Search results for "Regulatory requirements"

Vi söker nu 8 engagerade och ansvarstagande ställningsmontörer som vill bli en del av vårt team och arbeta i ett företag där säkerhet, kvalitet och samarbete står i centrum. I rollen som ställningsmontör ansvarar du för att arbetet utförs säkert, effektivt och enligt gällande regler och föreskrifter. Arbetet är fysiskt och varierande, och passar dig som trivs med ett aktivt jobb och att arbeta tillsammans med andra. Du behöver ha ett positivt och lösningsorienterat tänk. Du behöver också vara säkerhetsmedvetna, en lagspelare och ha god fysisk förmåga, Vi erbjuder en trygg anställning, konkurrenskraftig lön, möjlighet till utveckling och ett arbetslag med fokus på arbetsmiljö, gemenskap och säkerhetstänk.

Are you passionate about export compliance and eager to play a key role in enabling global trade for a world leader in network video? We're looking for an Export Control Advisor to join our Trade Compliance team at our headquarters in Lund, Sweden. In this role, you'll be at the heart of what makes Axis's global operations possible - ensuring our high-tech products reach customers worldwide, responsibly and compliantly. You'll work across borders, collaborate with teams from Legal to R&D to Sales, and directly shape the processes that keep Axis moving forward. Who is your future team? We are a highly performing diverse team consisting of fourteen skilled people of different ages, gender, nationality, knowledge, and background. The combination makes us strong and adds flavor and joy to our workplace. Four people focus on Export Compliance, ensuring that Axis complies with Export Control regulations worldwide and that our high-tech products are not supplied to restricted countries, parties, or users. The other people focus on Customs Compliance, securing that import and export activities are performed in a compliant and efficient manner and customs costs are minimized. Your focus will be on Export Compliance. What you will do as Export Control Advisor: In this role, you are central to safeguarding Axis's ability to operate and grow globally. By ensuring compliance with complex EU and US export control legislation, embargoes, and sanctions, you directly protect the company and enable our products to reach customers worldwide. You will work cross-functionally with Legal, R&D, Sourcing, Order, and Sales across regions. Below is example of tasks within the Axis Export Compliance team: Serve as primary point of contact for Export Control matters. Responsibility for ECCN classification of commodities under both EU and US legislation. Gather required information and submit export license applications and determinations. Conduct daily restricted party screenings. Develop and improve processes concerning Export Control both global and regional, including defining business requirements for IT tool development. Meet with Customs and Export Control Authorities where needed and represent Axis. Providing internal training within the company. Who are we looking for/Who are you? We believe that you are an analytical person with a strong personal drive and a get it done attitude. You are curious, actively searching for new information and want to develop and learn new things. You have a positive mindset and are a team player but also thrive working independently, planning, and managing your own activities and delivering results. You like to take responsibility and have good organizational skills as well as ability to see both the details and the big picture - making the right priorities. You easily co-operate across organizational borders, build strong collaboration and relations with key stakeholders. You are of course passionate about Export Compliance and Supply Chain. You wish to contribute and interact on a global level and be a part of an ambitious team where we make things happen! We'd love to hear that you have/are: Required: Several years' experience of Export Control (EU, US legislation) and International Trade. Detailed knowledge about ECCN, Restricted Party Screening, Embargo, Sanctions, and more… Demonstrated experience in export control, covering both EU and US legislation and international trade. In-depth knowledge of ECCN classification, restricted party screening, embargoes, and sanctions. Experience classifying products and software under ECCN frameworks. Experience working with ISP and/or BIS export license processes. Experience operating in a global business environment. Strong communication and collaboration skills, comfortable working with colleagues and stakeholders across cultures and regions. Fluency in English (written and spoken). Bonus points for: Working knowledge of electronics and/or software from a technical perspective. Familiarity with ERP systems and proficiency in Microsoft Office applications. Comfortable with continuous improvement methodologies and mindset. What Axis have to offer We are a world leader in network video, where cutting-edge technology meets global impact. Here, you'll contribute to meaningful projects that shape the future of security and surveillance - developing solutions used worldwide. As a fast-growing company, we offer exciting career opportunities. You'll grow professionally through continuous learning, supported by a collaborative team that values creativity, innovation, and work-life balance. Our Lund HQ Campus, including the impressive Grenden building, offers a dynamic environment with spaces crafted to encourage collaboration. Check it out: Axis HQ Ready to Act? Axis is a company realizing the benefits of a diverse workforce. We know that diversity in groups creates a better working environment and promotes creativity, something that is fundamental for our success. We welcome all applications. We go through applications continuously so don't wait - send in your application today! Vacation is important! At Axis we value work-life balance and that means that during summer many of us are on a well-deserved vacation. During this period, you can expect some delay in our response. We will review applications in August and get back to you as soon as possible. In case of questions, please reach out to recruiting manager Bill Eliasson at +46 46 272 1800

Are you a confident expert in regulatory compliance with a strong customer focus and a passion for sharing knowledge? In this role, you’ll act as a trusted advisor to our customers, guiding them through regulatory requirements for market access — particularly across Europe. You’ll lead compliance projects, deliver expert training, and help shape and grow our Regulatory Compliance Project Management service. Key Responsibilities: · Help define and continuously develop and evolve our advisory service “Regulatory Compliance Project Management” · Advise customers on CE marking, UKCA, and EU regulatory requirements · Perform strategic compliance project management projects · Deliver training sessions and courses online and in-person · Support the sales team by identifying opportunities and contributing to business growth · Collaborate with colleagues and customers across international markets · Take ownership of your professional development while actively contributing to the growth and advancement of your area of responsibility Your background should involve: · Post-secondary degree or diploma in a relevant field or equivalent work experience · Excellent knowledge and experience of work with regulatory requirements, testing and certification of electrical products for market access · Strong knowledge within LVD, EMC, RED and MD · Strong knowledge of the CE marking process, in both theory and practice · Excellent communication skills, in both Swedish and English Ability to teach within the area of regulatory requirements for electrical products You combine strong technical expertise with a consultative, customer-focused approach. You thrive in a fast-paced, evolving environment and are able to adapt to changing priorities. You are both detail-oriented and strategic in your thinking, enabling you to see the bigger picture while maintaining high accuracy. You build strong relationships and inspire trust among colleagues and customers alike. You take ownership of your work and are driven to deliver results. Intertek offers: Meaningful work that contributes to product safety and reliability Opportunities for professional development and long-term career growth A collaborative and supportive work environment Exposure to a wide range of products, technologies, and industries The chance to work within a truly global organization Intertek is a leading Total Quality Assurance provider to industries worldwide. With a 125-year legacy of excellence, our global network delivers innovative and bespoke Assurance, Testing, Inspection, and Certification solutions for our customers' operations and supply chains. Our extensive global network of accredited laboratories and world-class experts are dedicated to addressing quality, safety, and sustainability across a vast spectrum of industries, including Medical, Lighting, Renewable Energy, HVACR, Appliances & Electronics, Connected World (IoT), and many more. Global manufacturers trust Intertek for faster, simpler, and more cost-efficient services that clear a path for their product's success. Join us and be a part of a team that continually exceeds client expectations and sets the standard for quality and accuracy.

