Finden Sie Jobs für operational risk manager in Basel6
26/10/2026 Neu!
| Schweiz, Rupperswil, Aargau - Adecco |
| Suchen Sie einen Job mit Zukunft? Gestalten Sie diese bei unserem Kunden selbst mit als Aufgaben - Sie sind hauptverantwortlich für die Führung der Haupt- und Nebenbücher - Sie erstellen die quartalsweisen MwSt.-Abrechnungen - Sie optimieren und entwickeln die bestehenden Abläufe, Prozesse und Tools weiter - Sie unterstützen den Leiter Finanzen bei der Erstellung von Geschäftsabschlüssen, dem Risikomanagement, der internen und externen Compliance und vielem mehr - Sie überwachen die im Ausland erstellten Geschäftsabschlüsse der Tochtergesellschaften und erstellen Konsolidierungen der Firmengruppe - Sie unterstützen den jährlichen Budgetprozess nach Bedarf - Sie sind die Stellvertretung des Leiters Finanzen (CFO) Profil - Abgeschlossene kaufmännische Grundausbildung mit Weiterbildung im Finanzwesen (Fachmann/-frau im Finanz- und Rechnungswesen mit eidg. Fachausweis) - Mehrjährige Berufserfahrung in einer vergleichbaren Tätigkeit - Versierte Kenntnisse von MS-Office, insbesondere Excel - Sage-Kenntnisse von Vorteil - Der Verantwortung entsprechende Loyalität und Diskretion - Einwandfreie Kommunikation in Deutsch (Französischkenntnisse von Vorteil) - Hohe Leistungsbereitschaft mit entsprechendem Qualitätsanspruch und Verantwortungsbewusstsein Vorteile - Ein abwechslungsreiches herausforderndes Umfeld in einem spannenden Unternehmen - Eine einzigartige, wertschätzende Firmenkultur - 5 Wochen Ferien und attraktive Sozialleistungen Kontaktinformationen Falls du weitere Fragen zu diesem Stellenangebot (Referenz: JN -022025-714176) hast, kontaktiere bitte Filipa Videira unter 0582332000. Über uns Adecco ist Marktführer für Personallösungen in der Schweiz und weltweit. Jeden Tag sorgen unsere Teams in unseren rund 50 Standorten schweizweit für den besten Match zwischen Kandidat:innen und Kunden in unterschiedlichen Berufsfeldern und Branchen. Adecco Schweiz ist ein Unternehmen der Adecco Gruppe, dem weltweit führenden Unternehmen für Talent Advisory und Solutions. Wir glauben daran, jeden für die Zukunft fit zu machen und beschäftigen täglich über 3,5 Millionen Menschen. Wir rekrutieren, entwickeln und bilden Talente in 60 Ländern aus, und ermöglichen es Organisationen, die Zukunft der Arbeit mitzugestalten. PERM Bankwesen und Finanzdienstleistungen |
26/10/2026 Neu!
