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About us Mindler is one of Europe’s leading digital mental health providers, working to make evidence-based therapy accessible to everyone who needs it. In August 2025, we proudly acquired ieso, a pioneer in delivering online NHS talking therapies across the UK. Ieso holds several NHS contracts across England and Scotland through both typed and video sessions, making it easier for thousands of people to access effective, evidence-based treatment when they need it most. This role sits within the clinical affiliate network of Ieso - subsidiary of Mindler, meaning you’ll be part of a group with a strong track record in innovation, research, and delivering high-quality digital therapy to patients nationwide. The role We provide evidence-based Cognitive Behavioural Therapy (CBT) via video to NHS patients across the UK, from the Orkney Islands to Cornwall. Our mission is to make psychological therapies accessible to those who need them most, without significant waiting times. What do I need to have: To join our self-employed affiliate network, you’ll need: * To be a fully qualified CBT Therapist with BABCP accreditation. * Availability to accommodate a recommended minimum caseload of 5 patients per week. * An Enhanced DBS Certificate (including both barrings: Adults and Children) issued within the past 12 months OR registered with the Update Service. (We can support your application if you do not currently hold this) * Two satisfactory professional references (e.g., current supervisor and line manager) * Access to a secure laptop/PC with an auto-lock function (max 5-minute inactivity) * Personal email address (NHS email addresses cannot be accepted) **We cannot proceed if you do not have all of the above What can we offer? As a self-employed therapist, you’ll enjoy a range of benefits, including: * Flexibility: Work remotely and structure your caseload around your availability, with a recommended minimum of 5 patients. * Competitive Pay: Earn £62.90 per 60 minute Video session (including holiday pay), with half-pay for DNAs/late cancellations (up to two per episode of care). * Professional Development: Access to free regular high-quality supervision and opportunities to further develop your clinical skills. If you are passionate about providing high-quality therapy online and want to make a difference in digital mental healthcare, we’d love to hear from you! 👉To start your application today please respond with proof of the above requirements. Please don’t hesitate to reach out if you have any questions-we look forward to welcoming you to our network!
Gör skillnad. Varje dag. Är du sjuksköterska och intresserad av kardiologi? Letar du efter ett varierande arbete där du blir del av ett team med kompetenta och engagerade kollegor? Då är hjärtavdelningen rätt för dig! - Hjärtat! Ett av kroppens mest vitala och spännande organ enligt oss. Att få vara delaktig i ett bra hjärtteam har alltid varit vår önskan säger sjuksköterskorna Hannah och Madeleine, som tillsammans arbetar på hjärtavdelningen Kristianstad. Hjärtavdelningen är en vårdavdelning med 21 vårdplatser som diagnostiserar och behandlar patienter med kardiologiska sjukdomar. På enheten behandlas även patienter med allmänmedicinska åkommor. Vi har en dagvård knuten till avdelningen där vi vårdar patienter som tidigare krävt inneliggande vård. Patienterna vårdas över dagen och kan i de flesta fall gå hem samma dag. Vårdavdelningen har även ett nära samarbete med hjärtintensivavdelning (HIA). Vår arbetsplats kännetecknas av hög kompetens, god stämning och trevliga arbetskamrater. Vi har respekt för varandra och ser allas kompetens som lika viktig. Teamet runt patienterna består av läkare, sjuksköterska, undersköterska, fysioterapeut, arbetsterapeut, medicinsk sekreterare, kurator och dietist. Vi arbetar personcentrerat där patienten möter de olika yrkeskategorierna som behövs för att vården och behandlingen ska bli optimal. Hos oss får du en bred kompetens inom din specialitet. 1 plats(er). ARBETSUPPGIFTER Vi ser nu fram emot att välkomna en ny sjuksköterska till vårt härliga team. Tjänsten innebär även möjlighet till rotation Hjärtmottagning dagvård i Kristianstad. I rollen som sjuksköterska hos oss erbjuds du ett omväxlande arbete, där du kommer vara en viktig person i såväl den basala som den specifika omvårdnaden av patienten. Dina arbetsuppgifter hos oss innefattar bland annat den perioperativa vården av patienter som ska genomgå eller har genomgått kranskärloperation (CABG). Du förbereder även patienter inför pacemakeroperation och angiografi samt är med och assisterar vid elkonverteringar. På avdelningen ser vi utveckling som en naturlig del i arbetet, bland annat genom att erbjuda årliga utbildningsdagar samt att vi i arbetsgrupper förfinar och utvecklar samarbetsformer mellan professionerna. Här får du lära dig bland annat arytmitolkning då många av våra patienter har hjärtövervakning. Vi har en utbildningssjuksköterska på avdelningen som regelbundet håller i utbildningar och anordnar andra kompetensutvecklande insatser för att säkerställa en kontinuerlig utveckling och hög kompetens i arbetsgruppen. Det senaste året har våra sjuksköterskor bland annat fått möjlighet att genomföra simuleringsövningar kring väsentliga delar av vårdförloppet och delta på föreläsningar om hjärtsjukvård från våra kardiologer, något som varit mycket uppskattat. Vi har även daglig reflektion tillsammans med övriga kollegor i arbetslaget efter avslutat pass. På dagvården ger vi behandlingar som inte kräver inneliggande vård. Patienter kommer hit för bland annat intravenösa behandlingar, elkonvertering och förberedelse inför pacemakerinläggning som sker på operation. Oavsett om du är nyexaminerad eller har tidigare erfarenhet från yrket värdesätter vi att du får en trygg start på din nya anställning hos oss. När du börjar här lägger vår utbildningssjuksköterska upp en introduktionsplan tillsammans med dig utifrån dina tidigare erfarenheter och behov, och följer dig sedan under din första tid på avdelningen. KVALIFIKATIONER Du som söker är legitimerad sjuksköterska med behörighet att verka inom svensk sjukvård. Språkkunskaper i svenska lägst motsvarande nivå C1 enligt Europarådets nivåskala är ett krav. Vi ser det som meriterande om du tidigare har arbetat inom kardiologi. Vi söker dig som arbetar proaktivt och strukturerat samtidigt som du kan prioritera när en akut situation uppstår. För oss är det en självklarhet att du är noggrann och flexibel i din sjuksköterskeroll och tar hand om patienterna utifrån deras olika behov med ett gott bemötande. Som person är du engagerad, initiativrik och öppen för nya utmaningar och möjligheter. Vi vill även att du precis som vi värdesätter ett arbete som präglas av det egna ansvaret, delaktighet och ett gott samarbete mellan kollegor och närmaste chef. Stor vikt kommer att läggas vid personlig lämplighet. I denna rekrytering tillämpar vi löpande urval. Varmt välkommen med din ansökan redan idag, vi ser fram emot att lära känna dig! Anställningsform: Tillsvidareanställning. Varaktighet:, tillträde: Tillträde enligt överenskommelse. Region Skåne finns till för att alla som bor i Skåne ska må bra och känna framtidstro. Genom gränsöverskridande samarbeten och omtanke skapas de bästa förutsättningar för ett hälsosamt liv - inom näringsliv, kollektivtrafik, kultur och hälso- och sjukvård - i Skåne. Tillsammans gör vi livet mera möjligt. På https://www.skane.se/ledigajobb kan du se i vilket skede Region Skånes rekryteringar befinner sig och hur många som har sökt tjänsterna. Om du har skyddade personuppgifter ska du kontakta den kontaktperson som finns angiven i annonsen så att din ansökan blir hanterad enligt särskilda rutiner. När du söker ett jobb hos Region Skåne blir din ansökan en allmän handling enligt offentlighetsprincipen. Uppgifterna behandlas och sparas enligt dataskyddsförordningen (GDPR). Till bemannings- och rekryteringsföretag och till dig som är försäljare: Vi undanber oss vänligen men bestämt direktkontakt med bemannings- och rekryteringsföretag samt försäljare av ytterligare jobbannonser.
