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Gör det som du älskar, som konsult! Kvalifikationer Vi söker dig med minst två års erfarenhet. Vi ser gärna att du som konsult har god samarbetsförmåga, är noggrann, och ansvarstagande. Arbetsuppgifter Som ögonsjuksköterska hos Almia får du möjlighet att arbeta ute hos våra kunder med varierande arbetsuppgifter inom ögonsjukvård. Du kommer att assistera vid undersökningar, ge patientrådgivning och samarbeta med ögonläkare. Arbetsmiljön är dynamisk och varierar beroende på kund och klinik. Kontakta oss för mer information om detta uppdrag och din karriär med Almia. Finner du tjänsten som Ögonsjuksköterska till Sollefteå intressant är du är varmt välkommen att höra av dig direkt till Amanda Aletto eller någon av hennes kollegor på rekrytering@almia.se eller 08-410 250 50. Vi ser fram emot att höra från dig! Har du redan ett uppdrag men vet en klockren kandidat, tipsa vidare och ta del av en tipsbonus! Tillsammans med din konsultchef på Almia får du skapa det bästa upplägget som passar just dig och dina behov. Vi gör vårt yttersta för att lyssna och förstå vem du är, vad du vill och vad du behöver. Vi vill helt enkelt veta vad som är viktigt för dig. Därför är vi extra lyhörda för vad du har för behov och önskemål när det kommer till uppdragets period, omfattning, geografiskt område samt arbetstider. Det absolut viktigaste för oss är att vi tillsammans hittar ett upplägg som går att anpassa efter ditt livspussel. Personliga egenskaper: Du är en positiv och engagerad kollega som bidrar till en bra arbetsmiljö. Du är flexibel, ansvarsfull och har förmåga att arbeta både självständigt och i team. För att lyckas som konsult är det viktigt att du är prestigelös, lyhörd och trygg i dig själv. Du har du goda kunskaper i svenska och drivs av utmaningar och nya möjligheter. Vi erbjuder dig: Marknadskraftig lön En engagerad konsultchef Fördelaktiga förmånspaket Trygga villkor Tipsbonus Bli en del av Almia-familjen Almia Vårdbemanning är ett rikstäckande bolag med stort hjärta som gör allt för att du som konsult ska trivas och må bra. Tillsammans med dig följer vi dina önskemål och matchar uppdrag efter din erfarenhet. Du kommer alltid känna att du har ett stöd i din närmaste konsultchef, vars viktigaste uppgift är att se till att du mår bra. Hos oss på Almia får du ta del av en varm kultur där varje anställd är unik och får högsta prioritet från oss i form av engagemang, tillhörighet och tillgänglighet. I ditt dagliga jobb som konsult är du en del av ett vårdteam, med allt vad det innebär. Som konsult hos Almia är du också en viktig del av vårt team, och vår gemenskap. Vi håller kontakt, följer dig i uppdragen, finns alltid nära till hands och hjälper dig att lösa de eventuella problem som kan dyka upp längs vägen. Vi ser även till att du får träffa dina Almia-kollegor då och då för att utbyta tankar, tips och erfarenheter. Vi tar hand om varandra, lika självklart naturligt som att du tar hand om andra. Sista svarsdag Vi arbetar med löpande urval och kan komma att tillsätta uppdraget så fort vi hittat rätt person. Skicka därför in din ansökan så snart som möjligt! www.almia.se 08-410 250 50 rekrytering@almia.se
Välkommen till DocCura Vårdcentral! DocCura vårdcentral är en nyetablerad vårdcentral som snabbt har blivit ett uppskattat alternativ för patienter i expansiva Järfälla kommun samt närliggande kommuner. Vi söker dig som vill vara en nyckelperson i ett tvär-professionellt team på vår vårdcentral i Järfälla kommun. Som rehabkoordinator får du vara med från början och forma samverkan, rutiner och rehabiliteringsinsatser – alltid med patienten i centrum. DocCura vårdcentral är en nyetablerad vårdcentral i ett växande område i Järfälla kommun på uppgdrag av Region Stockholm, med målet att erbjuda den bästa vården och tillgänligheten för patienter. Hos oss får du möjligheten att arbeta i en modern och patientfokuserad verksamhet med korta beslutsvägar, teamkänsla och utvecklingsmöjligheter. Om tjänsten: Du ansvarar för att samordna och följa upp individanpassade rehabiliteringsplaner för patienter som är sjukskrivna eller i riskzonen. Arbetet sker enligt Region Stockholms riktlinjer och innefattar: Bedömning av rehabiliteringsbehov Samordning mellan vård, arbetsgivare, försäkringskassan och andra aktörer Journalföring och användning av KVÅ-koder Arbeta nära läkare och psykologer i teamet Vi söker dig som: Är legitimerad hälso- och sjukvårdspersonal, arbetsterapeut eller socionom Har erfarenhet av samordning eller vägledning inom sjukskrivning/rehabilitering Flerårig erfarenhet av rehabilitering och som genomgått Karolinska Institutets kurs "Koordineringsinsatser - att koordinera sjukskrivnings- & rehabiliteringsprocessen (7,5 hp)” eller ha motsvarande kännedom om försäkringsmedicin. Trivs i team, men är också självgående Vill vara med och forma ett vårdutbud från grunden Vi erbjuder: En ny vårdcentral i moderna lokaler i ett expansivt område Engagerat team i uppbyggnadsfas – här gör du skillnad på riktigt Individanpassad introduktion och möjlighet att påverka dina arbetsformer Kontinuerlig kompetensutveckling Ansökan Skicka in din ansökan med CV och personligt brev till ansokan@doccura.se. Urval sker löpande. Vid frågor är du välkommen att kontakta verksamhetschef Victoria Rouzdar via victoria.rouzdar@doccura.se. Välkommen till DocCura Vårdcentral!
