Recherche pour Industrie pharmaceutique en Suisse, Soloithurn:20

13/10/2026
Nouveau!
Suisse, Genève, Genève - Manpower
​ Nous recherchons pour notre client spécialisé dans l'industrie chimique, un technicien de laboratoire (H/F).  ​ Vos responsabilités seront par exemple :   - Analyser des produits (Matière première, Produits finis, en routine) selon les procédures qualité - Analyses physico-chimiques : densité, Acidité, teneur en eau ? - Analyses des eaux usées - Travail d'investigation et de synthèse des non-conformités   - Gérer le stock du laboratoire - etc Vous êtes :  - titulaire d'un CFC de Laborantin, ou diplôme de Technicien supérieur ou licence  en chimie ou biochimie avec minimum 2 années d'expériences confirmées en analyses et  analytique réfraction, couleur, filtration, RMN, DSC  (analyses, interprétation, méthodes, suivi des appareils) - Polyvalent et autonome pour travailler avec toutes les techniques du laboratoire et flux du laboratoire - Doté : d'un bon esprit d'équipe, du sens des responsabilités, d'organisation et de précision - rigoureux  - à l'aise avec les outils informatiques (Excel, Word, bases de données, etc...) - Bonne gestion du stress et des priorité ​ Si vous êtes intéressé(e) et correspondez au profil recherché, vous pouvez vous inscrire directement en transmettant votre dossier complet (CV - diplômes - certificat de travail).
13/10/2026
Nouveau!
Suisse, Tessin, Bellinzona - Work & Work SA
Per azienda cliente operante nel settore farmaceutico siamo alla ricerca di un Manutentore da inserire nel team di manutenzione.   Mansioni - Eseguire interventi di manutenzione ordinaria e straordinaria sugli impianti aziendali - Individuare e risolvere guasti e anomalie di natura elettrica - Effettuare attività di manutenzione preventiva per garantire il corretto funzionamento degli impianti - Supportare il team nelle attività di controllo e riparazione delle apparecchiature Requisiti - Formazione in ambito elettrico  - Esperienza, anche breve, nella manutenzione elettrica, preferibilmente in ambito industriale - Buona capacità di ricerca guasti e risoluzione di problemi tecnici
08/10/2026
Suisse, Bâle-Ville, Basel or Kaiseraugst - Manpower
​ Experis® ist ein weltweit führender Anbieter von IT-Personalvermittlung, Festanstellungen, Projektlösungen und Managed Services. Mit über 25 Jahren Erfahrung in der Schweiz und Standorten in Zürich, Basel und Genf verbinden wir führende Unternehmen mit erstklassigen IT-Fachkräften. Unsere Mission ist es, Talente dabei zu unterstützen, ihr Potenzial zu entfalten und erfolgreiche, zukunftsorientierte Karrieren zu gestalten. ​ In dieser Funktion stellen Sie mit Ihren Kollegen sicher, dass die Stammdaten die behördlichen Anforderungen abdecken sowie die Arbeitsabläufe der Kunden reflektieren. Durch den 1st Level Support tragen Sie entscheidend dazu bei, die Lead Time hinsichtlich der Produktion und Freigabe von Produkten einzuhalten. Allgemeine Informationen: - Startdatum: asap - Spätestmögliches Startdatum: 1.12.2026 - Geplante Dauer der Anstellung:12 Monate - Verlängerung (bei Befristung): wahrscheinlich (bei genehmigtem Budget, Projektverlängerung,...)  - Arbeitsplatz: Basel oder Kaiseraugst - Workload: 100% - Home Office: Nach Onboarding Minimum 50% On-site Pflicht Aufgaben & Verantwortlichkeiten: - 1st Level Support für SingleLIMS bei stammdaten-relevanten Anfragen im eigenen Verantwortungsbereich - Neuaufnahme, Anpassung und Review von Stammdaten und Methoden entsprechend den Bedürfnissen der Kunden bzw. der behördlichen Anforderungen - Review von Probenahmepläne und Kommunikation von Requirements an das Business - Erstellen und Aktualisieren von Konzepten, Arbeitsanweisungen (SOPs) und anderen relevanten GMP-Dokumenten - Schnittstelle zwischen dem Kunden (Business) und global IT (Entwickler, 2nd/3rd Level Support) Must Haves: - Voraussetzung für die abwechslungsreiche Stelle ist ein abgeschlossenes