Sökresultat för "Regulatory compliance"

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.

Kyowa Kirin is a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in four disease areas: bone and mineral; intractable hematologic; hematology oncology; and rare disease.  A Japan-based company, our goal is to translate science into smiles by delivering therapies where no adequate treatments currently exist, working from drug discovery to product development and commercialization. In North America, we are headquartered in Princeton, NJ, with offices in California, North Carolina, and Mississauga, Ontario. Summary: The Senior Director, GRA Development & Product Strategy Team Lead is responsible for the developing and implementing regulatory strategies, while leading people amd managing global projects. This role oversees a team of Global Regulatory Leads (GRL) supporting global products and may serve as a Regional Regulatory Lead (RRL) based on business needs. Essential Functions: •    Define and drive global regulatory strategies for all products within the assigned disease area, ensuring alignment with enterprise objectives and maximizing product value. •    Lead and develop a team of Global Regulatory Leads (GRLs), setting direction, building capabilities, and fostering a high-performance, accountable culture. •    Shape and integrate regulatory strategy into global product development and lifecycle plans in close partnership with cross-functional stakeholders. •    Oversee and ensure execution of regulatory strategies, including global submissions, approvals, and post-approval activities across assigned products and projects. •    Direct and represent the organization in interactions with health authorities, including leading negotiations and overseeing agency meeting strategy and execution. •    Guide and approve global regulatory submission plans, including marketing applications, labeling (e.g., CCDS), and key lifecycle deliverables. •    Manage and coordinate regulatory activities, timelines, and deliverables across internal teams and external partners, ensuring alignment and on-time execution. •    Ensure compliance with global regulatory requirements, internal policies, and GxP standards, including support for inspections, audits, and governance processes. •    Assess and communicate regulatory risks, emerging trends, and competitive intelligence, escalating issues and recommending mitigation strategies as appropriate. •    Drive operational excellence by leading process improvements, standardization efforts (e.g., SOPs/WIs), and adoption of best practices across Regulatory Affairs. •    Oversee external partnerships and due diligence activities, including vendor selection, alliance management, and regulatory support for business development transactions. •    Contribute to organizational leadership, including participation in RA Functional Teams (RAFTs), budget oversight, and fostering collaboration across Regulatory Affairs and the broader organization. •    Establish and maintain global labeling strategy, including oversight of Company Core Data Sheet (CCDS) development and alignment with regional labeling requirements. •    Allocate and optimize regulatory resources across the portfolio, ensuring effective prioritization and support for key business objectives. •    Recruit and build organizational capability by leading talent acquisition, succession planning, and ongoing training initiatives within the regulatory function. •    Ensure alignment with Vision 2030, company Core Values, Kabegoe Principles, and the Global Regulatory Affairs Vision. Requirements: Education Bachelor’s degree in life sciences, pharmacy, or a related scientific discipline required.  Advanced degree (e.g., MS, PhD, PharmD, MBA) is preferred but not required; relevant industry experience may be considered in lieu of advanced education. Experience •    Minimum 12+ years extensive regulatory affairs experience within the pharmaceutical, biotechnology, or related industry, including global development and lifecycle management, with a focus on bone and mineral disease areas.  •    Proven leadership experience, including managing and developing high-performing regulatory teams and/or leading through other leaders (e.g., GRLs) •    Demonstrated success in developing and executing global regulatory strategies across multiple regions and product stages (development through post-approval) •    Significant experience interacting with health authorities, including leading regulatory agency meetings and negotiations •    Cross-functional leadership experience, with a strong track record of influencing stakeholders and driving alignment across complex, matrixed organizations •    Experience supporting business development activities, including regulatory due diligence for in-licensing, out-licensing, or partnerships Strong collaboration across cross-functional teams including regulatory affairs, government affairs, clinical, legal, and R&D. Technical Skills •    Deep knowledge of global regulatory frameworks and guidelines, including major markets (e.g., FDA, EMA, ICH,PMDA) and their application to drug development and lifecycle management •    Expertise in regulatory submissions and approvals, including INDs/CTAs, NDAs/BLAs/MAAs, and post-approval variations •    Strong understanding of global labeling requirements, including development and maintenance of Company Core Data Sheets (CCDS) •    Advanced regulatory strategy development and risk management skills, with the ability to anticipate challenges and drive solutions •    Familiarity with GxP requirements and regulatory compliance standards, including inspection and audit readiness •    Proficiency in regulatory systems, tools, and document management platforms used for submissions, tracking, and compliance •    Strong organizational and project management skills with the ability to manage multiple initiatives simultaneously. •    Exceptional communication and influencing skills, with the ability to clearly articulate complex regulatory strategies, risks, and requirements to diverse audiences, including health authorities, senior leadership, and cross-functional teams, to drive alignment and informed decision-making. •    Strong proficiency MS Office Suite. Working Conditions: Requires up to domestic and international travel. The anticipated salary for this position will be $265,000-$285,000. The actual salary offered for this role at commencement of employment may vary based on several factors including but not limited to relevant experience, skill set, qualifications, education (including applicable licenses and certifications, job-based knowledge, location, and other business and organizational needs. The listed salary is just one component of the overall compensation package. At Kyowa Kirin North America we provide a comprehensive range of benefits including: * 401K with company match * Annual Bonus Program (Sales Bonus for Sales Jobs) * Generous PTO and Holiday Schedule which includes Summer and Winter Shut-Downs, Sick Days and, Volunteer Days * Healthcare Benefits (Medical, Dental, Prescription Drugs and Vision) * HSA & FSA Programs * Well-Being and Work/Life Programs * Life & Disability Insurance * Concierge Services * Long Term Incentive Program (subject to job level and performance) * Pet Insurance * Tuition Assistance * Employee Referral Awards The compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market. KKNA and all of its employees have an obligation to act in accordance with the law and with integrity in all our operations and interactions It is the policy of Kyowa Kirin North America, Inc. to provide equal employment opportunity to all qualified persons without regard to race, religion, creed, color, pregnancy, sex, age, national origin, disability, genetic trait or predisposition, veteran status, marital status, sexual orientation or affection preference or citizenship status or any other category protected by law. When you apply to a job on this site, the personal data contained in your application will be collected and stored by Kyowa Kirin, Inc. (“Controller”), which is located at 510 Carnegie Center Dr. Princeton, NJ 08540 USA and can be contacted by emailing kkus.talentacquisition.8h@kyowakirin.com. Controller’s data protection officer can be contacted at usprivacyoffice@kyowakirin.com. Your personal data will be processed for the purposes of managing Controller’s recruitment related activities, which include setting up and conducting interviews and tests for applicants, evaluating and assessing the results thereto, and as is otherwise needed in the recruitment and hiring processes. Such processing is legally permissible under Art. 6(1)(f) of General Data Protection Regulation (EU) 2016/679 (“GDPR”) as necessary for the purposes of the legitimate interests pursued by the Controller, which are the solicitation, evaluation, and selection of applicants for employment.  Your personal data will be shared with Greenhouse Software, Inc., a cloud services provider located in the United States of America and engaged by Controller to help manage its recruitment and hiring process on Controller’s behalf. Accordingly, if you are located outside of the United States, your personal data will be transferred to the United States once you submit it through this site. The transfer will be made using appropriate additional safeguards under the standard contractual clauses approved by regulators for transfers of personal data outside the European Union. Your personal data will be retained by Controller as long as Controller determines it is necessary to evaluate your application for employment.  Under the GDPR, if you are located in the European Union, you have the right to request access to your personal data, to request that your personal data be rectified or erased, and to request that processing of your personal data be restricted. You also have the right to data portability, and to lodge a complaint with an EU supervisory authority. If you have any questions about our use of your data, you may contact us by email at usprivacyoffice@kyowakirin.com. RECRUITMENT & STAFFING AGENCIES Kyowa Kirin does not accept agency resumes unless contacted directly by internal Kyowa Kirin Talent Acquisition. Please do not forward resumes to Kyowa Kirin employees or any other company location; Kyowa Kirin is not responsible for any fees related to unsolicited resumes. #LI-TT1 #Hybrid #Princeton

