Sökresultat för "clinical documentation"

Det här är ett jobb för dig som är driven, vill utvecklas i din yrkesroll och bidra till hälsa och livskvalitet för dem som bor hos oss. Här får du bra arbetstider, jobba självständigt och ha frihet att utforma dina arbetsdagar. Hos oss på Vardaga får du också engagerade kollegor och duktiga chefer, utbildningar, karriärmöjligheter samt flera förmåner. Här några av höjdpunkterna i vårt erbjudande till dig:  Bra schema och arbetstider: Dagtid mellan kl. 07.00-17.00. Helgtjänstgöring var tredje helg.  Hög kvalitet och stöd av tydliga rutiner: Lättillämpliga rutiner, styrdokument, checklistor och kvalitetsledningssystem ger dig ett omfattande stöd i arbetet.  Kompetensutveckling: Du har tillgång till Vardagas interna utbildningsorganisation Lära med en mängd kurser. Du har också möjlighet att ansöka om utbildningstjänst för att bli specialistsjuksköterska.  Karriärmöjligheter: Som sjuksköterska kan du gå vidare och bli enhetschef eller verksamhetschef för ett boende.  Bra ledning och korta beslutsvägar: Din chef finns nära till hands för stöd och för att bolla idéer. En av boendets sjuksköterskor sitter också alltid med i den lokala ledningsgruppen.  Gemenskap och stöd: Du jobbar nära sjuksköterskekollegor, gruppchefer och omvårdnadspersonal. Inom Vardaga finns ett nationellt nätverk för sjuksköterskor för att utväxla inspiration och kunskap.  Förmånsportal med rabatter: Köp till exempel biobiljetter och resor med kollektivtrafik till bra priser. Höjdpunkterna är baserade på svar från Vardagas 180 sjuksköterskor som listat sina bästa argument för att jobba hos oss. Läs mer om deras svar här. Om rollen Du är spindeln i nätet kring de boendes hälso- och sjukvårdsinsatser och jobbar för att ge livskvalitet. Du ansvarar för att medicinska ordinationer följs. Regelbundet genomför du riskbedömningar och uppföljningar för att säkerställa god kvalitet i verksamheten. Samarbete och stöd Du ingår i ett team med omsorgspersonal, sjuksköterskor, arbetsterapeut och fysioterapeut. En viktig roll för dig är att coacha och utbilda omsorgspersonalen så att ni tillsammans ger varje boende ett så gott liv som möjligt. I detta jobbar du nära boendets gruppchefer som är ansvariga för omsorgspersonalen. Våra gruppchefer coachar också och jobbar tillsammans med teamen i det dagliga arbetet. Vi satsar på ledarskapsutveckling för dig som sjuksköterska. En kurs vi kan erbjuda dig att gå är ”Att leda utan att vara chef”. Lära känna de boende Att förstå de boendes önskemål och se små förändring i deras hälsa och sjukdomstillstånd är många gånger avgörande för korrekta bedömningar och beslut. Tydliga rutiner För att skapa trygghet och tydlighet för dig som sjuksköterska finns ett omfattande stöd i form av praktiska och lättillämpliga rutiner, styrdokument och checklistor. Vårt kvalitetsledningssystem heter Qualimax och är branschledande. Som ny sjuksköterska hos oss deltar du i vårt digitala introduktionsprogram tillsammans med din mentor för att säkerställa att du får en tydlig introduktion med målet att snabbt komma in i arbetet och våra rutiner. "Bra samarbete är det allra viktigaste." - Annelie Stavås, sjuksköterska och gruppchef, Göteborg Om Villa Tule Villa Tule är beläget centralt i Sundbyberg med närhet till tunnelbana, tvärbana, pendeltåg och bussar. Vi har 63 platser i huset varav 36 st är för personer med kognitiv svikt och 27 st med somatisk inriktning. Som sjuksköterska är du omvårdnadsansvarig för 23 boende. Din erfarenhet och kunskap Du