MBE are expanding and are looking for creative, curious and senior software developers with system integration experience and strong competence in both embedded SW programming and automation test, to join our expert team towards our clients within Automotive, Energy and Medical Technology. REQUIRED QUALIFICATIONS: • M.Sc or B.Sc Computer Science, Software Engineering, Mechatronics engineering or equivalent. • Programming skills and technical documentation skills, likely more than 5 years’ experience as software developer. • Specific experience from C programming. • Specific experience from STM32 family of 32-bit Flash microcontrollers based on the Arm® Cortex®-M processor. • Experience from unit- and integration-level testing, automated testing and static code analysis PC-lint. • Experience from the Medical device industry within product development and from delivering products to IEC 62304, 60601-1 standards is meritorious. WORK DESCRIPTION: Our client designs, develops, manufactures and markets Scandinavian medical devices. The responsibilities consists of development of embedded SW (C), towards STM32 processors and to compile the code. Leading the simulation for the electrical medical device product. Perform unit tests on code, features and C-file. Lead the SW integration, Continuous integration (CI) and test code towards simulated environment. System testing SW/HW and Software Quality Assurance to integrate PCB with complete product. • Embedded SW development, C, towards STM32 family of 32-bit Flash microcontrollers based on the Arm® Cortex®-M processor • Unit- and integration-level testing, automated testing and static code analysis PC-lint. • Design, deploy and manage tools for test report for automated and manual tests. • Design, deploy and manage continuous integration systems which include automated testing and automated notification of results. • SW-development, Analysis&Verification is performed according to IEC 62304, 60601-1. MBE -10 years anniversary 2018!! MBE is awarded for growth and leadership such as DI Gazelle. We engage among the top engineers in the market of experienced experts as well as distinguished newly graduated engineers with personal values ​​for technically environmentally-friendly (Cleantech) solutions and for "Balance in Life" Successful companies build a well-planned business plan. MBE builds successful people through an individual "Personal Business Plan" focusing YOU! Through the MBE's recognized leadership model, our employees develops through long-term planning, between work, health and social life, challenging assignments, important contacts and supplementary courses to become the best they can be... with their own specific, individual conditions! We created and developed this leadership model together with professors at IHM Personal Leadership and Stephen R Covey's methodology already in 2001 Come in, Create and Develop Your Future With Us!

MBE are expanding and are looking for creative, curious and senior software developers with system integration experience and strong competence in both embedded SW programming and automation test, to join our expert team towards our clients within Automotive, Energy and Medical Technology. REQUIRED QUALIFICATIONS: • M.Sc or B.Sc Computer Science, Software Engineering, Mechatronics engineering or equivalent. • Programming skills and technical documentation skills, likely more than 5 years’ experience as software developer. • Specific experience from C programming. • Specific experience from STM32 family of 32-bit Flash microcontrollers based on the Arm® Cortex®-M processor. • Experience from unit- and integration-level testing, automated testing and static code analysis PC-lint. • Experience from the Medical device industry within product development and from delivering products to IEC 62304, 60601-1, 61010-1 standards is meritorious. WORK DESCRIPTION: Our client designs, develops, manufactures and markets Scandinavian medical devices. The responsibilities consists of development of embedded SW (C), towards STM32 processors and to compile the code. Leading the simulation for the electrical medical device product. Perform unit tests on code, features and C-file. Lead the SW integration, Continuous integration (CI) and test code towards simulated environment. System testing SW/HW and Software Quality Assurance to integrate PCB with complete product. • Embedded SW development, C, towards STM32 family of 32-bit Flash microcontrollers based on the Arm® Cortex®-M processor • Unit- and integration-level testing, automated testing and static code analysis PC-lint. • Design, deploy and manage tools for test report for automated and manual tests. • Design, deploy and manage continuous integration systems which include automated testing and automated notification of results. • SW-development, Analysis&Verification is performed according to IEC 62304, 60601-1, 61010-1. MBE -10 years anniversary 2018!! MBE is awarded for growth and leadership such as DI Gazelle. We engage among the top engineers in the market of experienced experts as well as distinguished newly graduated engineers with personal values ​​for technically environmentally-friendly (Cleantech) solutions and for "Balance in Life" Successful companies build a well-planned business plan. MBE builds successful people through an individual "Personal Business Plan" focusing YOU! Through the MBE's recognized leadership model, our employees develops through long-term planning, between work, health and social life, challenging assignments, important contacts and supplementary courses to become the best they can be... with their own specific, individual conditions! We created and developed this leadership model together with professors at IHM Personal Leadership and Stephen R Covey's methodology already in 2001 Come in, Create and Develop Your Future With Us!