Det här är tjänsten för dig som vill göra skillnad och bidra till förbättrad hälsa och livskvalitet för patienter. Vi söker en trygg och erfaren sjuksköterska med ett genuint intresse för äldreomsorgen till vår kvällsjour på Säbo och basala hemsjukvårdsuppdraget. Välkommen till ett härligt team! Om tjänsten Du arbetar tillsammans med en kollega under dina kvällspass. Till största delen kommer du sköta ditt arbete genom telefon med rådgivning, ordinationer, ställningstaganden och dylikt. Ni har tillgång till läkarstöd, bara ett telefonsamtal bort. Att åka ut på patientbesök ingår i tjänsten. De system vi arbetar i är bland andra TakeCare, Appva, Pascal och Lifecare. Vi är flexibla och öppna för önskemål kring tjänstgöringsgrad, tjänsten omfattar mestadels kvällar men går att kombinera med dagpass för att få högre sysselsättningsgrad. Placeringen kan variera mellan Norrtälje/Rimbo. Dina arbetsuppgifter omfattar bland annat: • Ge telefonrådgivning • Göra medicinska bedömningar • Utföra planerade patientbesök och ev. inskrivningar • Utföra dokumentation Om vårt erbjudande: Vi erbjuder friskvårdsbidrag på 5000 kr årligen. Du kan läsa mer om våra förmåner här. Om dig För den här tjänsten behöver du: • Vara legitimerad sjuksköterska • B-körkort och körvana • Goda kunskaper i svenska språket i tal och skrift Det är meriterande om du också har: • Specialistutbildning inom äldrevård eller palliativ vård • Erfarenhet från äldrevård/demensvård • Erfarenhet av telefonrådgivning Du arbetar med omtanke i allt du gör och du tar stort ansvar för ditt arbete. Du har förmåga att prioritera och leda andra vid förändrade omständigheter. Flexibelt och kollegialt samarbete är av stor vikt för dig och något du får stor nytta av i ditt uppdrag hos oss. Som person är du ansvarstagande, självständig och ödmjuk, med en stark förmåga att prioritera dina arbetsuppgifter. Du delar vår värdegrund som bygger på delaktighet, trygghet och respekt. Vi lägger stor vikt vid personlig lämplighet. Om oss Vi är en arbetsgrupp på runt 20 sjuksköterskor inom Tiohundra Säbo som tillsammans arbetar på våra åtta boenden, dagar, kvällar och nätter. Under kvällarna och nätterna har vi även det basala hemsjukvårdsuppdraget. Viktigt för oss är arbetet med patientsäkerhet och personcentrerad omvårdnad, vilket underlättas av att bolaget innehåller både äldrevård och akutvård. Gemensamt för alla våra boenden är att de drivs med engagemang och värme. Tillsammans vill vi erbjuda våra patienter den bästa äldreomsorgen i kommunen, en äldrevård vi alla känner stolthet över. Vi hoppas du vill bli en av oss. Vi är en del av Tiohundra – det kompletta vårdbolaget i Roslagen. 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. Ansök genom att klicka på knappen ”Ansök”. 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. Läs mer om hur det är att jobba hos oss i Region Stockholm
Department of Clinical Sciences We are seeking an clinically active veterinarian with broad experience in small animal practise and a particular interest in anesthesiology. About the position Your primary responsibilities will include responsibility for patients and patient safety in the daily clinical work and supervising students in anaesthesia and analgesia within the university clinics. Participation in the out-of-hours service is also expected. In your day-to-day role, you will be actively involved in the clinical teaching of veterinary students, interns, and residents. You will also provide guidance and support to veterinary nurses. Opportunities to engage in ongoing clinical research are available, and you may also contribute to lecturing, small group teaching, and assessing veterinary students. A crucial aspect of your work will involve advising and collaborating with veterinarians in other disciplines, such as intensive care and in patient care. Regular consultations with veterinarians, including referral veterinarians, are an integral part of this role. Your profile You have veterinary credentials from a university in Sweden or another EU/EEA country or in Switzerland and is eligible to practise veterinary medicine in Sweden. It is a merit, but not a requirement, if you hold credentials as an EBVS® European Veterinary Specialist in Veterinary Anaesthesia and Analgesia (or ACVAA board-certified specialist). Proficiency in English is required, and you either speak a Scandinavian language or are committed to learning Swedish within a time-period of ca 2-3 years. Significant emphasis will be placed on personal qualities. We value a professional approach and expect you to be flexible, appreciate teamwork, and contribute to the smooth operation of the surgical department. About us The Department of Clinical Sciences (KV), including the University Animal Hospital (UDS), serves as the centre for clinical research and education at SLU, Swedish University of Agricultural Sciences. The Swedish veterinary education recently celebrated 250 years. At UDS, veterinary students, veterinarians, and veterinary nurses receive hands-on training, while clinical research is actively conducted. The management team promotes a forward-thinking and supportive environment, encouraging employees to develop their skills and pursue their interests through ongoing professional development. At SLU University Animal Hospital (UDS), education, research, and advanced veterinary care go hand in hand. We train the veterinarians and veterinary nurses of tomorrow and provide first-class care to pets, competition animals, and livestock. We also share knowledge with the public. By combining established knowledge with the latest research results, we are developing the veterinary care of the future. Under one roof, we offer healthcare for horses, dogs, cats, and other small animals. In addition to modern, purpose-built facilities, we have access to advanced imaging diagnostics and a veterinary specialist laboratory. UDS's operations also include an outpatient clinic that travels to stables and farms to examine and treat horses and farm animals. Read more about our benefits and working at SLU by visiting: https://www.slu.se/en/about-slu/work-at-slu/ Location: Uppsala, Sweden Form of employment: Permanent employment. SLU may use 6 months probationary employment. Scope: 100% Start date: As soon as possible according to the agreement Application: Please submit your application before deadline 28 July 2026. You can submit your application by clicking the button below. Please include in your application: a letter of intent, a CV and copies of appropriate degree certificates. Union representatives: https://internt.slu.se/en/my-employment/employee-associations/kontaktpersoner-vid-rekrytering/ The Swedish University of Agricultural Sciences (SLU) has a key role in the development for sustainable life, based on science and education. Through our focus on the interaction between humans, animals and ecosystems and the responsible use of natural resources, we contribute to sustainable societal development and good living conditions on our planet. Our main campuses are located in Alnarp, Umeå and Uppsala, however, the university also operates at research stations, experimental forests and teaching sites throughout Sweden. SLU has around 4,000 employees, 6,000 students and doctoral students and a turnover of over SEK 4,5 billion. We are investing in attractive environments on all of our campuses. We strive to provide a work environment characterised by inclusivity and gender equality, where different experiences generate conversations between people and pave the way for science, creativity and development. Therefore, we welcome applications from people with diverse backgrounds and perspectives.Öppen för alla Vi fokuserar på din kompetens, inte dina övriga förutsättningar. Vi är öppna för att anpassa rollen eller arbetsplatsen efter dina behov.
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! Specialist in surgery/general surgery for permanent position in central Sweden Are you a skilled surgeon / general surgery specialist looking for your next career move? We are supporting a well-established healthcare provider in Sweden in their search for a motivated specialist to join their surgical team. About the role Work in a collaborative, multidisciplinary team with a focus on patient-centered care Manage a diverse mix of elective and acute surgical cases Opportunities to utilize your expertise fully and develop subspecialty skills Why this role is attractive Mentorship and professional guidance from experienced colleagues Regular opportunities for continued professional development Supportive work environment with wellness benefits Who we are looking for Certified Specialist in Surgery / General Surgery Team player who values collaboration across specialties Committed to delivering high-quality, safe surgical care Looking for a professionally rewarding role in a region offering an excellent quality of life What Dignus Medical Offers You: Ongoing support from a recruiter before, during, and after your employment Assistance with Swedish authorization and specialist recognition, if required Help with accommodation and relocation, including support for accompanying family members Access to a free Swedish language course with a private tutor via Teams/Skype Qualifications: EU-recognized specialist certification in surgery Good communication skills in English Willingness to learn Swedish Interested in new opportunities? Contact us to discuss available positions and find a role that fits your professional profile. We look forward to receiving your application! 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.