Vill du arbeta verksamhetsnära med juridiska frågor inom Trade Compliance och ESG? Vi söker en Legal Counsel som ska bevaka regulatoriska förändringar, ge kvalificerad juridisk rådgivning och bidra till fortsatt regelefterlevnad i en internationell organisation. Vi söker dig som 👤 Du har gedigen erfarenhet av både Trade Compliance och regulatoriska ESG-frågor. Du är självgående, kommunikativ och van att omsätta komplexa regelverk till konkreta åtgärder i verksamheten. Rollen kräver att du kan samarbeta effektivt med flera funktioner och intressenter i en global och tvärfunktionell miljö. Arbetsuppgifter ⚖️ Ge juridiskt stöd till tull- och handelsfunktioner, inklusive förbättring av processer. Bevaka och bedöma regulatorisk utveckling inom ESG. Stödja implementeringen av en styrmodell för 3PDD, inklusive CSDDD. Ge juridiskt stöd vid implementering av EUDR och EUBR. Hantera och följa upp nationella regelverk kopplade till modernt slaveri. Genomföra och stödja riskbedömningar inom Trade Compliance och leverantörskedjan. Kommunicera regulatoriska krav och rekommenderade åtgärder till relevanta delar av organisationen. Obligatoriska krav ✅ Minst 4–6 års relevant arbetslivserfarenhet inom både Trade Compliance och ESG. Praktisk erfarenhet av Trade Compliance-frågor, gärna inklusive operativt arbete och relaterade riskbedömningar. Erfarenhet av regulatorisk due diligence i leverantörskedjor. Erfarenhet av arbete i tvärfunktionella miljöer. Mycket god kommunikativ förmåga. Självgående arbetssätt. Engelska på expertnivå i tal och skrift. Meriterande krav ➕ Erfarenhet av CSDDD, EUDR eller EUBR. Erfarenhet av att utveckla processer inom tull och internationell handel. Erfarenhet av globala organisationer och regelverk i flera länder eller regioner. Erfarenhet av nationell lagstiftning kopplad till modernt slaveri. Om uppdraget 📌 Plats: Stockholm Distansarbete: 0 % Omfattning: 40 timmar per vecka Startdatum: 14 september 2026 Slutdatum: 1 oktober 2027 Sista ansökningsdag: 5 augusti 2026 Möjlighet till förlängning finns. Sway Sourcing är en innovativ rekryteringspartner som specialiserar sig på att matcha rätt talang med rätt företag – snabbt och effektivt. Vårt huvudfokus ligger inom Ekonomi, Administration, HR, Marknad och IT, men vi har även den breda expertis och flexibilitet som krävs för att leverera skräddarsydda rekryteringslösningar inom alla branscher. Trots att vi är en relativt ny aktör har vi redan byggt förtroende hos många av Sveriges största företag och arbetar både nationellt och internationellt. Med baser i Sverige och Spanien erbjuder vi en unik kombination av lokal expertis och global räckvidd. Vårt starka nätverk och djupa branschinsikter gör oss till en självklar partner för företag som vill ligga steget före i sin rekrytering.

About the Company At Avaron, you get the security of permanent employment combined with the variety of working at different customers. We place specialists across everything from tech, IT and industry to project management and business support – and whatever the assignment, you have a consultant manager who is there for you and your development. About the Role You will step into a role at the intersection of trade compliance, ESG, and regulatory change, helping a global organization stay ahead of evolving requirements across multiple regions. The legal landscape is moving quickly, and you will combine regulatory monitoring with hands-on advice to support implementation, governance, and continued compliance. This role suits you if you enjoy translating complex regulation into practical actions and working closely with the business in an international, cross-functional setting. It is an excellent opportunity to influence how compliance work is shaped across trade and ESG areas. Job DescriptionYou will monitor and assess regulatory developments within trade and ESG. You will support customs and trade teams with legal advice and process enhancements. You will provide legal support for the implementation of the 3PDD governance model, including CSDDD. You will support the implementation of EUDR and EUBR. You will manage national modern slavery reports. You will work closely with stakeholders across functions and regions to help secure continued compliance. RequirementsMinimum 4–6 years relevant work experience from both trade compliance and ESG areas. Experience from trade compliance matters. Experience from regulatory supply chain due diligence management. Experience from working in cross-functional environments. Good communication skills. Self driving attitude. Nice to haveExperience from operational trade compliance tasks. Experience with related risk assessments. What We OfferPermanent employment at Avaron AB Occupational pension Wellness allowance of SEK 5,000 per year Application Selections are made on an ongoing basis – apply as soon as you can.

📍 Göteborg | 🕒 Heltid | 🏢 On-site | 🌍 Engelska We are looking for a senior Financial Controller for an exciting consulting assignment within Operational Finance in a global organization. In this role, you will work closely with the business, FP&A and Accounting, supporting financial reporting, forecasting and follow-up. This is a hands-on role for someone who enjoys working with both numbers and stakeholders, turning financial data into clear insights and strong decision support. 🚀 About the assignment 💼 You will support operational finance activities with a focus on consolidated reporting, forecasting and financial follow-up. You will act as a trusted finance partner and work closely with stakeholders across the organization. Key responsibilities 📌 Monthly reporting and financial analysis for assigned operational areas Consolidation of actuals, forecasts and budgets Financial follow-up of spend, CAPEX and COGS Accruals, capitalization and internal control activities Audit documentation and compliance support Continuous dialogue with non-finance stakeholders We are looking for someone who has ✅ 5+ years of experience in financial controlling or operational finance Strong understanding of financial processes and governance Solid experience working with SAP and Excel Ability to explain financial data in a clear and structured way A proactive and structured mindset, with the ability to manage multiple priorities Assignment details 📅 Start: ASAP Location: Gothenburg Workload: Full-time Remote work: 0% (on-site) Language: English Assignment period: 09 Feb 2026 – 15 May 2026 ✨ Interested? Apply as soon as possible – the assignment starts immediately. Sway Sourcing är en innovativ rekryteringspartner som specialiserar sig på att matcha rätt talang med rätt företag – snabbt och effektivt. Vårt huvudfokus ligger inom Ekonomi, Administration, HR, Marknad och IT, men vi har även den breda expertis och flexibilitet som krävs för att leverera skräddarsydda rekryteringslösningar inom alla branscher. Trots att vi är en relativt ny aktör har vi redan byggt förtroende hos många av Sveriges största företag och arbetar både nationellt och internationellt. Med baser i Sverige och Spanien erbjuder vi en unik kombination av lokal expertis och global räckvidd. Vårt starka nätverk och djupa branschinsikter gör oss till en självklar partner för företag som vill ligga steget före i sin rekrytering. Öppen för alla Vi fokuserar på din kompetens, inte dina övriga förutsättningar. Vi är öppna för att anpassa rollen eller arbetsplatsen efter dina behov.

