Sökresultat för "Medical Documentation"

Gör skillnad. Varje dag. Söker du ett betydelsefullt och flexibelt arbete med en rad varierande arbetsuppgifter? Är du intresserad av egna ansvarsområden utöver de vardagliga sysslorna? Då kan den här tjänsten vara något för dig. Varmt välkommen till oss på vuxenpsykiatrin i Kristianstad! Verksamhetsområde (VO) vuxenpsykiatri Kristianstad bedriver specialistpsykiatri med cirka 350 medarbetare och vänder sig till vuxna från 18 år. Inom verksamhetsområdet bedrivs såväl heldygns- som öppenvård, Vårt upptagningsområde är fem kommuner i nordöstra Skåne. Vi är måna om att ha ett gott samarbete med kommunerna, vilket vi upprätthåller genom samverkansmöten och gemensamma vårdplaneringar. Öppenvårdsmottagningen i Kristianstad är placerad inom gångavstånd till Centralsjukhuset Kristianstad. Vi har ett nära samarbete där vi hjälps åt och arbetar med patienterna i fokus. Idag är vi cirka 80 medarbetare på mottagningen, varav nio medicinska sekreterare och två administratörer. Vi har även ett välutvecklat samarbete med psykiatriska akutmottagningen, heldygnsvården och andra externa samarbetspartners. 1 plats(er). ARBETSUPPGIFTER Vi söker dig som är redo för nya utmaningar och vill bli del av ett härligt gäng som hjälper och stöttar varandra! Som medicinsk sekreterare består ditt arbete till största delen av att organisera och strukturera det administrativa arbetet på mottagningen. I teamet samarbetar du med olika personalkategorier och medverkar aktivt till förbättring av rutiner, arbetssätt samt utveckling av enheten. Arbetsuppgifterna innefattar journalskrivning via MedSpeech i Melior, schemaläggning, registreringar i Pasis samt remiss- och teamkonferenshantering. I din roll har du viss patientkontakt med telefonpass samt hantering av inkomna ärenden via 1177. Du är ett stort stöd för dina kollegor arbetar även i ett nära samarbete med läkare och övrig vårdpersonal. Därutöver finns det möjlighet till egna ansvarsområden såsom Mina planer, Callguide med flera. När du börjar får du en introduktion, mentor och bredvidgång anpassad efter dina behov så din kompetens tas tillvara i vårt team. Vi erbjuder möjlighet till hemarbete, en dag per vecka. KVALIFIKATIONER Vi välkomnar dig som har en godkänd utbildning inom Hälso- och sjukvårdsadministration 80p KY/400p YH alternativt motsvarande utbildning som medicinsk sekreterare. Därtill har du goda kunskaper i medicinsk terminologi och goda kunskaper i svenska språket i såväl tal som skrift. Vi ser det som meriterande om du har god datorvana samt kunskaper i Melior, MedSpeech och/eller Pasis. För att trivas hos oss tror vi att du uppskattar en omväxlande arbetsplats lika mycket som vi gör. Ett spännande, variationsrikt och utvecklande arbete tilltalar dig. Du arbetar serviceinriktat och har ett flexibelt förhållningssätt där du snabbt kan ställa om när det behövs. Därtill har du god samarbetsförmåga och tycker om att arbeta i tvärprofessionella team. Givetvis arbetar du efter Region Skånes värderingar. Då vi är måna om att hitta rätt person för tjänsten lägger vi stor vikt vid personlig lämplighet. Som en del av den lämplighetsprövning, inför beslut att erbjuda arbete, kan det komma att göras en kontroll ur misstanke- och belastningsregistret. Läs mer här om när en kontroll kan bli aktuell: https://www.skane.se/jobb-och-utbildning/jobba-hos-oss/att-jobba-i-region-skane/villkor-och-formaner/#418025 I denna rekrytering tillämpar vi löpande urval. Varmt välkommen med din ansökan, vi ser fram emot att lära känna dig! Anställningsform: Tillsvidareanställning. Varaktighet:, tillträde: Tillträde enligt överenskommelse. . Region Skåne finns till för att alla som bor i Skåne ska må bra och känna framtidstro. Genom gränslösa samarbeten och omtanke skapas de bästa förutsättningar för ett hälsosamt liv inom näringsliv, kollektivtrafik, kultur och hälso- och sjukvård i Skåne. Tillsammans gör vi livet mera möjligt. Psykiatri, habilitering och hjälpmedel är den näst största förvaltningen med verksamheter runt om i hela Skåne. Vi har ett brett uppdrag där många olika kompetenser tillsammans ger våra patienter den bästa vården och omsorgen. Med nyfikenhet och stort intresse satsar vi också på utveckling och forskning. Uppdraget inom psykiatri är att bedriva specialiserad vård i den offentligt drivna barn-, vuxen- och rättspsykiatrin. Habiliteringen bedriver habilitering och rehabilitering inom den offentligt drivna barn-, ungdoms- och vuxenhabiliteringen. Hjälpmedel har i uppdrag att hantera hjälpmedel som föreskrivs till patienter i Skåne. Inom förvaltningen finns också syn-, hörsel och dövverksamhet och ungdomsmottagningarna i Skåne. På https://www.skane.se/ledigajobb kan du se i vilket skede Region Skånes rekryteringar befinner sig och hur många som har sökt tjänsterna. Till bemannings- och rekryteringsföretag och till dig som är försäljare: Vi undanber oss vänligen men bestämt direktkontakt med bemannings- och rekryteringsföretag samt försäljare av ytterligare jobbannonser.