är legitimerad sjuksköterska och vi ser gärna att du har arbetat några år inom äldreomsorgen. Våra boende är ofta multisjuka och det kräver att du har både översiktliga kunskaper kring olika sjukdomar och tillstånd samt ett intresse för den åldrande människan. God datorvana samt erfarenhet av dokumentation är viktigt. Vi önskar att du gillar att jobba självständigt och att ha friheten att utforma dina arbetsdagar  är trygg i din roll som sjuksköterska och kan fatta snabba beslut och föra en diskussion med ansvarig läkare  tar egna initiativ, har skinn på näsan och vågar ta för dig  tycker om att ha en ledarroll och att stötta dina kollegor  är van att strukturera och organisera ditt arbete. "Jag har alltid blivit trodd och satsad på och när man har idéer så lyssnar arbetsgivaren. " - Mårten Hedberg, Medicinskt ansvarig sjuksköterska, Stockholm Övrigt Lön: Vi tillämpar individuell lönesättning Tillträdesdatum: Enligt överenskommelse Sista ansökningsdag: 260820 Registerkontroll: Utdrag ur belastningsregister skall uppvisas vid en eventuell anställning. Som en del av vårt arbetsmiljöarbete kan slumpmässiga drogtester förekomma. Har du frågor? Kontakta gärna: Emma Walther på 076-551 78 86. Observera att det inte går att ansöka via E-post. Vi tillämpar 6 månaders provanställning. Om du vill veta mer om hur det är att jobba på Vardaga så läs gärna mer och träffa några av våra medarbetare här. Facklig kontakt: Vårdförbundet Mail: vardforbundet@ambea.se Ansökan Välkommen att ansöka via knappen ”Skicka ansökan” nedan. Vänta inte med att ansöka då vi gör urval löpande. Om du blir kallad till en intervju behöver du kunna styrka att du har rätt att arbeta i Sverige, genom att uppvisa att du har medborgarskap inom EU/EES eller ett giltigt arbetstillstånd. Läs mer om oss på www.vardaga.se

Vi söker nu nästa medlem i vårt team! Att arbeta som vaccinatör hos oss  Du är en legitimerad sjuksköterska som brinner för bra service och alltid gör det lilla extra för dina patienter. Du har förmågan till självständigt arbete och beslutsfattande utifrån din kompetens. Hos Min Doktor får du regelbundna vaccinationsutbildningar. Du arbetar nära kollegorna på Apotek Hjärtat och dina vaccinationskollegor runtom i landet. Erfarenhet av att arbeta med vaccinationer är meriterande men skall ej ses som ett krav. Vill du veta mer? Se vår film om hur det är att arbeta hos oss Det här söker vi hos dig Vi söker en utåtriktad sjuksköterska med god datorvana för arbete med vaccination på Apotek Hjärtat i Gislaved. Tjänsten omfattar 1-2 dagar i veckan på ett kontinuerligt schema. Arbetet hos oss är självständigt och innefattar bland annat: Vaccinering Journalföring Hantering av betalning Enklare inventering Övrig information Placering: Apotek Hjärtat på ICA Kvantum Gislaved Omfattning: Avtalad visstidsanställning/ tillsvidareanställning 1-2 dagar i veckan Tillträde: Omgående Välkommen med din ansökan Välkommen med din ansökan så snart som möjligt (urval och intervjuer sker löpande). Vi ser fram emot din ansökan! Om Min Doktor Min Doktor är Sveriges första digitala vårdgivare och erbjuder sedan 2013 snabba och trygga vårdbesök över nätet, oberoende av tid och plats. Idag är vi en av Sveriges största digitala vårdcentraler. Sedan 2018 bedriver vi även vaccinationsmottagningar i anslutning till Apotek Hjärtat och ICA, och är en av Sveriges största vaccinatörer. Min Doktor är registrerad vårdgivare och omfattas av hälso- och sjukvårdslagen, personuppgiftslagen, patientdatalagen och patientsäkerhetslagen.