Studium in den relevanten Bereichen (z.B. Pharma, Chemie, Verfahrenstechnik)  - Mindestens 1-3 Jahre Berufserfahrung im GMP Umfeld (vorzugsweise in den Bereichen Produktion oder Qualitätskontrolle) - Praxiserfahrung im Bereich der pharmazeutischen Herstellungsanalytik (IPC / QC) - Erfahrung mit der Pflege von Stammdaten im GMP Umfeld z.B. mit LIMS (Labware), MES, ERP  - Selbstständige, strukturierte, und proaktive Arbeitsweise, präzise Arbeit unter strengen Timelines und multiplen parallelen Aufgaben - Kommunikative und organisatorische Fähigkeiten und ein selbstsicheres Auftreten - Hohe Kunden- / Serviceorientierung - Sehr gute Deutsch Kenntnisse in Wort und Schrift (C1) ​​​​​​​Nice to Haves: - Grundkenntnisse von internen Systemen und Projektmanagement sind von Vorteil - Erfahrung im Bereich Business Analytics im GMP Manufacturing oder QC Umfeld - Englischkenntnisse in Wort und Schrift   ​ Weitere Schritte Interviews: 1 Runde On-site (wenn möglich) und 2te Runde Virtuell Klingt das nach der richtigen Herausforderung für dich? Wir freuen uns auf deine Bewerbung!     APPLY NOW • Interviews: 1 Runde On-site (wenn möglich) und 2te Runde Virtuell
07/10/2026
Suisse, Neuchâtel, Neuchatel - Manpower
​ Quality Control Analyst Start date: asap Duration: 9 months Location: Neuchatel ​ Vous apportez une expérience solide de laboratoire, y compris des méthodes biochimiques telles que ELISA, PCR. activité enzymatique, Western Blot, HPLC ou autre. Grâce à votre travail en tant que technicien de laboratoire, vous avez développé une bonne compréhension théorique et pratique des méthodes et de la technologie biochimiques. En particulier, nous attendons : - Vous travaillez de manière structurée et dans un souci de qualité. - Vous trouvez satisfaction et motivation dans les tâches routinières - Vous avez de l'expérience en matière de bonnes pratiques de fabrication (cGMP) et laboratoire controle qualité en industrie pharmaceutique Nous privilégions un environnement de proximité et détendu. Le travail s'effectue au sein d'une  équipe où les tâches changent très rapidement. On attend donc de vous que vous soyez motivé par un environnement en évolution rapide tout en étant capable de fournir des résultats de haut niveau. Missions principales : - Réaliser les activités d'analyses biochimique et de supervision selon les procédures en vigueur au laboratoire en respectant les règles GMP/BPD et/ou des projets en lien avec les activités du département Contrôle Qualité - Préparer des solutions utilisées pour nos analyses de laboratoire - Respecter l'ensemble des procédures en vigueur - Respecter et appliquer les règles EHS. - Renseigner les divers formulaires, logbooks et documents en respectant les Bonnes Pratiques de Fabrication et de Documentation et ALCOA + - Prévenir le Superviseur en cas de résultats non conformes et/ou invalides le jour même par oral et/ou écrit et initier l'évènement dans le système qualité dans les délais impartis. - Gérer les investigations laboratoires. - Appliquer les demandes planning et remonter tout soucis de manière proactive. - Exécuter les protocoles de qualifications des réactifs / consommables et de validation (méthode, système, équipements) - S'assurer que la calibration et la maintenance des équipements est en ordre lors de l'analyse - Respecter la gestion des Kanban en temps réel - Remonter au responsable de méthode/équipement et au Superviseur/délégué/Expert des écarts sur la procédure - Être capable d'identifier et résoudre certains problèmes peu complexes relatifs à son domaine d'expertise (Troubleshooting) - Réalisez les solutions ou approbation des solutions au laboratoire. - Gérez et ranger le laboratoire en général, respecter les normes de standardisation 5S.  - Supporter les initiatives d'amélioration continue Profil recherché : - Niveau d'études minimum : CFC laboratin/biologie ou un autre domaine scientifique pertinent. - 3 ans d'expérience minimum en laboratoire QC en environnement cGMP - Expérience en analyse Electrophorèse, HPLC, Elisa, ou en détermination de l'activité enzymatique souhaité - Francais courant et anglais technique - Nationalité suisse ou de l'UE, ou encore permis de travail suisse valide - Expérience en rédaction de protocole de validation de méthode est ​ If you are interested, please apply with your CV 
