Sökresultat för "medical documentation"

Stora Sköndals Neurologiska rehabiliteringsklinik erbjuder aktiv och intensiv rehabilitering för patienter med stroke, Parkinson, MS och andra neurologiska sjukdomar och skador. Rehabiliteringen är ett teamarbete där logoped, arbetsterapeut, fysioterapeut, kurator, psykolog, läkare, sjuksköterska och undersköterska arbetar tillsammans med patient och närstående. Förutom inneliggande rehabilitering tar vi emot patienter i öppenvård på neurologisk dagrehabilitering samt på vår logoped- och fysioterapimottagning. Vi söker nu vikarie till vår arbetsterapeutgrupp på dagrehabiliteringen. I första hand söker vi dig som är legitimerad arbetsterapeut, men det kan också finnas möjlighet för dig som är nästan färdig att arbeta under handledning av en erfaren arbetsterapeut. Tillsammans med fysioterapeut och det övriga teamet ansvarar du för att era patienter har en väl avvägd träningsmängd med patientens rehabiliteringsmål i rehabplanen i sikte. Träningen bedrivs såväl individuellt som i grupp med ett stort och varierat utbud av träningsformer. Träningslokalerna är utrustade med ett verkstäder för bland annat keramik och läder, ett träningskök samt flera mindre behandlingsrum. Vi använder också det naturnära läget och vår fantastiska terapiträdgård för träning utomhus när det passar. Vikariatet är 5 veckor på 50-80% från 27 april till 31 maj med stora möjligheter till förlängning över sommaren, då på heltid på vår inneliggande rehabilitering. Ansökningar och intervjuer kommer hanteras löpande och tillsättning kan ske innan sista ansökningsdag 2026-03-08. Du är arbetsterapeut, gärna med erfarenhet av neurologi. Goda kunskaper i svenska språket och vana att dokumentera är ett krav. Arbetet ställer höga krav på organisationsförmåga och samarbetsförmåga. Stor vikt läggs vid personlig lämplighet. Vi är en idéburen och icke vinstutdelande organisation inom stöd, vård, omsorg, utbildning och forskning. Att vi inte delar ut någon vinst gör att vi kan satsa alla resurser på att utföra vårt uppdrag så bra som möjligt. Sedan 1905 har verksamheter inom Stiftelsen Stora Sköndal utvecklats, förändrats och förbättras. Vissa verksamheter består, andra är helt nya. Men en sak förändras inte: Vi arbetar fortfarande utifrån övertygelsen om alla människors lika värde. Varje dag vill vi göra livet bättre för alla de människor vi möter i våra verksamheter. Idag är vi ca 750 medarbetare, både månadsanställda och timanställda som tillsammans arbetar mot vår vision - ett samhälle med en självklar plats för alla. Vår kultur genomsyras av våra värderingar - jämlikhet, omtanke och förändring. Läs mer om oss på www.storaskondal.se