MBE are expanding and are looking for creative, curious and senior software developers with system integration experience and strong competence in both embedded SW programming and automation test, to join our expert team towards our clients within Automotive, Energy and Medical Technology. REQUIRED QUALIFICATIONS: • M.Sc or B.Sc Computer Science, Software Engineering, Mechatronics engineering or equivalent. • Programming skills and technical documentation skills, likely more than 5 years’ experience as software developer. • Specific experience from C programming. • Specific experience from STM32 family of 32-bit Flash microcontrollers based on the Arm® Cortex®-M processor. • Experience from unit- and integration-level testing, automated testing and static code analysis PC-lint. • Experience from the Medical device industry within product development and from delivering products to IEC 62304, 60601-1, 61010-1 standards is meritorious. WORK DESCRIPTION: Our client designs, develops, manufactures and markets Scandinavian medical devices. The responsibilities consists of development of embedded SW (C), towards STM32 processors and to compile the code. Leading the simulation for the electrical medical device product. Perform unit tests on code, features and C-file. Lead the SW integration, Continuous integration (CI) and test code towards simulated environment. System testing SW/HW and Software Quality Assurance to integrate PCB with complete product. • Embedded SW development, C, towards STM32 family of 32-bit Flash microcontrollers based on the Arm® Cortex®-M processor • Unit- and integration-level testing, automated testing and static code analysis PC-lint. • Design, deploy and manage tools for test report for automated and manual tests. • Design, deploy and manage continuous integration systems which include automated testing and automated notification of results. • SW-development, Analysis&Verification is performed according to IEC 62304, 60601-1, 61010-1. MBE -10 years anniversary 2018!! MBE is awarded for growth and leadership such as DI Gazelle. We engage among the top engineers in the market of experienced experts as well as distinguished newly graduated engineers with personal values ​​for technically environmentally-friendly (Cleantech) solutions and for "Balance in Life" Successful companies build a well-planned business plan. MBE builds successful people through an individual "Personal Business Plan" focusing YOU! Through the MBE's recognized leadership model, our employees develops through long-term planning, between work, health and social life, challenging assignments, important contacts and supplementary courses to become the best they can be... with their own specific, individual conditions! We created and developed this leadership model together with professors at IHM Personal Leadership and Stephen R Covey's methodology already in 2001 Come in, Create and Develop Your Future With Us!

Requirements • MD Diploma plus Masters or PhD in Health Economics, Epidemiology or Public Health with broad medical knowledge within relevant therapeutic areas and real world evidence. The degree must have been approved or evaluated by the Swedish authorities (Socialstyrelsen). • Fluency in English and Swedish (written and spoken). Additional linguistic competence is a plus. • Competence in quantitative, qualitative and mixed method research methodologies along with data analysis packages like: STATA, Atlas Ti and Excel. Publication in peer reviewed journal or presentation in international conferences will be a merit. • Knowledgeable in all aspects of clinical trial methodology and GCP guidelines. • A minimum of 4 years clinical experience in an international setting. • Project management / evaluation experience focused on Health Economic Outcome Research. • Strong communication and public presentation skills. • Well demonstrated leadership, social and networking skills. The candidate should have the ability to work independently and in teams, including cross-functional settings. • Good moderation and negotiation skills together with a proactive approach and a high level of accountability. • Flexible and positive outgoing personality, with high level of drive and enthusiasm. • Innovative and entrepreneurial thinking. Job Responsibilities • Together with the Real-World Evidence Executive, Medical Advisor and Market Access Manager plan, co-ordinate and execute the medical activities in the Nordic countries according to the needs of the local business owners. Also, as per the global medical strategy develop a long-term medical strategy to implement on an account basis. • Understand the requirements of the Nordic client, prepare and present the deliverables: Communicating, gathering Health economic and clinical information in accordance with specific company guidelines. Prepares Proposals, Reviews and revises draft proposals that respond to client requirements, following standard formats used for previous engagements. Reviews Summaries: Reviews data; identifies patterns and implications. Develops Findings: Assists in using information and data to develop findings appropriate to client requirements. • Liaise with clinical trial investigators within the Nordic area, in collaboration with local clinical development, ensuring formation of effective working relationships. • Support marketing and sales departments with scientific information and in collaboration with them, actively liaise and interact with key opinion leaders and other key external stakeholders. Serve as medical contact person for local KOLs in the relevant activities when required. • Facilitate and co-ordinate investigator-initiated studies and other external investigator driven projects. • Attend local, national and international meetings and congresses. Scientific Solutions är ett konsult- och rekryteringsföretag med fokus på Life Science. Vi förser kunder inom läkemedels-, medicinteknik-, och bioteknikindustrin med medicinsk och naturvetenskaplig kompetens till verksamhetskritiska roller. Läs mer på www.scientificsolutions.se