07/10/2026
Suisse, Tessin, Lugano - Orienta SA
Orienta HealthCare, divisione specializzata nella ricerca e selezione, collocamento temporaneo e gestione di personale nel settore sanitario e socio-assistenziale pubblico e privato, ricerca    FARMACISTA   ATTIVITÀ/MANSIONI - Dispensazione di farmaci e prodotti parafarmaceutici - Consulenza al cliente/paziente su utilizzo e posologia dei medicinali - Gestione delle ricette e degli ordini - Controllo scorte e riordino prodotti - Collaborazione con il team della farmacia/struttura sanitaria   REQUISITI   - Diploma federale di farmacista o titolo estero equivalente - Buone competenze informatiche e una buona conoscenza del sistema sanitario svizzero - Buone capacità relazionali e orientamento al cliente - Precisione, affidabilità e capacità di lavorare in team - Conoscenza della lingua italiana   OFFERTA Tipologia di contratto: da definire Turni e orari: dispobilità sia full-time che part-time, turni su rotazione inclusi weekend e festivi   LUOGO DI LAVORO Distretto di Lugano
07/10/2026
Suisse, Tessin, Locarno - Orienta SA
  Orienta HealthCare, divisione specializzata nella ricerca e selezione, collocamento temporaneo e gestione di personale nel settore sanitario e socio-assistenziale pubblico e privato, ricerca   ASSISTENTE DI FARMACIA CON AFC (ATTESTATO FEDERALE CAPACITA')   ATTIVITÀ/MANSIONI   - Accoglienza e consulenza alla clientela - Gestione della vendita di prodotti farmaceutici e parafarmaceutici - Gestione cassa - Controllo, gestione del magazzino e monitoraggio scorte - Invio ordini e contatto con fornitori - Attività amministrative - Allestimento e cura degli spazi espositivi   REQUISITI   - Attestato federale capacità di Assistente di farmacia - Capacità di dispensazione sotto supervisione del farmacista - Gestione prodotti, stock e cassa - Conoscenza di base dei farmaci e parafarmaci - Conoscenza della lingua italiana   OFFERTA Tipologia di contratto: da definire Turni e orari: disponibilità sia full-time che part-time, turni su rotazione inclusi weekend e festivi   LUOGO DI LAVORO Distretto di Locarno
05/10/2026
Suisse, Tessin, Lugano - Manpower
​ 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 potenziamento della propria struttura il nostro cliente, ci ha affidato la selezione del seguente profilo: ​ Attività:  - Diploma di perito chimico / Attestato laboratorista in chimica /titolo equivalente - Laurea in Chimica o discipline Scientifiche - Conduzione di impianti chimici per la sintesi di composti altamente attivi - Applicazione delle norme cGMP e dei principi di Data Integrity - Compilazione della documentazione di linea (BPR, Logbook) - Utilizzo del sistema ERP Requisiti: - Esperienza almeno di 2 anni in posizioni analoghe, preferibilmente nel campo HPAPI/CDMO - Conduzione di impianti chimici per la sintesi di molecole altamente attive. - Esperienza di manipolazione di sostanze citotossiche. - Esperienza di lavoro in isolatori su reattori di taglia medio / piccola. - Conoscenza base di tecniche cromatografiche (Flash Chromatography, Cromatografia preparativa). - Preferibile conoscenza di tecniche di nanofiltrazione e/o liofilizzazione. - Conoscenza ed esperienza in analisi HPLC, TLC, KF, LOD - Conoscenza intermedia della lingua inglese (almeno B1) - Conoscenza software ERP Oracle e MS Office - Disponibilità al lavoro su turni   ​ SE RITIENE DI POSSEDERE TUTTI I REQUISITI RICHIESTI, NON ESITI AD ISCRIVERSI E A CANDIDARSI SUL NOSTRO SITO UFFICIALE: WWW.MANPOWER.CH, ALLEGANDO IL SUO CURRICULUM VITAE.  