Välkommen till Sundsvalls kommun! Inom Barn- och utbildningsförvaltningen möter våra cirka 3 000 medarbetare tillsammans cirka 14 000 barn och elever på fler än 100 förskolor och skolor runt om i kommunen varje dag. Varje barn och elev i Sundsvalls kommuns förskolor och skolor ska kunna utvecklas, lära sig och nå sina mål efter sina egna förutsättningar. Varje elev ska kunna lämna skolan med vilja, kunskap och goda förutsättningar att möta vuxenlivet och framtiden. Din nya arbetsplats Barn- och utbildningsförvaltningen i Sundsvalls kommun söker nu en skolläkare till Elevhälsans medicinska insats. Tjänsten är en utökning av verksamheten och erbjuder dig möjligheten att göra verklig skillnad för barns och ungas hälsa, utveckling och lärande. Som en del av elevhälsan arbetar du tillsammans med skolsköterskor, skolpsykologer, logopeder och övrig skolpersonal för att skapa goda förutsättningar för elevers hälsa och måluppfyllelse. Elevhälsans medicinska insats är HBTQI-certifierad och präglas av samverkan, kvalitet och utveckling. Du blir en del av ett professionsnätverk med kommunens övriga skolläkare och skolsköterskor där regelbundna möten, handledning och yrkesspecifik kompetensutveckling ingår som en naturlig del av arbetet. Så här bidrar du i rollen som Skolläkare Som skolläkare arbetar du främst hälsofrämjande och förebyggande, men också åtgärdande utifrån elevernas behov. Du utgår från de styrdokument som reglerar verksamheten, bland annat skollagen, hälso- och sjukvårdslagen samt Socialstyrelsens riktlinjer. I rollen kommer du bland annat att: bidra med medicinsk kompetens i elevhälsans tvärprofessionella arbete stödja elevernas utveckling mot utbildningens mål samverka med skolsköterskor, skolpersonal, vårdnadshavare och externa aktörer genomföra medicinska bedömningar och konsultationer arbeta med hälsofrämjande och förebyggande insatser på individ-, grupp- och organisationsnivå dokumentera i det digitala journalsystemet PMO delta i verksamhetens kvalitetsutveckling och utvecklingsarbete. Mottagningsarbetet sker på kommunens skolor i nära samarbete med skolsköterskorna. Tjänsten är i huvudsak förlagd på plats, med möjlighet till viss administrativ distansarbete efter dialog med chef. Tjänsten är en tillsvidareanställning. Omfattningen kan diskuteras och vara 100 procent eller annan överenskommen tjänstgöringsgrad, exempelvis 75 eller 50 procent. Din kompetens och erfarenhet Vi söker dig som är legitimerad läkare med specialistkompetens inom: allmänmedicin pediatrik, eller barn- och ungdomspsykiatri. Du har goda kunskaper i svenska samt grundläggande kunskaper i engelska. B-körkort är ett krav och du har erfarenhet av att arbeta i digitala journalsystem. Det är meriterande om du har erfarenhet av arbete som skolläkare och fördjupad kunskap inom områden såsom: tillväxt och utveckling psykisk hälsa vaccinations- och smittskyddsfrågor långvariga sjukdomstillstånd och funktionsnedsättningar specifika skolsvårigheter hälsofrämjande arbete i skolmiljö lagstiftning som styr skola och elevhälsa. För att trivas och lyckas i rollen ser vi att du är självständig och trygg i dina medicinska bedömningar. Du arbetar regelmedvetet och har god förståelse för de lagar och riktlinjer som styr verksamheten. Vidare är du stabil, flexibel och har lätt för att samarbeta med olika professioner. Du kommunicerar tydligt och har ett inkluderande förhållningssätt där du värdesätter människors olika bakgrunder och förutsättningar. Vi lägger stor vikt vid personlig lämplighet! Om rekryteringsprocessen Vid begäran ska läkarlegitimation och intyg om specialistkompetens kunna uppvisas. För anställning krävs även ett godkänt utdrag ur belastningsregistret. Bra att veta Lön: Månadslön/timlön Individuell och differentierad lönesättning tillämpas Villkor: Löneersättningar utöver månadslönen följer tillämpligt kollektivavtal. Centrala kollektivavtal finns på Sveriges Kommuner och Regioners hemsida, www.skr.se Kollektivavtal: HÖK-OFR Hälso- och sjukvård Förmåner: För mer information om förmåner och villkor inom Sundsvalls kommunen: https://sundsvall.se/kommun/jobb-och-foretagande/jobb-praktik-och-ideellt-arbete/kommunen-som-arbetsgivare/formaner?ae=förmÃ¥ner Är du intresserad av att läsa mer om Sundsvall? Klicka in på www.sundsvall.se eller är du intresserad av hur det vore att bo och arbeta i Sundsvall kan du läsa mer på www.nykommun.se/kommun/sundsvall/ Vid begäran skall betyg/examensbevis/studieintyg/lärarlegitimation som styrker att du har rätt kvalifikationer för tjänsten lämnas in. Tjänsten tillsätts under förutsättning att inte övertalighet uppkommer inom annan del av kommunen som gör att den tillsätts den vägen. Vi verkar för en drogfri arbetsmiljö och drogtest kan förekomma vid nyanställning av personal. Vi tillämpar rökfri arbetstid. I Sundsvalls kommun gillar vi olika och välkomnar medarbetare med olika bakgrund. Vi värnar om det värde som jämn könsfördelning samt mångfald tillför våra verksamheter och arbetar för att våra arbetsplatser ska vara tillgängliga för alla. För att kvalitetssäkra rekryteringsprocessen i Sundsvalls kommun samt möjliggöra god kommunikation med våra sökande ber vi dig söka tjänsten genom länken i denna annons. Är du även intresserad av att arbeta som räddningstjänstpersonal i beredskap/deltidsbrandman, klicka på länken: https://www.rtjmedelpad.se/om-oss/jobba-hos-oss/raddningstjanstpersonal-i-beredskap-rib Varmt välkommen med din ansökan! Vi undanber oss alla erbjudanden om annonsering- och rekryteringshjälp i samband med denna annons.