Vill du göra skillnad – på riktigt? Hos oss i Sollefteå kommun bidrar du varje dag till att samhället fungerar, växer och utvecklas. Vi är nära 2000 kollegor som tillsammans skapar trygghet, service och framtidstro för kommuninvånarna. Här får du mer än bara ett jobb: du blir en del av ett lag som präglas av mod, nytänkande och stolthet. Vi erbjuder goda möjligheter att utvecklas och påverka – och en arbetsmiljö som gör det lätt att hitta balansen mellan karriär och fritid. Som extra bonus får du tillgång till friskvårdsbidrag, fri längdskidåkning på Hallstaberget, gratis bad på flera av våra anläggningar och mycket mer. Och kanske det bästa av allt: du får arbeta i en kommun där storslagen natur möter småstadens charm, där gemenskapen är stark och framtidstron tydlig. Välkommen till Sollefteå – här gör vi skillnad, tillsammans. 1 plats(er). ARBETSUPPGIFTER Sollefteå kommun söker en Medicinskt ansvarig sjuksköterska (MAS) som vill vara med och utveckla en trygg, kvalitetssäkrad och patientsäker verksamhet för våra invånare. MAS tillhör den övergripande ledningen för Vård och social omsorg och hälso- och sjukvårdens ledningsgrupp där du tillsammans med andra arbetar med att förverkliga övergripande mål och visioner. Som MAS har du ett medicinskt ledningsansvar med mandat och ansvar för kvalitetsstyrning och kvalitetskontroll inom kommunal hälso- och sjukvård. Tillsammans med Verksamhetschef för hälso- och sjukvård och Medicinskt ansvarig för rehabilitering (MAR) ansvarar ni för att patienterna får en säker och ändamålsenlig vård och behandling av god kvalité. Du är en nyckelperson i kommunens kvalitets- och utvecklingsarbete och arbetar nära chefer, legitimerade professioner, interna och externa samarbetspartners. Du ansvarar för att patienten får säker och ändamålsenlig hälso- och sjukvård enligt Hälso- och sjukvårdslagen och Hälso- och sjukvårdsförordningen. Detta innefattar ansvar för läkemedelshantering, patientsäkerhet, delegering av vårduppgifter och att rutiner för rapportering fungerar väl. I ditt dagliga arbete kommer du bland annat: -Säkerställa att författningsbestämmelser, rutiner och riktlinjer efterlevs och är kända i verksamheterna -Utarbeta lokala anvisningar och rutiner för kommunal hälso- och sjukvård -Hantera avvikelser i hälso- och sjukvården -Anmäla allvarliga vårdskador till Inspektionen för vård- och omsorg -Skriva och samordna patientsäkerhetsberättelsen -Ansvara för medicintekniska produkter i samråd med MAR -Ge stöd och vägledning till verksamheter i frågor om patientvård, introduktion, utbildning och kompetensutveckling -Leda förändrings- och förbättringsarbeten -Samverka aktivt med kvalitetsledare, verksamhetschefer och ledning för att kvalitetssäkra och utveckla verksamheterna -Utforma tjänsteskrivelser och remissyttranden inom ditt ansvarsområde -Delta i olika dialogmöten, nätverk och samverkansgrupper där du bidrar med din medicinska kompetens. -I krissituationer, vid olyckor eller katastrofer arbetar du tillsammans med övrig ledning för att säkerställa att rutiner och planer finns på plats KVALIFIKATIONER Vi söker dig som har sjuksköterskeexamen och omfattande erfarenhet som sjuksköterska. Kunskap om och erfarenhet från kommunal eller regional hälso- och sjukvård är av stor betydelse. Vi värdesätter god kännedom om gällande lagstiftning inom området, särskilt Hälso- och sjukvårdslagen, Hälso- och sjukvårdsförordningen och den nya Socialtjänstlagen. Erfarenhet av att arbeta med patientsäkerhet, kvalitetsarbete och systematisk uppföljning är meriterande. Vi söker någon som tidigare arbetat som eller tillsammans med MAS eller liknande medicinskt ansvarig roll. Som person ser vi att du är både analytisk och pedagogisk, initiativrik och strukturerad. Du känner stort ansvar för dina uppdrag och deras genomförande. Du trivs med att arbeta självständigt och ta eget ansvar, men uppskattar och bidrar till goda samarbeten genom att vara lyhörd och tydlig i din kommunikation både muntligt och skriftligt. Du är en van användare av Officepaketet och har goda IT-kunskaper. Du behöver vara trygg i att förmedla och presentera information både muntligt och skriftligt i olika forum. Anställningsform: Tillsvidareanställning. Varaktighet:, tillträde: Tillträde enligt överenskommelse . I Sollefteå kommun är ett antal tjänster inplacerade i säkerhetsklass enligt säkerhetsskyddslagen (2018:585). För de tjänsterna ingår säkerhetsprövning i anställningsförfarandet. Registerutdrag: För tjänster inom äldreomsorg, verksamhet för personer med funktionsnedsättning samt verksamhet för barn och ungdomar, ingår kontroll av registerutdrag som en del av rekryteringsprocessen. Blankett för att beställa ett registerutdrag finns att ladda ner från Polisens webbplats: http://polisen.se Observera att vi endast tar emot ansökningar via Offentliga jobb. Första gången du söker ett jobb via Offentliga jobb, registrerar du dig på länken www.offentligajobb.se och skriver in dina uppgifter där. Du bör vara noggrann när du fyller i dina uppgifter, eftersom dina uppgifter ligger till grund för hanteringen. När vi mottagit din ansökan får du en bekräftelse via mejl. Vi strävar efter mångfald och jämn könsfördelning inom Sollefteå kommun. Vi undanber oss vänligt men bestämt att bli kontaktade av annons- och rekryteringsföretag.
Landskrona Omsorg AB är ett helägt kommunalt bolag i Landskrona. Vi erbjuder vård- och omsorgsboende, hälso- och sjukvård, hemtjänst samt stöd och service till personer med funktionsnedsättning. Med mod, uthållighet och handlingskraft sätter vi en stabil grund för våra medarbetare, vi möter våra brukare med nyfikenhet och respekt. För alla som bor här idag. Och för alla som kommer bo här i framtiden. Vi är 1 100 medarbetare som jobbar för att alla i kommunen ska kunna leva trygga och självständiga liv, även när de behöver hjälp. Vi arbetar efter vår värdegrund BRA, där B står för bemötande, R för resultat och A för ansvar. Vår värdegrund ska genomsyra all vår verksamhet och vi ska vara en arbetsplats där du känner arbetsglädje och stolthet. Vi är undersköterskor, stödassistenter, sjuksköterskor, arbetsterapeuter och många, många fler. Några är i början av karriären, andra har många års erfarenhet. Vi kommer från Landskrona, Skåne och hela världen. Tillsammans är vi Landskrona Omsorg. Välkommen! 4 plats(er). ARBETSUPPGIFTER Är du en trygg och engagerad sjuksköterska som vill arbeta med helhetsperspektiv och kvalitet i vården? Vill du vara en del av ett kompetent och stöttande team där du får möjlighet att påverka och utvecklas i din yrkesroll? Som omvårdnadsansvarig sjuksköterska hos Landskrona Omsorg AB ansvarar du för att säkerställa patientsäkerhet och hög kvalitet i vården för patienter inom hemsjukvård, LSS-boende och vård- och omsorgsboende. Dina huvudsakliga arbetsuppgifter inkluderar: • Omvårdnadsansvar - Bedöma, planera, genomföra och följa upp vårdinsatser för patienter med komplexa behov inom kommunal primärvård. • Samverkan och kommunikation - Samarbeta med interna team och externa aktörer (slutenvård, primärvård, ambulans) för att säkerställa en sammanhållen vårdprocess. • Stöd och handledning - Ge vägledning och stöd till omsorgspersonal, anhöriga och andra vårdgivare för att främja kvalitet och trygghet i vården. • Dokumentation och kvalitetssäkring - Säkerställa korrekt dokumentation och rapportering enligt lagar, riktlinjer och patientsäkerhetskrav. • Teknik och medicinteknik - Hantera medicinteknisk utrustning och använda digitala system för vård och administration. Du erbjuds ett stimulerande och varierande arbete där samarbete, engagemang och kvalitet står i fokus och blir del av ett kompetent och stöttande team där samarbete är en självklarhet. KVALIFIKATIONER Vi söker dig som är legitimerad sjuksköterska och som vill arbeta med människor utifrån ett etiskt och professionellt förhållningssätt. Du har utbildning och/eller erfarenhet av: • Omvårdnadsarbete och medicinteknik • Utbildad sjuksköterska (distriktssköterska, specialistsjuksköterska med inriktning mot äldre alternativt allmänsjuksköterska) • Dokumentation och arbete i digitala journalsystem • B-körkort för manuell växellåda är ett krav för tjänsten Du får gärna ha erfarenhet av: • Arbete inom kommunal vård, palliativ vård, slutenvård och/eller primärvård. • Samverkan med andra vårdgivare inom kommunal och regional vård • Bemötande av olika kulturer och de kulturella skillnader det innebär Vi tror att du är en person som: • Behärskar svenska språket flytande, både i tal och skrift • Är trygg i din yrkesroll och har ett gott bemötande • Arbetar strukturerat och tar ansvar • Har god samarbetsförmåga och har lätt för att skapa goda relationer • Är lösningsorienterad och har teknisk förståelse • Har ett genuint engagemang för kvalitet och patientsäkerhet I denna rekrytering ber vi dig att bifoga ditt CV samt besvara ett antal urvalsfrågor. Syftet med urvalsfrågorna är att skapa en effektivare och mer rättvis rekryteringsprocess, där alla kandidater bedöms utifrån samma kompetensbaserade kriterier. För en anställning i Landskrona Omsorg ska du uppvisa utdrag ur belastningsregister i ett obrutet kuvert. Det utdrag du skall beställa heter "Arbete i hemmet med äldre och personer med funktionsnedsättning". Välkommen med din ansökan! Löneform: Månadslön. Anställningsform: Tillsvidareanställning. Varaktighet: Tillsvidare, tillträde: 2026-09-01 Eller enligt överenskommelse. Arbetstid: Schema. 07:00-16:15, 30 minuters rast och flextid Arbetsgivarinformation: https://www.landskrona.se/jobbailandskronastad För att kvalitetssäkra rekryteringsprocessen i Landskrona stad använder vi rekryteringsverktyget Visma Recruit. Därför ber vi dig att skicka in din ansökan via Visma Recruit genom att klicka på ansökningslänken i annonsen. En ansökan till Landskrona stad är en allmän handling och dina personuppgifter hanteras enligt GDPR. Då vi inför denna rekrytering redan tagit ställning till de rekryteringskanaler vi önskar använda undanber vi oss att bli kontaktade för ytterligare erbjudanden om kompetensförmedling samt annonserings- och rekryteringshjälp. Om du som sökande har skyddade personuppgifter, behöver du kontakta rekryterande chef för att få tillgång till urvalsfrågorna. Du skickar din ansökan till HR-avdelningen via post eller lämnar in den i receptionen, ställd till HR-enheten där du också anger vilket referensnummer annonsen har. I din ansökan behöver du ange hur du vill bli kontaktad av rekryterande chef. Din ansökan kommer sekretessmarkeras och bevaras i två år även om du inte blir anställd hos oss. Därefter gallras handlingarna. Du kan läsa mer om hur vi behandlar dina personuppgifter på https://www.landskrona.se/kommun-och-politik/sa-behandlar-landskrona-stad-personuppgifter/.