05/10/2026
Suisse, Zurich, Zürich - Manpower
​ Experis® is a global leader in  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 talent with leading companies. Our mission is to help professionals unlock their potential and thrive in dynamic, future-ready careers. ​ Location: Zurich Start Date: 01.11.2026 End Date: 31.12.2027 Language requirement: English Essential: - Bachelor's Degree in an engineering related field; Packaging Engineers preferred - 5 years pharmaceutical experience (or equivalent) - Strong knowledge of cGMP documentation requirements - Strong technical,communication and leadership skills. - Knowledge of electronic documentation systems (MUST: Trackwise) Scope: - Knowledge of cGMP documentation requirements a must - Knowledge and experienced use of trackwise a must - Knowledge of developing and experience in qualifying packaging components on packaging equipment a must - Management (development, review and approval of) new and modifications to technical profile drawings and purchasing/release specifications a must - Ability to multi task and achieve tactical deliverables with little to no supervision, while understanding strategic impact training - Support team in substantiating and qualifying alternate component substrates, suppliers, and processes to mitigate risk of supply the development (input), launch, life cycle management and continuous improvement of primary and/or, - Lead or own change control, non-conformances and CAPA activities working with Quality and Global Labeling Operations - Manage implementation of platform (harmonization / standardization) components - Manage bill of materials, etc. Technical/Functional (Line) Expertise - cGMP SME in packaging - Technical specification, profile drawing development, review and approval - Packaging Process Validation - Specification development, review, approval and implementation - Managing quality documentation systems such as Veeva or Trackwise (change control, deviation/investigation and CAPA initiation, review and approval mechanisms a must)  - Must be a team player who can manage multiple tasks, a dynamic environment with a positive, outgoing spirit - Change agility and resilience; ability to work across time zones in matrix organization - Builds relationships based on integrity, fairness, honesty and perseverance - Interacts closely and builds strong relationships with internal cross functional team members as well as external technical experts at CMOs - Manages multiple tasks with focus on purpose and impact to strategy/business - Delivers on time, in full and right first time (compliance in highly regulated environment) ​ 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.
12/10/2026
Nouveau!
Suisse, Genève, Genève - Manpower
​ Nous recherchons pour notre client spécialisé dans l'industrie chimique, un cariste avec SUVA (H/F). ​ Vous allez : - travailler sur le quai d'arrivage ou d'expedition  - procéder à la palettisation et l'emballage des palettes  - procéder au chargement/déchargement des camions  - Remplissage des citernes (contrôle des vannes, prise d'échantillon) - trier des déchets - gérer les stocks (FIFO) - respecter des règles de sécurités  - être polyvalent sur un poste en équipe - Expérience professionnelle idéalement  dans le secteur de l'industrie       pharmaceutique, chimique ou agroalimentaire - Connaissance en logistique  - Connaissance SAP un atout - Français courant - Habitué au travail en équipe (2*8 / 3*8) - Vous devez OBLIGATOIREMENT détenir le permis cariste SUVA ​ Si vous êtes intéressé(e) et correspondez au profil recherché, vous pouvez vous inscrire directement en transmettant votre dossier complet (CV - diplômes - certificat de travail).