Join the Leadership Team at Velora Health Head of Growth Location: Stockholm Level: Senior, reporting directly to CEO Start: As soon as possible About Velora Health Velora Health is a rapidly growing AI HealthTech startup on a mission to address the leading causes of preventable death. Our goal is bold yet simple: a longer and healthier life for more people, through the fusion of personalized care and a holistic approach to health. We started our journey by tackling one of the biggest global health issues: obesity, which affects nearly 1 billion people worldwide. We're now expanding beyond obesity into broader chronic care. Through our platform and digital health clinic at Velora.se, we provide individuals access to the latest and most effective research-based treatments. We're AI-native. We use AI across the whole company. In Sweden alone, 2 million could live longer with Velora. Today we're a 20-person team across clinical care, engineering, growth and operations. Now we're hiring our Head of Growth to join our Leadership Team. The opportunity Reporting directly to the CEO, you'll be part of Velora's Leadership Team and a key voice in strategy and high-level decisions. This is not a support role, we're looking for a leader who challenges, sharpens, and helps drive the company forward. You combine sharp strategic thinking with hands-on execution. You'll help set direction, then take full ownership of growth and deliver measurable results. We're a subscription business, so retention and lifetime value matter as much as sign-ups. But for us the stakes are bigger than revenue. We're building the lifelong home for people with chronic disease, where staying in care means living longer: for someone with obesity, dropping out of treatment means 5 to 10 years of lost life. That is where great care and growth become the same job, and it is exactly what we built our platform and doctor-led care model to do. What you'll own The growth number, and the overall growth strategy including international expansion Acquisition and CAC across current channels (paid marketing, organic search, referral) Test and scale new growth avenues beyond B2C (B2B, B2B2C, payor and insurance) The in-product growth surface (onboarding, paywalls, activation) Retention, win-back and LTV, together with Medical Operations Referral and word-of-mouth Pricing, packaging and monetization Positioning and messaging Growth reporting and the insight the leadership team runs the business on The growth team and external partners What you'll do Co-shape strategy, priorities and operating rhythm with the CEO and leadership team Run a strong experimentation cadence Work AI-native: decide what in growth should run on AI and build the end-to-end workflows Default to agents: reach for AI agents before headcount, then hire people for the rest Treat growth as a product discipline: work in the product with engineering and clinical on onboarding, activation and retention, not just channels Bring structure, prioritization and momentum where things are undefined Lead cross-functional initiatives across commercial, clinical and product/tech Raise standards, remove bottlenecks, and increase execution speed Be hands-on, this is a builder role, not a "slide-only" role What success looks like First 30 days: Go deep on the product and the patient journey, the funnel and unit economics, and our patients and team. Come back with a growth model and your own read on where the biggest growth is. By 90 days: Deliver 2 to 3 clear improvements to acquisition or retention that move the numbers By 6 months: Growth runs as a gold-standard function with clear unit economics, a strong experimentation engine and a clear plan to scale revenue sharply from here. Who you are You're a high-ownership leader who can zoom out and zoom in, from strategy to execution, without losing quality. You likely have experience from one or more of these environments: A fast-moving scale-up/startup where you've built or scaled the growth function A high-standard organization where you've learned what "excellent" looks like A strategy/analysis-heavy role (e.g., consulting, corporate strategy, analytics) and you've proven you can operate and deliver Most importantly, you bring real craft in growth: Deep experience in B2C growth, since that's where we are today You've personally taken a consumer subscription business through a step-change in scale, while holding or improving CAC and payback You've diversified acquisition beyond paid marketing and organic search, and you treat retention and lifecycle as part of growth, not someone else's job You've built in-product growth with product and engineering: onboarding, activation, paywalls and retention loops You deploy budget against strict payback discipline, not into a target You're AI-forward, you think in automated workflows and in what's now possible in growth that wasn't possible before AI You're metrics-driven, structured, and decisive, and you execute with pace You're fluent in Swedish and English, since Sweden is our home market today, with international expansion ahead. Bonus (not required): Experience across B2B, B2B2C, insurance or partnership models, since those are routes we want to explore Experience in healthcare and HealthTech Experience scaling a function from early stage into growth Familiarity with Swedish/EU healthcare context Location We work together from our office in central Stockholm. Why Velora Real impact: help people live longer, healthier lives High ownership: run one of the most critical parts of the business The team: high standards, low ego, and plenty of fun along the way Meaningful option package (equity) Ready to build with us? Send your application (CV/LinkedIn) and a short note answering: What you would focus on first if you owned our growth, and why One example where you combined strategy + execution to drive measurable results How you use AI in your growth work today, and where do you think it goes next We're looking forward to hearing from you. Best, Vidar Laestadius CEO and Founder of Velora Health
Surgical Science is a global organisation and leading provider of medical training simulations and software solutions. 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, Stockholm, Tel Aviv, Cleveland, Cardiff, and Shenzen, 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. We’re looking for a Product Manager to lead the development and growth of our medical simulation products while contributing to and supporting our strategic initiatives. In this role, you’ll combine your expertise in product development, clinical workflows, technology, and customer insights to shape solutions that advance healthcare training and outcomes. You’ll own complex product initiatives, align cross-functional teams, and shape the roadmap for your product area, collaborating closely with engineering, clinical, marketing, and commercial partners. This is a chance to influence products that make healthcare education more effective, while working in a fast-moving, collaborative environment. This position will be based in our HQ in Gothenburg, reporting to Senior Director, Product Management. What you'll do: Own the end-to-end product lifecycle, from discovery and development to launch and iteration Translate customer, clinical, and technical needs into clear requirements and actionable plans Drive cross-functional execution across engineering, clinical, regulatory, and commercial teams Conduct market analysis and prioritization to inform roadmap and long-term strategy Support product strategy, value propositions, and core messaging as the source of truth Represent the product in key stakeholder engagements, both internally and externally Collaborate with Marketing on global events, exhibitions, and supporting materials Support go-to-market (GTM) strategy and execution, ensuring alignment and measurable launch success Support product marketing and sales enablement materials (e.g., positioning, demos, FAQs, competitive insights, clinical value) Act as the product authority, ensuring all materials are accurate, consistent, and strategically aligned Contribute to best practices and continuously improve ways of working Travel locally and globally as needed to engage with customers and partners (few times a year) What you'll bring: Around 2~5 years' experience as a technical Product Manager Experience in clinical/health care/medical industry/products, for example through education or work experience, ideally within an R&D software environment Strong technical and product expertise, with a track record of managing complex projects Proven ability to lead cross-functional collaboration and drive product execution Project management skills, with experience working in remote and global teams Excellent written and verbal communication skills in English. Swedish language is a plus Ability to work independently, take ownership, and make sound product decisions Strong interpersonal, stakeholder management, analytical, and problem-solving skills Why choose us? We operate at the intersection of innovative software and purpose-driven product development. We are a global organization with strong values and deep roots in Swedish work culture. We offer a high level of trust, autonomy, and true ownership over your work. Benefits: 🌍 Global environment (English as primary language) 💻 Hybrid work ⌚️ Flexible working hours 🏩 Optional Private healthcare 💚 Wellness allowance (Friskvårdsbidrag) 🚲 Optional bicycle lease 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.