Department of Clinical Sciences We are seeking a board-certified International specialist (European or American College of Veterinary Surgery (ECVS or ACVS Diplomate) in small animal surgery; alternatively, you hold a recognised national specialist title in small animal surgery. About the position As a specialist in surgery at UDS, you will primarily work in the surgery department, postoperative care unit, and ICU. You will provide clinical services in a broad range of surgery cases; orthopaedics, soft tissue, and neurosurgery cases. You are part of our surgical team, which works with excellent veterinary care, teaching, and research. It is a varied and stimulating everyday life in a round-the-clock operation at Sweden's only university animal hospital. You will support and develop the surgery team, provide guidance and support to veterinary nurses, ensure that the flow through the surgery department is efficient and safe for the patients, supervise and teach students as well as residents and junior veterinarians. You aim to get involved in strategic development and management of the clinic. Participation in the out-of-hours service is also expected. Collaboration with colleagues within your discipline and across the faculty is a part of the role. Opportunities to engage in ongoing clinical research are available, and you may contribute to lecturing, small group teaching, and assessing veterinary students. A crucial aspect of your work will involve advising and collaborating with veterinarians in other disciplines, such as intensive care and in-patient care. Regular consultations with veterinarians, including referral veterinarians, is an integral part of this role. You collaborate with our management team, subject representatives, and specialists with the goal of developing our employees in the discipline. Your profile We are seeking a board-certified International specialist (European or American College of Veterinary Surgery (ECVS or ACVS Diplomate) in small animal surgery; alternatively, you hold a recognised national specialist title in small animal surgery. You have veterinary credentials from a university in Sweden or another EU/EEA country or from Switzerland or other teaching institution with credentials that are accredited by the European Association of Establishments for Veterinary Education (EAEVE) or the American Veterinary Association (AVMA). It is an advantage if you also hold a PhD or have teaching experience. Proficiency in English is required, and you either speak a Scandinavian language or are committed to learning Swedish within a time-period of ca 2-3 years. You are communicative with a strong ability to create and maintain good relationships with customers and colleagues. You have a good ability to involve the surgery team in the daily patient flows. As a veterinarian at the University Animal Hospital, you have a scientific approach and an interest in evidence-based care and are positive about our learning environment. You are interested in teaching and participating in efforts to create good conditions for research. As a person, you are structured, methodical, have good self-awareness, can handle stressful situations well, and have a willingness to contribute to the organization. An out-of-hours service with irregular working hours is something you can manage. In this recruitment, we will place great emphasis on your personal abilities. About us The Department of Clinical Sciences (KV), including the University Animal Hospital (UDS), serves as the centre for clinical research and education at SLU, Swedish University of Agricultural Sciences. At UDS, veterinary students, veterinarians, and veterinary nurses receive hands-on training, while clinical research is actively conducted. The management team promotes a forward-thinking and supportive environment, encouraging employees to develop their skills and pursue their interests through ongoing professional development. At SLU University Animal Hospital (UDS), education, research, and advanced veterinary care go hand in hand. We train the veterinarians and veterinary nurses of tomorrow and provide first-class care to pets, competition animals, and livestock. We also share knowledge with the public. By combining established knowledge with the latest research results, we are developing the veterinary care of the future. Under one roof, we offer healthcare for horses, dogs, cats, and other small animals. In addition to modern, purpose-built facilities, we have access to advanced imaging diagnostics and a veterinary specialist laboratory. UDS's operations also include an outpatient clinic that travels to stables and farms to examine and treat horses and farm animals. Read more about our benefits and working at SLU by visiting: https://www.slu.se/en/about-slu/work-at-slu/ Location: Uppsala, Sweden Form of employment: Permanent employment. SLU may use probationary employment. Scope: 100% Start date: As soon as possible according to the agreement. Application: Please submit your application before deadline 2 July 2026. You can submit your application by clicking the button below. Please include in your application: a letter of intent, a CV and copies of appropriate degree certificates. Union representatives: https://internt.slu.se/en/my-employment/employee-associations/kontaktpersoner-vid-rekrytering/ The Swedish University of Agricultural Sciences (SLU) has a key role in the development for sustainable life, based on science and education. Through our focus on the interaction between humans, animals and ecosystems and the responsible use of natural resources, we contribute to sustainable societal development and good living conditions on our planet. Our main campuses are located in Alnarp, Umeå and Uppsala, however, the university also operates at research stations, experimental forests and teaching sites throughout Sweden. SLU has around 4,000 employees, 6,000 students and doctoral students and a turnover of over SEK 4,5 billion. We are investing in attractive environments on all of our campuses. We strive to provide a work environment characterised by inclusivity and gender equality, where different experiences generate conversations between people and pave the way for science, creativity and development. Therefore, we welcome applications from people with diverse backgrounds and perspectives.