01/10/2026
Suisse, Bâle-Ville, Kaiseraugst - 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. ​ General Information: - Start Date: asap - Latest Possible Start Date: Oct 30, 2026 - Planned Duration of Employment: 1 year - Extension (for temporary contracts): Likely - Workplace: Kaiseraugst - Workload: 100% - Home Office: Hybrid role - mandatory 3 days a week in office in Kaiseraugst Tasks & Responsibilities: As a Global Clinical Distribution Lead, you will play a variety of roles according to your experience, knowledge, and general business/team requirements, such as: - Manage the On-time Delivery Performance for network supply shipments in the distribution network to meet study requirements and patient demand. - Effective participation and engagement on Protocol Execution Teams (PETs), Global Supply Execution Teams (gSETs), and ad-hoc distribution-related meetings. - Drive resolution of operational and system matters impacting on-time delivery collaborating with providers internal and external - Execute and coordinate network depot supply in coordination with the Clinical Demand and Supply Leader and other partners as needed - Lead and participate in cross-functional and internal distribution-related projects and process improvement initiatives supporting the global distribution and PTDS strategy - Execute with the highest level of accuracy in the CLARA system and perform 1st and 2nd-level diagnostics  - Operate within a GMP-compliant environment, ensuring adherence to quality procedures in place - Processing event records such as quality incidents as well as CAPAs and Changes (Planned Events) if applicable Must Haves: - Degree (BA, BS, MS, MBA) in Business (Operations Management or Supply Chain Management), Biotechnology or relevant field   - 3-4 years' experience in Clinical Trial Management, logistics, warehouse management, or other Supply Chain disciplines, preferably in the Biotechnology / Pharmaceutical industry  - Strong SAP / ERP systems knowledge and experience  - Experience in cross-functional/cross-cultural and agile organizational models  - You are action-oriented and can influence both internal and external stakeholders - You demonstrate curiosity, active listening, and a willingness to experiment and test new ideas when appropriate, focusing on continuous learning and improvement - You have a collaborative and agile mindset, actively looking to contribute to cross-functional teams and develop a self-directed team organization - You solve problems and can manage complex situations autonomously Nice to Haves: - Operational Excellence/ Six Sigma/ Lean training a plus - APICS and/or SCOR certification a plus ​   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.     APPLY NOW
30/09/2026
Suisse, Soleure, 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.
25/09/2026
Suisse, Tessin, Locarno - Orienta SA
Il nostro cliente, società farmaceutica situata nel Distretto di Locarno, ci ha incaricato di selezionare un/una Perito Chimico Neodiplomato/a da inserire direttamente con il ruolo di operatore/trice di linea produttiva.     Attività - Conduzione e monitoraggio delle linee di produzione farmaceutica; - Carico delle materie prime e approvvigionamento della linea produttiva; - Controllo del corretto funzionamento degli impianti e delle apparecchiature di produzione; - Esecuzione di controlli visivi sul prodotto durante il processo produttivo; - Compilazione della documentazione di produzione; - Rispetto delle procedure aziendali e degli standard qualitativi; - Segnalazione di eventuali anomalie e supporto alle attività di miglioramento continuo.   Requisiti - Diploma di Perito Chimico; - Interesse per il settore farmaceutico e per le attività produttive; - Precisione, affidabilità e attenzione al dettaglio; - Predisposizione al lavoro in team; - Disponibilità a lavorare su turni a ciclo continuo   Si offre - Assunzione diretta presso l'azienda cliente con contratto a tempo indeterminato; - Percorso di formazione iniziale a giornata della durata di circa 2/3 mesi; - Successivo inserimento in turnazione a ciclo continuo; - Salario indicativo di CHF 3.500 lordi per 13 mensilità, oltre alle indennità previste per il lavoro a turni; - Opportunità di crescita professionale all'interno di una realtà farmaceutica strutturata e in continua evoluzione.   Luogo di lavoro: Distretto di Locarno.
23/09/2026
Suisse, Tessin, Lugano - Orienta SA
Orienta SA, filiale di Lugano, ricerca per importante realtà operante nel settore farmaceutico del distretto di Lugano   un/una Procurement Specialist Pharma.   ATTIVITÀ / MANSIONI - Gestione del processo di approvvigionamento di materiali, materie prime e servizi. - Negoziazione con fornitori nazionali e internazionali. - Analisi delle offerte commerciali e gestione delle richieste di acquisto. - Monitoraggio delle performance dei fornitori e dei livelli di servizio. - Collaborazione con i reparti Produzione, Qualità e Supply Chain. - Supporto alle attività di budgeting e controllo dei costi.   REQUISITI - Esperienza pregressa in ruolo analogo maturata nel settore Pharma o Life Science (requisito tassativo) - Conoscenza delle normative GMP. - Ottime capacità di negoziazione e gestione dei rapporti con i fornitori. - Buona conoscenza della lingua inglese. - Conoscenza della lingua tedesca considerata un plus, non vincolante. - Buona conoscenza dei principali strumenti informatici e dei sistemi ERP.   OFFERTA Tipologia di contratto - Assunzione a tempo indeterminato. - Inquadramento e pacchetto retributivo da valutare in base all'esperienza maturata.   Orari - Impiego a tempo pieno dal lunedì al venerdì.   Benefits - Formazione continua e aggiornamento professionale. - Opportunità di crescita in contesto internazionale. - Ambiente di lavoro dinamico e strutturato.   LUOGO DI LAVORO - Distretto di Lugano, Canton Ticino.