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! Specialists in Gastroenterology for hospital-based roles Dignus Medical is recruiting gastroenterologists for permanent positions at hospitals across Sweden. We welcome both specialists who wish to work broadly within gastroenterology and those who prefer to focus primarily on endoscopic procedures. The roles can be adapted depending on your professional interests and experience. Opportunities include: Outpatient clinic work only Combined outpatient and inpatient care Clinical work with a strong emphasis on endoscopy You will work in a structured hospital setting with access to modern diagnostic tools and established clinical routines. Collaboration with internal medicine, surgery, radiology, and pathology is an integral part of the work. What Dignus Medical Offers You: Ongoing support from a dedicated recruiter before, during, and after your employment. Assistance with obtaining Swedish authorization and specialist approvals, if required. Help with accommodation and travel arrangements, including support for your family, if necessary. Access to a free language course with a private tutor via Teams/Skype. Qualifications: EU-recognized specialist certification in gastroenterology Experience in clinical gastroenterology; endoscopy experience is an advantage Good communication skills in English Willingness to learn Swedish Contact us to discuss current gastroenterology positions in Sweden. We look forward to receiving your application! You can also register your CV (https://dignusmedical-en.recman.page/login) or sign up for our newsletter (https://www.dignusmedical.no/en/sign-up-for-newsletter/) to stay updated on future opportunities.
Kenvue is currently recruiting for a: Senior Manager, Clinical Science, Self Care What we do At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Who We Are Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here. Role reports to: EMEA Translational Science RD Director Location: Europe/Middle East/Africa, Sweden, Skane, Helsingborg Work Location: Fully Onsite What you will do Key responsibilities: Serves as clinical strategy lead for new product innovations and clinical programs in all phases of product development which include planning, design, execution, and reporting of clinical studies for assigned categories. Responsible for representing clinical strategies during health authority interactions. Shape and deliver claims, claims roadmaps, creative claims substantiation strategies and communication pipeline targeting both consumers and healthcare professionals. Play a claims subject matter expert role in understanding the relevant science to provide contributions and/or make recommendations to strengthen claims and or science storytelling to cross-functional project teams. Championing a human-centric innovation mindset Assures timely and quality completion of investigator brochures, study protocols, clinical study reports, and any documents needed for regulatory filing as well as timely and accurate publication of completed research. Build and maintain strong relationships with key stakeholders, including internal and external scientific partners, to advance research and development efforts. Responsible for clinical evaluation reports for medical devices in development and for post-market clinical follow up studies for in-market devices in their assigned need state. Support activities as needed including, but not limited to, Core Data Sheet, review of periodic safety reports, ingredient/product issue management, and benefit/risk challenges. Requirements: An advanced degree (e.g., PhD or PharmD or MD) is strongly preferred Experience in mapping out and leading full clinical development programs for regulatory submission is strongly preferred. Experience in developing clinical designs and methodologies, with execution of clinical studies. Experience in developing compelling claims & communication strategies and translating scientific evidence into robust claims substantiation. Demonstrated ability to understand the business context and work closely with commercial business partners in the development of over-the-counter medicinal products. Experience/leadership in a people/team management capacity is a plus. Must have ability and flexibility to work in a global environment. Ability to manage multiple projects and mentor junior colleagues. Excellent verbal and written communication skills Kenvue Helsingborg The Kenvue site in Helsingborg, Sweden is the home of the strong and growing brand NICORETTE®, a global market leader in smoking cessation. In 2021 our production facility was recognized as a Lighthouse by World Economic Forum, marking us as a beacon in The Fourth Industrial Revolution. The Helsingborg site is one of the largest employers in the city of Helsingborg, and the business is divided in two separate departments: Operations, where we house our manufacturing activities and R & D, our global development center for excellence working in three therapeutic areas for selfcare treatments: Smoking Cessation, Digestive Health and Cough & Cold. For more information, click here If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation
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.
