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.
Are you driven by a deep need to understand how systems work, from the kernel to the application layer? Do you see a working system not as an endpoint, but as a baseline for improvement, optimization, and hardening?
We are a specialized team of software and hardware experts at the heart of medical instrument development. We are seeking a senior engineer to join our team, someone who combines deep technical mastery with a passion for craftsmanship and a relentless drive to make things better.
In this role, you will be a core contributor and consultant, ensuring the foundational operating system is robust, secure, and perfectly tailored to the demanding world of MedTech. The perfect candidate is a systems thinker who effortlessly grasps the big picture and understands how individual components interact to form a cohesive, reliable whole. Driven by an innate curiosity, you are never satisfied with surface-level explanations; instead, you are a pragmatic problem-solver who uses a logical, structured mindset to independently track down root causes. Rather than waiting for direction, you are a proactive contributor who spots areas for improvement and takes the initiative to elevate the entire team. Finally, you are an excellent communicator with advanced English skills, fully capable of translating complex technical concepts into clear insights for both engineering peers and non-technical stakeholders alike.
General Information:
? Start date: Asap
? Planned duration: 12 months from start date
? Extension (in case of limitation): Possible
? Workplace: Rotkreuz
? Workload: 80-100%
? Home Office:Onsite 50% , home office possible
Tasks & Responsibilities:
? Architect and Engineer our Core OS Platform: Take ownership of our custom Debian-based distribution. This includes everything from kernel customization and driver integration to the creation, maintenance, and optimization of Debian packages.
? Master the Build and Release Pipeline: Evolve and improve the infrastructure and processes used to build, test, and release our Linux distribution, ensuring reliability and reproducibility.
? Be the Ultimate Escalation Point: Act as the go-to expert for complex, low-level system issues. Perform deep-dive troubleshooting, debugging, and root-cause analysis across both software and hardware.
? Consult and Empower Development Teams: Guide internal project teams on how to best leverage the Roche Linux platform.
? Proactively Drive Improvement: Constantly seek out opportunities to enhance our distribution, tools, and processes. Whether it‘s improving system performance, strengthening security, or automating a complex workflow, you will be expected to identify needs and champion solutions.
Must Haves:
? Deep, Hands-On Linux Mastery (10+ years): You are a seasoned professional who is comfortable across the entire Linux stack.
? Custom Distribution Engineering: Proven, extensive experience building, modifying, or maintaining a customized Linux distribution, with a strong preference for Debian ( ,using tools like debootstrap, molior, aptly).
? Expertise in Debian Packaging: You don‘t just apt-get install. You can create, patch, and maintain .deb packages from scratch, understanding policy, dependencies and best practices.
? Strong Scripting and Automation Skills: Fluency in Python and Shell scripting is essential for building tools and automating system tasks.
? Fundamental Systems Knowledge: A solid grasp of operating system theory (process management, memory, filesystems), software build systems (make, CMake), and the full testing and packaging lifecycle.
? Advanced English is mandatory; German is a welcome bonus.
Nice to Have:
? Proficiency in a systems programming language like C or C++.
? Experience with embedded systems, the ARM platform, hardware drivers, and low-level hardware/software integration.
? Knowledge of modern infrastructure: Virtualization (KVM), Containers (Docker, Kubernetes), CI/CD pipelines, and Infrastructure as Code (Terraform).
? Experience with cloud platforms ( , AWS).
If you are interested, please apply to the job with a copy of your CV.
Interviews will start from mid of September 2026, 2 rounds planed. 1st round online, 2nd round onsite.