SHL Medical is a world-leading provider in the design, development, and manufacturing of advanced self-injection devices. With a global team of 6,000 employees, we partner with leading pharmaceutical and biotech companies to deliver innovative autoinjectors, pen injectors, and other drug delivery systems that ensure effective treatment for patients. Headquartered in Switzerland since 2018, with key operations in Sweden, Taiwan, and the US, we are united by a commitment to innovation, impact, and growth. Together, we empower our people to develop solutions that make a meaningful difference in the lives of millions of patients while fostering a supportive, inclusive, and dynamic workplace for our colleagues. Job Overview The Sr Quality Engineer is responsible for acting as Workstream Lead Quality (QE Lead) in the Design & Development projects as responsible for design assurance activities across all project phases ensuring quality and robustness of the product design and manufacturing processes (including product care projects, design changes and design reviews). Furthermore, the Quality representative is responsible to assure compliance with applicable regulations and SHL Medical AB’s Quality Management System (QMS) in both Design & Development Projects and other Quality element tasks such as CAPAs and Change Control handling. Main Responsibilities Maintain and calibrate laboratory equipment and instruments to ensure operational reliability and compliance. To act as Workstream Lead Quality applying Quality Engineering principles in a dynamic way in development and production projects. To represent Workstream Lead Quality in all Design Controls and Product Development related aspects. To ensure that all design control and production/process control projects meet applicable (local and international) regulations, Corporate, Customer, and Local QMS requirements. To utilize Quality Engineering best practices, ensuring internal and external customers’ needs and requirements are built into new products and future product changes. To support SMEs in the identification and traceability of Critical to Quality attributes by applying Advanced Product Quality Planning/DFSS/Risk tools and techniques across all product development phases. To promote the use of statistics in testing and control of quality. To support and guide Risk Management activities (FMEAs). To assess and approve the risk mitigation techniques implemented and whether these are consistent with the product classification, potential defect types, defect frequency, severity, patient risk, process capability, product and process controls. To support Device product/process development and production activities, including the following: Develop or review product/process specifications and requirements. Develop or review product reliability specifications/predictions, and reliability test activities. To develop quality plans and work further with Manufacturing on the transfer of quality requirements. To contribute to compilation and maintenance of Design History Files (DHF). Minimum requirements Minimum 5+ years' work experience in relevant roles such as Quality Assurance, Quality Engineering Fluent in written and spoken English. Experience from working with interpretation of ISO Standards, e.g EN ISO 14971:2019 and EN ISO 13485:2016 Experience in establishing, reviewing and approving quality documentation Experience with model development, test method validation and statistical analysis. Green Belt practitioner, or demonstrated experience in application of Quality Methodologies such as DFSS, DMAIC, Lean Hands-on experience in product development from ideation to launch in the Medical Device Industry Preferred Qualifications Fluent in written and spoken Swedish. Experience with Design Controls and Design Transfer activities within the Medical Device industry Experience with injection molding and automated assembly manufacturing processes. Familiarity with validation activities including IQ/OQ/PQ and Test Method Validation (TMV). Experience working in cross-functional and international environments. We Offer Challenging assignments in a fast-growing and innovative industry. An exciting opportunity in a fast-growing international medical technology company. A modern working environment with multicultural and dynamic teams. A centrally located office in Zug, very close to the train station. Interested in joining SHL Medical and in supporting us with your expertise and personality? Then we look forward to receiving your application to our Talent Acquisition Department. Please note: We do not accept applications from recruitment agencies for this position

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.

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 leading University Hospital in Southwestern Sweden! Are you a pediatric ophthalmologist from the EU looking to grow your career in a modern, academic, and supportive environment? A leading university hospital in southwestern Sweden is now recruiting specialists in pediatric ophthalmology to strengthen its highly specialized eye care department. This is an exciting opportunity to work with advanced diagnostics and nationally designated care for pediatric glaucoma and cataract, while contributing to education, clinical development, and research within one of Sweden’s foremost ophthalmology units. About the role You will join a large ophthalmology department with more than 250 professionals, covering outpatient care, emergency eye services, inpatient wards, and surgical units. The pediatric ophthalmology section provides comprehensive diagnostic and therapeutic care for children and collaborates closely with electrophysiology and hereditary disease units. You will work in multidisciplinary teams that include physicians, orthoptists, nurses, optometrists, and technicians, all focused on delivering patient-centered, high-quality eye care. As part of a university hospital, you will also have the opportunity to participate in teaching, clinical research, and innovation projects. Requirements EU-recognized specialist certification in ophthalmology Minimum five years of clinical experience in ophthalmology Focus and competence in pediatric ophthalmology Strong interest in teaching, research, and clinical development Good communication skills in English and willingness to learn Swedish Team-oriented, responsible, and committed to providing high-quality patient care Experience or competence in medical retina is considered an advantage Language and relocation support A willingness and motivation to learn Swedish is important for your integration and clinical work. The relocation process begins once you reach language level B2. During this stage, you will work 50% clinically and study 50% Swedish until you achieve C1 level, which is required to apply for a Swedish specialist license (specialistbevis) to practice as a specialist doctor. Language training is provided free of charge once you have accepted an employment offer. You will receive full support throughout the licensing and relocation process, including assistance with documentation, Swedish authorization, and settling in Sweden. What Dignus Medical offers you Ongoing support from a recruiter before, during, and after your employment Assistance with obtaining Swedish authorization and specialist approvals, if required Help with accommodation and relocation, including support for your family Access to a free language course with a private tutor via Teams/Skype Why work in southwestern Sweden? Live and work in one of Sweden’s most beautiful and dynamic regions, combining city life, culture, and nature. Enjoy a high quality of life with short commutes, clean air, and a safe, family-friendly environment. You’ll have time for both professional development and personal wellbeing. Ready to take the next step in your career? We look forward to supporting your move to Sweden and helping you continue your professional journey as a pediatric ophthalmologist. Contact us for more information, or apply today! 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.

