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​ Established in 1948 in Milwaukee, Wisconsin (USA), Manpower is a global leader in the human resources industry. Operating in 82 countries with a network of over 3,900 offices, the company supports the workforce needs of more than 400,000 clients worldwide. As specialists in the recruitment and selection of permanent and temporary professionals across all major economic sectors, we have been operating in Switzerland for over 60 years, employing more than 260 professionals across 37 locations nationwide. On behalf of our client, we are looking for a QA Specialist. ​ Tasks and responsibilities: - Take ownership of all Quality Assurance aspects within company projects, with a strong focus on qualification and validation (e.g., moulding and assembly processes, new/modified manufacturing processes and environments, software systems). - Lead and support quality-related activities in projects by motivating collaborators, working across cross-functional and cross-site teams, and documenting decisions with clear justifications. - Apply relevant compliance standards (FDA, GMP, ISO 13485, ISO 15378, ICH) to ensure alignment with internal requirements and customer expectations. - Ensure the preparation, accuracy, and integrity of quality documentation related to qualifications and validations, maintaining traceability and compliance across all records. - Plan and prioritize qualification/validation project phases (e.g., DQ/IQ/OQ/PQ, risk assessments, protocols/reviews, Validation Master Plans) to meet critical deadlines, applying project management skills. - Investigate and resolve deviations and anomalies using a structured problem-solving approach, proactively proposing effective solutions. - Evaluate process data objectively with statistical tools to support risk-based and compliance-driven decisions. - Act as a key representative in managing qualification/validation strategies and activities with customers, notified bodies, regulatory authorities, and internal stakeholders. - Support the Quality Assurance team in other QA activities and processes (e.g., CAPA, Change Control, Complaints) as well as in Continuous Improvement initiatives. QUALIFICATIONS - Technical background (ideally with a degree in Mechanical Engineering or a related field) - Background in validation and qualification within pharmaceutical and/or medical devices environments - Good knowledge of pharmaceutical regulations such as GMP, ISO 13485, ISO 15378, FDA, ICH - Experience in industrial manufacturing processes (preferably components assembly and plastic moulding), quality control, and project management - Ability to use statistical and data analysis tools - Strong quality mindset with a risk-based decision-making approach - Proven leadership, teamwork and communication skills - Good command of English, both spoken and written ​ PLEASE REGISTER YOURSELF AND UPLOAD YOUR CV AT OUR OFFICIAL WEBSITE: WWW.MANPOWER.CH, IN ORDER TO PROCESS YOUR APPLICATION.

Votre mission : Position: At ED level, this cross-asset structurer role is an investment management position, sitting in the Markets and Cross-Asset structuring team. Your position focuses on designing and delivering sophisticated financial solutions spanning equities, fixed income, commodities, FX, and derivatives, tailored to client requirements. Flexible and hybrid working arrangements are available to accommodate different working styles. Key responsibilities include: - Mandates Management: Support the team in overseeing mandates, optimizing resource allocation, and providing data-driven insights to refine strategies and enhance client outcomes. - Product Development: Design and implement complex, cross-asset financial solutions, including derivatives, structured notes, swaps, and asset-backed securities. Engage with internal stakeholders to understand needs, present solutions, and communicate structures clearly. - Risk and Market Analysis: Evaluate market, credit, operational, and legal risks associated with proposed structures. Conduct quantitative and market research to identify trends, opportunities, and innovative structuring techniques. - Regulatory Support: Assist with monitoring and implementing regulatory changes, ensuring compliance across the organization while promoting efficient, cost-effective processes. - Innovation and Tools: Develop investment decision tools using back-testing and data analytics to support strategic decisions and enhance product offerings. Votre profil : Profile: - Master's degree in Economics, Physics, Mathematics or Finance. - At least 10 years+ experience in multi-asset financial structuring (ideally from investment banking. - Expertise in derivatives and structured products. - Proven analytical skills and ability to interpret complex data. - Excellent communication skills, capable of explaining complex concepts clearly to stakeholders. - Skilled in financial modeling, risk analysis, and quantitative methods, with Python and C++ proficiency. - Knowledge of regulatory frameworks affecting derivatives and structured products. - A proactive approach to innovation and process improvement. - Based in the Zurich area or open to relocating, motivated to bring your banking expertise to a global insurer. - Preference for candidates with, or eligible for, a Swiss work permit (EU/EFTA or equivalent); 3rd-country nationals will also be considered. A propos de Finders SA : Client: Our client is a leading global insurance and financial services group with a strong presence across multiple markets. Recognized for innovation and excellence, the organization is seeking a highly skilled financial structuring professional, ideally with a background in investment banking, structured products, or insurance investment solutions.