To Samsung we are currently looking for a Sustainability Officer who is curious, humble, and ready to grow in a challenging environment! In this role, you will join a dedicated and dynamic team that includes a Sustainability and Corporate Affairs Manager who leads the team, an Environmental Officer responsible for environmental reporting, and an external Public Affairs consultant. The role is a 12-month temporary position, covering parental leave, offering you the opportunity to contribute to impactful projects while gaining valuable experience in a global organization.   This role will achieve As the Sustainability Officer, you will contribute to impactful initiatives by providing sustainability expertise for cross-divisional sales efforts, supporting marketing and communication activities, managing sustainability reporting, ensuring compliance with evolving legislation, and empowering internal teams. Your contributions will be pivotal in securing new business and fostering customer confidence in our sustainability leadership.   Job scope and key deliverables In this role, you contribute to key sustainability efforts, including: Leading cross-divisional sales support: Provide sustainability expertise and documentation for tenders, customer requests, contract processes, and more. Supporting marketing and communication activities: Contribute to sustainability-related communications to e.g. customers, media, and internal stakeholders. Managing sustainability reporting: Project manage the creation of Samsung Nordic’s Sustainability report and take lead on other reporting activities, including quarterly GHG reports, Norwegian Transparency Act report, and external sustainability assessments (e.g. Ecovadis). Ensuring compliance with legislation: Monitor and analyze upcoming Nordic and EU sustainability-related legislation that affects Samsung business. Qualifications Higher academic qualification in environmental engineering, sustainability, business, marketing and communications, or an equivalent field. At least 2 years of practical experience in corporate sustainability, including areas such as environmental reporting and sales/marketing support. A proven track-record of leading projects successfully. Proficiency in PowerPoint and Excel with experience in presenting. Fluent in Swedish and English in speech and writing. Experience in a global company is a plus.   About the assignment For this assignment you will be hired as a full-time consultant by Digitalenta. We offer our consultants a generous package including healthcare allowance, insurance policy, paid vacation days and pension savings. In addition, you'll also have a dedicated consultant manager available throughout your employment with us, in addition to optional networking activities with our network of consultants. The assignment is full-time and for a period of 1 year, with possible extension. Start date around 2026-05-01.

Välkommen till jobbet som aktivt förbättrar Sveriges arbetsmarknad! Vårt uppdrag är att skapa samhällsnytta genom att sammanföra arbetssökande och arbetsgivare. Samtidigt värnar vi om att ge rättssäker och likvärdig service till våra medborgare. Tillsammans får vi Sverige i arbete! Vill du bli en av oss? Vårt uppdrag Inom Verksamhetsområdet Samordnat stöd ger vi samordnade insatser till arbetssökande och arbetsgivare för att förkorta tiden till varaktig sysselsättning och hållbar rekrytering samt motverka felaktiga utbetalningar och brott mot välfärdssystemen. Vi möter arbetssökande med stort stödbehov och arbetsgivare som vill bredda sin rekrytering, med utgångspunkt i vår lokala förankring och kunskap om arbetsmarknaden. Vår arbetsplats Den aktuella enheten har sin verksamhet i Karlstad, Torsby, Hagfors eller Arvika och består av cirka ANTAL medarbetare. Vi sitter tillsammans där samarbete och kollegialt stöd är centrala för att skapa en levande atmosfär. Placeringsort för tjänsten är Karlstad, Torsby, Hagfors eller Arvika. Tillsammans arbetar vi mot gemensamma mål och kan alltid räkna med varandras stöd i vårt dagliga arbete. Vårt ledarskap innebär att vi leder resultatinriktat med ett nära och coachande förhållningssätt som uppmuntrar till delaktighet, motivation och ansvarstagande. Beskrivning av tjänsten Som arbetsförmedlare inom Samordnat stöd arbetar du fördjupat med arbetssökande som behöver individuellt och ofta långsiktigt stöd för att komma in på eller stanna kvar på arbetsmarknaden. Arbetet sker främst genom fysiska möten och i nära samverkan med arbetsgivare, myndigheter och andra aktörer för att samordna insatser utifrån individens behov. Du arbetar även med arbetsgivare utifrån kompetensförsörjningsbehov och stöttar dem i att bredda sin rekrytering. En viktig del av uppdraget är att informera om Arbetsförmedlingens tjänster samt om rättigheter och skyldigheter, och ge stöd på vägen mot arbete. Du hanterar även inkommande ärenden via telefon från både arbetssökande och arbetsgivare med stort stödbehov. För att lyckas i rollen arbetar du strukturerat och är trygg i att tolka och tillämpa lagar och regelverk. Du dokumenterar rättssäkert, agerar professionellt i mötet med människor och kan navigera i flera system samtidigt. I uppdraget ingår att föra utredande, vägledande och ibland komplexa samtal samt att arbeta mot uppsatta mål. Eftersom arbetet innebär resor och besök runt om i länet, är B-körkort ett krav för tjänsten. Din anställning inleds med en introduktion som ger dig goda förutsättningar att lyckas i rollen som statstjänsteman. Vårt erbjudande Tjänsten är en tillsvidareanställning på heltid som inleds med sex månaders provanställning. Tillträde enligt överenskommelse. Placeringsorten är Karlstad, Torsby, Hagfors eller Arvika. Vi erbjuder förmånliga semesteravtal, möjlighet till flextid i överenskommelse med arbetsgivaren (efter avslutad introduktion på ca 9 veckor), friskvård på arbetstid samt friskvårdsbidrag. Läs mer om vår organisation och vårt uppdrag på vår webbplats Mer om att jobba hos oss. Grundläggande krav för tjänsten Universitets-/högskoleutbildning om lägst 180 högskolepoäng (120 poäng enligt tidigare system) Alternativt har du varit anställd som arbetsförmedlare på Arbetsförmedlingen samt bedöms ha goda förutsättningar att leva upp till dagens krav på arbetsförmedlare Samt Minst 2 års arbetslivserfarenhet, sammantaget arbete minst på 50 procent under sammanlagt 2 år Goda kunskaper i svenska, det vill säga god förmåga att kommunicera i tal och skrift, samt hög läsförståelse B-körkort Övriga meriter för tjänsten Erfarenhet av och kunskap om samverkan med andra aktörer, som t ex myndighet, kommun, samarbetspartners och arbetsgivare Arbetslivserfarenhet av att tolka och tillämpa regelverk Arbetslivserfarenhet av vägledning och coachning mot arbete eller utbildning för personer som står långt från arbetsmarknaden Den statliga värdegrunden guidar oss i vårt dagliga arbete. Som anställd hos oss förväntas du arbeta rättvist, opartiskt och med hög integritet, samt bidra till att upprätthålla och stärka förtroendet för vår myndighet. Mer om statliga värdegrunden Utöver detta har du personlig förmåga och fallenhet att arbeta i enlighet med Arbetsförmedlingens medarbetarkriterier. Som medarbetare på Arbetsförmedlingen förväntas du vara: Ansvarstagande – ta ansvar för ditt arbete, samarbeta och bidra till en god arbetsmiljöHandlingskraftig – ta initiativ, bidra till förbättringar och hantera förändringarResultatfokuserad – planera, följa upp och bidra till verksamhetsnytta och resultat Ansökan Välkommen med din ansökan senast 2026-08-17. Bifoga ditt CV där du specificerar årtal, månad och arbetsuppgifter för varje anställning, samt intyg som styrker kraven om utbildning och/eller arbetslivserfarenhet i din ansökan.Om efterfrågad information inte framgår riskerar du bli bortsållad i urvalet. Du behöver inte skicka in ett personligt brev. Under rekryteringsprocessen kan urvalstester förekomma. Vi kommer att hålla dig informerad genom hela rekryteringsprocessen. Mer om vår rekryteringsprocess. Har du skyddade personuppgifter kontaktar du rekryteringspartner. Vi arbetar aktivt för att vara en myndighet fri från diskriminering. Det är viktigt för oss att all kompetens tas tillvara och vi välkomnar alla sökande. Vi ser positivt på om du har kunskaper i något av våra nationella minoritetsspråk.