Strong governance and effective controls are fundamental to how we operate and succeed as a bank. You will therefore join an organization with a strong regulatory focus, where compliance is a top priority and there is a clear ambition to always do things the right way. Get an idea of the role You will be a key part of our Governance team, responsible for strengthening internal controls, supporting effective process management, and ensuring compliance with both internal policies and external regulations. As a Regulatory Specialist, you play an important role in ensuring that the bank’s governance framework and operational processes remain efficient and aligned with regulatory requirements. Working closely with the business, you help strengthen the control environment and drive meaningful improvements across processes and ways of working. Key responsibilities Coordinate horizon scanning, implementation and follow-up of regulatory requirements Develop, maintain, and ensure effective management of governance documents (policies, instructions, routines) Support the business with process mapping, controls, RACI models, and governance structures Lead projects and initiatives to strengthen internal controls, risk management, and compliance culture Prepare governance reporting and present materials to management and committees Contribute to digitalization and AI initiatives within governance and process frameworks On a personal level With a proactive and positive approach, you navigate complex environments and manage multiple priorities with confidence. You take clear ownership of initiatives, operate independently, and adapt easily to changing circumstances. Hands-on and action-oriented, you are unafraid of challenging existing ways of working to enhance efficiency and drive continuous improvement. You thrive in a dynamic and regulated environment where your balance of structure and flexibility makes a real impact. We believe you bring: At least 5 years experience from internal audit, regulatory or governance advisory, or a similar role within financial services or insurance. A background in Risk or Compliance is also highly relevant, particularly if you are interested in working more operationally with these topics. Experience with governance frameworks, document hierarchies, and process development Experience managing risk, incidents, and compliance requirements Proven ability within project and stakeholder management Interest or experience in digitalization and AI applied to governance or process work Resurs in brief At Resurs, we make everyday finances easier through innovative and customer-focused solutions. With customers across the Nordics and more than 800 colleagues, we are committed to creating long-term value for individuals, businesses, and society. Recognized as a career company for the past six years, we put strong emphasis on both personal and professional growth. We want to make a difference by striving to be our best, acting with kindness, and building trust through clarity and collaboration. Our heart beats strong and it shows in everything we do. Although we are based in the Nordics, our team is enriched by the breadth of perspectives brought by colleagues from different countries. We foster a welcoming and supportive culture, where collaboration drives us to achieve the best outcomes for our users. Apply today! Don’t wait to send in your application. Selection and interviews take place on an ongoing basis, and the position may be filled before the last application date. We look forward to hearing from you! Important information On final candidates, we carry out a detailed background check via an external company. #LI-LN1

At Nouryon, our global team takes positive action every day, to reach higher collectively and individually. We create innovative and sustainable solutions for our customers to answer society’s needs – today and in the future. We are looking for team members who bring ideas forward, champion others and work together to do better. Does that sound like you? About the job In this exiting role you will manage, drive and coordinate environmental investigations and remediation projects across Europe, ensuring compliance with regulatory requirements and responsible handling of soil and groundwater contamination. You will play a key part in managing environmental risks from both a sustainability and business perspective, while supporting sound financial planning through environmental reserves and contributing to the long-term strategy for managing environmental liabilities. You will be a part of the Nouryon Environmental Liability Management team, which is a part of corporate legal, with highly skilled and dedicated colleagues and partners around the globe. The role can be based in either Sweden Gothenburg or in the Netherlands, Amsterdam. In your future role as Environmental Liability Project Manager - Europe you will Be responsible for managing impaired sites and environmental liabilities across Nouryon’s European portfolio, ensuring compliance, cost control, and protection of company reputation. Monitor and control investigation and remediation costs, including invoice approval and environmental liability provisioning. Manage consultants and contractors, including scope definition, performance follow-up, cost control, and review of deliverables. Maintain relationships with Nouryon sites, regulatory authorities and key stakeholders. Support development of remediation strategies, including safety, budgeting, coordination with functions (Legal/Finance/HSE), and stakeholder engagement. Contribute to continuous improvement of ELM procedures and guidelines. Support M&A activities through environmental due diligence as needed. Travel as required for site visits (mainly Sweden, the Netherlands, Germany, Belgium and France) and stakeholder engagement. Travel varies but can during periods be expected to be up to 20%. We believe you bring Academic degree in science or engineering (e.g. MSc, master’s degree or equivalent in geology, chemistry, environmental science or similar) Extensive relevant experience from process, pharma, mining or oil industry and/or global technical consulting Project management experience of complex environmental matters from technical, financial and legal aspects Experience working across multiple countries (both technical and cultural contexts) Experience engaging with regulatory authorities in more than one European jurisdiction Fluent in English and either of Swedish or Dutch Drivers license We believe you are a confident and decisive professional who can act with clarity and authority when needed. You build trust quickly, including with senior stakeholders, by communicating with credibility and sound judgement. You are skilled at building and maintaining strong relationships across functions and geographies, and you navigate complex situations with a structured and forward-looking approach. You can balance and integrate multiple perspectives—technical, legal, and financial—when making decisions, and you demonstrate strong cultural awareness when working in an international environment. At the same time, you are organized and proactive, with the ability to manage issues systematically and anticipate challenges ahead of time. We offer you At Nouryon, we provide a great job and friendly coworkers, plus benefits in addition to salary. Our collective agreement is with IKEM. Plus, we offer unilateral perks, such as bonus, reduced hours, health care allowance, lunch allowance, and more. Have we got your interest? This is a permanent position on a full-time basis, reporting to Henrik Eriksson, Global Environmental Liability Manager and based in Sweden, Gothenburg at our Nordic Business Center or in The Netherlands Amsterdam. Please apply via our online recruitment system. We will not accept applications via e-mail. Once it's with us we will review to see if we have a match between your skills and the role! For more information about our hiring process, visit: nouryon.com/careers/how-we-hire/ As an applicant, you will be subject to a background check before employment. You will receive more information about this later in the recruitment process. We work actively and systematically with HSE matters to ensure a safe and sustainable working environment for our employees. As an employee, you may therefore be required to undergo drug testing on a random basis. This is part of our commitment to safeguarding the safety and well-being of our staff. We look forward to receiving your application! About Nouryon Explore careers and life at Nouryon If you’re looking for your next career move, apply today and join Nouryon’s worldwide team in providing essential solutions that our customers use to manufacture everyday products such as personal care, cleaning, paints and coatings, agriculture and food, pharmaceuticals, and building products. Our employees are driven by the wish to make an impact and actively drive positive change. If that describes you, we will gladly make way for your ambitions. From day one we support you with your personal growth, through challenging positions and comprehensive learning and development opportunities, in a dynamic, international, diverse, and proactive working environment. Visit our website and follow us on LinkedIn. Contact For additional information about the vacancy please contact hiring manager Henrik Eriksson, Global Environmental Liability Manager at henrik.eriksson1@nouryon.com If you have any questions about the recruitment process or your application or need assistance, please contact: Recruiting.SE@Nouryon.com For union contacts, please see below: Akademikerklubben: Katarina Risö – katarina.riso@nouryon.com Unionen: Helene Rosenlund helene.rosenlund@nouryon.com Ledarna: Sanna Backman – sanna.backman@nouryon.com #WeAreNouryon #GrowWithUs We have already chosen our sourcing channels for this recruitment and kindly ask not to be contacted by any advertisement agents, recruitment agencies or staffing companies.