We are seeking a Lecturer/Senior Lecturer in Medical Sciences (Anatomy) to contribute to high-quality teaching and academic development across the MBBS programme.

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.

Die ALTEN Consulting Services GmbH bietet mit über 20 Jahren Branchenerfahrung ihren namhaften Kunden aus Industrie und Wirtschaft hochspezialisierte Engineering- und IT-Dienstleistungen zur gemeinsamen Realisierung von branchen- und technologieübergreifenden Lösungen an. Kompetenz, Engagement und Leidenschaft verbinden alle unsere Mitarbeiter der ALTEN Consulting Services GmbH. Dabei stehen ein partnerschaftliches Miteinander, ein starkes WIR-Gefühl, der persönliche Kontakt zu unseren Kunden und die Kreativität jedes Einzelnen stets im Fokus. Werde auch Du Teil unserer Erfolgsgeschichte. Hardware Engineer - Medical Electronics (all gender) Make it happen DU... - unterstützt das Team im Support elektrischer Installationen des Produktportfolios - setzt Designänderungen um und begleitest deren technische Validierung - führst Retouren- und Fehleranalysen durch und entwickelst Lösungs- und Optimierungsvorschläge - erstellst und pflegst technische Dokumentationen wie Entwurfsdokumente, Testspezifikationen und Testprotokolle - arbeitest an der Sicherstellung und Verbesserung der Produktqualität im Rahmen des Product Sustainings - unterstützt bei technischen Abstimmungen im Umfeld von Entwicklung und Produktpflege Be our forward thinker DU... - hast ein abgeschlossenes Master- oder Diplomstudium der Elektrotechnik oder einer vergleichbaren Fachrichtung - verfügst über erste Berufserfahrung in der Entwicklung oder im Testing von elektronischen Systemen, idealerweise im MedTech-Umfeld - besitzt Kenntnisse in Messtechnik, Layout-Design und elektrischen Testverfahren - hast Erfahrung im Umgang mit Linux, Python sowie gängigen SAP- und MS-Office-Anwendungen - verfügst über sehr gute Deutsch- und gute bis sehr gute Englischkenntnisse in Wort und Schrift A home where people learn and thrive - Zukunftsorientierter Arbeitsplatz mit unbefristetem Arbeitsvertrag - Attraktive Vergütung - Mobiles Arbeiten nach Absprache - Individuelle interne und externe Weiterbildungen - Flexible Arbeitszeitgestaltung mit Gleitzeitkontenregelung - Persönlichen Ansprechpartner Weitere Informationen findest Du unter: www.alten-consulting.de Wir wertschätzen Vielfalt und begrüßen daher alle Bewerbungen - unabhängig von Geschlecht, Nationalität, ethnischer und sozialer Herkunft, Religion / Weltanschauung, Behinderung, Alter sowie sexueller Orientierung und Identität. Schwerbehinderte werden bei gleicher Eignung bevorzugt berücksichtigt. Bewirb dich jetzt über unser Online-Bewerbungsformular.