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 are building a future where health and technology move seamlessly together - and we are growing fast. As we prepare for a significant phase of growth, we are looking for an experienced Finance Director to join us. This is a high-impact, hands-on leadership role for someone who thrives in fast-moving startup environments and can quickly bring structure, clarity, and financial discipline during a pivotal stage of growth. You’ll oversee all core finance activities, from managing external accounting partners and financial operations to KPI ownership, forecasting, and fundraising support. Working closely with leadership, investors, and cross-functional teams, you’ll provide the financial insight and operational rigour needed to support Tandem’s ambitious growth plans during this interim period. We’re looking for someone who has been through startup scaling journeys before, including international expansion, evolving processes, and the realities of high-growth businesses. If you enjoy bringing order to complexity, building scalable foundations, and making an immediate impact, we’d love to hear from you. WHAT YOU WILL DO * Lead and develop a growing finance function, overseeing external accounting partners alongside internal finance operations across multiple countries, including bookkeeping, invoicing, and financial controls. * Own key financial KPIs (ARR, user growth, burn rate) and deliver regular, actionable reporting to leadership and investors. * Build and maintain FP&A models, historical data, and financial narratives to support fundraising and board discussions. * Design scalable finance systems and processes to support international expansion and rapid team growth. * Partner cross-functionally with leadership, People, Ops, and Product teams to align financial planning with business goals. * Provide experienced financial leadership during a key growth phase, helping establish the foundations for a scalable long-term finance function. WHAT YOU BRING * Proven experience operating as a senior finance leader within early-stage SaaS B2B companies, ideally in interim, fractional, or high-growth scaling environments. * Strong financial operations and strategic modelling skills, with experience across SaaS metrics (ARR, retention, CAC), FP&A, cash flow management, and investor readiness. * Demonstrated ability to quickly assess, stabilise, and improve finance processes in fast-paced or evolving businesses. * Hands-on, detail-oriented, and comfortable moving fluidly between day-to-day execution and strategic planning. * Clear communicator and collaborative partner, able to distill financial insights into actionable guidance for leadership and investors. * Growth mindset, adaptability, and enthusiasm for helping scaling teams navigate periods of rapid change. BONUS POINTS * Experience supporting international finance operations (multi-country invoicing, compliance, etc.) * Exposure to the health-tech or digital health sectors * CPA, CFA, ACA, ACCA, or equivalent qualifications (not required) * Previous experience in interim, contract, or transformation-focused finance leadership roles 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.
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 You care about things being done properly. Not just documented, but correct, traceable, and defensible. In previous roles, you were likely the person who made sure nothing slipped through the cracks - the one who understood that in regulated environments, details matter because they compound into trust. At Tandem, you’ll bring that mindset to the forefront of one of the most important challenges in modern healthcare: building AI-powered medical software that is not only fast-moving and innovative, but fully compliant with European regulation. As an MDR Compliance Associate, you’ll play a central role in maintaining and organizing the technical documentation behind our software as a medical device (SaMD) products, ensuring documentation stays accurate, up to date, and audit-ready as our products evolve. You'll support change management activities, collaborate closely with product and engineering teams, and help ensure that every update we ship remains compliant with MDR requirements. This is a hands-on role for someone who thrives on structure, takes real ownership, and wants to work close to both product and engineering, making sure our documentation reflects the reality of the product while enabling the team to move fast without compromising quality or compliance. If you get excited about bringing order to complex documentation, working closely with technical teams, and helping build systems that clinicians and patients can trust, we’d love to meet you. WHAT YOU WILL DO * Support on the day-to-day maintenance of MDR technical documentation files (Annex II/III) for our software as a medical device (SaMD) products. * Play a key role in our change management process. When software is updated or improved, ensure the technical file is assessed, updated, and remains compliant with MDR requirements. * Support the maintenance and updating of clinical evaluation documentation, including clinical data analysis, ensuring alignment with MDR requirements and MEDDEV/MDCG guidance. * Work within our traceability tools (Ketryx) and in-house eQMS to keep documentation audit-ready, version-controlled, and up to date. * Collaborate with engineering and product teams to capture design and development outputs and assess the regulatory impact of software changes. * Coordinate documentation updates across teams to ensure our technical files accurately reflect product changes. * Support internal audits and contribute to preparations for notified body assessments. WHAT YOU BRING * 1–3 years of experience in regulatory affairs, legal compliance, or MDR compliance operations * Familiarity with EU MDR requirements, particularly technical documentation (Annex II/III) * A genuine interest in software, AI, and how medical device regulations apply to digital health products * Enjoy working with structured documentation and have a strong eye for detail. You're the type of person who likes keeping things organized, accurate, and easy to follow. * Structured, detail-oriented, and willing to take real ownership of your work. This is a hands-on role in a fast-moving team where the pace is high and the work matters. * Understanding of clinical evaluation processes and clinical data. You will work closely with clinical documentation, so a baseline grasp of clinical evidence and its role in MDR compliance is important. * A high work ethic and drive. We are a startup building regulated AI medical software, and this role requires someone who thrives in an intense environment and is willing to go the extra mile. * Degree in law, biomedical engineering, medicine, or a related field, or equivalent practical experience. * Fluent in English (spoken and written). BONUS POINTS: * Understanding of change management processes for medical device software. * Experience with data analysis or research methodology. * Experience with traceability tools or eQMS platforms. * Comfortable working with LLM-based tools such as Claude and Codex in your daily workflow. * Experience with project management and collaboration tools such as Notion or Linear. * Ability to code or scripting experience. LOCATION We believe the best ideas happen when we’re together. This role is based in our vibrant HQ in the Epicenter building in the heart of Stockholm where you will work primarily from our office to collaborate, connect, and build our culture. 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. Interview with key stakeholder 3. Interview with hiring manager 4. Working Day - Join us in the Stockholm office for a half day to experience our our culture firsthand, collaborate with our team, and see how you work in action. We're currently in the middle of vacation season, which means it may take us a little longer to review applications and get back to you. Thanks for your patience - we're looking forward to reading your application! BENEFITS * Competitive salary & company stock options * 30 days/year of paid vacation * 5,000 SEK wellness allowance (friskvårdsbidrag) plus an additional 6,000 SEK yearly to spend on other health related initiatives * Generous Parental leave top-up for new parents * Private Medical Insurance to stay healthy * Mental health support through our partner Mindler * Pension program * 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.
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 You love solving problems with technology. At your previous job you were the person who really got stuff done, and because you understood how everything worked you were someone people often came to for help. At Tandem, those skills will be applied to problems that really matter - problems that help ensure our healthcare system functions properly. You’ll be designing, implementing, and debugging high-stakes, complex systems together with other engineers who are deeply engaged and care about both our mission and the technology we build. You’ll work across the stack and collaborate closely with multiple teams, contributing to technical decisions, supporting others through collaboration and knowledge sharing, and helping ensure our systems are performant, reliable, and continuously improving. This is a high-impact role where you’ll help shape both the product and the way we build it. You’ll be responsible for writing excellent code, taking ownership of well-defined problem areas, and driving features and improvements from design to production. If you’re excited about building meaningful products and tackling challenging technical problems in a fast-moving environment, we’d love to meet you. WHAT YOU WILL DO: * Design and develop complex systems - from data processing pipelines to APIs and client integrations that are critical to clinician workflows. * Contribute to building and scaling cloud infrastructure to ensure high availability, performance, and security. * Influence technical direction within your team through hands-on work, thoughtful design, and clear documentation. * Collaborate closely with stakeholders, including clinicians and designers, to ensure we're solving the right problems with the right solutions. * Make and contribute to technical decisions across backend and frontend systems, including Python, TypeScript, React, and Kubernetes. * Support and grow other engineers across the team through code reviews, design feedback, and strategic guidance. * Continuously improve engineering practices, tooling, and code quality within your team. WHAT YOU BRING * A strong track record of delivering technical projects end-to-end in a fast-moving product environment. * Solid experience building and deploying scalable backend systems. * Experience working with cloud infrastructure and distributed systems, combined with a strong product mindset — you care about impact, not just code. * A bias toward ownership, proactivity, and collaboration. * Clear and effective communication skills, and the ability to contribute to technical and product discussions. BONUS POINTS * Hands-on experience with LLM-based applications. * Experience working with streaming audio, transcription systems, or real-time media pipelines. * Experience building authentication servers and systems. * Experience with Kubernetes and Azure * Proficiency with modern frontend technologies, especially TypeScript and React. * Participation in open-source projects or technical communities. * Experience in health-tech. LOCATION We believe the best ideas happen when we’re together. This role is based in our vibrant HQ in the Epicenter building in the heart of Stockholm where you will work primarily from our office to collaborate, connect, and build our culture. 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. Technical interviews with some of our Engineering team 3. System Design Interview at our office - Join us in the Stockholm office for a lunch and a Product focused System Design interview to experience our culture firsthand, collaborate with our team, and see how you work in action. 4. Follow-up interview with our CTO & Co-Founder We're currently in the middle of vacation season, which means it may take us a little longer to review applications and get back to you. Thanks for your patience - we're looking forward to reading your application! BENEFITS * Competitive salary & company stock options * 30 days/year of paid vacation * 5,000 SEK wellness allowance (friskvårdsbidrag) plus an additional 6,000 SEK yearly to spend on other health related initiatives * Generous Parental leave top-up for new parents * Private Medical Insurance to stay healthy * Mental health support through our partner Mindler * Pension program * 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.