Hos oss i Region Dalarna får du ett meningsfullt arbete där du kan göra skillnad. Tillsammans arbetar vi för ett hållbart Dalarna med utvecklingskraft i länets alla delar. Om verksamheten Vill du arbeta på en stor klinik i ständig utveckling - med patienten i fokus? Nu söker vi en medicinsk sekreterare som vill bli en del av vårt administrativa team. Kirurgkliniken i Falun bedriver både planerad och akut verksamhet inom öppen- och slutenvård. Vi tar emot patienter inom flera specialistområden, bl a akutkirurgi, urologi, övre- och nedre gastrokirurgi, kärlkirurgi, plastikkirurgi, bröst- och endokrinkrirugi och onkologi. Kliniken består av tre slutenvårdsavdelningar, tre öppenvårdsmottagningar (kirurgi, onkologi och bariatrisk mottagning) och ett administrativt team. Arbetsuppgifter Arbetsuppgifterna för denna tjänst kommer främst att finnas på vår bariatriska mottagning och på vår kirurgmottagning. Som medicinsk sekreterare hos oss har du en central roll i verksamheten. Du arbetar nära kollegor från flera professioner och bidrar till struktur, kvalitet och utveckling i det dagliga arbetet. Arbetsuppgifterna omfattar bland annat: Medicinsk dokumentation Diagnoskodning Receptionsarbete på bariatrisk mottagning Utskick av kallelser på bariatrisk mottagning Tidbokning på bariatrisk mottagning Remiss- och posthantering Väntelisthantering Registrering i nationella kvalitetsregister Telefonservice Tjänsten erbjuder varierande arbetsuppgifter och goda möjligheter att utvecklas i din yrkesroll. Vi söker dig som: Är positiv, engagerad och lösningsfokuserad Har god samarbetsförmåga, kommunikationsförmåga och bidrar till gott arbetsklimat Är noggrann och ansvarstagande Kan arbeta både självständigt och i team Har en positiv inställning till att ta dig an nya arbetsuppgifter och bidra till utvecklingen av våra arbetssätt. Har god kommunikationsförmåga och ett gott bemötande. Kvalifikationer Du har någon av följande utbildningar: Medicinska sekreterarprogrammet, 120 hp Vårdadministrativa programmet, 180 hp Medicinsk sekreterare (YH), 400 p 1-årig eftergymnasial vårddokumentationsutbildning Du har även: Goda kunskaper i svenska språket Goda kunskaper i medicinsk terminologi Goda allmänna IT-kunskaper Meriterande: Erfarenhet av arbete i Cosmic samt av diagnos- och åtgärdsregistrering. Stor vikt läggs vid personlig lämplighet. AnsökanHar du skyddade personuppgifter ska du inte ansöka via systemet, utan kontakta rekryterande chef direkt Vi tar interna referenser på nuvarande och tidigare anställda i Region Dalarna På Att söka jobb hos oss - Region Dalarna kan du läsa mer om Region Dalarna som arbetsgivare, vår värdegrund, arbetsmiljö, förmåner samt vilka kontroller som görs inför anställning Vi har gjort vårt medieval och avböjer kontakt från sälj- och rekryteringsföretag Kontakter fritext Fackliga kontaktuppgifter Fackförbund - Region Dalarna

