Recherche pour Industrie pharmaceutique en Suisse, Soloithurn:20

23/09/2026
Nouveau!
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.  
23/09/2026
Nouveau!
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.
23/09/2026
Nouveau!
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
Nouveau!
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
Nouveau!
Suisse, Tessin, Lugano - Orienta SA
Orienta SA, filiale di Lugano, ricerca per importante realtà operante nel settore Pharma del distretto di Lugano   un/una Regulatory Affairs Specialist     ATTIVITÀ / MANSIONI - Gestione delle attività regolatorie relative ai prodotti Pharma. - Preparazione, revisione e sottomissione della documentazione alle autorità competenti. - Supporto ai processi di registrazione, rinnovo e variazione dei prodotti. - Monitoraggio degli aggiornamenti normativi e valutazione del relativo impatto sui prodotti aziendali. - Collaborazione con i reparti Quality Assurance, Ricerca & Sviluppo e Produzione. - Gestione dei rapporti con enti regolatori e partner esterni.   REQUISITI - Esperienza pregressa nel ruolo di Regulatory Affairs maturata nel settore Pharma. - Conoscenza della normativa svizzera ed europea applicabile ai prodotti farmaceutici. - Esperienza nella gestione di dossier regolatori e pratiche di registrazione. - Ottima conoscenza della lingua inglese. - La conoscenza della lingua tedesca sarà considerata un plus, ma non rappresenta un requisito vincolante. - Buone capacità organizzative, analitiche e relazionali. - Buona conoscenza dei principali strumenti informatici.   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 altamente specializzato.   $LUOGO DI LAVORO - Distretto di Lugano, Canton Ticino.
22/09/2026
Nouveau!
Suisse, Bâle-Ville, 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.   ​ Hintergrund: Als System Process Specialist (SPS) im Site Service SAP Support & Service Team sind Sie für den End-to-End-Support der SAP EWM- und MM-Systeme verantwortlich. Sie verfügen über ein fundiertes Verständnis der Warehouse Management (EWM)-, Logistik- für Ersatzteilprozesse (MM/Spare Parts) und arbeiten eng mit der Business Community zusammen, um IT-Anwendungen und tägliche Abläufe zu unterstützen und zu optimieren. Dabei agieren Sie als vertrauenswürdiger Ansprechpartner und Vermittler zwischen den Fachbereichen (Logistik/Lager/Ersatzteilwesen) und den globalen IT-Teams. Zusätzlich übernehmen Sie eine wichtige Rolle in der Fehleranalyse, Anwenderschulung, und der Begleitung von Prozessverbesserungen. Der oder die perfekte Kandidat:in:  Als ideale:r Kandidat:in bringen Sie ein Studium der Wirtschaftsinformatik oder eine logistische Ausbildung sowie mindestens 3 Jahre Erfahrung im Support von SAP EWM, MM und S/4HANA mit. Sie verfuegen ueber fundiertes Prozesswissen in der Intralogistik und steuern souveraen das Incident- sowie Change-Management an der Schnittstelle zwischen Endnutzern und 2nd-Level-Support. Mit starken analytischen Faehigkeiten loesen Sie Stoerungen im laufenden Lagerbetrieb rasch und wirken aktiv an Prozessoptimierungen mit.Fliessende Deutsch- und Englischkenntnisse sowie eine agile, kundenorientierte Arbeitsweise ? idealerweise ergaenzt durch Erfahrung im regulierten GxP-Umfeld ? runden Ihr Profil ab. Aufgaben & Verantwortlichkeiten: - End User Operation Support & Incident Management - First-Level-Support für SAP EWM, SAP MM (Spare Parts Management) und angrenzende Systeme (On-Site und teils Remote). - Troubleshooting und Fehlerbehebung für S/4HANA, SAP EWM sowie angrenzende IT-Systeme (z. B. MGD, mobile Datenerfassungsgeräte/Scanner, Warehouse-Automatisierungsschnittstellen). - Zentraler Point of Contact für Endnutzer und Business-Stakeholder bei IT-relevanten Fragen und Anfragen aus dem Bereich Lagerung, Materialwirtschaft und Ersatzteillogistik. - Schnittstelle zum 2nd-Level-Support und Global Team Support: Eskalation von Komplexproblemen, Unterstützung bei der Klärung von Anfragen und Ticket-Nachverfolgung zur Sicherstellung zeitnaher Lösungen. Prozessunterstützung & Optimierung - Unterstützung der Endnutzer bei der Einreichung neuer Prozessverbesserungsideen unter Berücksichtigung von Prozessabhängigkeiten (z. B. Schnittstelle Ersatzteilbeschaffung MM zu Instandhaltung EAM) und Systemauswirkungen.  Change Management & Schulungen - Mitwirkung bei Change-Prozessen mit Systemauswirkungen, inkl. Beschreibung, Abstimmung und Testen von Änderungen.  Must Haves: - IT-Studium (Wirtschaftsinformatik) oder eine logistische/kaufmännische Ausbildung (z.B. Fachkraft für Lagerlogistik) mit starker IT-Affinität - 3+ Jahre Erfahrung mit SAP R/3 sowie gute Kenntnisse in SAP S/4HANA (starker Fokus auf SAP EWM und SAP MM / Spare Parts Management). - Gutes Prozesswissen in Intralogistik, Lagerverwaltung, Wareneingang/-ausgang, Materialfluss sowie Ersatzteilmanagement / Instandhaltungsersatzteilen. - Erfahrung mit Support-Prozessen und Tools für Incident- und Change-Management (z. B. ServiceNow). - Starke analytische Fähigkeiten für Fehleranalyse, Troubleshooting und Problemlösung im laufenden Lager- und Materialbetrieb. - Sehr gute technische Dokumentations- und Kommunikationsfähigkeiten in Deutsch und Englisch. - Starke Kundenorientierung, agile Denkweise sowie eine hohe Stabilität, Flexibilität und Geschwindigkeit in der Lösungsfindung.  Nice to haves: - Erfahrung in der Pharma-Produktion oder einer vergleichbaren regulierten Industrie (GxP-Umfeld von Vorteil). ​ Klingt das nach der richtigen Herausforderung für dich? Wir freuen uns auf deine Bewerbung!