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. Location: Zurich
Start date: 01.10.2027 - flexible
Duration: 6 months ? with possibility of extension
Key Responsibilities
Track record in Program or large Project deliveries
Track record in migration programs with test, user change and business change experience
Profound understanding of transaction-related core processes such as order manager, corporate actions, deliveries, loans and OTC
Profound know-how in portfolio management and analysis capabilities, including rebalancing, allocation and performance calculation
Certified Project Manager or Agile Product Manager
Qualifications
Outstanding communication and presentation skills
Very strong planning, execution and delivery methodology
Reliable partner able to challenge and align with other streams, balancing strategic targets with feasibility
If you are interested in this opportunity, we look forward to receiving your CV or if you have any questions, contact Kaixi Jia at +41 44 229 99 43.
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.
Fondata nel 1948 a Milwaukee, Wisconsin, USA, Manpower è una società internazionale leader nel settore delle risorse umane. Presente a livello mondiale in 82 paesi con oltre 3'900 filiali risponde ai bisogni dei suoi 400'000 clienti.
Specialisti nel reclutamento e nella selezione di personale fisso e temporaneo in diversi settori dell'economia, siamo presenti in Svizzera da oltre 60 anni con più di 260 collaboratori in più di 37 sedi.
Nell'ottica di rafforzamento della propria struttura il nostro cliente, ci ha incaricato di selezionare il seguente profilo professionale: Il Preparatore è responsabile dell'esecuzione delle attività assegnate nel rispetto delle procedure e degli standard aziendali, con particolare riferimento a:
Preparazione di liquidi iniettabili secondo ricetta, Batch Record e procedure operative approvate
Gestione delle materie necessarie al processo, comprese materie prime in forma di polvere, filtri ed altra attrezzatura dedicata
Esecuzione delle attività di pesata, carico, dissoluzione, miscelazione, omogeneizzazione e trasferimento del prodotto, CIP e SIP, lavaggio e sterilizzazione componenti
Conduzione delle apparecchiature di preparazione e lavaggio/sterilizzazione
Supporto alle attività di allestimento e costituzione del semilavorato, garantendo il corretto flusso di materiali e prodotto
Assistenza alle linee di produzione e/o di riempimento, intervenendo nelle attività operative di supporto e nella gestione delle necessità di reparto
Competenze tecniche richieste
Conoscenza dei principi di produzione farmaceutica in ambiente controllato, in funzione del processo
Conoscenza delle principali GMP e della documentazione di produzione
Familiarità con i processi di preparazione di forme farmaceutiche liquide iniettabili
Capacità di lavorare con materie prime in polvere e principi attivi ad alta potenza
Capacità di interpretare e applicare SOP, Batch Record, istruzioni operative e ricette di produzione
Capacità di utilizzare apparecchiature e strumenti di produzione nel rispetto delle procedure
Attenzione alla corretta gestione di pesate, dosaggi, tempi, temperature, parametri di processo e trasferimenti
Conoscenza dei principi di controllo della contaminazione e prevenzione della cross-contamination
Competenze comportamentali
Precisione e attenzione al dettaglio, soprattutto nella gestione delle materie prime e della documentazione GMP
Elevato senso di responsabilità e orientamento alla qualità
VI PREGHIAMO DI ISCRIVERVI SUL NOSTRO SITO UFFICIALE: WWW.MANPOWER.CH, ALLEGANDO IL VOSTRO CURRICULUM VITAE PER POTER ESAMINARE LA VOSTRA CANDIDATURA.
Manpower recherche pour un de ses mandants de la place genevoise, une entreprise spécialisée dans la Chimie :
Laborantin en chimie junior avec CFC (H/F)
Missions:
Réaliser des analyses physico-chimiques sur matières premières, produits intermédiaires et produits finis.
Réaliser les analyses de routine sur GC-FID conformément aux procédures en vigueur
Préparer les échantillons et les réactifs nécessaires aux essais.
Effectuer les contrôles qualité conformément aux procédures internes.
Enregistrer et interpréter les résultats d'analyses.
Assurer la traçabilité des essais et rédiger les rapports associés.
Participer à l'entretien, au nettoyage et à la calibration des équipements de laboratoire.
Respecter les règles de sécurité, d'hygiène et d'environnement en vigueur.