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! Family medicine specialist career opportunities across Sweden Sweden has a growing demand for specialists in General Practice / Family Medicine within primary healthcare. Through Dignus Medical, a Scandinavian medical recruitment company with more than 20 years of experience, physicians from across Europe can explore long-term career opportunities within Swedish primary care. We collaborate with modern primary care centres across Sweden, from smaller community clinics to larger multidisciplinary healthcare centres. Our role is to help you find a position that matches your professional interests, preferred location and work-life balance. Primary care physicians in Sweden play a central role in the healthcare system and work with a broad variety of cases, long-term patient relationships and close collaboration with other healthcare professionals. Professional Development General practitioners in Sweden work in a clinically focused environment with opportunities to develop areas of special interest. Many clinics also offer opportunities to participate in teaching or supervision of junior doctors, particularly in larger healthcare centres. Relocation and Support Relocating to another country is a major step. Dignus Medical supports you throughout the entire process from the first conversation to being fully established in Sweden. Your personal advisor will assist with: medical licensing relocation planning practical matters related to moving and settling in Our services are completely free of charge for physicians. Support for Your Family Many physicians relocate with their families. We therefore provide guidance regarding schools, childcare, housing and everyday life in Sweden. We can also offer support for partners seeking employment, including opportunities within healthcare where relevant. Language Training To work independently as a physician in Sweden, Swedish language proficiency at C1 level is required. Dignus Medical provides intensive online Swedish language training with experienced instructors. The training is flexible and adapted to your schedule. Language courses can also be offered to accompanying partners and older children to support their integration. Living in Sweden Sweden offers a high quality of life, safe communities and excellent public services. Physicians often appreciate the balance between professional responsibility and personal life, with structured working hours and good opportunities for outdoor activities, sports and family life. Families benefit from high-quality childcare, subsidized preschool and free school meals for children. Requirements We are looking for physicians who: Hold an EU-recognised specialist certification in General Practice / Family Medicine Have good communication skills in English Are motivated to learn Swedish and relocate to Sweden Interested in learning more? We’d love to hear from you. Submit your application or contact us today to explore current openings. Let us help you take the next step in your career as a general practitioner specialist in Sweden! Send your CV and specialist certificate, and we will discuss suitable opportunities within our network of hospitals across Sweden. Dignus Medical will help match your profile with the right position and guide you throughout the entire process. We look forward to receiving your application! 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.
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! Combine meaningful work with a high quality of life Is it time for a change? Are you looking for a better worklife balance, shorter commuting times, and close access to nature without compromising on professional challenge and development? This opportunity may be the next step in your career. We are a recruitment company supporting a well-established healthcare provider in Sweden in their search for a radiologists. The position is based in a scenic and nature-rich region, offering a safe and calm living environment with excellent opportunities for outdoor activities year-round, while still providing access to culture, services, and activities for the whole family. About the role As a specialist in radiology, you will be a key member of a well-functioning multidisciplinary team, working in close collaboration with referring clinicians and other healthcare professionals. The workplace is characterized by a positive working climate, strong collaboration, and a shared commitment to high-quality, patient-centered diagnostics. Radiology services in Sweden are continuously evolving, with an increasing focus on: high-quality and timely diagnostic imaging advanced digital systems and efficient workflows close clinical collaboration and patient safety a sustainable and supportive work environment The department provides a broad range of diagnostic imaging services, including assessment, interpretation, and reporting across multiple modalities, supporting patient care throughout all stages of life. A varied and professionally rewarding position The radiology department handles both scheduled examinations and acute imaging, offering a diverse and stimulating workload. You will have the opportunity to work broadly within radiology or further develop subspecialty interests, depending on your experience and the department’s needs. The role is intellectually demanding and professionally rewarding, with strong opportunities for continuous learning, skills development, and long-term career growth. What the workplace offers In addition to a meaningful and stimulating role, the employer offers strong support for your professional development and well-being: Mentorship or professional guidance from an experienced radiologist Regular opportunities for professional development and continuing medical education A work environment that promotes good health, including a wellness allowance We are looking for you who Are a certified specialist in radiology Value collaboration and enjoy working in multidisciplinary teams Are committed to delivering high-quality diagnostic services Are interested in combining a professionally fulfilling role with a high quality of life What Dignus Medical Offers You: Ongoing support from a recruiter before, during, and after your employment Assistance with Swedish authorization and specialist recognition, if required Help with accommodation and relocation, including support for accompanying family members Access to a free Swedish language course with a private tutor via Teams/Skype Qualifications: EU-recognized specialist certification in radiology Good communication skills in English Willingness to learn Swedish Interested in new opportunities? Contact us to discuss available positions and find a role that fits your professional profile. We look forward to receiving your application! 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.
At the Vitrolife Group, we work every day to unlock the full potential of science and technology to reduce the barriers towards building a family. Together we help our customers and their patients to fulfill the dream of having a baby. Shape the Platform, Enable Domains, Build for Scale We are looking for a Senior Data Engineer to join our Group Analytics enabling team. This is a key role in establishing and evolving our global data platform, with Microsoft Fabric and the Azure ecosystem as the primary technology direction. You will combine hands-on data engineering with architectural responsibility, helping us build scalable, governed, and automated data platform capabilities. The role is central to our ambition to move from fragmented and manually maintained legacy solutions toward a modern, domain-oriented data platform that enables trusted analytics, self service, and future AI/ML use cases. This is an opportunity for someone who enjoys building for scale, setting technical direction, and enabling others through strong engineering standards, reusable patterns, and practical guidance. Your Mission As a Senior Data Engineer, you will help design, build, and mature our global data platform. You will work with Microsoft Fabric, lakehouse and medallion architecture, reusable data pipelines, analytical data models, and modern engineering practices. You will play an important role in enabling a federated, data mesh-inspired operating model, where domain teams can own and evolve their data products within clear technical and governance guardrails. Depending on your profile, you may also take architectural responsibility for selected platform capabilities, patterns, and technical decisions. Experience from other modern lakehouse platforms, such as Databricks, Spark, or PySpark, is highly relevant where it strengthens your ability to design scalable and automated data solutions. What You’ll Do • Help design, build, and evolve our Microsoft Fabric-based global data platform, including scalable pipelines, lakehouse patterns, and analytical data models. • Develop reusable engineering standards, templates, and governed data objects that enable domain teams to build and manage data products. • Apply modern engineering practices such as Git, CI/CD, monitoring, documentation, testing, and infrastructure-as-code principles such as Terraform. • Embed security, access control, GDPR/PII handling, lineage, and metadata requirements into platform delivery. • Work closely with enterprise architects, data engineers, data analysts, data scientists, business stakeholders, and domain teams. • Mentor colleagues and support the modernization and deprecation of legacy BI/DW solutions. What You Bring • Senior-level data engineering experience with strong hands-on delivery, architectural understanding, and ability to design scalable platform solutions. • Strong SQL and Python skills, with Microsoft Fabric experience or transferable lakehouse expertise from Databricks, Spark, PySpark, or Delta Lake. • Experience with production-grade data pipelines, medallion/lakehouse architecture, analytical data modeling, and domain-oriented data design. • Experience with modern engineering practices such as Git, CI/CD, DevOps, monitoring, and preferably infrastructure-as-code principles such as Terraform. • Good understanding of data governance, metadata, lineage, access control, GDPR, and PII handling. • Collaborative mindset, with the ability to create reusable patterns and translate business and analytical needs into scalable technical solutions. Why Join Us? You will be part of shaping the foundation for how data is managed, governed, and used across the organization. This is a chance to help build the platform many data engineers wish they could build from the start: scalable, secure, automated, metadata-driven, and designed for future AI and agent-enabled ways of working. You will influence platform architecture, establish reusable engineering patterns, and help domain teams become more self-sufficient with data. The role contributes directly to the shift from fragmented legacy solutions toward a trusted global data platform for analytics, self-service, and future AI/ML capabilities. You will join an enabling analytics team with a clear ambition: to make data more accessible, reusable, and reliable across the business. Please note that this role is based in Valencia or Gothenburg. Applications will be reviewed on an ongoing basis, so please submit your application as soon as possible. Vitrolife Group is a global provider of medical devices and genetic services. Based on science and advanced research capabilities, we develop services and products for personalized genetic information and medical device products. We support our customers by improving their clinical practice for the patient's outcome of fertility treatment. We are currently approximately 1 100 colleagues worldwide, with headquarters in Gothenburg, Sweden. Vitrolife Group's products and services are available in more than 110 countries through our own presence in 30 countries and a network of distributors. Vitrolife Group is a sustainable market leader and aims to be the preferred partner for IVF-clinics by providing superior products and services with the vision of fulfilling the dream of having a baby. The Vitrolife share is listed on Nasdaq Stockholm.