Are you a dental hygienist who loves combining clinical expertise with education and wants to make a global impact on oral health? We’re now looking for a Clinical & Education Advisor to join our Communication & Education Team in Malmö. At TePe, we’re committed to advancing oral health worldwide and we take pride in improving people’s well being, starting with our own co workers. Join us on our journey to become a science driven thought leader! What will you be working with? As a Clinical & Education Advisor, you will play a key role in developing and executing TePe’s global education plan. You will create impactful, evidence-based educational materials and help position TePe as a leading expert in oral health. You will work closely with internal teams and external stakeholders to deliver high-quality education, strengthen professional relationships, and help increase product recommendation rates worldwide. Key responsibilities Develop educational materials in collaboration with Marketing and global markets. Plan and deliver educational activities, training, and lectures for internal and external audiences. Support markets in building local networks with dental professionals. Promote global partnerships to build local engagement and strengthen professional credibility. Provide clinical expertise to stakeholders and contribute to product innovation. Review marketing and product documentation to ensure scientific accuracy. Represent TePe at international events and congressses. This position includes some planned travel, so we are looking for someone who is flexible and open to international travelling, including attending dental trade fairs and visiting customers. This role requires that you are based at our head office in Malmö with possibility to work from home 1-2 days per week in agreement with the manager and team. Who are you? You have strong communication and presentation skills, as well as the ability to translate clinical knowledge into commercial value. You have a passion for linking scientific evidence to your clinical experience and enjoy spreading the word about the importance of prevention and oral health. You are confident in building relationships and enjoy working collaboratively as part of a team. It’s an extra plus if you have experience from a specialist practice within periodontology. The role requires: Qualified Dental Hygienist with several years of clinical experience Fluent in English, both written and spoken; Swedish is considered a strong advantage Strong communication and presentation skills Why join TePe? Fast, stable growth & opportunities: As a rapidly expanding company, we seek dedicated people who want to grow with us and make a real impact. Learning never stops: We invest in personal and professional growth through mentorship, training, and career progression. Collaboration at our core: At TePe, science meets creativity in a knowledge-sharing environment where teamwork drives innovation. Sustainability and health are at the heart of everything we do. From our products to our workplace, we take a holistic approach – creating a better future for people, their smiles, and the planet. TePe Oral Hygiene Products, founded by the Eklund family in 1965, is an international company headquartered in Malmö, Sweden. TePe has around 520 employees and reported a turnover of MSEK 1,407 in 2024. Based on sustainable innovation and the vision to bring healthy smiles for life, TePe offers a complete range of high-quality self-care solutions, developed in partnership with the dental profession. Marketed by subsidiaries, sales and marketing offices in Singapore, Japan and Turkey, and business creators in more than 80 countries, TePe’s oral health products are available through dental practices, pharmacies, e-tail, and retail. All development and manufacturing take place in Malmö. For more information, visit www.tepe.com How to apply You are warmly welcome to submit your application via the link provided in this advertisement. We kindly ask you to submit your application in English. We will begin the selection process in week 32, and we will contact you at that time with further information. For this recruitment TePe is partnering up with ROI Rekrytering. For further questions please contact Senior Consultant Lisa Alsterberg at lisa.alsterberg@roirekrytering or 073-394 15 05 All information is handled confidentially in accordance with Roi Rekrytering integrity policy as well as the new data protection act, GDPR. This means that we can only process applications coming through the applications system. Thank you for your understanding. Assessment tools To find the best fit for both you and us, we use assessments from Alva Labs These science-based tools help us understand your potential beyond the CV. They make the selection process fairer and help us identify who is most likely to succeed and grow in the role. These assessments are carried out by the candidates TePe will meet for an interview. Background Check As part of our recruitment process, a background check is conducted on the final candidate before employment is confirmed. The check may include verification of employment history, education, professional qualifications, financial records, legal status, and the right to work. The background check is conducted through an external provider. All checks are carried out with the candidate’s consent and in accordance with applicable laws and data protection regulations.