| Schweiz, Aarau, Ag - Adecco |
| Möchten Sie die finanzielle Steuerung eines dynamischen KMU aktiv mitgestalten? Unser Kunde, ein etabliertes Handelsunternehmen in der Region Aarau, bietet Ihnen die Möglichkeit, als Fachbereichsleitung Finanzen die finanzielle Zukunft des Unternehmens strategisch weiterzuentwickeln und zu optimieren. Aufgaben - Gesamtverantwortung für das Finanz- und Rechnungswesen, Controlling sowie die Liquiditätssteuerung - Erstellung von Monats-, Quartals- und Jahresabschlüssen nach Schweizer Rechnungslegungsstandards - Entwicklung und Umsetzung von Finanzstrategien zur nachhaltigen Unternehmenssteuerung - Optimierung und Digitalisierung von Finanzprozessen zur Effizienzsteigerung - Budgetierung, Forecasting und Kostenkontrolle zur Sicherstellung der finanziellen Stabilität - Steuerung des Risikomanagements sowie Einhaltung gesetzlicher und regulatorischer Vorgaben - Enge Zusammenarbeit mit Banken, Steuerberatern und Wirtschaftsprüfern - Führung, Entwicklung und Motivation eines leistungsstarken Finanzteams Profil - Abgeschlossenes Studium in Betriebswirtschaft, Finanzen oder eine vergleichbare Ausbildung (z. B. Dipl. Finanzexperte/in, Experte/in Rechnungslegung & Controlling) - Mehrjährige Erfahrung in einer leitenden Finanzfunktion, idealerweise im Handel oder einem verwandten Sektor - Fundierte Kenntnisse in Rechnungslegung, Controlling, Finanzplanung und Budgetierung - Sicherer Umgang mit ERP-Systemen und Finanzsoftware, Erfahrung mit Digitalisierungsprojekten von Vorteil - Analytische und strategische Denkweise mit einer ausgeprägten Hands-on-Mentalität - Führungserfahrung mit ausgeprägten Kommunikations- und Verhandlungsfähigkeiten - Eigenverantwortliche, strukturierte und lösungsorientierte Arbeitsweise - Sehr gute Deutschkenntnisse, Englischkenntnisse von Vorteil Vorteile - Attraktives Vergütungspaket mit leistungsbezogenen Bonusmöglichkeiten - Strategischer Gestaltungsspielraum in einem zukunftsorientierten Handelsunternehmen - Moderne Arbeitsumgebung mit flexiblen Arbeitszeiten für eine optimale Work-Life-Balance - Individuelle Weiterbildungs- und Entwicklungsmöglichkeiten - Ein wertschätzendes, inklusives Arbeitsklima mit kurzen Entscheidungswegen Kontaktinformationen Falls du weitere Fragen zu diesem Stellenangebot (Referenz: JN -032025-724492) hast, kontaktiere bitte Filipa Videira unter 0582332000. Über uns Adecco ist Marktführer für Personallösungen in der Schweiz und weltweit. Jeden Tag sorgen unsere Teams in unseren rund 50 Standorten schweizweit für den besten Match zwischen Kandidat:innen und Kunden in unterschiedlichen Berufsfeldern und Branchen. Adecco Schweiz ist ein Unternehmen der Adecco Gruppe, dem weltweit führenden Unternehmen für Talent Advisory und Solutions. Wir glauben daran, jeden für die Zukunft fit zu machen und beschäftigen täglich über 3,5 Millionen Menschen. Wir rekrutieren, entwickeln und bilden Talente in 60 Ländern aus, und ermöglichen es Organisationen, die Zukunft der Arbeit mitzugestalten. PERM Finanzen und Buchhaltung |
26/10/2026 Neu!
| Schweiz, Basel - Work Selection AG |
| As a first-tier supplier to our renowned business partner F. Hoffmann-La Roche Ltd. in Basel, we are currently looking for a motivated and dedicated Regulatory Specialist ? Commercial / Post-Marketing & Remediation (CMC) for a temporary assignment of 12 months. A healthier future. It's what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That's what makes us Roche. At Roche, we believe in empowering you to thrive and do your best work. By bringing together our unique strengths in technical regulatory affairs, medicines, and technology, you will collaborate in an environment that nurtures growth, values your unique perspective, and drives sustainable innovation to transform healthcare for patients worldwide. In the position of Regulatory Specialist (CMC) in Pharma Technical Regulatory (PTR), you will support technical regulatory activities across the lifecycle of commercialized pharmaceutical products. This position is specifically focused on post-approval regulatory maintenance, change controls, regulatory deviations, system integration and remediation of legacy regulatory data and records. The role requires strong CMC regulatory expertise, experience working with marketed products and strong proficiency in the Veeva RIM environment. Tasks & Responsibilities - Independently manage and execute global technical regulatory submissions for commercial products, ensuring compliance with local and regional registration requirements, internal policies and audit standards - Manage the regulatory lifecycle of assigned commercial products - Assess technical change records for regulatory impact and coordinate required post-approval regulatory activities - Support post-marketing submissions, change controls and regulatory deviations - Maintain and remediate CMC regulatory documentation and data in Veeva RIM and related document management systems - Support system integration and clean-up of legacy regulatory information - Represent Pharma Technical Regulatory on cross-functional project teams and provide regulatory advice - Collaborate with local and global technical teams to ensure continued regulatory