JobCourier annunci per settore: Industria farmaceutica

​ Wir suchen einen Q/SHE Officer (m/w/d) zur Verstärkung eines führenden internationalen Unternehmens im Life-Sciences-Sektor in Kaiseraugst. ​ Description: Hauptaufgaben und Verantwortlichkeiten Change Control / Qualifizierungen 1. Betreuen von Anlagenänderungen und Umbauten in der Abteilung SP (Pharma) 2. Erstellung der Vorgabe- und Nachweisdokumente 3. Durchführung von Qualifizierungen und Validierungen Q/SHE-Aufgaben 4. Unterstützung beim Batchrecordreview 5. Bearbeitung von Abweichung und Kundenreklamationen 6. Vorbereitung und Ausarbeitung von Risikoanalysen verfahrenstechnischer Anlagen und chemischer Prozesse. 7. Verfassen von Sicherheitsanweisungen und Risikobewertungen 8. Erstellung & Review gelenkter GMP Dokumente OPTIONAL: Erstellung von Explosionsschutzdokumenten und Dokumentation der Explosionsschutzmassnahmen in enger Zusammenarbeit mit den Anlagenbetreibern ​ Erforderliche Ausbildung und Kenntnisse ? Abgeschlossenes Studium im naturwissenschaftlichen oder ingenieurwissenschaftlichen Bereich (z.B. als Verfahrens- oder Sicherheitsingenieur, Chemiker, Pharmazeut, oder vergleichbarer Hintergrund) ? Gute Kenntnisse der GMP- und Behördenanforderungen ? Sicheres Auftreten, ausgeprägte Kommunikationsfähigkeit und Kundenorientierung ? Hohes Maß an Teamfähigkeit, Eigeninitiative, Selbstständigkeit und Belastbarkeit Lohnrahmen ca CHF 8'000.- je nach Ausbildung und Erfahrung

​ We are recruiting for a Global Pricing Manager for one of our Pharma clients based in Glattpark-Opfikon. ​ Description: - Maternity leave cover. - In this role, you would manage global launch pricing strategy execution for zasocitinib in PsO, and collaborate with a variety of cross-functional stakeholders to support critical launch preparation activities - Drive global launch pricing strategy execution for zasocitinib in PsO - Coordinate with external vendor to manage final adjustments zasocitinib tiered pricing guidance, incorporating GPA leadership feedback - Facilitate global rollout of zasocitinib tiered pricing guidance to enable local launch and MRP27 planning - Monitor for global pricing policy and PsO market developments (e.g., icotrokinra launch ex-US) that could impact planned zasocitinib pricing strategy - Partner and collaborate as needed with access, health economics, global commercial, MCE, and key LOCs on cross-functional initiatives (including Global PsO Summit in September) - Share pricing perspectives and updates in relevant forums as needed (e.g., zasocitinib monthly and quarterly GPA GO2, cross-functional launch team meeting, franchise meeting) - Co-lead cross-functional launch schedule working group for zasocitinib in PsO - Collaborate to conduct international reference pricing analyses - Experience Requirements - Pharmaceutical industry experience is required, with a strong preference for direct experience in international pricing and reimbursement. Experience with country affiliates is preferred. - Internal contacts: Key member of the Global Market Access team and strategic pricing partner to Global Product Strategy Leads, Commercial Leads, IBU Market Access Leads. - External contacts: External consultants and vendors. ​ Contact: Alba Jansa alba.jansa@experis.ch