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.

VI VILL HA SVERIGES LYCKLIGASTE INVÅNARE. ÄR DU MED OSS? I Flens kommun satsar vi på att bygga något långsiktigt. Ett samhälle där människor trivs, växer och stannar kvar. Vår nya och modiga vision, Flen – Sveriges lyckligaste kommun, är mer än bara ord. Det är en riktning vi valt tillsammans och en påminnelse om vilka vi är till för. I varje möte med en invånare, i varje beslut vi fattar, i varje vardag vi formar – ska vi tänka med hjärtat. Och det börjar med oss. Nu söker vi en undersköterska med både kompetens och hjärta till Slottsängens särskilda boende i Flen! DET HÄR BLIR DINA ARBETSUPPGIFTER Som undersköterska hos oss har du en avgörande roll i att skapa en trygg och meningsfull vardag för våra boende. Ditt arbete präglas av ett nära och respektfullt bemötande, där du stöttar den enskilde med personlig omvårdnad, hygien och måltider – alltid med utgångspunkt i individuella behov och önskemål. Du arbetar för att bevara och stärka varje persons värdighet, självständighet och livskvalitet. I din yrkesroll utför du även medicinska insatser på delegation från legitimerad personal. Du fungerar som teamets ögon och öron genom att observera hälsotillstånd och dokumentera insatser enligt gällande lagstiftning. Utöver den fysiska omvårdnaden är du en viktig social kraft som bidrar till guldkant i vardagen genom samtal, aktiviteter och kontakt med anhöriga. Vi söker dig som kombinerar professionell kompetens med ett varmt hjärta och en god samarbetsförmåga. Vi lägger stor vikt vid personlig lämplighet. Arbetstiden är förlagd till dag, kväll och helg. FÖR DEN HÄR ROLLEN KRÄVS ATT DU: Har yrkesbevis som undersköterska. Har god datavana. Har goda kunskaper i svenska, både i tal och skrift, då dokumentation är en viktig del av arbetet. DET HÄR VÄRDERAR VI HÖGT: Mer än två års erfarenhet av arbete som undersköterska. Vidareutbildning som specialistundersköterska, exempelvis inom palliativ vård eller vård och omsorg av äldre. DINA PERSONLIGA EGENSKAPER Vi tror att du är en person som är flexibel och har lätt för att anpassa dig efter förändrade situationer i vardagen. Du är kommunikativ och har ett gott bemötande, vilket gör att du skapar trygga relationer med både brukare, anhöriga och kollegor. Som person är du samarbetsvillig men också självgående – du tar ansvar för dina arbetsuppgifter och driver dem framåt på ett strukturerat sätt. Du har en god problemlösningsförmåga och ser möjligheter även i utmanande situationer. Med ett stort engagemang i ditt arbete bidrar du till en positiv arbetsmiljö, och din fantasifullhet gör att du hittar kreativa lösningar som sätter individens behov i fokus. Vi lägger stor vikt vid personlig lämplighet. VARFÖR JOBBA HOS OSS? I Flens kommun vill vi ge dig goda förutsättningar att trivas både på och utanför jobbet. Vi erbjuder bland annat semesterväxling, friskvårdsbidrag och ersättning för patientavgifter upp till högkostnadsskydd – och det finns fler förmåner än så. Många av våra arbetsplatser har dessutom goda pendlingsmöjligheter. Du kan läsa mer om hur det är att jobba hos oss på kommunens webbplats: http://flen.se. Slottsängen är ett särskilt boende med tre avdelningar i markplan, beläget i ett naturskönt område i Flen. Här erbjuds en trivsam miljö som skapar goda förutsättningar för både boende och personal. REDO ATT SÖKA? Vi rekryterar kompetensbaserat och läser inte personliga brev. Ansök genom att bifoga ditt CV, eventuell intyg och besvara urvalsfrågorna. Som sökande ansvarar du för att dokumentera din kompetens tydligt i dina svar på frågorna, då dessa ligger till grund för vår bedömning. Var noga med att svara utförligt och undvik att hänvisa till ditt CV. Vid intervju behöver du visa giltig legitimation, till exempel pass eller nationellt ID-kort. Det går även bra med körkort tillsammans med personbevis (laddas ned via skatteverket). Om du inte är medborgare i Sverige, EU, EES eller Schweiz behöver du istället visa att du har giltigt arbetstillstånd eller att du är undantagen från kravet. Om tjänsten: För den här tjänsten förekommer arbetsprov. Omfattning: Heltid, tillsvidare (provanställning kan tillämpas). Tillträde: 261007 eller enligt överenskommelse. Sista ansökningsdag: 260726 Inför eventuell anställning: Vid anställning av medarbetare i ledande befattningar, verksamhetskritiska roller eller vid arbete i hemmet hos äldre och vuxna med funktionsnedsättning, kan arbetsgivaren begära utdrag ur misstanke- och belastningsregistret Fackliga ombud nås via Kontaktcenter, 0157-43 00 00. OBS! Om du har skyddade personuppgifter ska du inte skicka in ansökan via vårt system. Vänd dig till kommunens webbplats eller till Kontaktcenter för instruktioner. Varmt välkommen till Flen!