Unser Kunde ist ein globales pharmazeutisches Unternehmen, das sich der Entwicklung und Bereitstellung hochwertiger Arzneimittel widmet, die für Patientinnen und Patienten in kleinen, unterversorgten oder seltenen Krankheitsgruppen einen echten Unterschied machen. Unser Kunde ist davon überzeugt, dass jede Patientin und jeder Patient zählt. Kein Mensch sollte aufgrund der Größe der Patientengruppe oder der Komplexität seiner Erkrankung übersehen werden. Unser Kunde verfolgt einen einzigartigen Ansatz zur Bewältigung von Herausforderungen im Zusammenhang mit Produkten, die schwer herzustellen sind oder deren Einstellung droht und entwickelt zudem neue Produkte, um ungedeckten medizinischen Bedarf zu adressieren. Wir suchen einen erfahrenen Medical Science Liaison (m/w/d), der für den Aufbau und das Wachstum des Geschäfts in Deutschland verantwortlich zeichnet. Medical Science Liaison Süd (m/w/d) IHRE AUFGABEN ✓ Identifikation, Ansprache und Aufbau nachhaltiger Beziehungen zu führenden KOLs und einflussreichen HCPs in der deutschen kardiopulmonalen Community, einschließlich große CF‑Zentren, PAH‑Expertencentren und Universitätskliniken ✓ Therapiebereiche: Kardiopulmonales Portfolio, einschließlich Mukoviszidose, pulmonale arterielle Hypertonie ✓ Entwicklung und Umsetzung eines deutschen KOL‑Plans mit klar definierten Zielen ✓ Repräsentation des Kunden auf relevanten deutschen und internationalen Kongressen mit klar definiertem Interaktionsplan ✓ Unterstützung der Leitung Medical bei deutschen Advisory Boards, Speaker‑Programmen und Kongressaktivitäten ✓ Sammlung, Analyse und strukturierte Weitergabe umsetzbarer wissenschaftlicher, klinischer und wettbewerbsbezogener Erkenntnisse aus dem deutschen Feld ✓ Regelmäßige Rückmeldung von Insights an Medical Affairs, Sales und Marketing sowie Market Access ✓ Frühes Aufzeigen neuer Einwände, Änderungen deutscher und europäischer Leitlinien, Wettbewerberentwicklungen ✓ Arbeit in Übereinstimmung mit allen relevanten deutschen und europäischen Regularien und Verhaltenskodizes ✓ Erfüllung aller Pharmakovigilanz‑Meldepflichten, die sich aus Feldinteraktionen in Deutschland ergeben ✓ Abstimmung mit Global Medical und dem erweiterten Medical‑Affairs‑Team zur Ausrichtung der deutschen Aktivitäten an der Portfoliostrategie IHRE QUALIFIKATIONEN ✓ Abgeschlossenes Hochschulstudium (PhD, PharmD, MD oder vergleichbarer deutscher Abschluss); Masterabschluss (MSc) in den Life Sciences mit einschlägiger MSL‑Erfahrung ✓ Mindestens 3 – 5 Jahre MSL‑Erfahrung im deutschen Pharmamarkt, idealerweise in den Bereichen Atemwegserkrankungen, Mukoviszidose oder pulmonale Hypertonie ✓ Starkes bestehendes Netzwerk bzw. nachweisliche Fähigkeit zum Aufbau belastbarer Beziehungen zu deutschen kardiopulmonalen KOLs und Exzellenzzentren ✓ Fundierte Kenntnisse des deutschen Gesundheitssystems, einschließlich GKV, G‑BA‑Prozesse und Verordnungsumfeld ✓ Sehr gute Präsentations‑ und Kommunikationsfähigkeiten für ein deutsches klinisches Fachpublikum ✓ Sicheres, eigenständiges Arbeiten in einem spezialisierten, schnell wachsenden Pharmaunternehmen mit schlanken Strukturen ✓ Hohe Reisebereitschaft innerhalb Deutschlands bis zu 60–70 % ✓ Deutsch- und Englischkenntnisse auf muttersprachlichem oder verhandlungssicherem Niveau zwingend erforderlich UNSER ANGEBOT ✓ Attraktive Vergütung: Unbefristetes Arbeitsverhältnis mit einem wettbewerbsfähigen Gehalt und zusätzlichen Kunden-Prämien sowie 30 Tage Urlaub ✓ Moderner Firmenwagen: Nutzung auch privat mit unbegrenzten Freikilometern ✓ Umfassende Sozialleistungen: Volle vermögenswirksame Leistungen und 15% Zuschuss des Arbeitgebers zur betrieblichen Altersvorsorge inklusive umfassendem Unfallschutz – im Job, in der Freizeit, rund um die Uhr ✓ Corporate Benefits: Attraktive Einkaufsvorteile durch unse...(Lesen Sie die vollständige Jobbeschreibung auf der Seite des Partners) Homeoffice: Umfang: Maximal 100%