1 plats(er). Vill du vara med och främja människors hälsa och bidra till en hållbar miljö? Då är det dig vi söker! Miljö- och hälsoskyddsförvaltningen behöver nu en ny kollega till hälsoskyddsgruppen. Dina arbetsuppgifter Som miljö- och hälsoskyddsinspektör arbetar du med tillsyn enligt miljöbalken och utövar myndighetsuppdrag på ett respektfullt och sakligt sätt gentemot verksamheter och individer du möter ute på fältet. Den här tjänsten har inriktning mot hälsoskydd och innebär att du självständigt inspekterar verksamheter och bedömer om deras verksamhet uppfyller lagstiftningen. I rollen ställer du krav, informerar och fattar beslut, samtidigt som du bidrar till att skapa en hållbar och trygg miljö för alla. Du planerar och genomför tillsyn själv utifrån den beslutade tillsynsplanen samt driver dina egna ärenden från start till avslut. Som inspektör hos oss får du en varierande och utvecklande roll. Arbetet innebär många samarbetskontakter med andra aktörer, förvaltningar och privatpersoner vilket innebär att du behöver kunna kommunicera på ett anpassat och professionellt sätt. Dina arbetsuppgifter omfattar både planerad och händelsestyrd tillsyn. De tillsynsobjekt som är aktuella för tjänsten kan vara skolor, förskolor, skärande och stickande verksamheter med mera. Du kommer också handlägga inkommande ärenden som till exempel klagomål och anmälningsärenden. Du behöver på ett respektfullt sätt kunna informera, ställa krav och fatta beslut utifrån saklig grund. Du planerar din egen arbetsdag och driver dina ärenden både självständigt och i samverkan med andra. Du arbetar nära dina kollegor och ni ger och får stöd av varandra. Vi använder Ecos 2 som ärendehanteringssystem  Din kompetens Vi söker dig som har en högskoleutbildning om minst 180-240 hp från naturvetenskaplig, folkhälsovetenskaplig eller teknisk högskoleutbildning som bedöms lämplig alternativt motsvarande praktisk erfarenhet. Vi vill också att du har goda kunskaper i miljöbalken. Vi ser även att du har god datorvana och uttrycker dig väl i svenska både i tal och skrift. Har du utbildning i förvaltningsrätt på minst 15 högskolepoäng eller motsvarande praktisk erfarenhet ser vi det som ett plus. Erfarenhet av myndighetsutövning inom miljö- och hälsoskyddsområdet ser vi också som ett plus.  B-körkort är ett krav då tjänstebilar förekommer.  Som person är du trygg, stabil, lyhörd och kan behålla ditt lugn även i pressade situationer. Du har en god samarbetsförmåga och kommunicerar på ett konstruktivt sätt. Du tar ansvar för dina uppgifter och planerar samt organiserar ditt arbete på ett effektivt sätt. Du kan tänka riskbaserat och kritiskt samt har förmågan att anpassa dig efter nya rön och förändringar i lagstiftningen. Du kan uttrycka dig bra i tal och skrift på svenska, men det kan också hända att du behöver kommunicera på engelska. arbetet kräver mycket god datorvana” eller att det vävs in i befintlig text om kommunicering. Varmt välkommen med din ansökan! Vi erbjuder På miljö- och hälsoskyddsförvaltningen är vi cirka 50 personer som arbetar med tillsyn med stöd av bland annat miljöbalken, avfallslagstiftningen, kemikalielagstiftningen, strålskyddslagen, tobakslagen, alkohollagen, livsmedelslagen samt konsumentjuridisk rådgivning. Vi deltar i samhällsplaneringen genom exempelvis deltagande i interna styr- och projektgrupper och som remissinstans i planärenden. Vår verksamhet är utåtriktad och berör på något sätt alla som bor och verkar i Västerås. Vi som arbetar på miljö- och hälsoskyddsförvaltningen utför det operativa tillsynsarbetet som miljö- och konsumentnämnden ansvarar för. Här får du arbeta med engagerade och kompetenta kollegor som hjälper och är måna om varandra. Hos oss blir du en del av ett kompetent och engagerat team där samarbete och arbetsglädje står i centrum. Vi tror på frihet under ansvar, vilket innebär att du själv planerar och driver ditt arbete, samtidigt som vi värdesätter balans mellan arbete och fritid. Vi erbjuder därför flextid och möjlighet att arbeta hemifrån delar av veckan. Vårt kontor är centralt placerat med goda kommunikationsmöjligheter och vi har tjänstebilar och tjänstecyklar för resor i tjänsten. Dessutom erbjuds du även friskvårdsbidrag årligen. Läs gärna mer om förvaltningens arbete på: https://www.vasteras.se/miljoochhalsoskyddsforvaltningen Vi lever vår värdegrund i mötet med varandra och de vi är till för. Varje dag, året runt ser vi till att Västerås fungerar. Tillsammans med dina ca 11 500 kollegor runt om i staden får du Sveriges viktigaste jobb. Läs mer om möjligheter, karriärvägar och om vårt erbjudande här: https://www.vasteras.se/jobbochkarriär (https://www.vasteras.se/jobbochkarriär)   Övrig information I samband med intervju behöver du styrka ditt medborgarskap. Det kan du göra med pass alternativt personbevis tillsammans med ID-handling. Om du inte är medborgare i Sverige, EU, EES eller Schweiz måste du uppvisa att du har ett giltigt arbetstillstånd eller är undantagen från skyldigheten att ha arbetstillstånd. Anställning kan ske först efter kontroll av arbetstillstånd, vilket krävs enligt utlänningsförordningen. Alla erbjudanden om rekryterings- och annonseringshjälp undanbedes. Anställningsform: Tillsvidareanställning.