compliance - Support interactions with Health Authorities and external partners on assigned technical topics - Identify regulatory risks and proactively improve tracking, control systems and workflows - Monitor changes in global regulatory requirements and assess potential impacts on marketed products and lifecycle strategies Must Haves - Minimum Bachelor's degree in a relevant field - 3?4 years of CMC regulatory / technical regulatory experience - Experience supporting commercialized pharmaceutical products - Experience with post-approval / post-marketing regulatory maintenance - Experience with regulatory change controls - Experience managing or supporting regulatory deviations - Working knowledge of legacy / old product data clean-up and remediation - Strong proficiency in the Veeva RIM environment - Experience maintaining regulatory submission documentation in Veeva - Fluent English, written and spoken, minimum C1 - Proactive problem-solving ability and willingness to streamline legacy records and processes Nice to Haves - German language skills. - Previous Roche experience. - Experience with biologics. Benefits - Work with modern and up-to-date tools in an innovative work environment - Experience a work culture that promotes diversity and inclusion and where all employees feel valued - Benefit from financial support for your professional development plans - Take advantage of unbeatable, year-round discounts at renowned retailers and over 200 top brands - Benefit from fleet discounts when purchasing new cars or receive constant fuel discounts with our fuel card - Become part of one of the most prestigious pharmaceutical companies and actively shape the future of healthcare - Work on a state-of-the-art campus featuring green spaces, meeting areas, and an inspiring atmosphere - Take advantage of attractive fitness and swimming pool facilities or the gaming room as a creative retreat - Enjoy a selection of high-quality meals in modern staff restaurants - As part of a sustainable mobility concept, on-site parking spaces are available to you, provided you meet the relevant qualifications - Start with a professional onboarding process and a thorough introduction to your new role during the Welcome Days Are you interested? Don't hesitate and submit your complete application documents online today. We look forward to hearing from you! Wir wertschätzen Vielfalt und begrüssen daher alle Bewerbungen ? unabhängig von Geschlecht, sozialer Herkunft, Religion, Alter und Identität. Zur leichteren Lesbarkeit und besseren Verständlichkeit verwenden wir nur eine Gender-Form. Selbstverständlich sind im jeweiligen Kontext alle Genderformen gleichermassen gemeint. Temporär 100% Mitarbeiter |
26/10/2026 Neu!
| Schweiz, Basel - Work Selection AG |
| As a first-tier supplier to our renowned business partner F. Hoffmann-La Roche Ltd. in Basel, we are currently looking for a motivated and dedicated Regulatory Specialist ? Clinical / Early-Stage Development (CMC) for a temporary assignment of 12 months. A healthier future. It's what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That's what makes us Roche. At Roche, we believe in empowering you to thrive and do your best work. By bringing together our unique strengths in technical regulatory affairs, medicines, and technology, you will collaborate in an environment that nurtures growth, values your unique perspective, and drives sustainable innovation to transform healthcare for patients worldwide. In the position of Regulatory Specialist (CMC) in Pharma Technical Regulatory (PTR), you will be accountable for handling Health Authority interactions pertaining to CMC information, including IND, IMPD and related clinical regulatory submissions. This position is specifically focused on early clinical development, supporting Investigational Medicinal Products (IMPs), Investigational Medicinal Product Dossiers (IMPDs) and Clinical Trial Applications (CTAs). The role requires strong technical CMC regulatory expertise, close collaboration with global stakeholders and proficiency in Veeva Document Management to support compliant regulatory submissions. Tasks & Responsibilities - Independently manage and execute global technical regulatory submissions for clinical products, ensuring compliance with local and regional registration requirements, internal policies and audit standards. - Support CMC regulatory activities for early clinical development programs. - Prepare and coordinate IMPDs and other technical documentation required for Clinical Trial Applications. - Support regulatory strategies aimed at enabling timely approval of CTAs. - Evaluate technical information and changes for potential regulatory impact. - Maintain CMC documentation within Veeva Document Management. - Represent Pharma Technical Regulatory on cross-functional project teams and provide regulatory advice. - Collaborate with global technical teams, affiliates and other stakeholders. - Support interactions with Health Authorities and external partners on assigned technical topics. - Identify regulatory risks and support improvements to submission processes and workflows. - Monitor relevant changes in global regulatory requirements and assess their