Are you a psychologist with Danish authorization, or are you interested in applying for Danish authorization? If so, you could be our next colleague at our psychiatric clinic in Copenhagen. About the Position Althea Care is looking to expand our team with additional psychologists at our clinic in Copenhagen. We work with efficient and well-structured clinical pathways that support high-quality, coordinated, and individually tailored care. As a psychologist with us, you will have the opportunity to conduct neuropsychiatric assessments and provide treatment for conditions such as ADHD and autism. The position can be offered either as permanent employment or on a consultancy basis. We are currently looking for psychologists with experience in neuropsychiatric assessments of children and adolescents, as well as adults. The role combines on-site clinical work in Copenhagen with remote work. Qualification requirements: .Fluent in Swedish. .Danish authorization as a psychologist, or a willingness to begin the application process for Danish authorization. .Experience conducting neuropsychiatric assessments. About Althea Care Althea Care is a Danish psychiatric clinic based in Copenhagen, providing assessment and treatment services to both Danish and Swedish citizens. Founded in 2023, we offer psychiatric care for children, adolescents, and adults. Our clinic specializes primarily in the assessment and treatment of neurodevelopmental conditions. We do not provide services for patients with substance use disorders. Our clinical pathways are clearly structured and based on national clinical guidelines for each diagnosis. We combine high standards of patient safety with the flexibility to provide individualized, patient-centred care. Our multidisciplinary team includes psychiatrists, psychologists, nurses, and healthcare administrators. We are committed to creating a sustainable and supportive working environment. Our organization is characterized by clear routines, close collaboration, minimal administrative meetings, and a high degree of autonomy, allowing each team member to plan and manage their own work. Applications are reviewed on an ongoing basis, and the position may be filled before the application deadline. Working Environment & Benefits Working hours are generally scheduled during weekdays, with the possibility of adapting your schedule to include evenings and weekends if preferred. We strive for a balanced mix of digital and in-person consultations based on patients' needs. The role can be performed partly remotely. Employment Details Location: Copenhagen / Hybrid (partly remote) Employment type: Full-time or part-time Contract: Permanent (or consultancy agreement) Employer Althea Care ApS https://www.altheacare.se/ Contact Josephine Nemark Operations Manager / Licensed Psychologist info@altheacare.dk
Are you a psychologist with Danish authorization, or are you eligible to apply for Danish authorization? Would you like to work with a modern psychiatric clinic based in Copenhagen while providing treatment remotely? Althea Care is expanding and is looking for additional psychologists to join our team. We offer a structured, efficient, and evidence-based model of care that combines clear clinical pathways with individualized treatment. We are currently seeking psychologists with experience or interest in providing psychological treatment for children and adolescents via remote consultations. The position can be offered either as employment or as a consultancy assignment. Qualification requirements: .Fluent in Swedish. .Danish authorization as a psychologist, or willingness to apply for Danish authorization. About Althea Care Althea Care is a private psychiatric clinic based in Copenhagen, providing assessment and treatment for both Danish and Swedish patients. Established in 2023, we offer services to children, adolescents, and adults. Our clinical work primarily focuses on the assessment and treatment of neurodevelopmental conditions. We do not provide treatment for substance use disorders. Our care pathways are clearly structured and based on national clinical guidelines, ensuring high standards of patient safety while allowing for individualized treatment plans. Our multidisciplinary team consists of psychiatrists, psychologists, nurses, and healthcare administrators. We are committed to creating a sustainable and enjoyable working environment. Our organization is characterized by clear routines, close collaboration, minimal unnecessary meetings, and a high degree of autonomy, allowing each clinician to organize their own work. Recruitment is ongoing, and the position may be filled before the application deadline.
To Care City söker nu dig som är leg psykolog med erfarenhet från primärvården till ett längre föräldravikariat. Vi är en lagom stor vårdcentral med ca 9400 listade patienter i alla åldrar. Vi har allmänläkare, ST-läkare, hemsjukvård, sköterskemottagningar samt ett psykosocialt uppdrag för både barn och vuxna. Tillsammans bidrar till en trivsam och familjär arbetsplats med högt i tak, nära till skratt och en genuin omtanke om varandra och våra patienter. Vad erbjuder vi dig? En väl fungerande arbetsplats med en stark teamkänsla Ett väl uppbyggt psykosocialt team som arbetar efter tydliga rutiner, samverkar under regelbundna team-konferenser och har en nära samverkan inom såväl psykolog-gruppen som med övriga professioner. En arbetsplats som strävar mot att hålla en hög tillgänglighet och kvalitet samt ger möjlighet att påverka såväl arbetssätt som schemaläggning och därmed arbetsmiljö. Arbetet som psykolog på To Care City innefattar utredning och behandling av patienter inom det psykosociala uppdraget. Vi arbetar systematiskt och strukturerat enligt KBT med strävan om att alltid erbjuda våra patienter den bästa vården. Besöken kan vara planerade såväl som av kortare mer akut bedömnings-karaktär. Hos oss kommer du att arbeta i nära samarbete med samtliga professioner på mottagningen och du kommer att vara en viktig del i det fortlöpande förbättringsarbetet och utvecklingen av verksamheten. Vem söker vi? Vi söker dig som är legitimerad psykolog med intresse för och erfarenhet av arbete inom primärvården och det psykosociala uppdraget. Du är trygg i din yrkesroll och har förmågan att se verksamheten ur ett helhetsperspektiv med både patienten och mottagningen i fokus. Du är stabil, flexibel och anpassningsbar till olika situationer samt har lätt för att samarbeta. Du behöver ha en god kommunikationsförmåga i syfte att skapa goda relationer med patienter såväl som kollegor. Som person är du lyhörd för våra patienters behov och ditt bemötande är professionellt och ödmjukt. Det är meriterande om du har erfarenhet från och/eller intresse för arbete med såväl barn som vuxna. Rollen avser dock främst arbete med vuxna patienter. Anställning och ansökan: Intervjuer sker fortlöpande under rekryterings-tiden, så ansök gärna redan idag. Stor vikt läggs vid personlig lämplighet. Vi ser verkligen fram emot din ansökan! Mottagning To Care City ligger på Karlavägen 58, mitt på Östermalm. Verksamheten har ca 9000 listade patienter och består av husläkarmottagning, psykosocialt team och hemsjukvård. Personalgruppen består av 25 medarbetare. Om företaget Prima Vårds filosofi bygger på det lokala engagemanget och att den bästa kvalitetsutvecklingen sker genom lokalt engagemang. Prima Vård är ett familjegrundat vårdbolag med verksamhet inom primärvård, barn-och kvinnosjukvård, psykiatri samt företagshälsovård. I bolaget ingår omkring 100 lokala vårdenheter med stor bredd. Intresserad om att läsa mer om Prima Vård? Slå oss gärna en signal eller besök gärna vår hemsida: https://primavard.se/om-prima-vard