På 27 hektar gammal pappersbruksmark mitt i Mölndal bygger vi en ny stadsdel. När området står klart kommer 5-6 000 människor att bo här och 4 000 att arbeta här. Industrimiljön 400-åriga historia ska vävas samman med modern arkitektur till en plats människor söker sig till. Tio byggaktörer bygger sina egna kvarter. Mölndals stad ansvarar för allmän platsmark och skolor/förskolor. MölnDala Fastighets AB äger marken, leder utvecklingen och bygger besöksmålet Papyr med bas i den gamla industrimiljön. Den första detaljplanen har vunnit laga kraft. De första 600 bostäderna ska stå klara 2027–2028. Förskola och grundskola öppnar 2029. Bolaget har gått från planeringsfas till genomförande — och samtidigt fortsätter arbetet med kommande detaljplaner. Det är just nu ett tio-tal byggprojekt som ska köra parallellt på samma yta. Markarbeten, etableringar, byggtrafik, ledningar, schakter, transporter, störningar. Någon måste hålla ihop det. Det är dig vi söker. Vad du gör Du är MölnDalas operativa hjärna i samordningen av Forsåkers genomförande. Du har möten med byggaktörerna i området, identifierar konflikter innan de blir problem, driver fram lösningar när tidsplaner inte stämmer, hanterar gränssnitten mot Mölndals stads ansvar för allmän platsmark, och håller koll på störningarna mot omgivningen — Kvarnbyn, trafik, näringsliv och allmänhet. Du sitter inte vid sidan av — du är där det händer. Du äger agendan i områdets samordningsforum för MölnDalas räkning. Du hanterar myndighetskontakter och tillståndsfrågor som rör områdets infrastruktur. Du driver områdets gemensamma genomförandestrategi i det operativa. Mycket av samordningen sker fysiskt i Tibellska Villan — vårt samordningskontor där både MölnDala och våra entreprenörer arbetar tillsammans. Det är inte ett möte i månaden. Det är en arbetsplats där samverkan är inbyggd i hur vi jobbar. Du har inget formellt mandat över byggaktörerna. Det är hela poängen. Du får dem att samordna sig tack vare din erfarenhet, din strukturkänsla och din förmåga att läsa rum. När det funkar märks det inte. När det inte funkar märks det överallt. Vem vi tror att du är Du har minst åtta år bakom dig från större bygg- eller infrastrukturprojekt — gärna en bakgrund som senior projektledare på anläggningssidan, kommunal exploatering eller större exploatör. Du är civilingenjör eller har likvärdig bakgrund. Du vet hur kommunal kontext fungerar — detaljplaner, exploateringsavtal, allmän platsmark, politik. Du har stått i rum där fem entreprenörer drar åt fyra olika håll och fått dem att rikta sig åt samma. Du gillar detaljer och möten utan att fastna i dem. Du tar ansvar utan att behöva en chefstitel. Du är diplomatisk men du är inte mjuk. När du behöver hålla en linje gör du det, och du har relationerna kvar nästa vecka. Du är lyhörd, prestigelös och driven av själva uppdraget - av att vara med och bygga något som står kvar. Vad rollen inte är Det här är inte projektledning för enskilda byggprojekt - det är byggaktörernas eget ansvar. Det är inte heller en strategisk roll med fokus på vision och långsiktig utveckling. Det här är samordning. Det är operativt, detaljrikt och pågående - och det är hela poängen. Vad vi erbjuder Ett av de mest komplexa och spännande stadsutvecklingsuppdragen i Västsverige just nu. En ovanlig kombination av byggteknisk komplexitet, kommunal kontext och historisk plats. En liten organisation — femton personer som förvaltar enorma värden — där varje roll bär bredare än i ett större bolag. En nära ledningsgrupp och en kommande Avdelningschef att rapportera till — som rekryteras parallellt med dig. Och en plats i Mölndal som om tio år kommer vara en av Västsveriges mest omtalade nya stadsdelar — där du var med och såg till att den blev av. Vi är femton personer, och det märks. Du försvinner inte in i en hierarki — det du gör syns, och det räknas. Vi känner varandra. Vi äter lunch ihop, vi firar när ett kvarter står klart, och vi säger ifrån när något skaver. Det är en grupp där folk är kloka utan att behöva visa det, och hjälpsamma utan att hålla räkning. Du kommer till kollegor som kan sitt hantverk och som gärna delar med sig — och som förväntar sig detsamma av dig. Vi lär oss hela tiden — och just nu lär vi oss att använda AI i vår vardag. Vi är ett av de första bolagen i vår storlek som tar det på allvar, inte som en gimmick utan som ett sätt att få mer gjort med små resurser. Du behöver inte vara expert. Ingen av oss var det när vi började. Men du ska vara nyfiken och gilla att lära dig nytt — för det kommer vi att göra tillsammans, hela tiden. Praktiskt Tillsvidareanställning, 100 % Placering: Kvarnbygatan 2B, Villa Korndal, Mölndal. Mycket av det operativa arbetet sker i samordningskontoret Tibellska Villan, tillsammans med våra entreprenörer. Rapporterar till Avdelningschef Marknadsmässig lön efter erfarenhet och bakgrund Vi använder Antura för projekt- och portföljstyrning — det är en fördel om du är van vid det, men inget krav Om dig själv som digital användare Forsåker är ett informationstungt uppdrag — tidsplaner, kontaktytor, avtal, milstolpar, möten, beslut. Den som arbetar smart digitalt får mycket mer gjort utan att tappa kvalitet. Vi tror att du trivs med att vara den som hittar nya sätt att jobba med information och samordning, och som ser digitala verktyg som en självklar del av yrkesvardagen. Ansökan Vi arbetar med löpande urval och tillsätter snarast möjligt. Ansök här och bifoga ett kort brev där du berättar varför denna utmaning lockar dig just nu - vi vill veta hur du tänker, inte bara vad du gjort. För frågor om rollen, kontakta Jacob Bergström, HR-rådgivare. Det jag söker är inte den som har gjort den här rollen förut. Det är den som ser uppdraget och tänker "det här är precis vad jag är bra på". Hör av dig. Bjarne Fjellanger VD, MölnDala Fastighets AB