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

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.

Hansa Biopharma develops innovative treatments that give patients with rare and serious immune-mediated conditions a chance to a better life. We are now looking for an experienced Senior QA Manager Validation and Quality, to help shape our quality work at one of the most exciting biotech companies in the Nordics. About the role You will be a key player in a QA team of six dedicated colleagues, all based at our office in Lund. As Senior QA Manager, you will drive and approve validation activities - spanning process, cleaning and analytical method validation - with a clear quality perspective. You will act as subject matter expert supporting cross-functional teams, external partner management and regulatory authority inspections. This is the right role for you if you thrive with both strategic ownership and operational presence - where one day you are reviewing validation documentation and the next you are in dialogue with a CDMO or preparing a team for an authority inspection. Your responsibilities: Provide strategic and operational direction for quality management and validation across development, clinical and commercial manufacturing QA review and approval of validation documentation Supplier quality management: guide and qualify external manufacturing partners (CDMOs/CMOs) throughout the product lifecycle Support authority inspections and internal/external audits of suppliers and vendors Cross-functional collaboration with CMC, Regulatory, Clinical and Supply Chain Drive continuous improvement of the Quality Management System (QMS) and proactively identify areas for development Who are you? We believe you are a seasoned QA professional with broad experience across both drug substance (DS) and drug product (DP) manufacturing. You are thorough and results-oriented, but also a natural collaborator who knows when to take the lead and when to seek input from others. We are looking for someone with: Advanced degree (Ph.D. or M.Sc.) in Chemical Engineering, Chemistry, Pharmaceutical Sciences or a related discipline 10+ years of biopharmaceutical industry experience with a focus on QA, process development and validation Proven track record of leading validation activities for DS and DP through clinical and commercial stages Strong knowledge of aseptic manufacturing and biotechnology processes Deep understanding of regulatory requirements (FDA, EMA, ICH) related to manufacturing and validation Experience managing external partners and CDMOs/CMOs Experience of authority inspections (FDA, EMA) as presenter and/or coordinator Strong communication skills and the ability to influence across functions and organisational levels What we offer At Hansa, you will not just have a job - you will have a role where your work directly contributes to changing lives for patients with acute and complex immune disorders. A close-knit, welcoming culture in a mid-sized company where you can see how your contribution makes a difference The opportunity to help build a fully integrated biopharmaceutical company with global reach Talented, driven colleagues with an open and entrepreneurial mindset A strong pipeline built on Hansa’s proprietary IgG-cleaving enzyme technology platform Office in Lund, at the heart of a vibrant Life Science ecosystem Our values At Hansa, we are guided by our core values: Accountability, Courage, Integrity and Pioneering. We believe in the power of diversity and are committed to building an inclusive workplace where every perspective is valued. Appealing? Send in an application as soon as possible. In this recruitment, Hansa Biopharma is collaborating with SallyQ. For questions, please contact Ellinor Crafoord, Senior Recruitment Consultant, +46793554257 or ellinor.crafoord@sallyq.se.

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! 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.