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.

Välkommen till vård- och omsorgsförvaltningen. Vi arbetar med stöd och vård till äldre och till personer med funktionsnedsättning. Målet är att de ska kunna leva ett så aktivt och självständigt liv som möjligt. Vård- och omsorgsförvaltningen är en av Sveriges största arbetsgivare inom kommunal vård och omsorg. Här arbetar cirka 7 500 medarbetare utifrån vår värdegrund – göra skillnad, arbeta tillsammans och välkomna nyskapande. Hos oss finns stora möjligheter att ta eget ansvar, utvecklas och bidra med sin kompetens. Vi strävar mot en organisationskultur med en tilltro till varandra och en stolthet över verksamheten. Mer information om hur det är att arbeta i Uppsala kommun hittar du på https://www.uppsala.se/jobb/vard-halsa-omsorg/ Inom vård- och omsorgsförvaltningen har vi heltid som norm. Det innebär att alla tillsvidareanställda medarbetare i grunden har en heltidsanställning. Vid en eventuell intervju ges mer information om vad det innebär i denna tjänst. Undantagna från heltid som norm är personliga assistenter. 1 plats(er). Är du intresserad av eller har erfarenhet inom demens, psykiatri eller socialpsykiatri, och vill bli en del av ett sammansvetsat team där tydlig kommunikation och samarbete är centralt? Då kan Dalbyhemmet vara helt rätt arbetsplats för dig. Hos oss arbetar vi varje dag för att skapa en trygg och meningsfull vardag för våra brukare. Välkommen med din ansökan! Dalbyhemmet ligger i en naturnära miljö med en stor trädgård som skapar goda möjligheter för både aktiviteter och återhämtning. Här arbetar vi med ett rehabiliterande förhållningssätt och erbjuder våra brukare en aktiv vardag med utflykter och andra planerade inslag. Som medarbetare ingår du i ett team med nära samarbete mellan legitimerade kollegor, verksamhetschef och omvårdnadspersonal. En viktig och uppskattad del av vårt arbetssätt är att djur och odling ingår i verksamheten. Vi har höns, kaniner och katter som bor hos oss. Beskrivning av arbetsuppgifter Som sjuksköterska hos oss får du möjlighet att göra skillnad genom att med brukaren i centrum bidra med din kompetens, kunnande och engagemang. Din roll kommer innebära arbete med varierande arbetsuppgifter inom ditt område. Till dina mer konkreta arbetsuppgifter ingår: att bedöma och planera behovet av HSL insatser samt utvärdera behandlingsresultat att handleda omvårdnadspersonal att delegera HSL- uppgifter till omvårdnadspersonal att delta i teamsamverkan kring brukare till exempel beträffande fallriskbedömningar och Senior Alert Som sjuksköterska ingår du tillsammans med övrig legitimerad personal och teamombud i verksamhetschefens ledningsgrupp. Vår ambition är att du tillsammans med oss utvecklar verksamheten och dig själv i ett nära samarbeta med dina kollegor. Kvalifikationer Vi söker dig som har: svensk sjuksköterskelegitimation  dokumentations- och datorvana goda kunskaper i svenska, både i tal och skrift Det är meriterande om du har erfarenhet av arbete med äldre personer och åldrandets sjukdomar. Som person är du flexibel och har lätt för att anpassa dig till förändrade omständigheter där du ser möjligheter. Vidare är du mål- och resultatorienterad, med förmåga att arbeta strukturerat mot uppsatta mål och fokusera på att leverera resultat.  Du har en god samarbetsförmåga och trivs med att arbeta tillsammans med andra. Du är lyhörd, kommunicerar tydligt och bidrar till ett smidigt samarbete genom att lyssna, ge och ta feedback samt hantera eventuella konflikter på ett konstruktivt sätt. Slutligen är du beslutsam och trygg i att fatta snabba beslut även när informationen är begränsad eller situationen är komplex. Du visar gott omdöme under tidspress och omsätter dina beslut i handling. Upplysningar Har du frågor om tjänsten, kontakta: Enhetschef Emil Mattsson, 018-726 0309 Facklig företrädare: Vårdförbundet, Kristian