​ We are looking for an Investigational Product Delivery Lead for one of our  main clients in Kaiseraugst.  ​ Description: Key Responsibilities (6-8 bullet points): - Coordinate end‑to‑end investigational product delivery across 5?10 active clinical trials - Act as the single coordination point between various stakeholders, Clinical Trials Management, Clinical Operations, technical teams, Quality, Manufacturing, Supply Chain, Analytics, and external partners - Actively engage and follow up with functions to ensure execution against timelines, quality, and regulatory requirements - Maintain constant, structured communication with technical teams to translate clinical needs into executable technical actions, and keep all functions involved well informed and aware about changes in timelines - Ensure consistent application of the IP process with focus on: - Robustness - Adherence to approved processes - Traceability and documentation - Continuous improvement - Proactively identify risks, gaps, and dependencies and drive resolution through direct outreach - Support governance through clear reporting, visibility, and portfolio‑level tracking - Lead and facilitate monthly cross‑functional IP coordination meetings and contribute to portfolio reviews ​ You bring (6-8 bullet points): · - Degree in Pharmacy, Pharmaceutical Sciences, Chemical Engineering, Materials Science, Chemistry, or a related scientific discipline. - Good understanding on dietary supplement product development and manufacturing procedure from idea to product - 3?5 years hands‑on experience in: - Quality and/or Pharmaceutical Technology - Oral Solid Dosage Forms - Relevant regulatory frameworks (e.g. Pharmacopeia, GMP) - Dietary supplement experience - Solid understanding of clinical trial workflows - Experience with CTMS, Veeva, or equivalent clinical systems - Basic but practical project management capability - A strong understanding of materials and chemical sciences is considered an asset. - Process deployment, execution monitoring, and reporting Contact: alba Jansa: alba.jansa@experis.ch

​ Experis ist Teil der ManpowerGroup und spezialisiert auf Recruiting- und Projektlösungen im IT-Umfeld. Wir verbinden hochqualifizierte Fachkräfte mit spannenden Technologien und unterstützen Unternehmen dabei, ihre IT nachhaltig weiterzuentwickeln. Dabei setzen wir auf moderne Arbeitsmodelle, langfristige Perspektiven und individuelle Förderung. ​ Stellenbeschreibung Für unseren Pharma-Produktions- und Verpackungs Standort Kaiseraugst suchen wir eine/n motivierte/n, aufgeschlossene/n und technisch versierte/n System Engineer für unsere Data Historian & Rotronic Monitoring System, welcher die Rolle des System Owners übernehmen soll. Der oder die perfekte Kandidat Der perfekte Kandidat bringt ein Studium oder eine Ausbildung in Informatik oder Automation mit und verfügt über tiefe Expertise in der AVEVA PI Plattform (Konfiguration & Schnittstellen). Du bist versiert im Umgang mit SPS/PLS (Siemens S7), der IT-Qualifizierung (CSV) und dem Pharma-GxP-Umfeld. Projektmanagement, Active Directory und starke Qualitäten als Matrix-Leader runden dein Profil ab. Zudem bist du kommunikationsstark und sprichst fließend Deutsch und Englisch. Aufgaben & Verantwortlichkeiten - Betreuung der AVEVA Plant Information (PI) und Rotronic Monitoring Systeme (RMS) an den Standorten Basel und Kaiseraugst - Übernahme System Owner Rolle für PI und RMS - Erstellen und aktualisieren von Validierungsdokumentation - Incident-, Problem- und Change Management - Service Management - Deviation Management - Leitung / Mitarbeit bei Projekten - Audit & Inspektion Management - Implementieren von Equipment Schnittstellen an das PI System - Anbindung von Produktionsequipment an die Produktion Domain (Active Directory) Must Haves - Abgeschlossene Berufsausbildung, Techniker oder Ingenieur (Bachelor/Master) im Bereich Informatik, Automation oder ähnlich. - Sehr gute Kenntnisse der AVEVA PI Plattform ***** - Fortgeschrittene Erfahrungen bei der Konfiguration von PI Schnittstellen / PI System (PI Zertifizierung ist ein Plus) ***** - Erfahrung mit SPS Steuerungen und PLS Systemen (Mehrheitlich Siemens S7) ***** - Erfahrung in Computerised System Validation & IT Qualification - Erfahrung in Pharma Produktion / GxP Umfeld ***** - Erfahrung in Project Management - Kenntnisse mit Active Directory - Hoch entwickelte Kompetenzen als Matrix Leader - Sehr gute Kommunikationsfähigkeiten - Fliessende Deutsch und Englisch Kenntnisse Nice to Have - Kenntnisse in Netzwerktechnologie - Kenntnisse mit Rotronic Monitoring System (RMS) - Erfahrung mit Virtualisierungslösungen (VMware) - Erfahrung mit Backup / Restore Applikationen (Acronis) ​ Klingt das nach der richtigen Herausforderung für dich? Wir freuen uns auf deine Bewerbung!