Are you a qualified general nurse looking for professional growth and new life experiences? We offer numerous exciting opportunities for nurses who are interested in moving to Norway, a country known for its high-quality healthcare system, balanced work-life culture and beautiful natural landscapes. Your role: Providing holistic care to patients, addressing their medical, hygienic and social needs. Monitoring patients’ vital signs and keeping records of their health progress. Administering medications and treatments as prescribed by doctors. Performing blood draws and other routine medical procedures. Collaborating with a multidisciplinary team to deliver optimal care. Offering emotional support and clear communication to patients and their families. Working in both hospital and home care settings, adapting to each patient’s individual needs. Qualifications: Hold a valid nursing authorization from an EU country. Have previous work experience as a nurse, with a preference for those who have experience in hospitals or community care settings. Be proficient with basic computer skills, necessary for modern healthcare environments. Speak and write English fluently. Candidates must also be motivated to learn Norwegian. Hold a bachelor’s degree in nursing (BSN). A driver’s license may be required for certain home care positions. Personal qualities: Strong communication skills and the ability to work well in a team-oriented environment. A responsible, structured, and flexible approach to patient care. The ability to remain calm and perform under pressure, handling stressful situations with a professional attitude. Respect for patients’ individual needs and a compassionate approach to their care. A strong desire to move to Norway and integrate into Norwegian society, bringing your family along for a rewarding experience. A genuine passion for nursing, combined with a clear understanding of your professional responsibilities and limitations. The ability to prioritize tasks and maintain a solution-oriented mindset. What we offer: Competitive salary packages and pension plans. A permanent employment opportunity in a supportive and friendly environment. A clear path for professional growth and development. Free online Norwegian language courses with a private tutor to ease your transition. Full assistance with obtaining Norwegian nursing authorization. Comprehensive support with relocation logistics, including help with accommodation, schools, and childcare for your family. Guidance from professional headhunters with 19 years of experience, who will assist you throughout the entire process. Why choose Norway? Norway is consistently ranked as one of the best countries in the world for quality of life. Our healthcare system is publicly funded, providing patients with excellent care while offering healthcare professionals a structured and rewarding work environment. Nurses in Norway benefit from clear career progression, strong support from interdisciplinary teams, and the ability to spend quality time with each patient, contributing to better health outcomes. In addition to professional growth, moving to Norway offers a chance to experience a high standard of living, with clean air, a focus on outdoor activities and a family-friendly environment. If you see yourself thriving in this role and want to explore the possibilities of working in Norway, we encourage you to contact us. We look forward to guiding you through the next steps in your journey!
At the Vitrolife Group, we work every day to unlock the full potential of science and technology to reduce the barriers towards building a family. Together we help our customers and their patients to fulfill the dream of having a baby. Shape the Platform, Enable Domains, Build for Scale We are looking for a Senior Data Engineer to join our Group Analytics enabling team. This is a key role in establishing and evolving our global data platform, with Microsoft Fabric and the Azure ecosystem as the primary technology direction. You will combine hands-on data engineering with architectural responsibility, helping us build scalable, governed, and automated data platform capabilities. The role is central to our ambition to move from fragmented and manually maintained legacy solutions toward a modern, domain-oriented data platform that enables trusted analytics, self service, and future AI/ML use cases. This is an opportunity for someone who enjoys building for scale, setting technical direction, and enabling others through strong engineering standards, reusable patterns, and practical guidance. Your Mission As a Senior Data Engineer, you will help design, build, and mature our global data platform. You will work with Microsoft Fabric, lakehouse and medallion architecture, reusable data pipelines, analytical data models, and modern engineering practices. You will play an important role in enabling a federated, data mesh-inspired operating model, where domain teams can own and evolve their data products within clear technical and governance guardrails. Depending on your profile, you may also take architectural responsibility for selected platform capabilities, patterns, and technical decisions. Experience from other modern lakehouse platforms, such as Databricks, Spark, or PySpark, is highly relevant where it strengthens your ability to design scalable and automated data solutions. What You’ll Do • Help design, build, and evolve our Microsoft Fabric-based global data platform, including scalable pipelines, lakehouse patterns, and analytical data models. • Develop reusable engineering standards, templates, and governed data objects that enable domain teams to build and manage data products. • Apply modern engineering practices such as Git, CI/CD, monitoring, documentation, testing, and infrastructure-as-code principles such as Terraform. • Embed security, access control, GDPR/PII handling, lineage, and metadata requirements into platform delivery. • Work closely with enterprise architects, data engineers, data analysts, data scientists, business stakeholders, and domain teams. • Mentor colleagues and support the modernization and deprecation of legacy BI/DW solutions. What You Bring • Senior-level data engineering experience with strong hands-on delivery, architectural understanding, and ability to design scalable platform solutions. • Strong SQL and Python skills, with Microsoft Fabric experience or transferable lakehouse expertise from Databricks, Spark, PySpark, or Delta Lake. • Experience with production-grade data pipelines, medallion/lakehouse architecture, analytical data modeling, and domain-oriented data design. • Experience with modern engineering practices such as Git, CI/CD, DevOps, monitoring, and preferably infrastructure-as-code principles such as Terraform. • Good understanding of data governance, metadata, lineage, access control, GDPR, and PII handling. • Collaborative mindset, with the ability to create reusable patterns and translate business and analytical needs into scalable technical solutions. Why Join Us? You will be part of shaping the foundation for how data is managed, governed, and used across the organization. This is a chance to help build the platform many data engineers wish they could build from the start: scalable, secure, automated, metadata-driven, and designed for future AI and agent-enabled ways of working. You will influence platform architecture, establish reusable engineering patterns, and help domain teams become more self-sufficient with data. The role contributes directly to the shift from fragmented legacy solutions toward a trusted global data platform for analytics, self-service, and future AI/ML capabilities. You will join an enabling analytics team with a clear ambition: to make data more accessible, reusable, and reliable across the business. Please note that this role is based in Valencia or Gothenburg. Applications will be reviewed on an ongoing basis, so please submit your application as soon as possible. Vitrolife Group is a global provider of medical devices and genetic services. Based on science and advanced research capabilities, we develop services and products for personalized genetic information and medical device products. We support our customers by improving their clinical practice for the patient's outcome of fertility treatment. We are currently approximately 1 100 colleagues worldwide, with headquarters in Gothenburg, Sweden. Vitrolife Group's products and services are available in more than 110 countries through our own presence in 30 countries and a network of distributors. Vitrolife Group is a sustainable market leader and aims to be the preferred partner for IVF-clinics by providing superior products and services with the vision of fulfilling the dream of having a baby. The Vitrolife share is listed on Nasdaq Stockholm.