Hjertén, 018-67 70 47 Har du frågor gällande registrering av din ansökan eller rekryteringsprocessen, kontakta rekryteringsenheten: 018-726 37 19 Vi kommer att begära utdrag ur belastningsregistret innan anställning kan erbjudas. Uppsala kommun tillämpar individuell och differentierad lönesättning enligt gällande löneavtal. I din ansökan ska du ange medborgarskap. Om du inte är medborgare i Sverige, EU, EES eller Schweiz måste du också kunna styrka att du har ett giltigt arbetstillstånd eller är undantagen från skyldigheten att ha arbetstillstånd. Anställning kan ske först efter kontroll av arbetstillstånd, vilket krävs enligt utlänningsförordningen. En anställning hos Uppsala kommun kan komma att innebära en krigsplacering. Löneform: Månadslön. Anställningsform: Tillsvidareanställning. Varaktighet: Tillsvidare, tillträde: Enligt överenskommet.

About the role At Navinci, we are passionate about understanding biology and disease at a deeper level. We develop technologies and applications that help researchers study proteins, signaling pathways, cellular biology, and molecular mechanisms directly in biological samples. Our work spans tissue and cell-based systems and increasingly combines information from multiple technologies and data types to generate richer biological insight. We collaborate with leading academic groups, biotech companies, and pharmaceutical partners worldwide to advance research and translational science. As we continue to grow, we are looking for 2–3 scientists with different backgrounds and expertise to join our R&D team. We are interested in people who are excited by science, enjoy solving complex problems, and want to contribute to the development of innovative research tools and technologies. Whether your background is in cell biology, tissue biology, spatial biology, immunology, biomarker research, assay development, translational science, omics technologies, or technology development, we would love to hear from you. What you will do Design, execute, optimize, and troubleshoot biological assays and laboratory experiments Analyze and interpret data, generate robust and reproducible results, and communicate clear conclusions Document experimental work according to quality standards and contribute to scientific decision-making Collaborate across R&D, Operations, and Commercial teams Support development of new applications, products, technologies, and improved ways of working Must-have qualifications MSc or PhD in Biotechnology, Molecular Biology, Cell Biology, Biochemistry, Immunology, Medical Science, or a related field Hands-on experience with immunofluorescence, immunohistochemistry (IHC), and other in situ staining and detection methods Experience working with both tissue samples and cell-based models Experience designing, executing, and troubleshooting biological experiments Strong skills in data analysis and presentation, experimental planning, and scientific documentation Fluent in English, written and spoken Experience in one or more of the following areas Cell culture and primary cell models RNA-based methods, transcriptomics, or other omics technologies Flow cytometry Multiplex imaging, microscopy, image analysis, or digital pathology Protein biomarker analysis and antibody-based assays Assay, application, or product development Translational research, biomarker discovery, or disease biology (e.g., oncology, immunology, neuroscience) Statistical analysis, automation, quality systems Industrial R&D, scientific publications, grant writing or patent-related activities Who you are Curious, innovative, and eager to solve scientific challenges Agile and adaptable, with the ability to work in a fast-moving environment Structured, organized, and committed to high scientific quality Hands-on, proactive, and solution-oriented Collaborative, supportive, and comfortable taking ownership of your work