Für ein international orientiertes MVZ suchen wir Dich als: Medical Assistant/ MFA (m/w/d) Unser Kunde ist ein Neuropsychiatrisches Zentrum, das gemeinsam im Team von zehn Ärzten neurologische und psychiatrische Erkrankungen diagnostiziert und therapiert und auf Deine Unterstützung wartet. DAS ERWARTET DICH: - Als ausgebildete Medizinische Fachangestellte / Arzthelferin (m/w/d) mit fließenden Deutsch-Kenntnissen bringst du Deine Erfahrungen mit in die Praxis ein. - Du übernimmst die Terminkoordination und den Schriftverkehr und assistierst in den Behandlungen. - Mit Deinen ausgeprägten kommunikativen und organisatorischen Fähigkeiten unterstützt Du die Ärzte und verhilfst zu einem reibungslosen Praxisablauf. - Du betreust internationale Patienten und sorgst dabei für eine hohe Behandlungsqualität. Gegebenenfalls sprichst Du eine zweite Sprache (keine Voraussetzung) z.B. türkisch (Medikal Asistan), englisch, serbo-kroatisch, italienisch oder arabisch. UNSER MANDANT BIETET DIR: - Ein abwechslungsreiches und anspruchsvolles Aufgabengebiet der Neurologie und Psychiatrie - Eine langfristige Perspektive in einem modernen MVZ mit internationaler Ausrichtung - Eine übertarifliche Bezahlung DAS HÖRT SICH GUT FÜR DICH AN? Sende uns Deinen Lebenslauf an jobs@confianza-personal.de. Du hast noch Fragen, dann steht Dir Frau Süß gerne unter 089/5908380 zur Verfügung. Wir freuen uns darauf, mehr über deine beruflichen und persönlichen Ziele zu erfahren. Als spezialisierter Partner im Gesundheitswesen begleiten wir dich kostenfrei durch den gesamten Bewerbungsprozess ndash; bis du bei unserem Kunden startest.

Selection Criteria The ideal candidate will have the following profile: • A university degree in a field relevant to the position, • Minimum five years relevant work experience preferably with an international or regional organisation dealing with social and employment policies, particularly in active aging and lifelong learning • Experience in project development and international project management. Knowledge of funding requirements and rules of European Social Fund(ESF), knowledge of general funding rules will be an advantage. • Clear analytical skills and ability to make sound judgments, critical thinking and problem-solving skills; • Experience in reporting on project implementation and thematic issues. • Excellent command of written and spoken English and Swedish. • Excellent drafting and reporting skills; • Excellent communication and interpersonal skills. • Fluency in other languages of the CBSS Member States is an asset. • Computer literacy in MS office tools Job description - Project Officer for ESF Project the CBSS Secretariat is looking for a project manager for the newly approved ESF project “BSLF for Sustainable Working Life” embedded in CBSS long term priority Sustainable and Prosperous Region and EUS BSR Flagship “Baltic Sea Labour Forum (BSLF)”. Reporting to the Senior Adviser for Sustainable and Prosperous Region, the tasks and responsibilities of the Project Officer include the following: • Overall coordination for the flawless execution of project • Ensuring that project implementation is going in accordance with project proposal and activities’ plan as well as with ESF regulations • To ensure the maintenance of the project’s partnership and communication with project partners • Managing the relationship with related stakeholders • Developing detailed project plans to track progress • Preparation for and implementation of activities such as conferences, workshops and meetings. • Reporting on project implementation, conferences and meetings. • Presenting activities in various national and international events • Managing changes in project scope, schedule and costs • Performing risk management to minimize project risks • Reporting to management as needed • Create and maintain comprehensive project documentation • Performs other related duties as required The Council of the Baltic Sea States The Council of the Baltic Sea States (CBSS) serves as an overall regional forum for intergovernmental cooperation and coordination among the 11 CBSS Member States – Denmark, Estonia, Finland, Germany, Iceland, Latvia, Lithuania, Norway, Poland, Russia, Sweden, as well as the European Union. A Permanent International Secretariat was established in Stockholm in October 1998. The budget of the Secretariat is financed by annual contributions from the CBSS Member States as well as through project funds. The Secretariat is organised in a core team and specialised units. Currently there are 25 employees at the Secretariat. Additional information about the CBSS is available on www.cbss.org. The Secretariat’s work is guided by the three long-term priorities of the Council - Regional Identity; Sustainable & Prosperous Region and Safe & Secure Region.