Om Laholms kommun Det är i mötet med våra invånare som värdet av vårt arbete uppstår! Som medarbetare i Laholms kommun är du med och levererar tjänster och service till våra invånare – varje dag, året om. Laholms kommun rymmer allt från omsorg, stöd och utbildning för våra invånare till infrastruktur, underhåll, kulturliv och tillväxt. Vi tror på att varje medarbetare har drivkraften och förmågan att förbättra verksamheten och en vilja att utvecklas i sitt yrke.  Som medarbetare i Laholms kommun har du kollegor med många olika yrken och bakgrund, men det som förenar oss är vårt uppdrag och vår gemensamma värdegrund med ledorden glädje, mod, delaktighet, engagemang och gott föredöme Samhällsbyggnads-, kultur och folkhälsoförvaltningen (SKF) är en av landets bredaste och mest diversifierade förvaltningar och omfattar sju enheter (Räddningstjänst, Miljöenheten, Plan-och byggnadsenheten, Tekniska enheten, Måltidsenheten, Kulturenheten och Fritidsenheten) samt en Förvaltningsstab. Vår målsättning är att vara en framåtlutad, förändringsbenägen och serviceinriktad förvaltning som hålls samman av vårt gemensamma utvecklingsarbete och vår strävan att skickliggöra varandra i våra respektive professioner. På SKF arbetar vi i ett högt tempo med den bredaste palett av kommunala uppgifter vilket ställer krav på våra medarbetade att se utanför sina respektive verksamheter för att bidra till en helhet inom förvaltningen. I vår verksamhet svarar vi mot tre politiska nämnder: Samhällsbyggnadsnämnden, Kultur- & folkhälsonämnden samt jävsnämnden. Plan- och byggnadsenheten består av 21 personer som med olika kompetenser och egenskaper bidrar till samhällsbyggandet i Laholms kommun. Inom enheten finns planarkitekter, bygglovshandläggare, handläggare för bostadsanpassning, kart- och mätningsingenjörer samt GIS - ingenjörer. Enheten ansvarar för en stor del av samhällsbyggnadsprocessen och inom vårt uppdrag ligger detaljplan, bygglov och genomförande delen, tillsyn enligt PBL, bostadsanpassningsbidrag, upprättande och ajourhållning av kommunens kartverk, mätverksamhet, utveckling av GIS med mera. Om tjänsten Som bygglovshandläggare kommer du att bli en del i ett kontor där alla bidrar till att skapa den fysiska miljön i Laholms kommun. Du kommer att ingå i plan- och byggnadsenhetens bygglovsavdelning som tillsammans diskuterar och stöttar varandra i det dagliga arbetet. Utöver dina närmsta kollegor som arbetar med bygglov så kommer du att ha kollegor som arbetar med bostadsanpassningsbidrag, detaljplaner och kart-, mät- och GIS verksamhet. För tjänsten behöver du ha god insikt i plan- och bygglagstiftningen och du arbetar i första hand med bygglov. Du handlägger självständigt ärenden och ansvarar för dessa fram till bygglovsbeslut och i vissa ärendegrupper hanterar du även start- och slutbesked. Du förbereder och föredrar ärenden som behandlas i samhällsbyggnadsnämnden. Du arbetar med rådgivning till allmänheten per telefon och vid fysiska och digitala möten. Det kan även förekomma andra arbetsuppgifter som ligger inom ramen för en bygglovshandläggare så som till exempel tillsynsarbete enligt plan- och bygglagen. Du kommer arbeta självständigt men också tillsammans med kollegor för att utveckla processer och rutiner och ajourhålla fackkunskaper. Är du den vi söker? Vi söker dig som är högskoleutbildad, utbildad bygglovshandläggare eller har annan utbildningsbakgrund eller erfarenhet som vi bedömer vara likvärdig. Vi ser gärna att du har goda kunskaper om plan- och bygglagen och närliggande lagstiftning och erfarenhet av myndighetsutövning. Du har lätt för att hantera digitala system och har en snabb inlärningsförmåga. Vi arbetar i ärendehanteringssystemet Nova. Som person är du initiativrik, strukturerad och noggrann. Du tar stort eget ansvar och arbetar både självständigt och i grupp. Du har lätt för att planera ditt arbete och göra prioriteringar så att du kan leverera rätt kvalitet i rätt tid. Du har förståelse för arbete i en politisk styrd organisation I ditt arbete kommer du att ha många kontakter med kommuninvånare, företag och myndigheter vilket ställer krav på din förmåga att vara lyhörd och serviceinriktad och ha ett professionellt och anpassat bemötande. Du kommunicerar tydligt och enkelt. Har lätt för att uttrycka dig på svenska både i tal och skrift. Vi lägger stor vikt vid din personliga lämplighet. Körkort krävs för tjänsten. Urval kan komma att ske löpande under rekryteringsprocessen, vänta därför inte med att skicka in din ansökan!   Om anställningen Lönespridning för tjänsten lönesättning 2026: Lägst 37 000 kr/mån Medel 41 400 kr/mån Högsta 45 000 kr/mån. Lönesättning påverkas av erfarenhet och kunskap.      Antal tjänster: 1   Enligt överenskommelse Övriga upplysningar Är du intresserad utav uppdraget som RIB brandman i Laholms kommun kan du gå in på: Räddningstjänst - Laholms kommun Till följd av lag om belastningsregister ska utdrag ur polisens belastningsregister uppvisas vid anställning inom LSS, barnomsorg samt skola. Arbete i hemmet med äldre och personer med funktionsnedsättning | Polismyndigheten Arbete inom skola eller förskola | Polismyndigheten Du som söker jobb och har skyddade personuppgifter ska kontakta rekryterande chef i annonsen som kommer guida dig vidare för en säker ansökningsprocess. Du ska inte ansöka digitalt via ansökningslänken Information till annonssäljare Vi undanber oss alla erbjudanden om annonserings- och rekryteringshjälp i samband med denna annons. Vi erbjuder ett utvecklande arbete och friskvård i olika former samt tillämpar rökfri arbetstid. Laholms kommun verkar för att alla medarbetare ska ha lika rättigheter och möjligheter och vi välkomnar alla sökande oavsett kön, könsöverskridande identitet eller uttryck, etnisk tillhörighet, funktionsnedsättning, sexuell läggning, religion eller annan trosuppfattning.