Are you interested in medical images and image analysis? Would you like to work in a growing company devoted to making a real difference in drug development through ground-breaking imaging? A company where you would contribute and be a part of a collaborative team? If this ticks your boxes, you should continue reading. At Antaros Medical, we are pioneering imaging methodologies, such as Magnetic Resonance Imaging (MRI), Positron Emission Tomography (PET), and Dual-energy X-ray (DXA) to design and deliver clinical studies for decision making and differentiation in drug development. We value competence and development as well as ideas and solutions. Relations and trust are keys to success, and it is equally important for us to have fun while doing a meaningful job. We have currently around 140 employees working at our offices in Mölndal, Uppsala and Lund, and we are continuously growing and developing. As a part of our growth journey, we are looking for an analytical and detail-focused Image Analyst for 6 month-employment (with possibility of extension) to join our team based in Mölndal. As an Image Analyst, you will be responsible for quality control and segmentation of medical images from MR, PET and DXA investigations in a technical and research-intensive environment. You will work in a team that together analyse and deliver data for clinical trials using tools to segment organs and structures in the medical images. Your responsibility also includes communication with national and international imaging centres. You do not need any previous experience from image analysis and will, as part of your on-boarding, receive a mentor and undergo an extensive training programme. Your main responsibilities will be: Quality control of images and related documentation from the MR, PET and DXA investigations in the clinical trials Segmentation of images from the MR, PET and DXA investigations including documentation of this Communication with national and international imaging centres on image quality Who are we looking for? We emphasize personal suitability and believe that you are a structured and organized person with attention to details, who likes to work in an environment with high demands on quality. We further believe that you are a positive and communicative person who collaborates well with others and enjoys working against a deadline. Desired qualifications and skills: High school grade, preferably in natural science, possibly any relevant higher education, for example as a biomedical analyst or in healthcare (or equivalent or similar skills gained through work experience), higher education is not a requirement Computer proficiency Good knowledge of spoken and written English Are you interested? Great to hear! Please submit your application via this link. Interviews will be held on a rolling basis throughout the application period. Application deadline: 31 July. For more information about the position, please contact: Anna Ringheim Cadete, Head of Corelab, anna.ringheim@antarosmedical.com The recruitment refers to temporary (6 months) full-time (100%) employment. We only handle applications via our recruitment system Teamtailor. The recruitment is managed by Antaros Medical. We kindly decline any contact from recruitment- or staffing firms. About Antaros Medical At Antaros Medical, we combine ground-breaking imaging with profound experience in drug development and deep knowledge of disease mechanisms. We are specialized in cardiorenal & metabolic diseases and oncology. We have a global network of collaboration partners and customers, including both Big Pharma and Biotech, and several European collaboration initiatives such as Innovative Medicine Initiative (IMI) and COST. Antaros Medical has delivered small complex, mechanistic studies as well as multi-center clinical trials worldwide utilizing our innovative imaging methods. Our global headquarter and imaging Corelab are based in Sweden, and we have recently opened a subsidiary in the US. If you want to find out more about our company, go to our website: www.antarosmedical.com. Our culture is our people, and our values makes us everything that we are. Please feel free to have a look upon our Culture Handbook to get to know us even more: Our culture - Antaros Medical.

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

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.

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).

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