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! Dignus Medical connects family medicine specialists with long-term GP jobs across Sweden. We specialize in matching your medical qualifications and personal preferences with clinics and healthcare providers that value your contribution and support your professional development. We are now seeking specialists in family medicine/general practice for permanent positions in primary care centers located in southwestern Sweden. The clinics are well-established and work with clear structures, stable patient lists, and predictable schedules. The position focuses on daytime work with continuity of care and collaboration within a multidisciplinary team. Work environment You will work closely with nurses, physiotherapists, psychologists, and other healthcare professionals. Digital systems support documentation, referrals, and follow-up, allowing more time for clinical work. Patient care covers all age groups and includes both acute and long-term medical conditions. Location and lifestyle The area offers proximity to the sea, open landscapes, and towns with good infrastructure. Housing options are varied, commuting times are short, and access to schools, services, and leisure activities is strong. The location suits physicians who want balance between professional life and everyday living. What is included Permanent employment in public or private primary care Competitive salary and regulated working hours Relocation assistance for you and your family Swedish language training Support throughout licensing, recruitment, and relocation Requirements EU-recognized specialist qualification in family medicine or general practice Good English skills Willingness to learn Swedish Structured and patient-oriented  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 in Sweden! You can also register your CV (https://dignusmedical-en.recman.page/login) or sign up for our newsletter (https://www.dignusmedical.no/en/sign-up-for-newsletter/) to stay updated on future opportunities.

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! Join a long-term ENT position on a beautiful Swedish-speaking island belonging to Finland, located between Sweden and mainland Finland.  The island offers a peaceful, family-friendly environment with about 30,000 inhabitants, clean sea air, and an exceptional work-life balance. Role overview A clinical, on-site specialist ENT position with broad responsibility for both adult and pediatric patients. The work environment is supportive, well-equipped, and designed for stable professional development. Requirements EU-recognized specialist certification in ENT/Otolaryngology Minimum 3 years of post-specialization experience Broad independent competence, including pediatric ENT Experience with routine and complex ENT diagnostics and surgery Strong communication and teamwork skills Willingness to learn Swedish Clinical scope and workload Approximately 10 outpatient visits per day. Most common diagnoses are benign otologic, rhinologic, and throat conditions. No thyroid cases. Malignancies are referred to mainland university hospitals. Approximately 50% of patients have an audiological diagnosis. Typical surgical procedures include tonsillectomy, tympanostomy tube insertion, septoplasty, and FESS. Facial surgery for cutaneous malignancies is performed. No on-call duties. Operating theatre time 1–2 days per week. Work conditions Competitive salary in euros, adjusted individually by experience Standard working hours: 38–38.5 hours/week Excellent work environment in a calm, scenic location Regular professional development opportunities What the hospital offers Stimulating clinical work in a safe, tranquil island setting Supportive team and high-quality working conditions Strong focus on work-life balance What Dignus Medical provides Dedicated recruiter support before, during, and after relocation Full relocation assistance: accommodation, travel, family support, school applications Free personalized Swedish language training (4–6 hours/week, online with tutor) Assistance with documentation and practical matters Fully arranged study visit to the clinic and local area, including travel and accommodation Ready to embrace a new professional adventure and a beautiful lifestyle? Apply now! 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! Ophthalmologist in a Unique Archipelago Environment Have you considered changing jobs but have not quite found that extra something? Are you looking for a workplace where work-life balance truly goes hand in hand? We are currently seeking a Specialist in Ophthalmology with a few years of experience to join a unique archipelago environment, where you will have the opportunity to work clinically with a primary focus on outpatient care. We are looking for someone who: Is a certified Specialist in Ophthalmology. Has broad experience with both adult and pediatric patients. Is able to work independently in a broad role that includes outpatient consultations, minor surgical procedures, management of diabetes-related eye conditions, and injections. Enjoys working independently and taking significant responsibility, while also having strong communication skills and the ability to collaborate well with colleagues. Requirements EU-recognized specialist certification in Ophthalmology. Minimum 3 years of post-specialization experience. Broad independent clinical competence, including pediatric ophthalmology. Experience with routine and advanced ophthalmological diagnostics and procedures. Strong communication and teamwork skills. Willingness to learn Swedish. What the hospital offers: A stimulating workplace with an excellent working environment in a unique archipelago setting. Regular opportunities for professional development. Attractive employment conditions and working hours that promote a healthy work-life balance (38.25 hours per week). If you have a family and school-aged children, some of the best schools in the Nordic region are available locally, along with excellent childcare services. In the event of relocation, we provide assistance with housing, finding schools and childcare for accompanying children, as well as support in finding employment for an accompanying partner. If you are ready for a new challenge in an inspiring environment where quality of life and professional pride are highly valued, we look forward to receiving your application. You can also register your CV or subscribe to our newsletter to stay updated on future opportunities. What Dignus Medical provides Dedicated recruiter support before, during, and after relocation Full relocation assistance: accommodation, travel, family support, school applications Free personalized Swedish language training (4–6 hours/week, online with tutor) Assistance with documentation and practical matters Fully arranged study visit to the clinic and local area, including travel and accommodation Ready to embrace a new professional adventure and a beautiful lifestyle? Apply now! 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.