Nanexa is now recruiting a Quality Assurance (QA) Manager. The position is full-time and based at our headquarters in Uppsala, and we are looking for a new colleague to join our growing organisation. As a QA Manager at Nanexa, you will play a key role in building and shaping the quality function in a growing pharmaceutical company. This is not a traditional QA role in a large organisation – instead, you will be part of a small, highly skilled team where your contributions will have a direct and visible impact on how we work and grow. You will have the opportunity to develop, implement and continuously improve our Quality Management System while being actively involved in the full product lifecycle – from early development to manufacturing of clinical trial material. The role combines strategic responsibility with hands-on work and close collaboration across functions. At Nanexa, you will not work in a silo. You will be involved across the organisation, working closely with colleagues in development, production and analytics, gaining a broad understanding of our technology, products and processes. As a company of approximately 15 employees, we offer an environment where each individual plays an important role, and where you will actively contribute to building something new. Responsibilities The QA Manager will have a central role in the oversight of manufacturing and analytical activities from a quality perspective, covering the entire chain from development to clinical supply. You will report directly to the Head of Quality Assurance and be an important contributor to the continued development of the QA function and the company as a whole. Your responsibilities will include: - Develop, implement and continuously improve the Quality Management System in line with company growth and regulatory requirements - Assess and approve batch-related documentation such as specifications, batch records, deviations and change requests - Ensure that production and testing of clinical trial materials are conducted in accordance with applicable GMP requirements - Review and approve SOPs, manage periodic reviews and support supplier qualification and re-evaluation - Lead and participate in internal audits and audits of external service providers - Represent QA in cross-functional project teams and contribute to project execution - Provide guidance and support to the organisation in quality-related matters - Perform internal training within GMP and quality systems - Contribute to the strategic development of the QA function and quality processes Your Profile We are looking for a driven and quality-minded professional who enjoys working in a dynamic and developing environment. Key qualifications include: - MSc in Pharmacy, Biology, Chemistry, Engineering, or a related field - Several years of experience within QA in a GMP-regulated pharmaceutical or biotech environment - Experience in development and/or validation of manufacturing or analytical processes - Experience in authoring and reviewing GxP-critical documentation, including SOPs, deviations, CAPAs and change controls - Strong knowledge of Quality Systems and applicable GMP regulations - Fluency in Swedish and English As a person, you are proactive, structured and solution-oriented, with a strong sense of ownership and accountability. You thrive in a dynamic organisation where processes are still being developed, and where you have the opportunity to make a real impact. You are comfortable taking on multiple responsibilities and enjoy working both independently and in close collaboration with others. At Nanexa, each employee contributes to the overall success of the company and you will have the opportunity to influence not only your own area of responsibility, but also the development of the company as a whole. About Nanexa AB Nanexa is a Swedish pharmaceutical company developing long-acting injectable drugs based on our proprietary PharmaShell® technology. We operate at the intersection of material science and drug development, taking projects from early idea through development to proof-of-concept in clinical trials. In addition to our own pipeline, we collaborate with leading pharmaceutical companies to develop new products based on our technology. To learn more about Nanexa, please visit www.nanexa.com For more information about the position, please contact: Krishan Johansson Haque, PhD Sr Recruitment Consultant, QRIOS Life Science & Engineering T: +46 (0)72-070 16 53 E: krishan.johansson-haque@qrios.se