På Psykiatri Sydväst har vi fem heldygnsvårdsavdelningar med olika uppdrag, där samarbete mellan avdelningarna är en självklar del av vårt arbete. Vår vård präglas av ett personcentrerat förhållningssätt och vi arbetar enligt konceptet Safewards. Här finns tid för reflektion och vi erbjuder löpande kompetensutveckling. Vi har frågat klinikens medarbetare vad som gör det attraktivt att arbeta här. Läs deras svar här: 10 skäl att jobba på Psykiatri Sydväst Tror du som vi på ett personcentrerat arbetssätt där bemötande och trygghet är centralt – även nattetid? Har du ett medmänskligt engagemang och vill vara del i att utveckla omvårdnad inom psykiatrisk heldygnsvård? Vi söker dig som vill göra skillnad tillsammans med oss på M77. Vi söker dig som Är legitimerad sjuksköterska. Har erfarenhet från psykiatrisk heldygnsvård och vill utveckla omvårdnaden på individ och gruppnivå. Har ett genuint intresse för psykiatrisk omvårdnad och vill arbetsleda på ett strukturerat och tryggt sätt med hög grad av ansvar. Har lätt för att samarbeta och bygga relationer och kan bidra till en hög kvalitet av psykiatrisk omvårdnad. Är trygg även kring somatisk vård. Arbetsuppgifter Din roll – sjuksköterska natt Omvårdnadsansvar med patientcentrerat fokus Ta vid där kvällen slutar Aktivt verka för patientens delaktighet Medicinhantering och dokumentation i TakeCare Arbetsledning i samarbete med undersköterskor Skapa trygghet och god sömnhygien för patienterna Du arbetar självständigt men i nära team med dag- och kvällspersonal för att ge kontinuitet i vården. Kvalifikationer Vi söker dig som Är legitimerad sjuksköterska Har erfarenhet från psykiatrisk heldygnsvård och vill utveckla omvårdnaden på individ och gruppnivå Har ett genuint intresse för psykiatrisk omvårdnad och vill arbetsleda på ett strukturerat och tryggt sätt med hög grad av ansvar Har lätt för att samarbeta och bygga relationer och kan bidra till en hög kvalitet av psykiatrisk omvårdnad Är trygg även kring somatisk vård Meriterande Specialistutbildning i psykiatri. Vi lägger stor vikt vid personlig lämplighet. Vårt erbjudande till dig Utbildning i arbetsledning – kunskap om hur du får teamet att fungera optimalt Mentorskap – är du intresserad paras du ihop med en av sektionens erfarna sjuksköterskor som kan stödja dig i ditt arbete och professionella utveckling. Anpassad introduktion utifrån dina behov och din bakgrund. Vårt mål är att du ska vara trygg med arbetsuppgifterna innan du arbetar självständigt. Kvarstannandebonus (ATK) enligt regionens avtal med vårdförbundet. Det innebär att du får 40 h/år i en timbank som du kan ta ut i lön, ledighet eller pensionsavsättning. Som legitimerad sjuksköterska med specialistutbildning i psykiatrisk vård har du möjlighet att ta på dig extra uppdrag. Upp till 20% av arbetstiden kan läggas på uppdraget och det utgår även ett lönetillägg om 2500 kr/månad. Som arbetsgivare är vi måna om att du ska må bra. Därför erbjuder vi bland annat friskvårdstimme, ett friskvårdsbidrag på 5 000 kr per år, ett mycket förmånligt pensionsavtal samt föräldraförmåner. Läs mer om alla våra förmåner här. Är du nyfiken på tjänsten? Sök idag eller kontakta oss för mer information! Tillsvidare, 100% natt-tjänst enligt schema 5 veckors rullande schema. Du söker tjänsten med CV, personligt brev och kopia av din sjuksköterskelegitimation. Urval och intervjuer sker löpande. Varmt välkommen med din ansökan! Om Psykiatri Sydväst Universitetskliniken Psykiatri Sydväst drivs av visionen att erbjuda den bästa psykiatriska vården i Sverige. Vi är en del av SLSO psykiatri och har omfattande samverkan med Karolinska Institutet. Kliniken och präglas av forskning, nytänkande, innovationer och ständig utveckling. Psykiatri Sydväst är i sin helhet samlad i Flemingsberg vid Karolinska Universitetssjukhuset Huddinge. Läs mer om Psykiatri Sydväst här. Att söka jobb i Region Stockholm Vi eftersträvar jämställdhet och jämlikhet på vår arbetsplats och ser gärna sökande med olika bakgrund och förutsättningar. Vi tar endast emot ansökningar via detta system. Ansök genom att klicka på knappen ”Ansök”. Ansökningar per brev eller e-post beaktas inte. Vi undanber oss direktkontakt med bemannings- och rekryteringsföretag samt säljare av ytterligare jobbannonser. Vårt rekryteringssystem kan inte hantera anonyma ansökningar eller sökande med skyddade personuppgifter. Om du har skyddade personuppgifter ber vi dig att kontakta den kontaktpersonen som finns angiven i annonsen. Din ansökan kommer då att hanteras utanför rekryteringssystemet. Du bör även vara försiktig med vilken information du lämnar i din ansökan och endast ta med information som är relevant för den aktuella befattningen. Region Stockholm ansvarar för hälso- och sjukvård, kollektivtrafik, regional utveckling och bidrar till kulturlivet. Varje dag, dygnet runt. I landets snabbaste växande region. Tillsammans skapar vi Europas attraktivaste storstadsregion. Läs mer om hur det är att jobba hos oss i Region Stockholm
ABOUT MINDLER At Mindler, our mission is to transform and democratize access to mental health care, making it available for everyone, when they need it. We are on a bold journey to change lives for the better by breaking the stigma surrounding mental illness and empowering people across Europe with high-quality tech-enabled human-led mental healthcare. Deeply rooted in human compassion and clinical excellence, we combine evidence-based digital therapy with innovative technology - supporting clinicians to deliver and patients to receive the best possible mental healthcare. Today we're delivering healthcare across five European markets, and we're just getting started. We're looking for great people who want to grow with us! THE ROLE As Accounting Manager, you'll play a key role in strengthening and scaling Mindler's finance function as we continue to grow internationally. Reporting to the CFO, you'll lead our accounting team, ensure accurate, high-quality financial reporting across multiple markets, and play a key role in developing an accounting function that scales with our business. This role is ideal for someone who enjoys combining strategic thinking with hands-on execution. You've experienced both the pace of a fast-growing company and the structure of a larger organisation, giving you a strong understanding of what good looks like when it comes to accounting processes and controls. Now you're excited to bring that experience to an ambitious, purpose-driven company where you can make a real impact. WHAT YOU’LL BE RESPONSIBLE FOR Financial Reporting & Close Lead the monthly, quarterly, and annual close processes across our entities, ensuring timely and accurate financial reporting. You'll oversee group consolidation and ensure compliance with K3, IFRS, and local GAAP. Accounting Operations Lead day-to-day accounting operations while continuously improving processes, controls, and ways of working to support a growing international business. Compliance & Controls Ensure compliance with statutory and regulatory requirements across our markets, maintain a strong internal control environment, and coordinate external audits. Team Leadership & Development Lead and develop the accounting team, fostering collaboration, accountability, and continuous learning. Cross-Functional Collaboration Partner closely with the CFO and colleagues across Finance, Legal, HR, and Operations to support business growth, improve processes, and provide accounting expertise on key business initiatives. Systems & Data Drive the continued development of our accounting systems and tools, improving efficiency, data quality, and scalability as we grow. WHO WE’RE LOOKING FOR We're looking for someone who thrives in a growing and complex business, who enjoys improving, simplifying, and building better ways of working and who takes accountability and ownership. You'll likely bring: * A degree in Accounting, Finance, or a related field (professional accounting qualification is a plus). * Solid accounting experience, including leadership responsibilities. * Experience from an international, multi-entity environment. * Experience from both a larger organisation and a fast-growing company. * Strong technical accounting knowledge and experience with financial reporting and close processes. * A pragmatic mindset with the ability to balance accuracy, structure, and business needs in a fast-moving environment. * Experience working with ERP systems and driving process improvements. * A collaborative leadership style with the ability to coach and develop others. * Strong communication skills and the ability to explain financial matters to non-finance stakeholders. * Fluency in English and Swedish, both written and spoken. Most importantly, you're curious, pragmatic, and enjoy rolling up your sleeves to help build a finance function that's ready for what's next. WHY JOIN MINDLER? At Mindler, you'll be part of a company with an ambitious mission: making high-quality mental healthcare accessible to more people. As Accounting Manager, you'll have the opportunity to influence how we shape and scale our business and finance function while working closely with an experienced CFO and colleagues across Europe. We offer a collaborative, low-ego culture where people care deeply about both results and each other. You'll have the freedom to take ownership, make an impact and grow alongside an ambitious international team. LOCATION Based in Stockholm with a minimum of three days per week in the office. We'll be reviewing applications on a rolling basis. As many of us are enjoying some summer holiday, the recruitment process may take a little longer than usual. We look forward to hearing from you! Mindler is an equal opportunity employer. All qualified applicants will be considered for employment without regard to gender, gender identity or expression, national origin, religion or other beliefs, disability, sexual orientation or age.