Drivs du av att se dina idéer bli verklighet? Välkommen till vår spännande och teknikintensiva värld. Din roll Vi söker miljötålighetsingenjör och i rollen ingår att ta fram kravspecifikationer för mekaniken i våra missilprodukter. Du kommer delta i planering och genomförande av att verifiera satta miljökrav samt i det tekniska utvecklingsarbetet för våra framtida missilprodukter. Arbetet spänner över hela produktutvecklingscykeln och innefattar således en bred palett av uppgifter. Exempel på arbetsuppgifter för gruppen kan vara att: Prediktera och definiera miljökrav för apparater, komponenter och kompletta produkter Utreda utfall och ta fram åtgärdsförslag Verifiera och validera att framtagen design möter aktuell kravbild och är säker och sund ur ett miljötålighetsperspektiv Vi erbjuder dig en stimulerande miljö där du arbetar i en mängd olika utvecklings- och kundprojekt. Du kommer att tillhöra ett team där ni tillsammans planerar och fördelar era arbetsuppgifter. Ofta löser man sina arbetsuppgifter tillsammans med utvecklare som arbetar i andra team. Arbetet innebär att du arbetar nära hårdvaran och hantering av denna i framförallt verifieringsarbetet. Teamet som du kommer att ingå i har mångårig erfarenhet och expertis inom miljötålighet. Arbetet sker i en miljö med kompetenta medarbetare där vi är generösa med vår kunskap vilket främjar såväl karriären som den personliga utvecklingen. Vi värnar om att vara en arbetsplats där gemenskap, stimulerande arbetsuppgifter och trivsel står högt i kurs. Din profil Vi söker dig med en civilingenjörsutbildning gärna inom maskinteknik, teknisk fysik eller farkostteknik. Vi lägger stor vikt vid personliga egenskaper och intressen. Med förmågan att samarbeta och med viljan att utvecklas så kommer du att komma långt i denna roll. Har du erfarenhet av miljötålighetsarbete eller verifierande provning är det meriterande. Vi ser gärna att du har erfarenheter inom något eller några av följande områden: Mekanikkonstruktion Systemdesign Metoder för verifiering av miljökrav För att vara framgångsrik i någon av våra roller behöver du kunna läsa och skriva teknisk dokumentation på både svenska och engelska. Befattningen kräver att du genomgår och godkänns enligt vid var tid gällande bestämmelser för säkerhetsskydd. För befattningar där Saab har krav på säkerhetsklassinplacering kan, i förekommande fall, medföra krav på visst medborgarskap. Vad du blir en del av Upptäck oändliga möjligheter. Anta utmaningar, skapa smarta innovationer och uppgradera dina förmågor. Det här är en plats för kluriga tänkare, modiga pionjärer och alla däremellan. Tillsammans uppnår vi det extraordinära, var och en tar med sitt unika perspektiv. Varje bidrag räknas. Saab är ett ledande försvars- och säkerhetsföretag med syfte att hjälpa nationer att skydda sin befolkning och bidra till trygghet för människor och samhällen. Med 28 000 talangfulla medarbetare utvecklar Saab teknik och lösningar för en säkrare och mer hållbar värld. Saab utvecklar, tillverkar och underhåller avancerade system inom flygteknik, vapen, ledningssystem, sensorer och undervattenssystem. Saab har sitt huvudkontor i Sverige men en global verksamhet där Saab är en del av många nationers försvarsförmåga. Läs mer om oss här Mekanikavdelningen för missilsystem har drygt 100 medarbetare som arbetar inom hela utvecklingskedjan från teknik- och produktstudier till färdig produkt och produktvård. Området är fördelat på tre geografiskt skilda platser; Linköping, Karlskoga och Karlstad. Den aktuella tjänsten är placerad i Linköping. Sektionen för mekanisk analys i Linköping består av ca 20 medarbetare som förutom miljötålighetsteknik även arbetar med simuleringar gällande t ex hållfasthet, strukturdynamik och termodynamik, systemarbete inom mekanikområdet samt materialteknik. Karakteristiskt för sektionen är att medarbetarna arbetar med många olika produkter vilket innebär stor variation i arbetsuppgifter.