Would you like to work in an international environment where you’ll make a difference every day? At Permobil, we’re looking for game-changers to join us as we innovate for individuals and develop the world’s most advanced assistive solutions. At Permobil, the people who use our products come first. Our purpose is to create advanced assistive solutions that make the lives of adults and children living with disabilities more enriching. Our people are passionate about pushing the boundaries of technology to deliver innovations that improve lives. We are a sustainable and responsible business committed to continuous improvement, and our customers can trust us to provide market-leading solutions driven by insights-based clinical data. Position Overview We are seeking a Senior Infrastructure Engineer - Cloud to help build, operate, and evolve our global hybrid cloud platform on Microsoft Azure. In this role, you will design and implement scalable, secure cloud infrastructure supporting business-critical applications and services across our global footprint. You will play a key role in areas such as Azure landing zones, governance, Azure Policy, hybrid connectivity, and Azure Arc capabilities, while collaborating closely with infrastructure, platform, and security teams to deliver reliable enterprise cloud services. Key Responsibilities: Design, deploy, and manage Azure hybrid cloud infrastructure Develop and maintain Azure landing zones and governance models Implement Azure Policy, RBAC, and Azure Arc capabilities Drive adoption of containers, AKS, and hybrid runtime solutions Manage Azure networking, connectivity, and security services Monitor cloud performance, costs, and optimization opportunities Implement observability solutions using Azure Monitor and Application Insights Manage secrets, certificates, and keys using Azure Key Vault Build and maintain Infrastructure as Code using Terraform, Bicep, or ARM Operate and improve CI/CD pipelines using Azure DevOps or GitHub Actions Evaluate new Azure services and provide technical guidance and documentation Qualifications & Skills: Bachelor’s or Master’s degree in Computer Science, Information Technology, or a related field. Relevant Azure certifications (AZ-104, AZ-305, AZ-500) are highly valued, 5+ years of hands on experience with Microsoft Azure infrastructure (networking, compute, storage, identity), Proven experience designing and evolving enterprise cloud platforms, Strong experience with hybrid cloud architectures, including Azure Arc and datacenter integration, Deep understanding of Azure networking (VNets, NSGs, private endpoints, ExpressRoute, Firewall, Application Gateway), Experience implementing governance and security controls (Azure Policy, RBAC, Entra ID, Key Vault), Solid experience with Infrastructure as Code (Terraform, Bicep, ARM), Experience supporting application and DevOps teams with cloud platforms, containers, or CI/CD, Fluent in English. Meriting experience & skills: Experience with containers and Kubernetes (AKS) in enterprise environments, Exposure to secondary cloud platforms (e.g., AWS) in a hybrid or multi cloud context, Experience with disaster recovery design in hybrid environments, Experience in regulated or global enterprise environments, Fluent in Swedish. Who are you? You are a structured and analytical problem solver who thrives in complex hybrid cloud environments. You combine strong technical depth with clear communication, making it easy for both technical and non-technical stakeholders to understand and act on your guidance. Comfortable working across global teams and time zones, you bring a proactive and curious mindset, continuously looking for ways to improve platform maturity, standards, and overall cloud capability. Why is Permobil the next step for you? You’ll make a difference. Every day. Everything we do leads to understanding and improving the lives of our users. Through our evidence-based innovation, we make a difference to people’s lives. You’ll make your mark as part of our future. We collaborate with colleagues across borders to Innovate for Individuals. The impact you make personally could lead change around the world. You’ll feel welcome from day one. We’re known for being great colleagues, who are collaborative, fun and at the cutting-edge. Everyone at Permobil cares as much as you do about making a positive difference. Application Process We will conduct selection continuously so send us your application today or before July 26th at the latest! Permobil is an equal opportunity employer committed to diversity and inclusion. We welcome applications from all qualified individuals. For more information about the position, please contact Erik Jensen, Manager Global Infrastructure, Erik.Jensen@permobil.com For information about the recruitment process, please contact Zivile Mitkute, Talent Acquisition Partner, zivile.mitkute@permobil.com Please respect that we do not wish recruitment assistance or advertising, we decline calls from recruitment and advertising providers. More about Permobil Permobil founder Dr. Per Uddén believed that helping people achieve the greatest level of independence is a basic human right and, for over 50 years, Permobil has held fast to that belief. Permobil is a global leader in advanced rehabilitation technology, passionate about better understanding our users’ needs and improving their quality of life through state-of-the-art healthcare solutions. Today, those solutions include power wheelchairs, seating and positioning products, power assist, and manual wheelchairs. Permobil is part of Patricia Industries, a subsidiary of Investor AB, and is headquartered in Sweden. Permobil has 2 000 team members in 18 countries around the world. For more information regarding the company’s storied history and complete product line, visit permobil.com.