BUILD SOMETHING MONUMENTAL FOR HEALTHCARE! At Tandem Health we’re reimagining healthcare by putting clinicians first. Our platform - designed by clinicians, for clinicians - is built on deep insight into real-world pain points, with intuitive medical notes and workflows that truly support patient care. We’re a fast-scaling health-tech company backed by top investors and expanding globally. We move fast, stay curious, and believe building something that matters starts with an extraordinary team. If you're passionate about impact and innovation, we'd love to meet you! ABOUT THE ROLE Tandem is building the clinical operating system for European healthcare. As we scale across countries and health systems, rigorous, fast-moving clinical research is critical to proving impact, shaping product direction, and positioning Tandem as a leader in healthcare AI. We are now looking for a Clinical Research Lead to own and drive Tandem’s clinical research strategy end-to-end. You will lead research efforts across customers and markets, design and execute high-impact studies, and ensure Tandem is at the forefront of clinical evidence generation within European healthcare.This is a hands-on leadership role for someone who thrives in a fast-paced environment, enjoys shipping research (not just planning it), and wants to see their work directly influence real-world clinical practice. WHAT YOU WILL DO * Own and execute Tandem’s clinical research strategy across multiple countries and customers * Plan, coordinate, and lead clinical studies in collaboration with healthcare providers, internal product teams, and external partners * Design robust study protocols that balance scientific rigor with speed and operational feasibility * Lead data analysis, interpretation, and dissemination of results * Publish high-quality research in leading journals and conferences within healthcare and AI * Support regulatory, commercial, and product teams with clinical evidence and insights * Represent Tandem externally in scientific and clinical forums, strengthening our reputation as a research leader * Continuously improve how we run research - making it faster, more scalable, and more impactful WHAT YOU BRING * A medical background (MD or equivalent) * PhD (required) in a relevant field (e.g. clinical research, epidemiology, biostatistics, computer science/ML, biomedical engineering), with a strong publication record * Strong experience leading clinical research projects end-to-end * A proven publication track record in high-quality journals, ideally within healthcare AI or digital health * Experience working with real-world clinical data and healthcare systems * Comfort operating in a fast-paced, ambiguous environment where priorities evolve quickly * A bias toward action and impact - you value rapid, high-quality research over multi-year academic timelines * Excellent communication skills and the ability to work cross-functionally across clinical, product, and commercial teams BONUS POINTS * Experience working in or with European healthcare systems across multiple countries * Background in health tech, AI, or a high-growth scale-up * Prior experience running multi-site or multi-country clinical studies * A strong external network within clinical research or healthcare AI * Deep technical understanding within AI, incl. programming expertise LOCATION We believe the best ideas happen when we’re together. This role is based in our vibrant HQ in the Epicenter building in the heart of Stockholm where you will work primarily from our office to collaborate, connect, and build our culture. HOW TO APPLY We adopt a continuous selection process, so please make sure to apply with your CV in English. Our interview process consists of 4 stages: 1. Screening interview with Talent Acquisition 2. First interview with our CEO and Co-Founder 3. Follow-up interview with one of our Medical Operations Clinician 4. Working Day - Join us in the Stockholm office for a half-day to experience our culture firsthand, collaborate with our team, and see how you work in action. BENEFITS * Competitive salary & company stock options * 25 days/year of paid vacation * 5,000 SEK wellness allowance (friskvårdsbidrag) * Social and team-building activities (off-sites, after works, winter/summer parties) * An opportunity to make a real positive impact in the world of healthcare * Work with some of the best minds in AI, healthcare, and engineering. We review our benefits packages on a regular basis and might modify our benefits from time to time. CULTURE AT TANDEM At Tandem, we move fast, think big, and take ownership. We're a high-performing, diverse team with a shared drive to change the future of healthcare - and we’re just getting started. Our culture is built on action, ambition, and learning. You'll be trusted to take the lead, challenge yourself, and make an impact from day one. We believe real growth happens when you're stretched, supported, and surrounded by smart, passionate teammates who want to win together. Even though we’re spread across countries, we come together often in Sweden for team meetings, social events, and offsites - blending global reach with real human connection. We hire for talent, potential, and attitude - valuing different backgrounds and fresh perspectives. Great ideas come from everywhere, and we’re building a team that reflects the world we want to change. Tandem handles sensitive patient data and will conduct a background check before hiring any candidate.