Vill du bidra till en tryggare och säkrare vård? Hos Inspektionen för vård och omsorg (IVO) får du arbeta med tillsyn som gör verklig skillnad. Vi söker nu inspektörer med juristkompetens till vårt kontor i Umeå.   Om jobbet Som inspektör arbetar du med att utreda och bedöma legitimerad hälso- och sjukvårdspersonals yrkesutövning utifrån gällande regelverk. Arbetsuppgifter:                   utreda ärenden som rör legitimerad hälso- och sjukvårdspersonals yrkesutövning, exempelvis kopplat till sjukdom (t.ex. beroende), kompetens, läkemedelsförskrivning, vård och behandling eller journalföring, granska patientjournaler, förskrivningar och annan relevant dokumentation, genomföra samtal och möten med enskilda yrkesutövare som står under IVO:s tillsyn, vara huvudhandläggare i vissa ärenden och medhandläggare i andra, beroende på ärendenas omfattning och karaktär, arbeta i nära samverkan med kollegor nationellt, inklusive inspektörer med olika professioner samt tillsynstandläkare och tillsynsläkare, bidra till tvärprofessionella bedömningar och gemensamma ställningstaganden, bereda beslut i ärenden samt skriva anmälningar till Hälso- och sjukvårdens ansvarsnämnd (HSAN).   Kvalifikationer Vi söker dig som har: juristexamen, minst två års aktuell och för rollen relevant erfarenhet av juridiskt utredningsarbete, handläggning, beslutsberedning eller myndighetsutövning inom offentlig sektor, god förmåga att uttrycka dig på svenska i tal och skrift.     Det är meriterande om du har: erfarenhet från domstol, exempelvis notarietjänstgöring eller arbete som föredragande jurist erfarenhet av tillsynsarbete, erfarenhet av arbete i beslutsfattande eller beslutsberedande roller, erfarenhet av arbete inom IVO:s tillsynsområde hälso- och sjukvård, erfarenhet av att granska och analysera journaler, medicinska underlag eller annan omfattande dokumentation,   Personliga egenskaper För att lyckas i rollen behöver du ha god analytisk förmåga och kunna göra välgrundade bedömningar utifrån komplexa underlag. Du behöver vara noggrann och kvalitetsmedveten, med förmåga att arbeta sakligt, rättssäkert och med hög integritet. Rollen kräver även gott omdöme, särskilt i ärenden som kan vara känsliga eller innebära svåra avvägningar.   Du behöver vara strukturerad och kunna driva ärenden framåt, både självständigt och tillsammans med andra. Eftersom arbetet sker i nära samverkan med kollegor nationellt och i tvärprofessionella sammanhang behöver du också ha god samarbetsförmåga och kunna bidra med ditt professionella perspektiv i gemensamma bedömningar.   Vid rekryteringen kommer vi att lägga stor vikt vid dina personliga egenskaper.    Detta kan IVO erbjuda dig Vi erbjuder en utvecklande roll i en dynamisk kunskapsorganisation där du bidrar till att utveckla en modern och effektiv tillsyn. Vi förbättrar ständigt våra arbetssätt och strävar efter en sammansättning av medarbetare som speglar samhällets mångfald. Läs om våra avtalsvillkor och förmåner här: https://www.ivo.se/om-ivo/arbeta-hos-oss/   Ansökan Du ansöker genom att besvara våra urvalsfrågor och bifoga ditt CV. Ansökan ska skickas in på svenska. Svara tydligt och utförligt på frågorna, eftersom de ligger till grund för urvalet, hänvisa inte till andra handlingar som CV.   Att besvara frågorna är en förutsättning för att din ansökan ska anses komplett.   Ansök senast den 7 augusti 2026.    Läs mer om vår rekryteringsprocess här: https://www.ivo.se/om-ivo/arbeta-hos-oss/   Övrigt Befattning: Inspektör Anställningsform: tillsvidareanställning med sex månaders provanställning Placeringsort: Umeå Arbetstid: Flextid Tillträde: Efter överenskommelse   Resor i tjänsten kan förekomma.   IVO bidrar till en trygg och säker vård och omsorg IVO står för engagemang och bred kunskap om svensk vård och omsorg. Vi granskar, drar lärdomar och arbetar för att vården och omsorgen ska bli bättre och säkrare – alltid med fokus på patienter och brukare.   Vi är drygt 850 anställda. Arbetet med tillsyn bedrivs vid sex regionala kontor på orterna Umeå, Stockholm, Örebro, Jönköping, Göteborg och Malmö.   I Stockholm finns även myndighetsövergripande avdelningar för aktörskontroll, verksamhetsstöd, rättsligt stöd, analys, planering och kommunikation samt generaldirektörens stab.   Samtal från externa rekryteringsföretag och säljare undanbedes.

Juridiska institutionen utlyser en postdoktoral anställning i rättsinformatik, inom ramen för forskningsprogrammet WASP-HS (Wallenberg AI, Autonomous Systems and Software Program – Humanity and Society). Postdoktorn kommer att vara anställd vid Juridiska institutionen. Juridiska institutionenär en av de större institutionerna vid Stockholms universitet med ca 150 anställda och ca 5 500 studenter. Drygt 100 lärare är på heltid engagerade för att undervisa och bedriva den forskning som utbildningen vilar på. Ett fyrtiotal professorer med olika rättsvetenskapliga inriktningar finns vid institutionen. Som forskare hos oss blir du en viktig del i en dynamisk miljö med forskning av högsta klass och med stark internationell prägel. Mer information om oss finns på:  Juridiska institutionen.  Projektbeskrivning Stockholms universitet bygger upp en stark och dynamisk miljö för rättsvetenskaplig forskning om artificiell intelligens och har en ledande position i Sverige och Norden. Anställningen är knuten till WASP-HS forskningskluster The Rule of AI – AI, Regulation, and Society. Visionen för WASP-HS är att främja ny tvärvetenskaplig kunskap inom humaniora och samhällsvetenskap om AI och autonoma system samt deras påverkan på människan och samhällsutvecklingen. WASP-HS möjliggör forskning i framkant, expertis och kompetensuppbyggnad inom humaniora och samhällsvetenskap. Forskningsklustret leds av Uppsala universitet, Örebro universitet och Stockholms universitet och studerar hur AI omformar regleringsprocesser, med fokus på utformningen av, tillsynen över samt efterlevnaden av regler (www.oru.se/english/research/research-groups/rg/?rdb=g481). Postdoktorn kommer att vara en del av klustret och vara placerad vid Juridiska institutionen, men utforma och genomföra sitt postdoktorala projekt självständigt. Arbetsuppgifter En postdoktor ska i första hand ägna sin tid åt egen postdoktoral forskning (3 år på heltid).  Andra arbetsuppgifter kan ingå, såsom undervisning av studenter, arbete i undervisningsteam samt administration (högst 20 % av anställningen). Behörighetskrav För att vara behörig för anställning som postdoktor krävs avlagd doktorsexamen eller utländsk examen som bedöms motsvara relevant doktorsexamen. Examen ska vara avlagd senast då anställningsbeslutet fattas. Bedömningsgrunder Det är meriterande om doktorsexamen eller motsvarande är avlagd högst tre år före sista ansökningsdag. Om det finns särskilda skäl, kan en tidigare avlagd examen också anses vara meriterande. Med särskilda skäl avses ledighet på grund av sjukdom, föräldraledighet, förtroendeuppdrag inom fackliga organisationer, tjänstgöring inom totalförsvaret, eller andra liknande omständigheter samt klinisk tjänstgöring eller för ämnesområdet relevant tjänstgöring/uppdrag. Sökande ska ha avlagt doktorsexamen inom ett samhällsvetenskapligt eller humanistiskt ämne (SCB: 501–509, 601–603, 60407–60410, 605). Sökande ska ha tillräckliga kunskaper i svenska eller engelska. Vid tillsättningen kommer särskild vikt att fästas vid vetenskaplig skicklighet. Antagning sker på grundval av en bedömning av den sökandes förmåga att framgångsrikt genomföra det postdoktorala projektet. Bedömningen fokuserar i första hand på projektbeskrivningen samt annat relevant vetenskapligt skriftligt material (publicerat eller opublicerat). Vetenskapligt material som inte är juridiskt kan också vara meriterande i den mån det är relevant för projektet. Analytisk förmåga, förmågan att strukturera materialet och att självständigt arbeta med det föreslagna projektet, samt projektets vetenskapliga värde, är av avgörande betydelse. Utöver det skriftliga materialet kan även andra meriter, såsom betyg, examina, genomförda kurser m.m., vara av betydelse i bedömningen. Vidare kan den sökandes samarbetsförmåga i olika avseenden, t.ex. i undervisning, beaktas. Det är meriterande att ha praktisk och/eller teoretisk erfarenhet inom området rättsinformatik, särskilt i relation till AI. Om anställningen Anställningen avser heltid och gäller tre år, med möjlighet till förlängning om det finns särskilda skäl. Tillträde 1 januari 2027 eller enligt överenskommelse. Vi erbjuder Hos oss får du dynamiken i samspelet mellan högre utbildning och forskning som gör Stockholms universitet till en spännande och kreativ miljö. Du arbetar i en internationell miljö och får förmånliga villkor. Universitetet ligger beläget i Nationalstadsparken med goda förbindelser till city. Stockholms universitet värnar om att vara en arbetsplats som är fri från diskriminering och ger lika rättigheter och möjligheter för alla. Kontakt Upplysningar om anställningen och projektet lämnas av projektledaren, Liane Colonna, liane.colonna@juridicum.su.se.  Ansökan Du söker anställningen via Stockholms universitets rekryteringssystem. Bifoga personligt brev och CV samt de bilagor som efterfrågas i ansökningsformuläret. Du som sökande ansvarar för att ansökan är komplett och att den är universitetet tillhanda senast sista ansökningsdag. Anvisningar för sökande finns på webbsidan: att söka en anställning. Stockholms universitet bidrar till det hållbara demokratiska samhällets utveckling genom kunskap, upplysning och sanningssökande.