Profil recherché:
Diplôme de CFC en Chimie, Chimie Analytique, Mesures Physiques ou domaine similaire.
Première expérience en laboratoire (stage, alternance ou emploi) appréciée.
Connaissance des techniques d'analyse de base et des bonnes pratiques de laboratoire.
Maîtrise des outils informatiques courants (MS Office).
Rigueur, organisation et esprit d'équipe.
Curiosité scientifique et volonté d'apprendre.
Résistance au stress
Si vous correspondez à cette offre, merci de postuler via le formulaire en ligne avec un dossier complet (CV, certificats de travail...)
Pour le compte de l'un de nos clients, acteur reconnu dans le secteur agroalimentaire, nous recherchons un(e) Boulanger(ère) Industriel(le) afin de renforcer son équipe de production. Vos responsabilités
Réaliser les différentes étapes de fabrication des produits de boulangerie.
Préparer, peser et mélanger les matières premières selon les recettes définies.
Assurer le pétrissage, le façonnage et le suivi de la fermentation.
Alimenter et surveiller les lignes de production automatisées.
Contrôler la qualité des produits finis et semi-finis.
Effectuer les contrôles de conformité tout au long du processus de fabrication.
Respecter strictement les normes d'hygiène, de sécurité et de qualité.
Votre profil
Formation de boulanger ou expérience significative dans un poste similaire.
Une expérience en environnement industriel ou agroalimentaire constitue un réel atout.
Bonne compréhension des procédés de fabrication en boulangerie.
Personne rigoureuse, autonome et dotée d'un bon esprit d'équipe.
Bonne condition physique.
Permis de conduire et véhicule personnel souhaités afin de faciliter les déplacements et l'accès au site de production.
Vous vous reconnaissez dans ce profil ? Nous nous réjouissons de recevoir votre dossier de candidature complet en ligne
MANPOWER AG ist spezialisiert auf Temporär- und Dauerstellen und bietet umfassende Personaldienstleistungen an. Mit Standorten in der ganzen Schweiz unterstützen wir unsere Kunden, um deren Aufträge und Projekte erfolgreich zu realisieren. Für unseren Kunden in der Region Bubikon suchen wir einen/eine
HR Generalist 80-100%
Ihre Aufgaben
Flexible Übernahme weiterer HR-Aufgaben und Projekte zur Unterstützung des Teams
Unterstützung in der HR-Administration entlang des gesamten Employee Lifecycles
Zuständig für die termingerechte monatliche Lohnverarbeitung
Unterstützung beim Thema Zeitwirtschaft (Monatsabschlüsse und Mutationen)
Planung, Organisation und Koordination von Firmenanlässen sowie Mitarbeitergeschenken
Aktive Mitarbeit in HR-Projekten (Prozessgestaltung, Weiterentwicklung von Reglementen usw.)
Aufbereitung von HR-Kennzahlen, Auswertungen und Statistiken
Ihr Profil
Mehrjährige Erfahrung im HR-Bereich, idealerweise als HR Business Partner oder HR Manager
Sehr gute Deutsch- und Französischkenntnisse
Fähigkeit, Rekrutierungsprozesse in französischer Sprache zu führen
Hohe Eigeninitiative, Kommunikationsstärke und Freude an der Arbeit in einem dynamischen Umfeld
Bei unserem Kunden erwartet Sie ein verantwortungsvolles und motivierendes Arbeitsumfeld sowie attraktive Anstellungsbedingungen.
Ich freue mich auf Ihre vollständigen Bewerbungsunterlagen über den Online-Bewerbungsbutton.
Bei Fragen stehe ich Daniel Gade Ihnen gerne unter der folgenden Telefonnummer zur Verfügung: +41 58 307 23 07.
Wir freuen uns auf Ihre Bewerbung.
Experis is recruiting a Production Planner to supports manufacturing planning, scheduling and changeover activities.
In this role, you will Develops the site manufacturing schedule for day to day operations and supports planning activities for long term timelines.
