vi även att du har en god verktygsvana då handgripligt tekniskt arbete är förekommande. Vi ser gärna att du har erfarenhet av medicintekniskt relaterat arbete inom dialysverksamhet. Om du tidigare har arbetat med IT, data och elektronik så är det ett plus. Vi ser också det som ett plus att du har erfarenhet från offentliga upphandlingar och projektarbete. Vi lägger stor vikt vid dina personliga egenskaper och söker någon som är nyfiken, prestigelös, bra på att samarbeta, tar ett egenansvar för sin utveckling och som vill bidra till vårt positiva arbetsklimat. I ditt arbete behöver du vara noggrann och ansvarstagande, samt ha förmåga att självständigt planera och genomföra ditt arbete. Vidare är du strukturerad, engagerad, serviceinriktad och ansvarsfull. Arbetet kräver stor hänsyn till verksamheten och fallenhet för service åtagande. Du är van vid att arbeta självständigt samtidigt som det är viktigt att du trivs och fungerar väl med att arbeta i team tillsammans med medarbetare inom både din egen och andra professioner. Planen för dagen kan snabbt förändras om situationer inträffa därför uppskattar vi även egenskaper som flexibilitet och förmåga att hantera oförutsedda händelser. I den här rekryteringen tillämpas löpande urval. Varmt välkommen med dina ansökan, vi ser fram emot att lära känna dig! Anställningsform: Tillsvidareanställning. Varaktighet:, tillträde: Tillträde enligt överenskommelse. Region Skåne ansvarar för hälso- och sjukvård, kollektivtrafik och en hållbar utveckling i hela Skåne. Vårt högsta beslutande organ är regionfullmäktige, som väljs direkt av invånarna i Skåne. Region Skåne är en värderingsstyrd organisation som arbetar med värderingarna välkomnande, drivande, omtanke och respekt i allt vi gör. Skånes universitetssjukhus (Sus) finns i Lund och Malmö och är landets tredje största sjukhus. Sus är ett kunskapsnav för hälso- och sjukvård i livets alla skeden på regional, nationell och internationell nivå. Våra 12 000 medarbetare är med och driver utvecklingen inom universitetssjukhusets tre uppdragsområden: vård, forskning och utbildning. Hos oss får du arbeta i en värderingsstyrd organisation som utvecklar hälso- och sjukvården tillsammans med patienter och deras närstående. Välkommen! På https://www.skane.se/ledigajobb kan du se i vilket skede Region Skånes rekryteringar befinner sig och hur många som har sökt tjänsterna. Om du har skyddade personuppgifter ska du kontakta den kontaktperson som finns angiven i annonsen så att din ansökan blir hanterad enligt särskilda rutiner. När du söker ett jobb hos Region Skåne blir din ansökan en allmän handling enligt offentlighetsprincipen. Uppgifterna behandlas och sparas enligt dataskyddsförordningen (GDPR). Till bemannings- och rekryteringsföretag och till dig som är försäljare: Vi undanber oss vänligen men bestämt direktkontakt med bemannings- och rekryteringsföretag samt försäljare av ytterligare jobbannonser.

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 Overview This role focuses on hands-on support of our medical simulators throughout the customer lifecycle. You will be involved in pre-sale demonstrations, post-sale Installation and training, and ongoing customer education. The position is customer-facing, requires frequent travel, and involves close collaboration with internal teams and regional partners.   This position will be based in Gothenburg, Sweden, but we may also consider candidates based in Stockholm.   Responsibilities Deliver pre-sale product demonstrations to customers, partners, and distributors, often with doctors, clinicians and medical industry professionals. Conduct post-sale training sessions, including on-site and online trainings Support simulator installations, workshops, and customer onboarding activities Serve as a product and application expert, providing guidance on system usage and best practices Participate in regional and international conferences, exhibitions, and customer events Share customer feedback and field insights with Sales, Product, and R&D teams   Your profile We are looking for a dynamic and adaptable professional with experience in clinical or field-based training. Prior clinical experience is highly valued, enabling effective collaboration with healthcare and industry professionals. You thrive in a fast-paced international environment and combine strong technical aptitude with excellent communication, organizational, and training skills.   Qualifications & Experience Educational or professional background in healthcare, life sciences, medical technology, or related fields (e.g., biology, medical sciences, biomedical/medical engineering, nursing, or medicine) Experience in customer-facing roles such as training, clinical support, application support, or education is advantageous Experience working with medical devices, simulators, or other advanced technical systems is considered a strong asset Strong presentation, communication, and instructional skills Technical aptitude with the ability to troubleshoot and resolve system-related issues Excellent organizational and time-management skills Fluent in English; additional languages are an advantage Willingness and ability to travel frequently (approximately 50–60%), often on short notice, primarily within Europe   Personal Attributes Self-driven, reliable, and responsible Customer-oriented with strong interpersonal and relationship-building skills Adaptable and comfortable working in an international environment with changing priorities and schedules Curious, hands-on, and motivated to continuously learn new technologies   Why join us? A meaningful and technology driven mission. Our technology combines the intersection of software and healthcare. A role like nothing you will have experienced. Travel around the world to support global healthcare institutions. We offer trust, autonomy, and career growth.   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.

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!