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.
About the position As a Global Regulatory Specialist, you will join our client's global Quality & Regulatory Affairs function and play a key role in ensuring that medical devices and mounting systems comply with regulatory requirements across international markets. You will become part of a central regulatory team based in Stockholm, supporting a global organization that operates in more than 80 countries and holds a market-leading position within assistive communication solutions. The role combines operational responsibilities with strategic influence. While maintaining existing regulatory processes, you will also support the organization by interpreting regulatory changes, providing expert guidance, and ensuring continued market access for the company's products. Key responsibilities: Maintain and improve technical documentation, including Annex II & III documentation and EU Declarations of Conformity. Coordinate product registrations and device listings with regulatory authorities, including the FDA, Authorized Representatives, and distributors. Support regulatory compliance activities related to EU MDR Class I products and FDA 510(k)-exempt Class II devices. Review device classifications and assess regulatory implications across global markets. Coordinate internal and external audits and support audit readiness activities. Monitor changes in global regulatory requirements and communicate their impact throughout the organization. Collaborate closely with Product Development, Quality, Operations, and other cross-functional teams to ensure regulatory compliance throughout the product lifecycle. This is a highly collaborative global role with frequent interaction with colleagues across Europe, North America, Asia, and Australia. While most collaboration takes place virtually, occasional international travel may occur, primarily within Europe. We are looking for someone whoHolds a Bachelor's degree in Regulatory Affairs, Life Sciences, Electrical Engineering, Electronics, or a related field. Has at least five years of experience working within Medical Device Regulatory Affairs. Has solid hands-on experience with EU MDR (Class I) and FDA Quality System Regulations (QSR). Has experience working with regulatory systems, document management tools, QMS platforms, technical documentation, and regulatory audits. Is comfortable interpreting complex regulatory requirements and translating them into practical guidance for different stakeholders. Communicates fluently in English, both verbally and in writing. Experience working with embedded systems, IEC 62304, EU MDR Class II/III products, or additional languages such as German is considered highly meritorious. We believe you areOur client place great emphasis on personal qualities, as success in this role depends on your ability to work collaboratively across a global organization while maintaining high regulatory standards. You are analytical, structured, and patient, with a genuine interest in understanding evolving regulations and staying up to date with industry developments. You enjoy reading, interpreting, and applying complex regulatory documentation and are comfortable working independently while supporting stakeholders throughout the business. You are confident in communicating regulatory requirements and able to influence others through facts and expertise. Rather than seeking a managerial position, you enjoy being the subject matter expert that colleagues rely on when navigating regulatory challenges. Curiosity and a willingness to continuously learn are highly valued, as regulations continue to evolve across global markets. About the partner company Our client is a global MedTech company headquartered in Stockholm and a world leader within assistive communication solutions. Every day, their products empower people with disabilities to communicate, connect with others, and live more independent lives. With approximately 1,400 employees worldwide, the company operates across multiple international markets and develops innovative medical devices used both in healthcare environments and at home. Their products hold a leading global market position, and regulatory compliance plays a critical role in ensuring continued market access across different regions. The Quality & Regulatory Affairs function is centrally located in Stockholm and collaborates closely with colleagues across Europe, North America, Asia, and Australia. You will join an experienced international organization where expertise, collaboration, and continuous learning are highly valued. About the employment This is a consulting assignment with employment through OIO. The assignment is expected to run for 6-12 months, with excellent opportunities for a permanent position with the client if both parties are satisfied. Scope: Full-time Start: August 2026 (for the right candidate, some flexibility is available) Location: Stockholm, Östermalm (hybrid, 1-3 days per week in the office) Working hours: Primarily office hours with flexible working arrangements Salary: Fixed monthly salary Apply today! Submit your application as soon as possible, as we review candidates continuously and the advertisement may close before the recruitment process is completed. About OIO Our passion is helping people find the right role and workplace. At the same time, we understand that choosing your next career move is an important decision. That's why we dedicate ourselves to getting to know both our candidates and their ambitions throughout the recruitment process. We believe that people have the greatest opportunity to reach their full potential when they're in the right environment. Through fair employment terms, close leadership, and continuous support, we actively contribute to your engagement and professional development. We are as picky as you are.
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.
Plusfamiljen är ett familjeägt assistansbolag som i närmare 20 år har stöttat människor med funktionsvariation att leva livet fullt ut – på sina egna villkor. Hos oss möter du värme, engagemang och en kultur där vi sätter både kunder och medarbetare först. Vårt uppdrag är att skapa en personlig och kvalitativ assistans där omtanke, professionalitet och engagemang går hand i hand. Att arbeta hos oss innebär att bli en del av något större – vi gör skillnad för människor som behöver det allra mest. Personal Care Assistants for a 16-Year-Old Girl Living in Bromma We are currently looking for a Personal Care Assistant to support an active 16-year-old girl who lives with her wonderful family in Bromma, Stockholm. As a Personal Care Assistant, you will play an important role in creating a safe, supportive, and enjoyable everyday life based on her individual needs and abilities. You will provide active support in daily activities, play, and communication, while also assisting with all aspects of personal care, transfers, and mealtimes. To be a good match for our client, you should be a positive, warm, calm, reliable, attentive, and patient person. You are proactive, able to read different situations, and comfortable working independently. We also appreciate someone who is creative and enjoys coming up with new activities and experiences. As our client is very active, it is essential that you do not have any physical limitations that would prevent you from keeping up with her daily activities. We are looking for someone who wants to make a meaningful difference in another person's life over the long term. You should be responsible, compassionate, and responsive to the needs of others. To apply for this position, you must: Be at least 18 years old. Be able to provide a criminal record extract. Provide two relevant references. At the request of our client, we are only accepting applications from female candidates. As the family has a dog, applicants must not have a dog allergy. Position Details The position begins in early August and offers approximately 80% employment. Working hours vary and include: Morning shifts: 2–4 mornings per week (7:00 AM–9:00 AM) Evening shifts: 4:00 PM–9:00 PM Weekend shifts with varying hours:Daytime: 9:00 AM–2:30 PM Evening: 2:30 PM–9:00 PM Additional hours are available during school holidays. Flexibility is appreciated, as there may occasionally be a need to cover extra shifts. What We Offer Many of our employees have been with us since our company was founded in 2006, something we are very proud of. We want our employees to enjoy their work and feel that what they do truly makes a difference. As a Personal Care Assistant, you play an invaluable role in another person's life—and often in the life of an entire family. As part of our team, you will receive: A dedicated contact person—your manager—who will provide practical guidance and ongoing support. A collective bargaining agreement, ensuring both your current and future employment security. Occupational insurance and a wellness allowance. Training and support whenever needed. A fixed hourly salary. Holiday pay and evening/weekend supplements in accordance with the collective bargaining agreement. We warmly welcome your application! To learn more about us and why you should choose Plusfamiljen as your employer, please visit our website at www.plusfamiljen.se. The application deadline is 31 August, but positions may be filled before this date. If you have any questions, please contact the Client Manager at alexander@plusfamiljen.se.
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