Summary
The incumbent supports manufacturing planning, scheduling and changeover activities for the SOL DS Manufacturing Site supporting both clinical and commercial programs and CQV phase. Responsible for creating and maintaining accurate, detailed daily production schedules and the medium-term production plans used by Manufacturing, Materials, Quality, Engineering, Validation and Plant Management. The incumbent also supports facility readiness, changeover and maintenance project schedules. Confirming resource requirements, proactively identifying and communicating constraints with suggested alternative solutions are also responsibilities of this position. The incumbent also drives issue resolution for project success and reports project status to team and manager.
Description
Develops the site manufacturing schedule for day to day operations and supports planning activities for long term timelines. Responsible for tactical day-to-day scheduling and product changeover timelines that meet the production demand plan. Interacts with manufacturing personnel to determine current completion state of production operation activities and to clarify any schedule updates/changes. Supports facility project schedules for shutdown work, commissioning, validation, change-over, routine/non-routine facilities maintenance activities.
Min Education and experience Requirements
- Minimum Associate's degree (AA) in Chemical/Biochemical Engineering, Supply Chain Management, or related business/science/technical field;
- Bachelor's degree (BS) preferred
- Minimum 3-5 years of relevant experience in a GMP regulated industry or an equivalent combination of education and experience. Skills
- Independent worker with minimal supervision; customer focused and team player ? Clearly and actively communicates planning, scheduling and changeover information or process issues with affected parties in a timely manner.
? Ability to recognize opportunities for improvement in systems or processes and recommend solutions
? Ability to identify obstacles and escalate appropriately
? Working knowledge with planning and scheduling in a GMP manufacturing facility
? Understanding of protein biologics manufacturing process knowledge and related activities
? Recognizes and performs regular responsibilities, while pursuing learning of new skills and/or processes
? Ability to influence without authority, pro-actively builds healthy working relationships between their department and other groups
? Familiarity with enterprise applications (e.g. Infor, Oracle)
- Strong Experience with software packages (Office Package - Excel Macro)
Duration: 12 Months
Location: Solothurn
If you are interested, please apply with a copy of your CV.
2 rounds of interviews.
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.
We are looking for a highly motivated Project Manager with experience in Product Launch or development of Medical Device.
Language requirement: Fluent in English and German.
Main Responsibilities
? Responsible for leading product development projects from concept through product launch
? Responsible for creating, monitoring, and maintaining project plans
? Identifying critical paths, project risks, and roadblocks, and proposing corrective actions
? Preparing and presenting project status reports and presentations
? Collaborating with internal service providers and external suppliers
Description of Duties and Responsibilities
? Develop project plans in collaboration with the project team
? Manage the execution of project plans together with the project team
? Work with internal service providers and external suppliers to ensure project progress
? Responsible for meeting project plans and milestones on time
? Report on project progress and status
? Escalation of critical issues
? Identify critical paths, project risks, and roadblocks, and work with the project team to develop solutions
? Support product launch and market introduction activities
? Collaborate with U.S.-based project management teams and project teams
? Manage particularly complex and strategically significant projects within the division
? Act as deputy for the supervisor and assume managerial responsibilities when required
? Understand and comply with policies regarding the Code of Conduct, Ethics & Compliance programs, and other relevant regulations.
Qualifications / Requirements
? Bachelor's or Master's degree in Engineering (Medical Technology, Mechatronics, Electrical Engineering, Mechanical Engineering, or related field)
? Minimum of 5 years of experience in project management and/or the development of medical devices
? Project Management certification is preferred
? Strong facilitation, influencing, and leadership skills
? Excellent German and English language skills
? Self-motivated and proactive
? Strong team player
? Able to work effectively under pressure
? Customer-oriented mindset.
For this position we can only consider applicants with a Swiss work permit or a Swiss/EU passport and enrolled in a University program.
Kindly send us your CV today through the link in the advert.