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

We pull medical technology from the future to solve human health.   Authorised by governments around the world to assess medical AI, we remove unnecessary delays from every regulatory approval we do so patients get devices from the future, today. We are proud to count the world’s most ambitious companies building medical technology as customers. You will be joining a team with product-market fit, flowing data, and exponentially growing revenue. ABOUT THE ROLE Scarlet’s Quality Team ensures that innovative medical device companies meet the highest regulatory standards. We support cutting-edge healthtech through efficient, high-quality QMS audits. We’re expanding our auditor pool and are looking for part-time/contractor lead auditors who can independently deliver audits in line with Scarlet’s standards, approach, and culture. This role is suited for auditors who fulfil the relevant criteria to be authorised as a Lead Auditor in a Certification or Notified Body under ISO 13485, EU MDR, and UK MDR. You will work flexibly, supporting audit delivery as part of Scarlet’s notified body activities. YOUR RESPONSIBILITIES * Conduct remote audits of medical device manufacturers’ Quality Management Systems under ISO 13485, EU MDR, and UK MDR. * Provide clear, structured audit documentation and evidence-based conclusions. * Contribute to consistent, high-quality audit experiences aligned with Scarlet’s audit methodology and values. REQUIRED QUALIFICATIONS & EXPERIENCE * Education * Bachelor’s degree in: * software engineering * computer science * physics or biophysics * biology or microbiology * chemistry or biochemistry * electrical, electronic, mechanical engineering or bioengineering * human physiology * medicine * pharmacy * Professional experience * Minimum 4 years of experience in the medical device industry * Minimum 2 years of experience auditing or managing QMSs under: * ISO 13485 * EU MDR and/or UK MDR * Preferred: Practical experience working with software. * Auditing experience * Prior work with notified bodies or accreditation bodies as a Lead Auditor * Technical experience * Experience with software medical devices (SaMD) is strongly preferred * Working knowledge of relevant standards, such as: * ISO 14971 * IEC 62304 * IEC 82304 * Cybersecurity WHAT WE’RE LOOKING FOR * Strong regulatory judgement — you are confident in interpreting and applying regulatory requirements. * Consistency & quality focus — you care deeply about audit quality and repeatability. * Clear communicator — you explain findings and requirements clearly and constructively. * Independent & reliable — you can deliver audits with minimal oversight * Aligned mindset — you are open to adopting Scarlet’s values, audit methods and tooling. ENGAGEMENT MODEL * Consultant auditor role * Fully remote * Flexible scheduling, subject to audit demand and availability INTERVIEW PROCESS * Introductory call with Emily (45 min) * Auditor competence & regulatory interview with a Scarlet auditor (45 min) * Case study with Johan * Complete a case study (maximum 60 min) * Present the case study (30 min) * References * Offer & onboarding