potential impact on development programs. Must Haves - Minimum Bachelor's degree in a relevant field - 3?4 years of CMC regulatory / technical regulatory experience - Experience in CMC regulatory support for early clinical trials - Experience with Investigational Medicinal Products (IMPs) - Hands-on experience preparing or supporting Investigational Medicinal Product Dossiers (IMPDs) - Experience with Clinical Trial Applications for early- to mid-stage development programs - Solid hands-on experience with Veeva Document Management for regulatory submissions - Fluent English, written and spoken, minimum C1 Nice to Haves - German language skills - Previous Roche experience - Experience with biologics Benefits - Work with modern and up-to-date tools in an innovative work environment - Experience a work culture that promotes diversity and inclusion and where all employees feel valued - Benefit from financial support for your professional development plans - Take advantage of unbeatable, year-round discounts at renowned retailers and over 200 top brands - Benefit from fleet discounts when purchasing new cars or receive constant fuel discounts with our fuel card - Become part of one of the most prestigious pharmaceutical companies and actively shape the future of healthcare - Work on a state-of-the-art campus featuring green spaces, meeting areas, and an inspiring atmosphere - Take advantage of attractive fitness and swimming pool facilities or the gaming room as a creative retreat - Enjoy a selection of high-quality meals in modern staff restaurants - As part of a sustainable mobility concept, on-site parking spaces are available to you, provided you meet the relevant qualifications - Start with a professional onboarding process and a thorough introduction to your new role during the Welcome Days Are you interested? Don't hesitate and submit your complete application documents online today. We look forward to hearing from you! Wir wertschätzen Vielfalt und begrüssen daher alle Bewerbungen ? unabhängig von Geschlecht, sozialer Herkunft, Religion, Alter und Identität. Zur leichteren Lesbarkeit und besseren Verständlichkeit verwenden wir nur eine Gender-Form. Selbstverständlich sind im jeweiligen Kontext alle Genderformen gleichermassen gemeint. Temporär 100% Mitarbeiter |
05/10/2026
| Schweiz, Basel-Land, Basel - Finders SA | |
Anstellungsart:Festanstellung | |
| Client: Our client is a well-established international private banking and asset management group with a strong presence across key financial centres. The organisation combines the stability and heritage of a long-standing financial institution with an entrepreneurial approach to investment and client service. The team operates in an international environment where collaboration, personal accountability and high professional standards are important. There is also a clear focus on sustainable investment and creating long-term value for clients. Position: This is an opportunity to join a highly regarded, long-established financial institution combining stability, innovation and an entrepreneurial culture — based in the beautiful Swiss city of Basel. We are currently looking for an experienced Risk & Performance Specialist to join an established analytics function supporting Asset Management. This is a role for someone who enjoys working at the intersection of investment risk, performance analysis, data and portfolio management. You will have exposure to a broad range of investment strategies and will play an important role in turning complex portfolio data into meaningful insight for investment and senior stakeholders. Responsibilities: - Carry out both forward-looking and historical risk analysis across equity, fixed income, multi-asset and alternative investment strategies - Assess portfolio exposures including VaR, tracking error, factor risk, concentration and liquidity - Prepare performance attribution and contribution analysis, translating results into clear investment insights - Work closely with Portfolio Management, Investment Compliance and Operations to maintain robust data quality and ensure reporting is delivered accurately and on time - Support the continued enhancement of risk and performance analytics, including methodologies, tools and underlying infrastructure - Present findings and analysis to relevant internal stakeholders, including investment professionals and senior management - Contribute ideas and practical solutions to improve the way investment risk and performance are measured and communicated Why apply? This is an opportunity to join a sophisticated investment environment where your analysis will have direct relevance to portfolio decisions and senior stakeholders. You will have the opportunity to work across multiple asset classes rather than being restricted to a narrow product area, while also contributing to the evolution of the firm's risk and performance capabilities. The culture is suited to someone who takes ownership, enjoys solving problems pragmatically and values accuracy without losing sight of the bigger investment picture. An entrepreneurial mindset, integrity and a collaborative approach are valued, alongside the opportunity to develop