At Neoventa, we develop fetal monitoring solutions that help clinicians make critical decisions during childbirth. We are looking for a Technical Product Manager to take lifecycle responsibility for our fetal/maternal monitoring platform. About the role You will own our fetal/maternal monitoring platform, including CTG and fetal ECG/ST analysis, and guide it throughout its lifecycle—from requirements to development, release, and continuous improvements. Working closely with R&D, Clinical, Regulatory, Quality, Commercial teams, and external partners, you will turn user needs into safe, compliant, and meaningful products. The role is based at our HQ in Mölndal, reporting to the Chief Technology Officer. What you will do Own the products' roadmap and technical backlog Translate clinical and user needs into product and system requirements Drive technical decisions together with the rest of the R&D team Ensure solutions meet safety, regulatory, and commercial requirements Contribute to verification, validation, and product release Analyze field performance and drive continuous improvement Act as the technical expert internally and externally Your profile Engineering degree (Biomedical, Electrical, Software, Systems or similar) 8+ years of experience in technical product management, systems engineering or similar Experience from active medical devices (or other regulated industries) Strong understanding of embedded systems, signal processing, and HW/SW integration Fluent in professional English Who you are You combine deep technical curiosity with a strong sense of ownership You are comfortable navigating complexity and making sound decisions with incomplete information You are a collaborative problemsolver with a can-do attitude You communicate with clarity and adapt your message to your audience You focus on what creates real value - balancing technical possibilities with clinical and business needs Why join us? This is a unique opportunity to become the techincal product manager for a complex medical device and help shape the future of fetal monitoring. You'll work at the intersection of technology, clinical practice, and innovation - where your professionallism will have a direct impact on healthcare professionals, mothers, and babies worldwide. To apply Neoventa is committed to sustainability and diversity and encourages applicants from all backgrounds. The application deadline is August 9th, 2026. Due to the summer vacation candidate selection and interviews will be done after the application period. We do not accept applications via email or phone; instead, we kindly ask you to apply directly through our career website. If you have any questions regarding the recruitment process or the position, you are welcome to contact Thomas Börstell, Chief Technology Officer, thomas.borstell@neoventa.com or Frida Svenningsson, Chief People & Culture Officer, frida.svenningsson@neoventa.com. We look forward to receiving your application!
We are looking for a Head of Marketing & Communications to strengthen our product marketing and drive commercial impact globally. The role is based at our HQ in Mölndal, reporting to the Chief Commercial Officer, with responsibility for a marketing team of two. Your impact You will play a key role in strengthening our commercial impact, by shaping how we position our products, how we communicate their value, and how we support our sales teams and distributors globally. You are comfortable switching between thinking long-term and getting things done yourself – whether that means shaping a message, creating material, or supporting a launch together with sales. You will play a key role in strengthening our global presence, supporting sales, and positioning Neoventa as a trusted partner in obstetric care. What you will do Strengthen how we position our product offer and ensure our messaging is clear and consistent across markets and distributors Own and drive Neoventa’s global marketing and communications strategy Partner and contribute closely with Sales/distributors, R&D and Clinical teams to translate customer and market insights into impactful communication Develop marketing campaigns and sales materials to support distributors and sales teams Contribute to the development of Neoventa Academy for education and engagement together with KOL’s and the Clinical team. Develop our digital channels and content, including growing our e-learning offering Own and drive product launches and portfolio communication together with sales Define budget, team goals and KPIs, measure performance and continuously improve marketing effectiveness Lead and develop the marketing team, create clear priorities, a positive work environment, and strong execution across global marketing and communications activities. Your profile We believe you are commercially minded, collaborative, and comfortable working close to both products and sales. You likely bring: Degree within Marketing or a related field Minimum 5 years experience from marketing within MedTech or other Life Science business Experience from international marketing in a commercial and product-focused environment Experience working closely with sales teams and distributors Track record of translating strategy into execution and results Experience leading projects and teams Experience in service selling is considered an advantage Who you are A strategic thinker with a hands-on approach and a strong sense of ownership Collaborative and proactive, with ease in working across teams and functions Driven and structured, able to create clarity in dynamic environments You can take complex clinical and product information and turn it into clear, simple messaging Curious about customers and markets, with a focus on creating real impact Unpretentious, warm, and considerate in how you engage with others Why Join Neoventa? This is an opportunity to join a purpose-driven company where your work truly matters. You will shape the future of a growing global brand while contributing to better healthcare outcomes for families around the world. To apply Neoventa is committed to sustainability and diversity and encourages applicants from all backgrounds. The application deadline is July 26th, 2026. Selection will be done during the application period, and interviews will start after the summer period in August, so please do not wait to submit your application. We do not accept applications via email or phone; instead, we kindly ask you to apply directly through our career website. If you have any questions regarding the recruitment process or the position, you are welcome to contact Josefine Wihlborg, Chief Commercial Officer, josefine.wihlborg@neoventa.com or Frida Svenningsson, Chief People & Culture Officer, frida.svenningsson@neoventa.com. We look forward to receiving your application!
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.
Thermo Fisher Scientific is looking for an experienced clinical project management leader to oversee complex, international clinical research projects. You may work as a Project Lead, provide strategic project oversight, manage and develop colleagues, or combine elements of these responsibilities according to business needs. You will be accountable for delivering projects to agreed standards of quality, time and cost while maintaining strong relationships with customers and cross-functional teams. Our Mission is to enable our customers to make the world healthier, cleaner and safer. In this role, your leadership will help customers progress promising medicines through clinical development and bring potentially life-changing therapies to patients. Main responsibilities You will: Lead complex clinical projects involving multiple services, countries or regions. Act as the principal contact for customers and manage expectations throughout the project. Take responsibility for project quality, timelines, budgets, forecasts and resources. Identify and manage risks, issues and changes to project scope. Lead and motivate international, cross-functional project teams. Ensure projects comply with company procedures, regulatory requirements and ICH-GCP standards. Support proposal development, customer strategy and business growth opportunities. Coach and develop project leaders and other colleagues. Where applicable, manage employees, including recruitment, objective setting, performance management and career development. Build trusted relationships with senior customers, internal leaders and key stakeholders. Skills and experience You should have: A bachelor’s degree, relevant vocational qualification or equivalent practical experience. Experience comparable to at least 10 years in clinical development, clinical research or a related field. At least five years of management or significant leadership responsibility. Strong knowledge of clinical development and relevant regulatory requirements. Expert understanding of cross-functional project management, including time, quality and cost. Experience managing budgets, forecasts, resources and contractual changes. Excellent communication, presentation, negotiation and relationship-building skills. The ability to lead, coach and motivate international teams. Strong judgement, problem-solving and strategic thinking skills. Confidence working in complex, changing or ambiguous situations. Competence using Microsoft Office and relevant clinical project management systems. A combination of suitable education, training and directly related experience may also be considered. Working environment This is a permanent, remote role based in Sweden. The position may also involve occasional work in office, laboratory or clinical environments, depending on project requirements. Why join Thermo Fisher Scientific? You will have the opportunity to lead important work, develop global talent and build a career with meaningful impact.