Do you want to help ensure the safety and compliance of innovative energy solutions? At NIBE, we develop market-leading products that contribute to a more sustainable future. We are now looking for a Safety Compliance Engineer to Markaryd who is passionate about product safety, regulatory compliance, and technical excellence. In this role, you will work closely with colleagues across development, testing, and certification to ensure our products meet applicable legal and safety requirements throughout their lifecycle. About the Role As a Safety Compliance Engineer, you will play a key role in ensuring that NIBE products comply with relevant legislation, harmonised standards, and internal compliance requirements. You will coordinate testing activities, maintain technical documentation, support certification processes, and contribute to standardisation work at both national and international levels. This is a collaborative role where you will work closely with engineering, product development, testing teams, and external certification bodies to identify, assess, and resolve compliance-related matters. Location: Markaryd Your Responsibilities Ensure compliance with applicable safety legislation, including LVD, RED, and MD, as well as safety requirements within the IEC 60335 standards relevant to heat pumps and related accessories. Plan, conduct, and follow up compliance testing and technical evaluations, both in-house and in collaboration with external laboratories. Coordinate certification activities and manage relationships with testing and certification partners. Support engineering and product development teams in identifying and resolving compliance and safety-related challenges throughout the product lifecycle. Develop, maintain, and update technical compliance documentation in accordance with regulatory and internal requirements. Monitor developments in legislation, standards, and regulatory requirements affecting NIBE products. Provide guidance, training, and support to colleagues regarding compliance processes and product safety requirements. Your Profile We are looking for a structured and proactive professional with a genuine interest in product safety and regulatory compliance. You are comfortable working independently while also collaborating effectively across different functions and stakeholders. To succeed in this role, you likely have: A relevant degree or professional experience within electrical engineering, mechanical engineering, product safety, compliance engineering, or a related technical field. Knowledge of regulatory frameworks such as LVD, RED, Machinery Directive, or similar product compliance requirements. Experience working with CE marking and European regulatory requirements. Strong analytical and problem-solving skills. Excellent communication skills and the ability to build strong relationships with both internal and external stakeholders. Fluency in spoken and written English. Why Join NIBE? NIBE is one of Europe's leading manufacturers of sustainable energy solutions. We combine innovation, technical expertise, and a strong commitment to quality to create products that make a real difference for our customers and for the environment. At NIBE, you will have the opportunity to work in an international environment where your expertise contributes directly to the development of safe, reliable, and sustainable products for the future. More about us We exist to provide the world with better energy solutions. Since 1952, we have worked with passion and determination to develop new methods for improved energy efficiency. In doing so, we play an important role in the global transition to a more sustainable society. Our products are built on the finest Swedish engineering expertise. We have a strong market position and are making significant investments for the future. Our corporate culture is characterized by a family-oriented and entrepreneurial spirit, built on a long tradition and rich history where simplicity, humility, and reliability are key values. We take a long-term view of your employment and offer a workplace with excellent career opportunities. Together, we ensure that you can make the most of your talent, creativity, and expertise. NIBE in numbers NIBE AB is a modern and successful industrial company with annual revenues of over SEK 5 billion and more than 1,250 employees in Markaryd. NIBE is one of the market leaders in Europe, offering one of the industry’s broadest product ranges, including heat pumps, water heaters, solar panels, biofuel products, ventilation solutions, district heating equipment and more. NIBE AB is part of the publicly listed NIBE Industrier Group, which has annual revenues of approximately SEK 40 billion and more than 21,000 employees across over 30 countries. Application Does this sound like the right opportunity for you? Apply via our website under Available positions at NIBE. We review applications on an ongoing basis, so we encourage you to apply as soon as possible. The final application date is August 9. Please note that due to the holiday period (weeks 28–31), there will be a temporary pause in the recruitment process. The selection process will resume at the beginning of August. Questions? If you have any questions or would like to know more, please feel free to contact one of the persons listed below. Please note that due to the holiday period (weeks 28–31), there will be a temporary pause in the recruitment process. The selection process will resume at the beginning of August. Welcome with your application!

Om din roll Som Information Security, Compliance & Risk Specialist arbetar du strukturerat och verksamhetsnära med att omsätta krav inom informationssäkerhet, regelefterlevnad och riskhantering till praktiskt värde. Du bidrar till att säkerställa efterlevnad av regelverk och är en viktig del i arbetet med att identifiera, förebygga och följa upp risker i en komplex omnichannel-verksamhet. Du samarbetar tätt med funktioner inom verksamheten och externa aktörer och verkar i gränslandet mellan teknik, regelverk och affär i frågor som rör dataskydd, compliance och risk. Rollen kombinerar operativt arbete med analys, uppföljning och utveckling av arbetssätt inom säkerhet och compliance. Exempel på arbetsuppgifter:  Stödja och vidareutveckla Åhléns arbete inom informationssäkerhet, compliance och risk Säkerställa efterlevnad av lagar, regelverk och interna policys som berör GDPR och PCI DSS Genomföra och följa upp riskbedömningar kopplade till informationssäkerhet, betalflöden, system och leverantörer Delta i arbete kring bedrägeririsker (fraud), incidenthantering och uppföljning av förbättringsåtgärder Analys och följa upp säkerhetsincidenter, avvikelser och identifierade förbättringsåtgärder Bidra till framtagning och uppdatering av styrande dokument, riktlinjer och utbildningsmaterial Delta i bedömning av säkerhets-, risk- och compliancekrav vid upphandling, onboarding och uppföljning av externa leverantörer. Omvärldsbevaka relevanta förändringar inom regelverk och praxis avseende informationssäkerhet, dataskydd och betalningar, samt bidra med analyser och rekommendationer kring nödvändiga åtgärder. Vi erbjuder dig: Åhléns är ett välkänt retailbolag med över 120 års historia och en tydlig ambition att fortsätta utvecklas genom digitalisering, innovation och hållbara arbetssätt. Hos oss får du arbeta i en affärsnära roll där säkerhet, risk och compliance är en självklar del av vår tillväxtresa. Du blir en del av ett engagerat team och får möjlighet att påverka, samarbeta tvärfunktionellt och utveckla arbetssätt i en organisation med högt tempo och stort kundfokus. Till oss tar du med dig: Några års erfarenhet av arbete inom informationssäkerhet, IT-risk eller compliance God kunskap om GDPR och dataskydd Erfarenhet av eller god förståelse för PCI DSS och betalrelaterade säkerhetskrav Erfarenhet av riskanalyser och uppföljning av säkerhets- och complianceåtgärder Meriterande: erfarenhet från retail, e-handel eller betalningsintensiv verksamhet samt kännedom om standarder som ISO/IEC 27001. För att lyckas i rollen krävs att du är strukturerad, analytisk och lösningsorienterad, med god kommunikativ förmåga och ett affärsmedvetet förhållningssätt. Du trivs med att arbeta självständigt och tvärfunktionellt i en föränderlig miljö. Om rekryteringen Tjänsten är en tillsvidareanställning på heltid. Du är placerad på vårt huvudkontor på Dalagatan 100 och vi ser gärna att du kan börja hos oss så snart som möjligt. Urval och intervjuer kan komma att ske löpande och tjänsten kan tillsättas innan sista ansökningsdag, så skicka in din ansökan redan idag! Som Information Security, Compliance & Risk Specialist på Åhléns blir du en del av ett passionerat team som drivs av affärsmannaskap och entreprenörskap. Vi ger dig förtroende och möjligheten att växa i en utvecklande miljö. Med det hälsar vi dig varmt välkommen till Åhléns!