Do you want to develop embedded software for medical devices that improve and save lives? Nexer Engineering is looking for Embedded Software Developers for assignments within the MedTech industry in Sweden. The focus is on embedded software development in regulated environments, with strong emphasis on product quality, patient safety, risk management, and compliance with medical device standards. Your role You will work throughout the embedded software development lifecycle, contributing to the development of safety-critical medical devices and systems. Responsibilities include: Developing and maintaining embedded software for medical devices Participating in software architecture and technical design activities Working with software verification, validation, and unit testing Contributing to risk management activities throughout the development process Supporting regulatory compliance and software documentation activities Collaborating closely with system engineers, quality teams, and cross-functional development teams Ensuring compliance with applicable medical device standards and development processes Your profile Proven experience in embedded software development Experience from the MedTech, Medical Device, Life Science, or other highly regulated industries Strong programming skills in Embedded C and/or C++ Experience developing software for embedded systems Understanding of software development in safety-critical or regulated environments Experience with software verification, validation, and testing activities Experience working throughout the complete software development lifecycle Ability to work in multidisciplinary product development teams Nice to have Experience working according to IEC 62304 Knowledge of medical device development processes and regulatory requirements Experience with risk management activities in product development Experience working with quality management systems in regulated environments Experience supporting audits, certifications, or regulatory submissions Swedish language skills Experience working within Swedish MedTech organizations Why Nexer Engineering? At Nexer Engineering, you will have the opportunity to work with innovative MedTech companies and contribute to products that have a direct impact on people's health and quality of life. We offer long-term assignments, strong technical communities, and opportunities to develop your expertise within embedded software, safety-critical systems, and regulated product development. Apply If you have experience in embedded software development and MedTech environments, and want to work with advanced products in a highly regulated industry, we would like to hear from you.

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.   What if your attention to detail helped a surgeon perform better — and a patient recover faster?   At Surgical Science, we build the simulators that train surgeons before they ever step into an operating room. Our haptic feedback devices, anatomical models, and instrument simulators are used by healthcare professionals across the globe to sharpen their skills in a safe, controlled environment. The stakes are real — and so is the impact of getting quality right.   We're looking for a QC Engineer to join our Quality Control team at our production facility in Gothenburg, Sweden. You will work at the heart of our manufacturing operations — where precision meets purpose.   What you'll actually do Own end-to-end QC test plans: analyze product requirements and design detailed test cases that cover functional, integration, regression, and system scenarios Validate surgical instrument simulators, anatomical models with sensors, and haptic feedback devices — making sure every unit that leaves our facility meets the highest standards Calibrate measurement equipment and simulator components to maintain accuracy across the production line Perform acceptance testing on incoming components and vendor-supplied parts Conduct production line quality checks and sign off on systems meeting specification Dig into complex defects — trace root causes, document findings, and work with production and development to resolve them Participate in requirements reviews, bringing the QC lens early in the product lifecycle Maintain and improve test documentation, calibration procedures, and QC processes   What you need to bring 2–5 years of hands-on QC testing experience, ideally in a hardware/software environment Solid knowledge of QC testing methodologies and test documentation standards (STD/STP/STR) Experience with calibration procedures and measurement equipment Proficiency in quality management tools such as Dynamics and iAuditor Comfortable working in both Windows and Linux environments Strong written and spoken English — you'll collaborate across teams and time zones A sharp analytical mind and the ability to manage multiple priorities without dropping the ball This role is on-site at our Gothenburg, Sweden facility   Even better if you have Background in medical devices, simulators, or similar hardware/software industries Previous QC experience at a company with a comparable product complexity Familiarity with full product development lifecycles in a regulated environment   Where this can take you The QC Engineer role is a real foundation for growth. You could develop into a Senior QC Engineer or take on a team lead position as we scale. Our cross-functional setup means you'll build deep relationships across production, R&D, and software — opening doors to specialized paths in quality systems, validation engineering, or product development.   You'll also work with colleagues across Sweden, the US, and beyond, giving you exposure to international ways of working in a company that's been at the forefront of medical simulation for over 25 years.   Life at Surgical Science 🌍 Truly global environment — we're a team of 10+ nationalities united by a shared mission 🏥 Work that matters — every simulator we build contributes to safer patient outcomes 🤝 Collaborative culture grounded in respect, curiosity, and perseverance 📈 A growing company with real opportunities to develop your career 🔬 Work with cutting-edge simulation technology that's backed by 400+ scientific publications   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.

Are you passionate about quality, contamination control, and medical device manufacturing? We are looking for a Cleanliness & Sterility Assurance Engineer to join our team and support the cleanliness and sterility assurance of dental implant products manufactured at our sites in Karlskoga, Sweden, and Yorba Linda, USA. In this role, you will play a key part in ensuring compliance with regulatory requirements and industry standards while contributing to the safety and quality of products that improve patients' lives worldwide. Key Responsibilities As a Cleanliness & Sterility Assurance Engineer, you will: Define validation studies related to microbiological, physical, and chemical cleanliness for new equipment and equipment modifications. Lead and execute cleanliness process validations for new and updated manufacturing equipment. Develop and implement cleanliness monitoring activities in collaboration with the Contamination Control Manager. Maintain and update contact material mapping documentation. Establish and maintain procedures, templates, and best practices to ensure standardized cleanliness validation and monitoring processes. Support biological and microbiological safety strategies across the organization. Coordinate and manage external testing activities with approved laboratories and vendors when required. Collaborate with cross-functional teams to support continuous improvement and regulatory compliance initiatives. Qualifications and Experience To succeed in this role, you should have: A Master's degree (MSc) or equivalent in Biotechnology, Biomedical Engineering, Microbiology, Toxicology, Biology, Chemistry, or another relevant scientific discipline. At least 5 years of experience within the Medical Device industry or a comparable regulated environment. Strong knowledge of contamination control, cleanliness assurance, and applicable regulatory standards, or the ability to quickly develop expertise and work independently with limited supervision. Experience with relevant standards such as ISO 13485 and ISO 11137-1 & 2. A solid understanding of manufacturing processes and process validation methodologies. Strong expertise in statistical analysis and interpretation of technical data. Excellent communication skills, both written and verbal. Fluency in English. Swedish language skills are considered an advantage. A structured, analytical, and problem-solving mindset.