Would you like to work in an international environment where you’ll make a difference every day? At Permobil, we’re looking for game-changers to join us as we innovate for individuals and develop the world’s most advanced assistive solutions. At Permobil, the people who use our products come first. Our purpose is to create advanced assistive solutions that make the lives of adults and children living with disabilities more enriching. Our people are passionate about pushing the boundaries of technology to deliver innovations that improve lives. We are a sustainable and responsible business committed to continuous improvement, and our customers can trust us to provide market-leading solutions driven by insights-based clinical data. Position Overview We are looking for a Senior Infrastructure Engineer – Windows Server to be the global technical owner of our Windows Server platform, and the primary escalation point for complex and high‑impact issues. You are responsible for ensuring that the Windows Server environment is secure, standardized, resilient, and fit for long‑term hybrid operation. In addition, you govern the MS SQL Server platform together with application teams and DBAs, defining standards, lifecycle rules, and architectural guardrails while execution remains distributed. The role combines deep hands‑on technical expertise with platform ownership. You will lead consolidation, modernization, and risk‑reduction efforts across a large enterprise Windows footprint, working as part of the Hybrid Cloud team. A key focus is enabling a long‑term hybrid Windows model, including integration with Azure Arc, while reducing operational overhead and unplanned work. This is a hybrid role based in Sundsvall (Birsta). Key Responsibilities: Own the global Windows Server platform, including engineering standards, lifecycle management, consolidation, and technical escalation for complex incidents. Define and govern SQL Server platform standards in partnership with application teams and DBAs Enable and evolve a hybrid Windows Server model, integrating on‑prem environments with Azure through Azure Arc and collaborating with Cloud and Security teams on governance, identity, monitoring, and vulnerability management. Design and maintain core Windows services like Group Policy, DHCP, certificate services (PKI), and Windows file/print services to enterprise standards. Operate and improve the enterprise Windows patching programme Harden Windows servers against organizational and industry baselines Maintain accurate CMDB and infrastructure inventory for compliance Build Infrastructure as Code using Ansible, Terraform, or equivalent tools Develop PowerShell automation for operational efficiency and reliability Improve documentation, runbooks, and knowledge sharing across the team Mentor junior engineers and support continuous platform improvement Qualifications & Skills: Bachelor’s or Master’s degree in Computer Science, Information Technology, or a related field, Relevant certifications such as Microsoft Certified: Windows Server Hybrid Administrator Associate or Red Hat Certified Specialist in Ansible Automation are highly valued, 5+ years of hands-on experience engineering and operating Windows Server environments at enterprise scale, Strong expertise in Windows Server 2016/2019/2022/2025, Active Directory, Group Policy, DNS, DHCP and other core windows services Proven experience operating an enterprise patching programme, including patch testing, deployment, and reporting (e.g., WSUS, SCCM/MECM or third-party patch tools), Strong PowerShell scripting skills for automation, reporting, and operational tooling, Working knowledge of Windows server hardening and vulnerability management (CIS Benchmarks, Defender for Endpoint/Servers, vulnerability scanners), Experience with backup and disaster recovery for Windows workloads, including recovery testing, Fluent in English Meriting experience & skills: Experience with Azure infrastructure services and hybrid identity (Entra ID, Entra Connect, Azure Arc for Servers), Hands-on experience with Infrastructure as Code tooling: Ansible, and Terraform or equivalent for Windows infrastructure, Experience with virtualization platforms and storage administration, Working knowledge of CI/CD pipelines (Azure DevOps, GitHub Actions) applied to infrastructure changes. Who are you? You are a structured and analytical problem solver who stays calm and focused even during high-pressure incidents. You communicate complex technical infrastructure topics in a clear and simple way that both technical and non-technical stakeholders can understand. With a strong process mindset and attention to detail, you value good documentation and always look for ways to automate repetitive work. Curious by nature, you continuously learn and stay up to date with developments in Windows Server and infrastructure automation. Application Process We will conduct selection continuously so send us your application today or before July 26th at the latest! Permobil is an equal opportunity employer committed to diversity and inclusion. We welcome applications from all qualified individuals. For more information about the position, please contact Erik Jensen, Manager Global Infrastructure, Erik.Jensen@permobil.com For information about the recruitment process, please contact Zivile Mitkute, Talent Acquisition Partner, zivile.mitkute@permobil.com Please respect that we do not wish recruitment assistance or advertising, we decline calls from recruitment and advertising providers. More about Permobil Permobil founder Dr. Per Uddén believed that helping people achieve the greatest level of independence is a basic human right and, for over 50 years, Permobil has held fast to that belief. Permobil is a global leader in advanced rehabilitation technology, passionate about better understanding our users’ needs and improving their quality of life through state-of-the-art healthcare solutions. Today, those solutions include power wheelchairs, seating and positioning products, power assist, and manual wheelchairs.