Company description: Getinge is a leading global provider of products and systems that contribute to quality enhancement and cost efficiency within healthcare and life sciences. We employ more than 10,000 people, and have operations in more than 40 countries. Saving lives is the greatest job in the world. Everything we do, from architectural planning to the equipment, therapies and solutions aim to secure the safest and most reliable care. As a leading medtech company, we focus every talent and resource towards helping our customers save as many lives as possible. Job description:About this opportunity At Getinge, the Infection Control business area plays a critical role in ensuring that our products meet global regulatory requirements and continue to support healthcare providers in delivering safe and effective patient care. The Regulatory Affairs function works closely with Quality, R&D, Operations, and global stakeholders to ensure compliance throughout the product lifecycle. As RA Manager Infection Control, you will be part of the Quality compliance, Regulatory & Medical organization. You will collaborate extensively across functions and sites within Infection control business area, as well as with global Regulatory Affairs teams and external regulatory bodies. The role offers a unique opportunity to influence regulatory strategy, strengthen cross-site collaboration, and drive regulatory excellence within a highly regulated MedTech environment. In this role, your primary responsibility will be to lead and drive regulatory affairs activities across Infection Control sites, providing strategic direction, ensuring regulatory compliance, and enhancing cross-site collaboration and efficiency.   What you will do As RA Manager Infection Control, you will lead regulatory activities supporting both business objectives and compliance requirements. You will act as a key regulatory expert and partner across the organization. Key responsibilities include: Develop and implement regulatory strategies to ensure products comply with applicable regulations and standards. Lead and support regulatory submissions and approvals, including CE marking, 510(k) submissions, and other market authorization activities. Act as the primary contact for notified bodies during technical documentation assessments and regulatory reviews. Review and approve technical files, regulatory documentation, labeling, packaging, and product claims. Drive regulatory intelligence activities, provide training, manage regulatory risks, and support audits, inspections, and non-compliance investigations. The preferred location for this role is Sweden. However, for the right candidate, we are open to a remote and/or hybrid working arrangement. No regular travel is required for this position.   You will bring To be successful in this position, we believe you have the following qualifications: Bachelor’s or master’s degree in quality management, Life Science, Industrial Technology, or a related field. At least 3 years of experience in Regulatory Affairs or a related function within a regulated industry. Previous leadership experience (minimum 1 year) with the ability to lead projects and cross-functional teams. Strong knowledge of regulatory compliance, risk assessment, gap analysis, and compliance auditing. Experience working with regulatory databases and advanced Microsoft Office skills. Experience supporting internal and external audits. Meritorious experience includes knowledge of regulatory frameworks and standards such as ISO 13485, ISO 14971, MDR, MDD, MDSAP, and ISO 14001. In addition to your technical expertise, we highly value your personality. We are looking for someone who combines strong analytical thinking with excellent written communication skills and can translate complex regulatory requirements into clear guidance for non-technical stakeholders. You have the ability to build relationships, influence stakeholders, and lead regulatory initiatives across multiple functions and locations. We believe you have a passion for continuous learning and an eagerness to stay up to date with evolving global regulatory requirements, standards, and best practices within the MedTech industry. At Getinge we see ourselves as proactive and self-driven in learning and contributing to the continued development of our products and our organization's capabilities. We are Team Players, Forward Thinkers and Game Changers. We think you will thrive in a high-expectation environment and have an interest in our products.   Why join Getinge Getinge offers a job in a safe and informal work environment, where we appreciate close team collaboration. We keep an open dialogue between leaders and employees, as well as between teams. We are focused on developing people, and together we will create a plan for learning and competence development when you start your career with us. We offer a competitive compensation and benefits package, including wellness allowances, generous family benefits and joint company activities. Everything to ensure we support your well-being and goals. Application Applications will be reviewed continually, and we therefore recommend sending us your application as soon as possible, but no later than 16th August. We kindly ask you to submit your application in our recruitment system by clicking the “apply now” button. Due to GDPR regulations we do not accept applications via e-mail. If you have any questions regarding the role, please contact responsible recruiter Emma Paulsson at email: emma.paulsson@getinge.com We look forward to receiving your application. We hope you will join us on our journey to become the world's most desired MedTech company.

Are you a structured and service-minded engineer with an eye for detail and regulations? Now you have the chance to become the regulatory anchor for our R&D projects and help our hardware products reach markets across the globe. Welcome to the Regulatory team within R&D in Lund! Your future team You'll become part of our Regulatory team within R&D in Lund - a group of seven experienced and knowledgeable colleagues who together play a crucial role in enabling Axis hardware products to reach markets globally. The team is the hub that our R&D projects and colleagues worldwide turn to when it comes to certification and regulatory requirements for our hardware products. Here, high competence is combined with a helpful and welcoming atmosphere - we're happy to share our knowledge and enjoy ourselves together along the way. What you'll do here as Regulatory Engineer R&D As a Regulatory Engineer R&D, your main task is to support our R&D projects with knowledge around the certification of our hardware products. The projects teams are responsible for scheduling and coordination, while you act as their regulatory anchor. You help the projects understand the requirement frameworks, provide regulatory support during external testing, and ensure that all documentation is handled correctly for global market access. In this role, you will: Support to R&D projects: Assist the projects with knowledge regarding regulatory requirements according to LVD, EMC, RED and equivalent requirements in other countries. Regulatory support toward test houses: Act as the projects' regulatory support in the dialogue with external test houses. Global Market Access & certification support: Contribute regulatory knowledge for global certifications and handle the documentation required for international market access. Global support within Axis: Answer questions from Axis' global organization regarding products' certification status and regulatory conditions in different markets. Administration: Ensure that the project's regulatory deliverables (test reports, certificates, Declaration of Conformity) are uploaded to the correct databases and that all documentation is complete ahead of launch. Who we are looking for We're looking for a thorough and structured team player who thrives in a supportive role and is motivated by making others successful. You have an eye for detail and find satisfaction in making sure the documentation is complete and in the right place - even when supporting several projects at the same time. You are analytical, enjoy digging deep into directives and standards, and find it easy to collaborate with colleagues around the world. We'd love to hear that you have/are: Good knowledge of regulations such as LVD, EMC and RED, as well as equivalent global requirements Experienced within the area of regulatory compliance and certification A strong communicator in English, both spoken and written, as you support the global organization and review international documentation Bonus points for (but not required): Experience of or familiarity with the certification of products with Bluetooth. What Axis has 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, whether through informal "fika" chats, formal meetings, or after-hours activities. Check it out: Axis HQ Your well-being matters to us. We offer a range of benefits, including a company bonus, Friday cake, wellness allowance, health insurance - and even your own Axis bicycle. To learn more about Axis, our innovative products, solutions, and vibrant company culture, explore: Life at Axis blog Engineering at Axis blog Innovation at Axis 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 of time, you can expect some delay in our response, but we will get back to you as soon as possible! In case of questions, please reach out to Maria Lindblad, Engineering Manager Regulatory at +46 (0) 708 68 12 36 (Not available w. 32)