professionally within an international organisation. Candidate Profile - A university or equivalent higher education qualification in Finance, Economics, Mathematics or a related discipline - 5+ years' relevant experience in investment risk, performance analysis, investment analytics or a related field - Strong understanding of portfolio risk and performance measurement, ideally across multiple asset classes - A hands-on, "get things done" mindset, with the initiative and flexibility to roll up their sleeves, take ownership and find practical solutions - Experience with Bloomberg PORT Enterprise or a comparable platform, alongside Bloomberg and other relevant investment analytics tools - Working knowledge of Python and SQL a must - Professional qualifications such as FRM, CFA, CAIA or CIPM would be advantageous - A pragmatic, analytical and detail-oriented approach, with strong communication skills and a focus on data accuracy - Fluent English; German would be a plus but not a must - Swiss work permit eligibility required; cross-border candidates are welcome. The role is fully office-based, with a commitment to living in or near Basel expected |
30/09/2026
| Schweiz, Solothurn, Solothurn - Manpower |
| Experis® is a global leader in IT professional resourcing, permanent recruitment, project solutions, and managed services. With over 25 years of experience in Switzerland and offices in Zürich, Basel, and Geneva, we connect top IT talent with leading companies. Our mission is to help professionals unlock their potential and thrive in dynamic, future-ready careers. As a Quality Assurance Associate, you will contribute to maintaining and strengthening the Quality Management System at the Solothurn site. In this role, you'll support core quality activities, help coordinate routine governance processes, and assist in maintaining inspection readiness. You will collaborate with various site or global functions to ensure smooth execution of essential quality tasks. This position allows you to play an important part in sustaining a strong culture of compliance without carrying full ownership of operational responsibilities. The holder of this position will be responsible for the following activities: 1. Audit and Inspection Support - Coordinate and monitor audit and inspection commitments to ensure timely closure and proper documentation in line with Biogen QMS requirements. - Organize and facilitate meetings with SMEs to review action status, gather updates, and maintain alignment on deliverables. 2. Site Meeting Governance - Schedule and manage logistics for site governance meetings (e.g., Investigation Review Board), including agenda preparation, pre‑read collection, and documentation of decisions. - Support governance forums related to deviations, change controls, CAPAs, and other QMS review boards to ensure consistent application of Biogen standards. - Contribute to improving and optimizing governance meetings in line with site objectives 3. Self‑Inspection Program Execution - Assist in planning, implementing, and tracking the Self‑Inspection Program, including scheduling activities with SMEs and ensuring timely documentation and follow‑up of observations. - Maintain tools and trackers supporting inspection readiness and compliance monitoring. 4. QMS Administration & Operational Support - Support QMS processes including deviations, CAPAs, change controls, training assignments, and quality risk management in accordance with Biogen procedures. - Collaborate with cross‑functional stakeholders (QA, QC, Manufacturing, Engineering, etc.) to ensure compliance and timely completion of required actions. - Support on KPIs reporting and monitoring 5. Documentation & Data Management - Ensure accurate and compliant documentation of QMS activities in systems such as TrackWise, Veeva, and myCIMS. - Maintain logs, trackers, meeting minutes, dashboards, and metrics related to QMS processes and governance activities. - Identify opportunities to streamline QMS processes, improve documentation quality, and enhance visibility of compliance commitments. This position requires co-operation with people at every level of the organization and from multiple functions, including engineering, automation, validation, Manufacturing personnel, SME's on equipment and knowledge of biotechnology API production. Good communication skills in English, verbally and written. Self-driven and take ownership and responsibility for own assignments. Value teamwork at all levels, performs work with an open-mind and ability to value input from colleagues and peers. Able to drive discussion to solve problems with cross functional teams. Be confident in making technical decisions. In addition, must be able to prioritize tasks, be flexible and able to keep many activities running at a time. If you are interested in this opportunity, we look forward to receiving your CV or if you have any questions, contact Elaine Kanwar at +41 61 282 22 23. Check out all open positions at Experis at www.experis.ch Due to Swiss work permit restrictions, we can only consider applications from EU citizens or holders of valid working permit in Switzerland. |
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