23/09/2026
Suisse, Soleure, Soloithurn - 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.     ​ Location: Solothurn Start date: ASAP Duration: 12 months  Key Responsibilities The Warehouse Operator/Materials Handler performs and documents daily Materials Management operations and internal material flow activities in a cGMP environment. The role involves all floor operations in the Warehouse & Weigh & Dispense department. The associate maintains a safe, efficient, and productive environment across warehouse and dispensary operations, with strong attention to detail and documentation while maintaining required trai ning levels. The Material Handler is expected to support cross-functional operations, with movement between the Warehouse and Weigh & Dispense areas determined by business needs and Supervisor direction. Other information: -Team structure: The team consists of 17 members. -Languages: English is mandatory. -Certifications: Forklift license is required. -Tools: Experience with Oracle and Syncade is required. -Schedule: Standard hours; no shift work is expected.   ​ 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.
23/09/2026
Suisse, Zoug, Rotkreuz - 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. ​ We are looking for a Scrum Master to join the PCR Hardware Abstraction team and part of an Agile Release train(ART) following SAFe, developing C++ based real-time control software that drives the mechatronics, thermal, fluidic and optical subsystems of our in-vitro diagnostic (IVD) PCR instruments.   The Perfect Candidate:     The perfect candidate is a proactive team player who drives continuous improvement and seeks a workplace where a job title is just the starting point. You must be a certified Scrum Master (CSM/PSMI) with a technical degree, practical Git experience, and a strong willingness to write thorough documentation for highly regulated environments like medical devices. While experience with C++, containerization, or event-driven architectures is a great bonus, this role requires an eagerness to engage with physical hardware and low-level systems rather than pure web, UI, or cloud-native development.     General Information:    - Start Date: 1.11.2026 - Latest Possible Start Date: 1.1.2027 - Planned Duration of Employment:1 year (Extension very likely) - Workplace: Rotkreuz  - Workload:Minimum working capacity is 50% and maximum 80% ;   100% is possible if open to further activities in software development or other activities if no software development background. - Home Office: Yes: 1-2 day required on-site depending on workload   Tasks & Responsibilities: - Act as a Scrum Master and team coach for the SW development team, facilitating progress, resolving blockers, and increasing workplace transparency. - Empower the team by applying proven Agile techniques, fostering conflict resolution, situational awareness, and continuous improvement. - Collaborate proactively within self-organizing teams to define, estimate, and plan high-impact work packages. - Leverage modern AI-supporting tools throughout the entire development lifecycle to optimize coding, testing, and troubleshooting workflows. - You ensure compliance with processes, propose improvements, and stay informed about regulatory and market standards. Must Haves:    You're a self motivated team player, it is natural for you to be proactive in working with your teammates and in working with other parts of the organization. You like sharing your Know-how to help the whole team advance. Bringing in new ideas to improve existing products with new functions and cost optimization is important to you. You're looking for a company where you have the opportunity to pursue your interests across functions and geographies. Where a job title is not considered the final definition of who you are, but the starting point.     - A Bachelor's degree in Computer Science, IT, or a related technical field (or equivalent practical experience). - Min 4 years experience serving as a Scrum Master for a software development team diligently applying Scrum practices and theory. - Certification in Scrum methodologies (such as CSM or PSMI) alongside deep knowledge of servant leadership, facilitation, and team empowerment techniques. - Practical understanding of modern development ecosystems, including Git/GitHub version control and setting up basic build environments. - Basic Experience with C++ programming. - Exceptional communication and interpersonal skills, with a natural ability to connect teams and resolve conflicts. - Highly motivated, deadline-focused, with a proactive and thorough way of working. - Willingness to work in a regulated environment (medical device, automotive, aerospace or industrial safety) and follow structured development processes. - Excellent communication and teamwork skills; willingness to write good documentation and drive work to conclusion. - Fluent in English.   Nice to Have:    - Experience with IEC 62304, ISO 13485 or IVDR (medical device software lifecycle standards). - Experience with event-driven architectures and message brokers (RabbitMQ, Domain Driven Design). - Kubernetes, Docker for CI/build environments. - Experience in agile development environments. - German language skills.   ​ 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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