Camurus is an international, science-led biopharmaceutical company committed to developing and commercializing innovative, long-acting medicines for improving the lives of patients with severe and chronic diseases. New drug products with best-in-class potential are conceived based on the company’s proprietary FluidCrystal® technology and its extensive R&D expertise. The R&D pipeline includes products for the treatment of dependence, pain, cancer, and endocrine diseases. Camurus has operations across Europe, the US, and Australia, with headquarters in Lund Sweden. The company’s shares are listed on Nasdaq Stockholm under the ticker CAMX. For more information, visit www.camurus.com and LinkedIn. In this role, you will get the opportunity to work with committed colleagues in a collaborative team, close to both commercialised products and development projects. Camurus is a rapidly growing and innovative company, and you will have a strong impact on the outsourced manufacturing processes throughout the product lifecycle. We are looking for an experienced Senior Process Engineer to join our Manufacturing Operations team. In this role, you will be responsible for leading technology transfer activities for manufacturing processes for injectable pharmaceutical products, from development into manufacturing environments at Contract Manufacturing Organizations (CMOs). You will support products from clinical development through to commercial supply. As Senior Process Engineer, you will act as a subject matter expert in pharmaceutical manufacturing processes, working closely with internal stakeholders and external partners to ensure robust, scalable, and GMP-compliant manufacturing operations. You will report to the Director Manufacturing Operations. Main responsibility Among others, your responsibilities will include: · Lead technology transfers of injectable pharmaceutical products from development into commercial manufacturing at CMOs. · Partner with R&D to ensure that formulation and process development activities support successful scale-up, manufacturability, and long-term process robustness. · Provide technical support for process development, scale-up, validation, and commercial manufacturing activities at CMOs. · Act as technical lead for investigations and troubleshooting of process deviations, OOS results, manufacturing failures, and other complex technical challenges. · Contribute to CMC documentation in support of global regulatory submissions and product lifecycle management. · Ensure that manufacturing processes are executed in accordance with applicable GMP requirements and regulatory expectations. Candidate profile We are looking for a professional with at least 7 years of experience from pharmaceutical manufacturing operations. You hold a Master’s degree in Engineering, Life Sciences, or a related scientific discipline. You have hands-on experience from manufacturing process development, technology transfer, and GMP-regulated pharmaceutical manufacturing, preferably within sterile or injectable products. Experience from fill-finish operations and combination products development is considered a strong merit. As a person, you are collaborative, responsible, and driven by solving problems. You enjoy getting to the bottom of complex technical challenges and you are a pragmatic team player who takes ownership and follows through on commitments. At the same time, you are humble and low-prestige, always willing to support colleagues and contribute wherever needed. You thrive in a dynamic environment where technical expertise, collaboration, and problem-solving go hand in hand. Fluency in spoken and written English is required. Camurus offers This a great opportunity to join a highly dynamic company during a very exciting phase of growth. Camurus has been very successful in bringing pharmaceutical products to the market – and the ambitions are not to be lowered. With a diversified project portfolio in different stages, the commercial potential is considerable. The position offers an international work environment and corporate culture, with the possibility for individual development and growth. You will have great opportunities to influence, and you will work together with highly competent colleagues, caring for each other. Camurus has almost 300 employees with the head office located in Lund. The corporate culture is driven by our core values of innovation, collaboration, ownership, quality, and passion for realizing our patient-centric commitment. Information and application For more information about this job-opening, please contact recruitment consultant Tobias Lorentzon at TOBLOR Consulting, phone: +46 735 11 10 60. You apply for this position through TOBLOR’s career site, https://career.toblor.se/, by uploading your CV and personal letter. For more information about Camurus, please visit: https://www.camurus.com/. We are looking forward to seeing your application!
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.
Drive innovation where it matters Make your next move matter At Mölnlycke, we believe that real impact starts with people. People who are bold enough to challenge the status quo. People who care deeply about their work, their colleagues, and the world around them. People who know exactly why they do what they do. As a global medical solutions company, we design and deliver innovative products and services across wound care, operating room solutions, gloves, and antiseptics. Our mission is to advance performance in healthcare by supporting professionals, improving outcomes, and making a difference where it matters most. In Wound Care, we help to prevent, manage and accelerate the healing of wounds. Where you’ll make a difference Mölnlycke is now looking for a Packaging Developer to join our R&D Wound Care Packaging & Artwork team at our headquarters. In this role, you’ll contribute to meaningful work that improves lives. You will collaborate across teams, bring your ideas to the table, and help shape innovative packaging solutions that support both patients and healthcare professionals. Here’s how you’ll make an impact: Drive and execute packaging change projects with defined scope and impact Develop and implement new or improved packaging solutions to meet customer needs and regulatory requirements Own technical documentation and ensure compliance with global standards for medical device packaging Collaborate with procurement and suppliers, leading technical discussions, support audits, and build partnerships Identify and propose new packaging technologies, materials, and suppliers Act as a key contributor in cross-functional teams including R&D, project management, and process development Support sustainability initiatives through development of smarter, more sustainable packaging solutions What you’ll get Be part of a culture built on trust, care, and shared ownership. Your growth and development Opportunities to expand your expertise in packaging and medical device development Exposure to cross-functional collaboration and strategic decision-making Potential career paths into senior development roles, project management, or leadership Flexibility, wellbeing and benefits A collaborative, supportive, and highly experienced team environment Opportunities to make a real difference for customers, patients, and the environment Competitive compensation and benefits package A workplace that values wellbeing, inclusion, and continuous improvement What you bring We’re looking for someone who combines technical expertise with curiosity and a collaborative mindset. Must-haves Bachelor’s or Master’s degree in engineering, chemistry, life sciences, or equivalent Around 5 years’ experience in product/material development from medical devices, or packaging development from other regulated industry Fluent English, written and spoken Strong communication and stakeholder collaboration skills Key strengths and mindset High level of accuracy and attention to detail A collaborative, positive, and solution-oriented approach Curiosity and a genuine interest in sustainable packaging innovation and development Ability to balance technical rigor with business needs Nice to have Experience working with packaging materials such as paper, plastics, or bottles Interest or experience in sustainable packaging solutions Strong knowledge of design control and regulated environments Understanding of global regulatory requirements for packaging Please submit your application by August 9th. As we approach the holiday season, interviews are planned to take place in August. Our approach to Diversity & Inclusion We’re building a workplace where everyone feels seen, heard, and valued. We believe that a diverse mix of people makes us stronger—bringing fresh perspectives, driving better decisions, and helping us deliver solutions that reflect the world we serve. Inclusion isn’t just a value—it’s how we work, grow, and lead together. About Mölnlycke Mölnlycke is a world-leading medical products and solutions company that equips healthcare professionals to achieve the best patient, clinical and economic outcomes. Our business is organised in four business areas: Wound Care, Operating Room Solutions, Gloves and Antiseptics, with customer centricity, sustainability and digitalisation at the heart of everything we do. We employ around 8,700 people globally, with headquarters in Gothenburg, Sweden, and operations in more than 100 countries. Mölnlycke is a founding partner of GoCo Health Innovation City and has been part of Investor AB since 2007.
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