We are recruiting registered nurses for permanent full-time positions in the Østfold region in southeastern Norway, on behalf of several municipalities. Østfold is a welcoming region in southeastern Norway, known for its beautiful coastline, scenic landscapes and close proximity to Oslo and Sweden. The municipalities have a continuous need for qualified nurses in both home care services and nursing homes, where you will play an important role in providing safe and reliable care to patients of all ages. These positions offer a stable job, a meaningful everyday working life and good opportunities for professional development within the Norwegian public healthcare system. You will work in well-organised teams that focus on cooperation, clear routines and high professional standards. Your responsibilities Clinical nursing in home care, nursing homes or assisted living facilities Observation, assessment, medication management and accurate documentation Follow-up of patients with diverse medical conditions and functional levels Collaboration with relatives, coordinating units and external partners Interdisciplinary cooperation with doctors, therapists and other health professionals Contributing to service development, improvement work and quality assurance Qualifications: Hold a valid nursing authorization from an EU country Relevant experience as a nurse (hospital or community care is an advantage) Be proficient with basic computer skills, necessary for modern healthcare environments Speak and write English fluently Motivated to learn Norwegian Hold a bachelor’s degree in nursing (BSN) Driving licence category B is an advantage for home visits Personal qualities: Responsible, structured and solution oriented Positive attitude and good teamwork skills Flexible and comfortable with varied tasks Motivated to contribute to a small but highly competent interdisciplinary team We offer: A full-time permanent position in the Norwegian public healthcare system Competitive salary and working conditions A supportive work environment that values cooperation and professional confidence Opportunities for further development and specialization Free online Norwegian language course with a private teacher Relocation assistance and help with housing Personal follow-up throughout the recruitment and relocation process Why choose this opportunity? Combine a rewarding nursing career with a great quality of life in Østfold. Enjoy the region’s beautiful coastline, peaceful surroundings and easy access to Oslo and Sweden. We will support you throughout the process to help you succeed in your new role. Ready to apply? Send us your application, and we will evaluate candidates continuously. Feel free to reach out for more information, I look forward to hearing from you!

On behalf of municipalities in Southern Norway, we are recruiting qualified nurses for permanent full-time positions in municipal healthcare services. Depending on your experience and interests, you may work in a nursing home, GP practice or public health clinic. These positions offer a varied workday, close patient contact and the opportunity to develop your skills as part of an experienced healthcare team. Your responsibilities Nursing duties in a nursing home, GP practice or public health clinic Medication management, clinical observation and professional documentation Collaboration with patients’ relatives and external partners Interdisciplinary work with doctors, therapists and other healthcare staff Contributing to quality improvement and development of local healthcare services We are looking for nurses who: Hold a valid license as a nurse from an EU/EEA country Are motivated to obtain Norwegian authorisation (we assist with the process) Speak fluent English and are highly motivated to learn Norwegian Are willing to complete our free Norwegian language course Work independently and in a structured manner Enjoys teamwork and has genuine compassion for patients Is flexible and able to adapt to different work situations Holds a driver’s license (preferred) We offer: A full-time permanent position in the Norwegian public healthcare system Competitive salary and working conditions A supportive work environment that values cooperation and professional confidence Opportunities for further development and specialization Free online Norwegian language course with a private teacher Relocation assistance and help with housing Personal follow-up throughout the recruitment and relocation process Life in Vest-Agder Southern Norway is known for its coastline, mild climate and relaxed way of life. The region offers a good balance between work and leisure, with easy access to nature, outdoor activities and local communities. Many international healthcare professionals appreciate the combination of a safe environment, short commuting distances and a well-organised healthcare system. The area also offers good schools, modern public services and a wide range of cultural and recreational activities. You can read more about the region here.

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.

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!