41 compliance jobs found for you.

We are looking for a Compliance Manufacturing Specialist for our client based in Corsier-sur-Vevey, for a 5-month assignment. Your role:As a Compliance Manufacturing Specialist, you will play a key role in supporting Manufacturing Operations on all quality and compliance aspects.You will lead and support compliance activities across Dispensing, Media/Buffer, USP, and DSP areas, ensuring operational excellence and adherence to GMP standards.You will

Location: Hinwil (Zurich), SwitzerlandProject Category: R&DRole Category: EngineeringWorkload: 100%Start Date: 03 November 2025End Date: 30 September 2026 (with extension option of 6 months)Remote Share: 60%About the RoleWe are seeking an experienced expert to lead and orchestrate the practical application of Cyber Resilience Act (CRA) requirements, transforming our gap analysis into a concrete, auditable compliance program. With the support of the team,

Are you a compliance expert with a knack for precise labeling and a passion for ensuring product integrity?For one of our Clients, a medical diagnostics company, we are looking for a dedicated and proactive Labeling and Compliance Specialist to join a Subchapter of Compliance Support team in Rotkreuz.In this pivotal role, you will be working with other members in our sub-chapter in ensuring seamless product labeling and process integration during the

Für einen unserer Kunden, ein führendes, globales Pharmaunternehmen, suchen wir aktuell einen Flex Team Member für den Bereich Laborunterstützung und Compliance.Allgemeine Informationen:Startdatum: 01.11.2025 Spätestmögliches Startdatum: 01.12.2025Geplante Dauer der Anstellung: 12 Monate mit einer VerlängerungsmöglichkeitArbeitsort: Basel Arbeitspensum: 100%Home-Office:  Möglich nach vereinbarung, eine regelmässige Anwesenheit vor Ort ist

Hast du Lust auf einen Job in der Herstellung von Medizinalprodukten? Wir suchen für unseren Kunden in der Nähe von Burgdorf eine/n motivierte/n Mitarbeiter/in Medizinaltechnik 80-100%Deine Aufgaben:Qualitätssicherung in der SerienfertigungAuftragsausführung nach Managementsystemen (ISO 13485 u.a.)Prozessoptimierung in Zusammenarbeit mit anderen AbteilungenQualitätskontrollen, Messungen, DokumentationBedienen von Anlagen,

Ihre Erfahrung ist Ihr Kapital - möchten Sie diese nutzen, um in der Gesundheitsbranche nachhaltig die Qualität zu sichern und weiterzuentwickeln? Als Fachperson im Qualitätsmanagement leisten Sie einen entscheidenden Beitrag für zwei etablierte Standorte unseres Kunden in Walzenhausen und St. Gallen. Was diese Aufgabe besonders macht:Sie arbeiten an zwei Standorten und sorgen für die reibungslose Umsetzung der Qualitätsziele.Ihre Erfahrung ist gefragt:

Bereich Assembly ? PrüfstandZur Verstärkung unseres Teams im Bereich Prüfstand suchen wir per sofort oder nach Vereinbarung eine zuverlässige, teamorientierte und qualitätsbewusste Persönlichkeit. In dieser spannenden Funktion sind Sie direkt an der finalen Prüfung unserer technisch hochstehenden Kompressoren beteiligt. Ihr zukünftiger Arbeitsalltag:Einrichten, Aufstellen und Einfahren der Kompressoren auf dem PrüfstandDurchführung von Probeläufen ? auch

Location: Bulle, SwitzerlandActivity rate : 100%Contract type: Temporary - full year 2026 (potential renewal)Activity rate: 80% - 100% We are looking for an experienced MES Specialist to join the Technical Services department of UCB. In this role, you will develop and maintain MES recipes within the Syncade system (Emerson), ensuring compliance with GMP and site quality standards. You will work closely with cross-functional teams including QA, Compliance,

For our client based in Corsier-sur-Vevey, we are currently looking for a Warehouse Specialist for an 8-month assignment.This role offers an exciting opportunity to contribute to a critical part of pharmaceutical operations while driving continuous improvement across the warehouse. Your role:  Goods Reception: Verify accuracy of incoming shipments, conduct inspections, and document discrepancies or damage.Sampling: Perform material sampling to meet