About the Role As a Global Regulatory Specialist, you will join our Quality & Regulatory Affairs team to help ensure our medical devices and mounting systems meet global regulatory requirements. Please note: This is a hybrid role with 1–3 days per week onsite at our Stockholm office in Östermalm, especially during onboarding. Occasional international travel (10–20%) may be required and will be communicated in advance. In this role you will: Streamline regulatory processes and set a roadmap in collaboration Product & Development, QA, and Operations teams. Coordinate with internal and external auditors to support audit readiness. Review device classifications and regulatory challenges across markets. Maintain and update technical documentation (Annex II & III) and declarations of conformity, including EU Declaration of Conformity, in alignment with the associated technical documentation. Coordinate establishment of registrations and device listings with the FDA, Authorized Representatives, and Importers/Distributors. Support product registrations and market access activities (EU MDR Class I, FDA 510(k)-exempt Class II). Monitor regulatory changes and communicate implications to relevant teams. What We’re Looking For We are looking for a structured and collaborative regulatory professional who enjoys solving problems with a logical approach, works autonomously while contributing to strategic initiatives, and thrives in a dynamic, cross-functional environment. We’re looking for a detail-oriented and analytical professional with: A bachelor’s degree in Regulatory Affairs, Life Sciences, Electrical-Electronics or a related field. At least 5 years of experience in medical device regulatory affairs with hands-on experience with EU MDR (Class I) and FDA QSR. Experience with regulatory systems, document control tools, and QMS platforms and exposure to technical documentation, internal and external audits for regulatory compliance Strong organization, coordination and communication skills to engage auditors and communicating with stakeholders across functions and levels. Ability to break down complex regulatory topics clearly for both technical and non-technical stakeholders. Proficiency in both spoken and written communication in English. Ideal candidates will bring: Familiarity with embedded systems and experience with IEC 62304. Experience with EU MDR (Class II/III).

Velora Bemanning söker legitimerade sjuksköterskor till uppdrag inom kommunal primärvård i Skåne. Arbetet omfattar hemsjukvård och insatser i kommunala verksamheter, där du utför sedvanliga sjuksköterskeuppgifter och samarbetar med andra yrkesgrupper inom vård och omsorg. Arbetsuppgifter Arbetet innefattar sedvanliga sjuksköterskeuppgifter inom kommunal primärvård, exempelvis: Medicinska bedömningar och omvårdnadsinsatser Läkemedelshantering och uppföljning Samarbete med omsorgspersonal, läkare och andra professioner Dokumentation och journalföring i aktuella verksamhetssystem Planering och uppföljning av patientinsatser i hemsjukvård Kvalifikationer Legitimerad sjuksköterska Erfarenhet av arbete inom kommunal primärvård är meriterande Goda kunskaper i svenska i tal och skrift Omfattning 100 % Arbetstider Dag/kväll/Natt/Helg Om Velora Bemanning Velora Bemanning är ett bemanningsföretag inom hälso- och sjukvård som samarbetar med verksamheter över hela Sverige. Vi erbjuder trygga uppdrag, personlig kontakt och konkurrenskraftiga villkor. Ansökan Är du intresserad av uppdraget? Skicka in din ansökan eller kontakta Velora Bemanning för mer information.