18/09/2026
Suisse, Soleure, Solothurn - Manpower
​ The role: The Associate III within the Integrated Downstream Quality Operations team is being part of the Quality Department at the new Large-Scale Manufacturing facility located at the Solothurn/Switzerland site. He/She focuses on Quality Operations and Quality Engineering activities for downstream manufacturing and equipment. The Solothurn site is intended to operate with a fully integrated electronic batch record for all commercial, clinical and PPQ campaigns. ​ General Information:  Start Date: 01.11.2026 End Date: 31.03.2027 (extension planned) Location: Solothurn Department: Quality Assurance, Integrated Downstream Quality Operations Responsibilities: - Executes QA activities related to downstream operations, GMP manufacturing,  and downstream equipment to ensure the safety, efficacy and purity of the products manufactured by Biogen - Reviews and approves GMP Engineering and Manufacturing documents during both project and operational phases of the site, specifically related to procedures, work instructions, CAPAs, deviations, change control, equipment (work orders, P&IDs, qualification protocols, calibration deviations..,) etc. - Partners with Manufacturing, Manufacturing Sciences, Process Engineering, Automation SMEs during deviation management and investigations. - Take part to the monitoring and release activities for Column Packing / Unpacking and Chromatography Review. - Ensures adherence to internal procedures during downstream manufacturing operations or for equipment controls and release before and during GMP CAPEX and OPEX project (i.e., shutdowns, construction projects) or New product introduction - Take part of the Quality On-Call duty rotation for Quality  - Participates in batch record review and close out in the view of batch release. - Experience with Quality Assurance, Equipment Qualification, Downstream Process is preferred. - Demonstrated ability to work autonomously with cross-functional team members. - Strong presentation and organizational skills - Demonstrated writing skills - Demonstrated problem solving skills - English B1 as a minimum. ​ If you are interested, please apply with a copy of your CV.  
21/09/2026
Nouveau!
Suisse, Genève, Geneva - Manpower
​ Pour l'un de nos clients, une entreprise internationale active dans l'industrie chimique et des ingrédients, basée à Genève, nous recherchons un Ingénieur Projet Medium/Senior qui saura piloter des projets complexes tout en garantissant l'excellence technique, la sécurité et la durabilité. ​ Description: Chez dsm-firmenich Geneva, nous investissons dans l'innovation et la performance industrielle. Pour accompagner notre croissance, nous recherchons un Ingénieur Projet Medieum/Senior qui saura piloter des projets complexes en garantissant excellence technique, sécurité et durabilité. Missions diverses: - Gestion de projets industriels de 10 kCHF à plusieurs centaines de kCHF sur un site de production international. - Responsabilité complète des projets : technique, budget, planning, sécurité et durabilité. - Pilotage des études, achats, installations, mises en service et transferts aux opérations. - Expertise procédés et sécurité industrielle (ATEX, DESP, HAZOP, conformité machine). - Ingénieur en génie chimique expérimenté, autonome, collaboratif et bilingue français/anglais. L'expérience/la connaissance du procédé de séchage par atomisation (spray drying) ainsi qu'une bonne compréhension des risques d'explosion sont indispensables. ​ Si vous êtes intéressé(e) par cette opportunité et pensez correspondre au profil recherché, n'hésitez pas à m'envoyer directement votre CV à alba.jansa@experis.ch
16/09/2026
Suisse, Glaris, Meyrin - Manpower
​ Nous recherchons pour notre client spécialisé dans l'industrie chimique, un technologue en production chimique (H/F) ayant un diplôme en chimie.  ​ Tâches :  - Assurer la conduite des réacteurs de synthèse et/ou équipements de distillation lors d'opérations batch - Travail en zone ATEX dans le strict respect des règles HSE - Chargement manuel des matières dans les appareils à partir de fûts, conteneur mobiles et sacs - Différentes opérations a réalisé : dosage de réactifs, décantation, distillation, concentration, transfert, filtration, lavage, etc ... - Surveillance et ajustement des appareils - Contrôle des produits en cours de fabrication (prise d'échantillon, interprétation des résultats) - Utilisation de SAP  Vous êtes : - Diplomé en chimie ( CFC, TFIC, CAIC...) - Autonome sur les différents process de la chimie - Mobile sur le canton de Genève - Disponible sur des horaires de journée ou d'équipe ​ 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).