For one of our clients, a world leader in in-vitro diagnostics, we are currently looking for a Product Safety Specialist - Electronic Diagnostics Instruments.General Information: Start date: asapLatest possible start date: 01.02.2026Duration: 1 year with the possibility of extensionWorkplace: Rotkreuz Workload: 80-100%Remote/Home Office: possible, at least 3 days on site work per week is expectedWorking hours: StandardDepartment: Compliance Operations,

For one of our clients, a global pioneer in pharmaceuticals, we are currently looking for a Quality Assurance Manager (Manufacturing Unit Monoclonal Antibodies).General Information: Start date: 01.01.2026Latest possible start date: 01.02.2026Duration: until 09.2026 with the possibility of extensionWorkplace: BaselWorkload: 80-100%Remote/Home Office: possible after consultation, on-site requiredWorking hours: StandardTeam: 6 peopleAbout the job:The Basel

Per importante società nel settore della revisione contabile e della consulenza aziendale ricerchiamo un Senior Audit Consultant (LICol).La risorsa selezionata opererà con piena autonomia e responsabilità sulle attività di revisione e consulenza in ambito finanziario, con particolare focus su compliance e risk management. Sarà punto di riferimento tecnico e gestionale per i progetti affidati. Responsabilità principaliPianificazione e conduzione di audit

Location: Bulle, SwitzerlandActivity rate : 100%Type of contract: Temporary contractStart date: 05.01.2026End date: 30.06.2026 (potential extensions)We are looking for an experienced Electronic Data Integrity QA Specialist to join the Quality Assurance team of UCB.In this role, you will act as a QA subject matter expert in data integrity, computerized system validation (CSV), and automation within a biotech manufacturing environment. You will review and

For a leading pharmaceutical wholesaler in Switzerland, we are seeking an FvP Associate for a permanent position, based in Bale Canton. This is a pivotal role at the intersection of quality and logistics, where you will assist the Responsible Person and ensure the pharmaceutical products are always available, correctly documented, and safely transported in compliance with Good Distribution Practice (GDP) requirements. You will act as the key interface

Assume project management responsibility for CMMC,  DFARS and NIST 800.171 implementation within the IT and IS/ cybersecurity domain – review and update IT & IS policies, process/ SOPs and execute relevant change management activities that arose from these requirements. Develop overarching strategy for IT and IS and implement country-wide technical solutions to support the compliance, i.e. enclaves.Lead development of GRC policies and their

For our client in Rotkreuz, a major player in the pharmaceutical sector, we are looking for an experienced and motivated Sourcing Manager. In this role, you will be responsible for managing procurement activities, ensuring compliance with internal policies, and building strong partnerships with suppliers and stakeholders.Your Responsibilities:Manage procurement requests in line with category strategies, company policies, and supplier agreementsCollaborate

Per conto di una società di revisione e consulenza aziendale, in fase di consolidamento nel settore Financial Services, si ricerca un/a Consulente Revisore Junior da inserire nel proprio organico.Il Ruolo e le ResponsabilitàLa risorsa selezionata supporterà il team di consulenza e revisione, svolgendo prevalentemente le seguenti attività:- Audit di Vigilanza: Esecuzione di audit di vigilanza FINMA (Autorità federale di vigilanza sui mercati finanziari) e

We are looking for a motivated and detail-oriented Senior Analyst, Procurement to support the management of a global $300M sourcing portfolio in Oils & Fats and Coconut. This role is key in ensuring accurate contract data and delivering insights to support strategic decisions.Key ResponsibilitiesContract & Data ManagementMaintain all physical Oils and Coconut contract data in commodities trading systems, ensuring alignment with supplier agreements (price,

Are you an experienced Full-Stack Software Developer with a passion for shaping the next generation of our instruments?We're looking for you to build the bridge between C# backend and React frontend, developing innovative software in a strictly regulated environment!General Information:Start date: asaplatest Start Date: 1.1.2026Planned duration: 12 monthsExtension (in case of limitation): possibleWorkload: 80-100%Home Office: 50% remote possibleTravel:

For our client based in Zürich, we are looking for an Interim HR Generalist with a focus on PayrollKey Responsibilities and DutiesHR Processes and Administration:Responsible for managing the payroll process in SwitzerlandSupport the implementation of a new payroll system and closely collaborate with the vendor to ensure timely and accurate data processingServe as the first point of contact for employees and managers regarding HR and labor law-related

For one of our clients, a global pharmaceutical company, we are looking for a Junior QC Analyst.General Information:Start date: 01.12.2025Duration: 30.06.2026Workplace: NeuchatelWorkload: 100%Remote/Home Office: Not possible, onsite presence requiredWorking hours: StandardWorking at weekend 1 time/monthAbout the job:As a QC Analyst you are the entry point for the QC laboratories, your main role is to provide the laboratories with all the samples,

For our client, an international company based in Klingnau, Aargau, we are looking for a dedicated Quality & OpEx Engineer 80 – 100% (f/m/d). General Information: Location: Klingnau, AargauStart Date: ASAPDuration: permanentWorking Hours: 80- 100%  Your Responsibilities: Oversee product and service quality, including decisions on non-conforming materialsManage customer complaints from acknowledgment to resolution and reportingEnsure compliance with

For one of our clients in the Scientific Sector, we are recruiting a Purchasing & Supplier Strategy Manager (100%) based in the canton of Fribourg. Your Responsibilities: Lead and develop the regional purchasing team, ensuring efficient sourcing strategies and operational performance.Secure supply continuity by proactively managing critical situations and ensuring timely material availability.Implement initiatives to optimize purchasing costs and improve

Per conto di azienda cliente attiva nel settore biomedicale con sede nell'area nord del Bellinzonese ricerchiamo una figura di Validation Engineer per un contratto temporaneo di 6 mesi.Il ruolo è cruciale per garantire che tutte le attività di convalida siano eseguite in piena conformità con gli standard normativi e i requisiti interni di qualità del cliente.Pianificazione e Sviluppo Protocolli: Sviluppare e implementare piani e protocolli di convalida

Start/End Dates: 10/1/2025 - 9/30/2026Location: BaselHrs/Wk:40.00Role OverviewWe are seeking a proactive and service-oriented Office Management & Hospitality Specialist to join our team in Basel. In this role, you will be the first point of contact for employees, clients, and guests, ensuring a welcoming and professional environment. You will manage daily office operations, contribute to internal projects, and support facility and hospitality services

Tasks:Drive the development of embedded software solutions in C/C++ and RTOS environments, ensuring code quality, performance, and compliance with project requirementsGuide and mentor embedded software engineers in day-to-day development tasks, quality control, effort estimation, and technical decision-makingSupport or lead the adoption of model-based development approaches (e.g. Simulink), including automated code generation for embedded targetsTranslate

Linux/Unix Systems EngineerWe are looking for a skilled Linux/Unix Systems Engineer to join our IT Systems team. In this role, you will be responsible for administering a large environment of virtual Linux (RHEL) and Unix (AIX) servers, along with the associated management tools.You will ensure the availability, performance, and security of the infrastructure, while maintaining compliance with internal standards and best practices.Your

Im Auftrag unseren Kunden, ein führendes und innovatives Unternehmen in der Pharmabranche, suchen wir dich als engagierten Beschaffungsspezialist (100%).Deine AufgabenSicherstellung, dass alle Beschaffungsanfragen gemäss den Richtlinien der jeweiligen Kategorie und unter Einhaltung der relevanten Richtlinien, Standards, Vorgaben und Betriebsabläufe ausgeführt werden, einschliesslich bevorzugter Lieferantenvereinbarungen und

For our Client in Visp we are searching for a Technical Document Manager who is responsible for coordinating the creation, adaptation, version control, and approval workflows of key project documentation throughout all project phases.  Key Responsibilities: Responsible for performance qualification (PQ) from detailed design through execution. This includes both CapEx-driven mechanical adaptations managed by external engineering (EPCM) partner and OpEx

On behalf of our client, we are looking for a QS Analyst (Training & Document Control). Contract: Temporary unlimitedLocation: Le LocleHome office: max 1 day per weekAvailability: ASAP or with maximum 1-month noticeLanguages: French and English fluency requiredResponsibilities:Manage and maintain the electronic training system (assignment, data entry)Support the maintenance of the document control systemManage circulation of documents for approvalReview