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
General Information:
Start Date: 21.09.2026
End Date: 28.02.2027
Location: Luterbach, Solothurn
Shift work: 5 Shift rotation (including nights)
- Performs and documents daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, revising cGMP documents.
- Ensuring compliance to cGMP as well as maintaining equipment and facilities.
- The Manufacturing Associate is detail-oriented with strong documentation skills. Maintain training level to the required level and support other functions on site.
- Assist with daily manufacturing operations in manufacturing facility. Typically requires 3-5 years of experience.
- The employee will be responsible for executing manufacturing related work within Solothurn as per procedures and policies.
- The employee will be accountable for maintaining and complying with the environmental, health and safety regulations.
- The employee will be responsible for maintaining his/hers training curriculum and not perform tasks that the employee is not trained to perform.
- Be able to work independently and with minimal direction. Has moderate responsibility.
- The employee will be responsible for maintaining equipment and perform manufacturing activities. Erroneous work can impact product integrity result in batch failures and consequently harm patients.
- The employee must be able to demonstrate the ability to independently document and record information related to their job functions.
- The employee must at all times make sure that if the employee is in doubt that the employee's supervisor or manager is consulted. Good verbal and written skills are required to ensure proper description of any issues.
- Employee must collaborate well with supporting functions and seek to define best outcomes for patients and the facility.
- A basic knowledge of biopharmaceutical technology and processes. The employee must be able to follow and comply with procedures and protocols.
- The employee should occasionally be able to make routine decisions based on gained experience. The employee must have a solid understanding of the requirements within correct and timely documentation within a cGMP environment.
- The employee must be trained and skilled in all operational and regulatory procedures of manufacturing department.
- Employee understands importance of safety and can teach saftey principles to less experienced colleagues.
If you are interested, please reply with a copy of your CV.
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.
We are looking for a highly motivated Master student to support strategic AI and Knowledge Management initiatives within a global biopharmaceutical environment.
The role will work closely with the MSAT Knowledge Management Lead and contribute to the design and deployment of the AI Academy, Data Academy, Process Wiki / Knowledge Navigator, and related AI-enabled knowledge solutions.
The assignment is ideal for a student who enjoys building at the intersection of AI tools, knowledge management, knowledge graph design, information architecture, and user-centric digital product design.
Purpose of the assignment
Support the preparation of MSAT AI and Data Academies and the development of a Process Wiki / Knowledge Navigator by combining generative AI, knowledge engineering, knowledge graph design, and modern web experience design.
Required Qualification:
Education. Currently enrolled in a Master programme at ETH Zürich preferably in the field of Computer Science, Data Science, Information Systems, Computational Science, Knowledge Engineering, Digital Design or a related field.
Technical experience. Practical experience in several of the following areas is recommended:
- Generative AI and large language model usage in real work scenarios.
- Microsoft Copilot, Cowork or comparable AI assistant / agent platforms.
- Knowledge graphs, semantic models, taxonomies or metadata modelling.
- RAG architectures, semantic search or AI-enabled knowledge retrieval.
- Web page creation and design using HTML, CSS, JavaScript or modern web frameworks.
- SharePoint Online, Microsoft 365 or enterprise collaboration platforms.
- UX/UI design, wireframing and user journey development.
- Python, data visualisation or graph database concepts are a plus. What you will gain?
- Hands-on experience in enterprise AI transformation and AI-enabled knowledge management.
- Exposure to strategic academy development, capability building and community enablement.
- Opportunity to work on a visible Process Wiki / Knowledge Navigator MVP with real business impact.
- Experience with modern AI tools, knowledge graph concepts and digital product design in a regulated global environment.
- Close collaboration with experts in MSAT, Process Intelligence, Knowledge Management, Digital & Data Science.
For this position we can only consider applicants with a Swiss work permit or a Swiss/EU passport and enrolled in a University program.
Are you interested in this opportunity? Kindly send us your CV today through the link in the advert.