Location: THG Labs, Meridian Business Park, Trowbridge, BA14 0BP About THG Labs THG acquired Acheson & Acheson in 2018 to bring full service, product development & manufacturing in-house to supply innovative branded and THG Beauty Brand products to the industry. In 2022 Acheson & Acheson became THG Labs. Capabilities include: * In-house market knowledge & trends * End-to-end service from idea generation through to manufacturing and launch * Technical, commercial and production expertise * Outstanding customer service About The Regulatory Compliance Team Based within the Beauty division of the business, The Regulatory Compliance Team is responsible for reviewing and assessing current and new cosmetic regulations globally including horizon scanning to make sure our clients have the latest information.  The team are responsible for checking and tracking the compliance to these regulations of all the ingredients, materials and formulations sourced and manufactured by THG Labs.  As well as managing and monitoring various certifications including audits, as well as processing and managing complaints and testing of products. Why be a Technical Information Officer at THG Labs?  Reporting to Snr Compliance Officer, the Technical Information Officer is responsible for assisting the team in accurate data collection, reporting, maintenance and researching compliance of raw materials and finished cosmetic products.  They will provide support to all members of the Regulatory Compliance Team to facilitate the delivery of projects assigned, ensuring products are safe, legal and sustainable. As a Technical Information Officer you will: * Collection of data relating to raw materials and finished goods to support the Regulatory Compliance team in the requirements for full compliance to all countries and regions as well as certifications as needed by the business and clients. * Ensuring accurate management of data in systems required for development and maintenance of cosmetic regulatory documentation. In accordance with company service level agreements and customer briefs. * Maintenance and collation of data relating to external certification of products including COSMOS, RSPO,  VEGAN SOCIETY, Halal and Cruelty Free International. * Reporting and maintaining data relating to sustainability of raw materials and finished products. * Developing knowledge of regulations relating to the development, manufacture, and sale of Cosmetic and toiletry products * Communicating with suppliers, requesting up to date and accurate information is received and processed in accordance with service level agreements. * Follow company work instructions and procedures. * Communicating effectively and positively with all teams, colleagues, and managers. * Take reasonable care for the health and safety for yourself and other persons who may be affected by your work * To cooperate with regards to all company health & safety measures, following H&S training when using equipment * Report to a person in authority any work situation which may represent a serious or imminent danger to health & safety or any shortcomings in the protection arrangements to health & safety. In respect of any hazards remember ‘see it, report it’ * Helping to promote a positive working atmosphere within the company. * Any other duties that may be required from time to time. What skills and experience do I need for this role? * Experience within the cosmetics, personal care, chemical, pharmaceutical, food, or regulatory compliance sectors. * Knowledge of cosmetic regulations, ingredient compliance, or product certification requirements. * Familiarity with certification schemes such as COSMOS, RSPO, Vegan Society, Halal, and Cruelty Free International. * Understanding of sustainability reporting and environmental data management. * Experience liaising with suppliers to obtain technical, regulatory, or compliance documentation. What’s in it for me? Career Development * Access bespoke development programmes that have been designed and developed by our in-house L&D team. * Continued development through our upskilling programme that is delivered in partnership with an industry-leading training provider. Enhanced Leave * 25 days annual leave plus bank holidays. * Don’t want to work on your birthday? We don’t either! Enjoy your day off on us! * Enhanced maternity and paternity pay, depending on length of service. * Up to 10 days compassionate leave. * Buy back up to 3 days each year. * Unlock 2 days volunteer leave after 12-months. Wellbeing Support * Access face-to-face and virtual appointments with our in-house GP (Manchester Head Office). * Access our 247 Employee Assistance Programme (EAP) which is provided by Bupa. Other Perks * Save up to 12% on the cost of personal tech through our salary sacrifice scheme. * Up to 50% staff discount on THG brands. * Know someone who would be perfect for THG? Refer them and get up to £1000 when they pass their probation. * Anniversary gifts when you hit 5 and 10 years of service.

Ideal start date: 01/11/2026 Contract duration (in months): 60 Grade range: 6 Benchmark job: 5A0020 - Communications/Public Relations /External Relations Professional Job flexibility: Fully Onsite What you'll do: Reporting directly to the Territorial Integration Pillar Coordinator of the FCC Project, you will be responsible for the project's regulatory authorisations and permitting activities. In this role, you will contribute directly to the objective of ensuring that the FCC project is ready to obtain all necessary regulatory approvals in both France and Switzerland within the required timeframe. Your responsibilities: - Contribute to the definition and implementation of the FCC project's regulatory authorisation strategy in France and Switzerland, in close collaboration with the competent authorities. - Coordinate cross-functional working groups on regulatory matters and identify issues requiring strategic decision-making. - Lead the development of the land acquisition and property strategy in collaboration with the relevant stakeholders. - Contribute to the preparation of the regulatory documentation required for the implementation of the FCC project, including permits, authorisations, exemptions and safety-related approvals, ensuring consistency in the positions presented to the authorities. - Contribute to project reviews and monitor the project master schedule for regulatory activities, identifying coordination needs and issues requiring management decisions. - Produce consolidated reporting on the progress of regulatory activities and contribute to the development of project monitoring tools, including indicators, risks and dashboards. Your profile: - Significant experience managing regulatory authorisation and permitting processes for major infrastructure projects in France and/or Switzerland, including land acquisition and property-related matters. Experience in cross-border projects or complex institutional environments would be an asset. - Proven experience managing complex projects involving multiple institutional stakeholders in structured and demanding environments. - Experience designing and implementing regulatory compliance frameworks in close collaboration with technical, legal and institutional teams. - Experience as a project owner or providing project definition and governance support for complex projects, including risk and opportunity assessment, development of implementation approaches and coordination of multiple stakeholders. - Master's degree or equivalent relevant experience in the field of Engineering, Law, Urban Planning, Spatial Planning (or Regional Planning) or a related field. Your skills: - Project management. - Use of office software packages. - Knowledge of regulatory frameworks applicable to major infrastructure projects. - Has a structured and organised approach towards work; is able to set priorities and plan tasks with results in mind. - Is willing to work on different projects simultaneously. - Expresses opinions, ideas and suggestions with conviction and in a logical/structured manner; keeps to the point. - Identifies, defines and assesses problems, takes action to address them. - Spoken and written French, with a commitment to learn English. For the full job description and application process please visit the following webstie: https://careers.cern/jobs/sr-se-2026-156-ld/

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.