​ Für unseren Kunden in der Region Dorneck, ein renommiertes Unternehmen der chemischen Produktion, suchen wir einen engagierten und erfahrenen Teamleiter (m/w/d). In dieser verantwortungsvollen Schlüsselposition übernehmen Sie die fachliche und disziplinarische Führung eines Schichtteams und stellen einen reibungslosen Ablauf der chemischen Herstellungsprozesse in einem anspruchsvollen Produktionsumfeld sicher. Angesprochen sind Persönlichkeiten mit Erfahrung in der chemischen oder pharmazeutischen Produktion, die eine Führungsaufgabe mit hoher Eigenverantwortung, klaren Entscheidungsbefugnissen und attraktiven Entwicklungsmöglichkeiten übernehmen möchten.   ​ Ihre Hauptaufgaben: - Führung, Förderung und Weiterentwicklung der Schichtteams sowohl fachlich als auch disziplinarisch - Planung und Koordination von Ressourcen, Schichten, Ferien sowie Instandhaltungsmassnahmen - Sicherstellung eines sicheren, effizienten und qualitätsorientierten Produktionsablaufs - Koordination der Abläufe zwischen den Schichten sowie der Produktionsplanung - Analyse von Qualitäts- und Sicherheitsereignissen und Ableitung geeigneter Massnahmen - Mitarbeit bei Investitions- und Verbesserungsprojekten - Verantwortung für korrekte Zeiterfassung und Anwesenheitsmanagement - Enge Zusammenarbeit mit den Bereichen Produktion, Engineering, Logistik, HSE, Qualität und HR Ihr Profil: - Abgeschlossene Berufsausbildung als Chemie- und Pharmatechnologe EFZ oder vergleichbare Qualifikation - Mindestens 5 Jahre Berufserfahrung, davon mindestens 3 Jahre in einer Führungsrolle (Schichtleiter oder Stellvertreter) in der chemischen Produktion oder Fertigung - Starkes technisches Verständnis für Maschinen, Anlagen und Produktionsprozesse - Hohe Entscheidungsfähigkeit, schnelle Auffassungsgabe und Überblick auch in komplexen Situationen - Ausgeprägte Sozial- und Kommunikationskompetenz sowie hohe Eigenmotivation - Sicherer Umgang mit ERP-Systemen (vorzugsweise SAP) und MS Office - Sehr gute Deutschkenntnisse; Englischkenntnisse von Vorteil ​ Interessiert? Wenn Sie bereit sind, Verantwortung zu übernehmen und Ihre Führungskompetenz in einem dynamischen Umfeld einzubringen, freuen wir uns auf Ihre Bewerbung. Bitte laden Sie diese über unsere Bewerbungsplattform hoch.  

​ Pour notre client, une entreprise biopharmaceutique de pointe, nous recherchons un(e) QC Lab Analyst HPLC pour intégrer leurs équipes du laboratoire Contrôle Qualité. ​ Vos missions : En tant que QC Lab Analyst, vous jouerez un rôle clé dans le contrôle qualité des produits. Vos responsabilités incluront : - Réaliser les analyses physico-chimiques sur les produits intermédiaires et semi-finis à l'aide de méthodes chromatographiques (HPLC, GC). - Effectuer la revue analytique des données brutes et des dossiers de lot QC pour garantir leur conformité. - Écrire et mettre à jour la documentation liée au contrôle qualité. - Participer à la déclaration et aux investigations en cas de non-conformités. - Proposer des solutions d'amélioration continue et contribuer à leur mise en ?uvre dans le cadre du Lean. - Participer à l'implémentation des CAPA et des change controls. - Veiller à ce que le laboratoire reste un environnement sûr et conforme aux standards 6S. Profil recherché : - CFC en Chimie ou diplôme équivalent, avec 3 à 5 ans d'expérience dans l'industrie pharmaceutique. - Solides connaissances des méthodes chromatographiques, notamment en HPLC et GC. - Capacité à communiquer efficacement, à rédiger avec rigueur et à faire preuve de précision. - Esprit d'équipe et aptitude à rechercher des solutions en collaboration. ​ Contrat temporaire  Lieu : Saint-Prex, VD, Suisse

​ Our client Philip Morris is looking for a Data Analyst based in Neuchatel or Lausanne (hybrid). ​ Role Purpose: Enable data informed decisions by transforming raw business data (in particular IP Law internal data & publicly available patent data) into trustworthy and actionable insights and intuitive analytics report or dashboard. The role owns the end to end BI lifecycle ? from requirement collection and data acquisition to secure publishing using Power BI, Excel, and out-of-the box reporting capability from operational tool. Key Accountabilities: ? Requirement Capture the needs via interview and translate the needs into a plan of action ? Data sourcing & integration Understand the enterprise data sources landscape, contribute to the definition of the extract/refresh strategies (if required), and build simple transformations scripts. ? Visualization & storytelling Build accessible dashboards and reports using native operational reporting tool (e.g. Salesforce reporting framework), or Power BI or advanced Excel where appropriate with focus on business relevance; iterate based on stakeholder feedback. ? Stakeholder engagement Partner with IP Law stakeholders to translate requirement into reports and/or dashboard Core Technical Competencies (Know?Do?Teach): Must Have: ? Power BI ? design reusable, documented models for BI reporting and apply templates and best practices. ? Excel (Advanced) ? Power Pivot, complex formulas, pivot tables, and data modeling for analytical workbooks. ? At least 3- 5 years of experience in a related field Nice to have: ? Salesforce Reporting ? build/maintain Salesforce reports and dashboards; ? Experience with ETL, RPA or programing language like python is considered an additional asset for implementing automated data extraction and transformation procedures. Soft Skills Must have: ? Agile ? listen, experiment, adapt, and learn from mistakes Nice to have: ? Embrace Challenge ? take thoughtful risks to innovate and disrupt ? Drive for Impact ? act with energy to deliver outcomes despite adversity ​ We are looking forward your application !