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 Tandem’s AI assistant empowers empowers social workers by generating relevant documentation (journalanteckningar, utredningar enligt IBIC, BBIC) directly from conversations. We are now looking for a Social Worker (socialsekreterare) to join our team in Sweden, with a focus on social services. This is a hybrid role combining project delivery, customer onboarding, and commercial support, with additional scope to shape how our product and go-to-market approach evolves for municipalities. This role is ideal for someone who became a social worker because they wanted to make a real difference, and who now wants to scale that impact through technology. WHAT YOU WILL DO * Lead onboarding and implementation projects for municipal social services customers, ensuring a smooth and successful rollout. * Act as a trusted advisor to customers, helping teams adopt new ways of working and realise value quickly. * Tailor Tandem’s product setup, workflows, and templates to the needs of different social services teams and municipalities. * Work closely with Product and Engineering to translate customer needs into product improvements and new features. * Help shape Tandem’s positioning, messaging, and marketing approach for the social services segment. * Support the Sales team in strategic customer conversations, demos, and key deals by bringing domain expertise. * Deliver user training sessions and ongoing support to ensure high engagement and confidence among users. WHAT YOU BRING * Qualified Social Worker / Socialsekreterare with experience working in social services. * Strong intrinsic motivation. You entered this field to help people and make a difference. * Tech-savvy and curious about how digital tools can improve how social workers work. * Experience working with digitalisation, systems implementation, operational development, or process improvement within a municipality. * Strong project management skills. * Commercial mindset and confidence supporting customer conversations. * Excellent stakeholder management skills, with the ability to build trust with Tandem users, as well as senior decision-makers. * Proactive, resourceful, and willing to go beyond what is expected to get things done. * Comfortable in a fast-moving startup environment where priorities evolve quickly. * Fluency in Swedish and strong communication skills in English. 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: * Screening interview with Talent Acquisition (Ellie) * First interview with our MedOps Lead (Jenny) * Second interview with our Country Manager (Roy) * Working Day — Join us in the Stockholm office for a day to experience our culture firsthand, collaborate with our team, and see how you work in action. 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.

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

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! Please Note: As we enter the summer vacation period, responses to applications will be delayed throughout July. We appreciate your patience while the team takes a well-earned break. We'll be back in full force from August! ABOUT THE ROLE Tandem Health is building technology that helps clinicians work more effectively, safely, and sustainably. As we scale, we want our support experience to be fast, reliable, and increasingly automated. Today, much of our clinician support is handled manually, with trained clinicians and internal teams responding to questions through Intercom. We are looking for a Technical Customer Support Lead to improve this. In this role, you will leverage the latest developments in AI to build a tech-enabled customer support function that is as automated as possible, while still maintaining excellent clinician satisfaction and clear human escalation paths when needed. You will own and improve our support setup in Intercom, creating better triage, automation, documentation, routing, and escalation processes. Your work will help clinicians get faster, higher-quality support, while giving our Engineering and Medical Operations teams more time back. This role is based in Stockholm and requires strong Swedish and English language skills. You will support clinicians in Sweden as well as other markets, including the UK. WHAT YOU WILL DO * Build an AI-enabled first line of support for clinicians, using Intercom and other tools to automate common questions and workflows. * Own and improve our Intercom setup, including inbox structure, workflows, bots, macros, tagging, routing, and reporting. * Create a clear triage and escalation system so support issues are prioritised and routed to the right team. * Identify recurring support themes and turn them into automation, help centre content, playbooks, or product feedback. * Work closely with Product & Engineering and Medical Operations teams to resolve issues and reduce manual support load. * Build and maintain support documentation, internal guides, clinician-facing content, and troubleshooting workflows. * Define when support should be automated, when a human should step in, and when issues should escalate. * Track support performance, including response times, resolution times, automation rate, escalation rate, and clinician satisfaction. WHAT YOU BRING * Experience in technical support, customer operations, support operations, product operations, or a similar role. * Strong interest in AI and automation, with excitement about applying new tools to real operational problems. * Experience working with Intercom or a similar customer support platform. * A technical mindset: you can investigate issues, understand product behaviour, and work effectively with Product and Engineering. * A systems mindset: you do not just want to answer the same question repeatedly; you want to build a better support system. * Strong written and verbal communication skills in Swedish and English. * Good judgement around when to automate, when to involve a human, and when to escalate. * Comfort creating documentation, workflows, playbooks, and support processes from scratch. * A strong customer focus and care for delivering a high-quality clinician experience. BONUS POINTS * Experience building AI-powered or highly automated support workflows. * Experience with Intercom Fin, Zendesk AI, Ada, Decagon, Sierra, ChatGPT-based workflows, or similar tools. * Experience in healthcare, clinical operations, regulated products, or other safety-sensitive environments. * Familiarity with support analytics, product feedback loops, bug reporting, or QA processes. * Experience helping a support function move from manual and reactive to structured, scalable, and automated. LOCATION We believe the best ideas happen when we’re together. This is a full-time role based in either Stockholm or London (with strong preference for Stockholm) where you will work primarily in order 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 stages: 1. Screening interview with Talent Acquisition 2. First interview with Head of Commercial Excellence 3. Second interview with our CEO 4. Working Day - Join us in the Stockholm office for a day to experience our culture firsthand, collaborate with our team, and see how you work in action. BENEFITS * Competitive salary & 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.