David Kennedy Recruitment is working with an innovative global Customer Experience company currently looking to hire a Head of Compliance to join their growing international team. Position: Head of Compliance Location: Limassol, Cyprus Employment type: Full-time DUTIES AND RESPONSIBILITIES: Lead the development, implementation, and continuous improvement of compliance frameworks, policies, and governance processes across the business Ensure full compliance with all applicable regulatory, legal, AML, KYC, Responsible Gambling, and data protection requirements across multiple jurisdictions Monitor regulatory developments and support the business in adapting policies, procedures, and controls in line with evolving regulations and operational initiatives Conduct regular compliance risk assessments and implement corrective actions to address identified gaps and regulatory requirements Oversee marketing compliance approvals to ensure alignment with industry standards and responsible gaming regulations Manage and coordinate new licence applications in collaboration with legal partners and regulatory authorities Act as the primary point of contact for regulators across multiple jurisdictions including the UK, Spain, Sweden, Portugal, and other regulated markets Prepare and deliver compliance reports, updates, and regulatory insights to senior leadership and key stakeholders Manage regulatory inspections, audits, examinations, and reporting obligations Develop and deliver compliance training programmes for employees across the organisation Lead, mentor, and support the compliance team, fostering a culture of accountability, collaboration, and continuous improvement Collaborate closely with development and operational teams to ensure customer-facing journeys, systems, and services remain aligned with compliance and regulatory requirements. REQUIREMENTS: Bachelor's degree in Law, Finance, Business Administration, or a related field, with a strong preference for a legal background Minimum 4 years of experience within iGaming compliance environments Strong understanding of multi-jurisdictional licensing frameworks including MGA, UKGC, SGA, DGA, and other regulated markets In-depth knowledge of AML, KYC, Responsible Gambling, and regulatory compliance obligations Proven experience working directly with regulators, managing audits, inspections, and regulatory reporting processes Strong leadership and people management experience with the ability to mentor and develop high-performing teams Experience handling customer-related decision-making processes connected to Safer Gambling and AML matters Strong analytical, organisational, and problem-solving skills Excellent communication and stakeholder management abilities across technical, operational, and executive teams Ability to maintain a high level of confidentiality, professionalism, trust, and credibility in sensitive matters Proactive mindset with the ability to drive process improvements and operational excellence within a regulated environment. OFFER: Excellent working environment within an international organisation. Medical insurance and pension plan options. Birthday vouchers and additional perks for special occasions. Fully equipped kitchen and in-house entertainment space. Monthly lunches, corporate events, sports teams, competitions, and social activities. Daily snacks and a casual dress code. Strong opportunities for professional growth and career progression within a global organisation.