16/09/2026
Suisse, Genève, Genève - Manpower
​ Nous recherchons pour notre client spécialisé dans l'industrie chimique, un opérateur de production (H/F). ​ Vos responsabilités seront : - pratiquer des mélanges de poudre, de produits liquides et matières premières - régler les paramètres de certaines machines - s'assurer du bon fonctionnement des machines - réalisation de la production en suivant les procédures - respect des normes HSE (hygiène sécurité environnement) - Expérience professionnelle idéalement dans le secteur de l'industrie pharmaceutique, chimique ou agroalimentaire - Connaissance des bonnes pratiques de fabrication  - Connaissance SAP un atout - Français courant - Habitué au travail en équipe (2*8 / 3*8) - Permis SUVA un atout  ​ 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).
09/09/2026
Suisse, Tessin, Biasca - 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: ​ Responsabilità - Diagnosi e riparazione guasti, manutenzione e messa in servizio impianti industriali e ausiliari - Manutenzione degli impianti di distribuzione di servizi (energie, acqua, aria compressa) - Gestione strumenti di misura, tarature e documentazione tecnica - Coordinamento ditte esterne per lavori specializzati - Pianificazione attività e implementazione miglioramenti impiantistici - Assicurare rispetto di sicurezza, qualità e procedure aziendali Competenze - Formazione Polimeccanico AFC o Meccanico di Produzione AFC; conoscenze PED, ATEX e GMP - Ottime capacità relazionali, lavoro in team, metodo e precisione - Organizzazione, gestione delle priorità e attenzione al dettaglio - Comunicazione efficace e reporting a vari livelli ​ 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.  
09/09/2026
Suisse, Genève, Genève - Manpower
​ 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...)
09/09/2026
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 ​ 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.
09/09/2026
Suisse, Tessin, Lugano - Manpower
​ Lead Marketing Manager About the Role We are looking for an experienced Lead Marketing Manager to drive the performance of marketing campaigns across a portfolio of events and initiatives. Leading a team of marketing professionals, you will be responsible for developing and executing data-driven campaigns that increase engagement, generate leads, improve conversion rates, and maximize marketing ROI. ​ Key Responsibilities - Lead, coach, and develop a team of marketing professionals. - Plan and execute multi-channel marketing campaigns. - Monitor campaign performance and optimize results through data analysis. - Manage the marketing funnel, from audience acquisition to conversion. - Oversee marketing budgets and ensure efficient resource allocation. - Drive continuous improvement through testing, analytics, and best practices. - Collaborate with internal stakeholders and external partners to deliver successful campaigns. Your Profile - Degree in Marketing, Communications, Business, or a related field. - Several years of experience in marketing, campaign management, or performance marketing. - Previous experience leading teams and managing KPI-driven projects. - Strong analytical mindset and passion for data-driven decision-making. - Solid understanding of digital marketing channels, including email and social media. - Fluent English; additional languages are an asset. What We Offer - A strategic leadership role with visible business impact. - An international and collaborative environment. - The opportunity to lead high-profile marketing initiatives and contribute to organizational growth. ​ PLEASE REGISTER YOURSELF AND UPLOAD YOUR CV AT OUR OFFICIAL WEBSITE: WWW.MANPOWER.CH, IN ORDER TO PROCESS YOUR APPLICATION. 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.  
08/09/2026
Suisse, Tessin, Luganese - Work & Work SA
Per azienda chimico-farmaceutico selezioniamo OPERAIO/A SETTORE FARMACEUTICO  Mansioni: - Supporto alle attività di produzione - Controllo qualità dei prodotti - Confezionamento e gestione materiali Requisiti: - Esperienza minima di 1 anno in ambito produttivo (preferibilmente farmaceutico) - Precisione e attenzione ai dettagli - Disponibilità immediata a lavorare su 3 turni   API HPAPI GMP Logbook BPR principi attivi  glovesbox confezionamento 
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