Are you structured, analytical, and passionate about aviation safety and regulatory compliance? Do you thrive in a highly regulated environment where attention to detail, continuous improvement, and collaboration are essential? At Avincis, safety is at the heart of everything we do. We are now looking for a Safety & Compliance Monitoring Officer to support our Safety Management and Compliance activities within our Nordic Part-145 maintenance organization. This is an exciting opportunity to join an international aviation environment and contribute to maintaining the highest standards of safety, compliance, and operational excellence. Location: The preferred location is Sweden. However, for the right candidate, remote working arrangements may be considered within Norway or Finland. About the role As Safety & Compliance Officer, you will support the Safety Director Nordics in the day-to-day management of safety and compliance activities within the Nordic Part-145 organization. The role focuses on administration, monitoring, reporting, and continuous improvement of safety management and compliance processes. The Nordic Part-145 organization includes Base and Line Maintenance Operations in Sweden, Norway, and Finland, with potential future expansion into Denmark. You will help ensure effective oversight, regulatory compliance, and operational resilience across multiple countries. This role reports directly to the Safety Director Nordics. Key Responsibilities Safety Management & Compliance Monitoring Support the daily operation of the Safety Management System (SMS) and Compliance Monitoring Programme. Monitor safety performance, compliance activities, and reporting requirements. Support the development of safety processes, procedures, and documentation. Maintain safety and compliance manuals and documentation. Support compliance with EASA regulations, company procedures, and internal standards. Occurrence Management & Risk Assessment Support occurrence reporting, investigations, and safety follow-up. Coordinate and monitor Corrective and Preventive Actions (CAPAs). Assist with hazard identification, risk assessments, and risk management. Support trend analysis, safety performance monitoring, and Management of Change (MoC) activities. Audits, Reporting & Continuous Improvement Support internal audits, authority inspections, and external assessments. Prepare safety reports, statistics, KPIs, and management presentations. Participate in improvement projects and management reviews. Promote a strong Just Culture and positive safety culture throughout the organization. Who We Are Looking For We are seeking an aviation professional with experience in Part-145 maintenance and Continuing Airworthiness Management (CAMO), combined with a genuine interest in aviation safety, compliance, and continuous improvement. You are comfortable working in a regulated environment and understand the challenges of maintaining compliance across multiple approvals and jurisdictions. You are structured, analytical, collaborative, and proactive. To succeed in this role, you are: A person of high integrity with a strong commitment to safety and compliance. Structured, organised, and able to manage multiple priorities. Analytical and solution-oriented. Comfortable working independently and across multiple functions. A strong communicator who builds trust and effective relationships. Committed to promoting a positive safety culture and Just Culture. Qualifications & Experience We are looking for candidates with: Experience within an EASA Part-145 maintenance organisation. Experience within CAMO or continuing airworthiness management. Good knowledge of EASA regulations and aviation regulatory requirements. Understanding of Safety Management Systems (SMS) and risk management. Experience with occurrence reporting, compliance monitoring, or auditing. Good understanding of aviation maintenance and continuing airworthiness. Good knowledge of Microsoft 365 and digital reporting tools. Strong organisational, administrative, and English communication skills. The following would be considered an advantage: Experience with aviation occurrence reporting systems. Auditor training or audit experience. Experience in multi-site or multi-country aviation organisations. Knowledge of Nordic aviation authority oversight. Why Join Avincis? At Avincis, our mission is to save lives. Every day, our teams deliver critical aviation services including Helicopter Emergency Medical Services (HEMS), Search and Rescue (SAR), and other mission-critical operations across Europe. As Safety & Compliance Officer, you will: Strengthen safety and regulatory compliance across Nordic maintenance operations. Work closely with experienced aviation safety leaders. Develop your expertise in a highly specialised aviation environment. Contribute directly to operational safety and organisational resilience. Be part of an international organisation where safety is always the highest priority. We Offer A challenging and rewarding position in an international aviation environment. Opportunities for professional and personal development. A collaborative and supportive working environment. Competitive terms and conditions. The opportunity to contribute to an organisation with a meaningful, life-saving mission.

Company description: Who are we?Volvo Cars is a company on a mission; to bring traditional car manufacturing into a connected, sustainable and smart future.Since 1927, we have been a brand known for our commitment to safety, creating innovative cars that make life less complicated for our consumers. In 2010, we decided to transform our business, resulting in a totally new generation of cars and technologies, as well as steady growth and record sales. Today, we’re expanding our global footprint in Europe, China and the US, and we’re on the lookout for new talent. We are constantly pushing our own skills and abilities to drive change in the automobile industry like never before. We are looking for innovative, committed people to join us in this endeavour and create safe, sustainable and connected cars. Job description: Let's introduce ourselves The Trade Compliance, Anti-Corruption & Human Rights team, organised under Compliance & Ethics, is responsible for overseeing Volvo Cars’ global Trade Sanctions and Export Control Compliance Program as part of the broader Compliance & Ethics framework. We operate in a fast-changing regulatory environment and work closely with Engineering, Digital, Procurement, Commercial, Cyber Security, and Logistics to provide clear, practical, and risk-based guidance to the business. We are now looking for a Senior Export Control & Sanctions Compliance Specialist to strengthen our team at Volvo Cars headquarters in Gothenburg.  This role focuses on supporting advanced automotive technologies, including connected vehicles, software-defined features, and digital services, in a complex multi-jurisdictional environment spanning the EU, U.S., and China. You will address some of the most challenging export control and sanctions questions in the industry, driven by evolving software, connectivity, and global supply chains. In this role, you will act as a key subject matter expert on export control and trade sanctions, supporting the organization in navigating complex regulatory requirements and influencing high-impact business and product-related decisions. This role involves matters with direct impact on Volvo Cars’ global product strategy and market access. You will play a central role in shaping how Volvo Cars manages export control and sanctions risks in a rapidly evolving technological and geopolitical landscape, ensuring compliant and efficient global operations.  What you'll do You will primarily work with export control and trade sanctions matters across multiple jurisdictions, including the EU and the U.S., in close collaboration with stakeholders across the organization, with exposure to and involvement in adjacent areas such as anti-corruption and human rights.  Your responsibilities will include: Provide advanced subject matter expertise on complex and high-risk export control scenarios, including classification of goods, software, and technology under EU Dual-Use and U.S. EAR frameworks Lead and support strategic export control decision-making, including licensing approaches and risk management in sensitive or high-impact cases Develop, implement, and maintain a global export control and trade sanctions compliance framework Establish and continuously improve policies, procedures, and internal controls aligned with applicable regulations Act as a trusted advisor to business teams on export control and trade sanctions requirements, including end-use, end-user, and restricted party considerations Oversee export classification, license determination, and transaction screening processes Monitor and interpret emerging export control and sanctions developments, including geopolitical shifts, and translate these into actionable business guidance Perform risk assessments and gap analyses, and coordinate remediation plans and corrective actions  Support export control assessments related to software, connectivity, cloud solutions, and technology transfers, including development and deployment scenarios Design and deliver training programs tailored to different business functions and risk profiles Prepare management reporting on export control and sanctions risks, KPIs, and compliance performance Profile description:What you'll bring Required qualifications University degree in Law, Business, International Trade, Engineering, or a related field At least 5–10 years of experience in export controls and sanctions, including hands-on experience with classification, licensing, and regulatory interpretation Strong working knowledge of EU and U.S. export control and sanctions laws and regulations, including dual-use and information security (encryption) controls Experience working with both technology/software and hardware-related export control matters Demonstrated experience handling complex, cross-border export control and sanctions matters involving multiple jurisdictions   Preferred qualifications Experience working in a multinational organization Experience working with or supporting technology-driven products or platforms, including software, connectivity, or digital solutions Familiarity with cloud-based solutions and technology transfer considerations Professional certification, such as Certified Export Control Manager (CECM), or equivalent Experience engaging with senior stakeholders and supporting decision-making   Who you are You demonstrate strong integrity and sound professional judgment, combined with a pragmatic and solution-oriented approach to compliance You bring an analytical, risk-based mindset and are comfortable navigating complex and evolving regulatory environments You excel in stakeholder management and communication, and build trust across business and functional teams You are able to work independently, prioritize effectively, and manage competing demands in a fast-paced environment We offer:

David Kennedy Recruitment is working with an innovative global Customer Experience company currently looking to hire a Senior Regulatory Compliance Manager to join their growing international team. Position: Senior Regulatory Compliance Manager Location: Limassol, Cyprus Work model: on-site (possibility of hybrid work arrangements after passign 6 mo probation period) Employment type: Full-time. DUTIES AND RESPONSIBILITIES: Lead regulatory compliance activities across multiple jurisdictions including UKGC, MGA, SGA, DGA, DGOJ, GGL, AGCO, LOTBA, Brazil, Peru, and others Ensure company policies, procedures, and operational processes remain aligned with local regulatory requirements Manage communication with regulatory authorities, including licence applications, renewals, notifications, and complaint handling Oversee recurring and ad-hoc regulatory reporting obligation Conduct internal compliance audits and reviews while maintaining accurate documentation and audit trails Provide regulatory and compliance guidance to internal stakeholders across Marketing, Payments, Product, Operations, and other departments Monitor regulatory updates and assess potential operational and compliance impact on the business Coordinate with external legal advisors and compliance consultants when required Maintain internal compliance documentation and evidence to support audit readiness Review and approve high-level customer complaints and regulatory complaint submissions. REQUIREMENTS: 5+ years of experience in a regulatory compliance role within the online gambling industry Strong understanding of multi-jurisdictional regulatory frameworks and compliance requirements Experience communicating directly with regulatory authorities is considered a strong advantage Bachelor's degree in Law, Finance, Risk Management, Business, or a related field is preferred Excellent communication, presentation, and report writing skills Strong organisational, analytical, and problem-solving abilities with high attention to detail Ability to work independently, manage multiple priorities, and exercise sound judgement High ethical standards with a methodical and professional approach. OFFER: Attractive salary package Relocation support for the candidates relocating from abroad Excellent work environment within a globally recognised iGaming organisation Medical insurance plan options Pension plan options Monetary vouchers for birthdays and special occasions Monthly lunches, corporate events, football team activities, competitions, and team gatherings Long-term professional growth and career development opportunities And many others!

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

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

RaySearch develops innovative software solutions to improve cancer care. About 1000 clinics in more than 40 countries use RaySearch software to improve treatments and quality of life for patients. RaySearch was founded in 2000 and is listed on Nasdaq Stockholm. The headquarters is located in Stockholm, with subsidiaries in the US, Europe and Asia - Pacific. Today we are more than 400 employees with a common vision of improving cancer care with innovative software. Our great staff is crucial for our success and we offer a fantastic working environment in modern offices, flexibility and good opportunities for development. We believe in equal opportunities, value diversity and work actively to prevent discrimination. Are you an experienced regulatory leader who enjoys developing people, improving processes, and driving regulatory excellence in a global medical device environment? Then this could be the right role for you.About the role We are looking for an experienced Regulatory Affairs Manager to lead a team of 5 Regulatory Affairs Specialists supporting our global medical device portfolio. This is a key leadership role for someone who combines deep global regulatory expertise with proven people leadership. You will lead and develop a team responsible for global regulatory submissions and registrations, regulatory compliance, vigilance, post-market regulatory activities, and regulatory intelligence. Success in this role requires a leader who is strategic, pragmatic, hands-on, and passionate about developing people while driving operational excellence.   What you'll do   Manage a team of 5 Regulatory Affairs Specialists.   Manage resource planning and allocation across global regulatory activities.   Ensure high-quality execution of global regulatory submissions, product registrations, and other regulatory operational activities.   Own and continuously improve core regulatory processes and ways of working.   Support global post-market regulatory activities, including vigilance, Post-Market Surveillance (PMS), Periodic Safety Update Reports (PSURs), regulatory compliance, and regulatory intelligence.   Provide technical guidance and hands-on support to the team on complex regulatory matters.   Foster a collaborative, engaged, and high-performing team focused on delivering regulatory excellence.  Your profile  You are an experienced regulatory leader with a passion for developing people, improving processes, and supporting a global medical device organization. You are a pragmatic and collaborative leader who translates regulatory requirements into practical, efficient processes that ensure compliance while supporting the business. You thrive in dynamic environments, focus on what matters most, build strong cross-functional relationships, and are motivated by developing talent and driving the continued success of the organization. Experience & skills  Extensive Regulatory Affairs experience within the medical device industry,   Proven people management experience, with the ability to lead, coach, and develop regulatory professionals.  Expert knowledge of the European Medical Device Regulation (EU MDR).   Demonstrated experience leading global regulatory submissions and product registrations, experience with at least one of the following regulatory authorities is required: China (NMPA), Japan (PMDA), India (CDSCO), US (FDA)   Experience with medical device software and IEC 62304.   Experience with medical device standards such as ISO 13485 and ISO 14971.  Strong understanding of global medical device regulations throughout the product lifecycle, including medical device product development and design control processes.  Demonstrated ability to optimize regulatory operations, improve processes, and lead teams through organizational change.   Excellent planning, prioritization, and stakeholder management skills.   A pragmatic, positive, and solution-oriented leader who leads by example, takes ownership, and thrives in a dynamic environment.   Proficiency in English.  Meriting experience  US regulatory experience, Experience with FDA submissions, including eSTAR/510(k).  Experience with IEC 62366 and ISO 14155  Experience with regulatory intelligence, regulatory signal monitoring, and evolving global regulatory requirements.   Experience with Cybersecurity requirements for medical devices.  Experience with AI/ML-enabled medical devices.  Our Culture Culture at RaySearch is the driving force behind our organization, where everything we do is driven by a shared passion for innovation and the fight against cancer. Our dedication is reflected in our ability to deliver exceptional results, pay close attention to detail, and consistently go the extra mile. Our employees stand out as experts in their field, driven by a relentless focus on solving problems - no matter how complex. At RaySearch, we take pride in leading the way in cancer treatment, leveraging cutting-edge technology to develop innovative solutions that make a real difference in patient care. Our Offer At RaySearch, we offer a diverse and inclusive work environment, fostering openness, sincerity, and collaboration. Located in Hagastaden, Stockholm's Life Science Hub, our modern and creative workspace includes an in-house gym, yoga, and social activities like ping pong, table football, and regular after-work events. Our bistro serves a fantastic lunch buffet, and we offer morning- and afternoon-fika every day. Our rooftop terrace also provides a stunning 360-degree view of Stockholm, enhancing the work experience. All of this comes attached with a competitive compensation and benefits package. Application Please apply to the position through the application form below. Selection and interviews will be ongoing. We do not accept applications by e-mail.