​ 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 Start Date: 03.08.26 Planned duration: 12 months from start date Extension (in case of limitation): possible Workplace: Rotkreuz Workload: 100% Home Office: 2?3 days remote Travel: less than 10% (occasional travel to Germany for project team meetings) Team size: 6?7 Working hours: Standard Background: We are looking for a collaborative and inspiring individual to join our diverse, interdisciplinary and international Customer Experience and Solution Design (CXSD) Chapter of more than 50 designers. The CXSD team is supporting all business areas with four main sub-chapters: CX research & strategy, Digital Design & User Testing Services, Solution Management and Physical & Sustainable Design. The Solution UX Lead is responsible for leading the user experience, planning, coordination, and design delivery for complex healthcare solutions across multiple products, services, and customer touchpoints. This role acts as the design backbone for solution development, ensuring that customer needs, business objectives, regulatory context, technical feasibility, and delivery constraints are translated into coherent, high-quality experiences for users and customers. The Solution UX Lead partners closely with Product Management, Engineering, Design, Research, Clinical/Medical, Regulatory, Service, and business stakeholders to define the UX direction, structure design work, manage design dependencies, and enable customer-centric decision-making throughout the solution lifecycle. The role combines strong UX leadership with project management, design estimation, resource planning, delivery tracking, and stakeholder alignment. Experience embedding design teams into Agile Release Trains, PI Planning, and SAFe ways of working is considered a strong plus. The perfect candidate brings 8+ years of experience in UX, product, or service design, backed by a degree in HCI, Industrial Design, or a related field. You have a proven track record of leading UX for complex digital, hardware, or healthcare solutions, combining deep design expertise with strong project management skills to plan, prioritize, and drive delivery. An exceptional collaborator and storyteller, you effortlessly translate complex insights into clear design direction while partnering with cross-functional stakeholders across global, matrixed teams. You thrive in agile environments?familiarity with SAFe or Lean UX is a major plus. Experience in healthcare, diagnostics, or regulated industries is highly desirable, along with fluent English (German is a plus). Tasks & Responsibilities: Lead UX workstreams across discovery, concept development, validation, implementation support, and launch preparation. Translate business objectives, customer insights, workflow needs, and regulatory context into actionable design decisions. Plan, estimate, structure, and manage UX activities, deliverables, dependencies, timelines, and resource needs. Coordinate designers, researchers, and cross-functional contributors across multiple workstreams. Ensure design deliverables are high quality, consistent, evidence-based, and ready for development and validation. Partner with Product Management, Engineering, Regulatory, Quality, Clinical, Service, and business stakeholders. Integrate UX work into agile delivery, including backlog refinement, sprint planning, PI Planning, system demos, and release planning. Identify risks, interdependencies, scope changes, and bottlenecks early, and propose mitigation actions or prepare escalation. Facilitate workshops, design reviews, prioritization sessions, and stakeholder alignment meetings. Coach designers and cross-functional teams on UX methods, customer-centricity, and design best practices. Represent UX in governance meetings, project reviews, customer engagements, and strategic discussions. Contribute to improving design leadership operations, estimation practices, team rituals, and delivery efficiency. Must Haves: 8+ years of experience in UX design, product design, service design, human factors, design research, or a related field. Degree in UX Design, Human-Computer Interaction, Industrial Design, Service Design, Human Factors or a related field. Proven experience leading UX for complex digital or hardware products, services, platforms, or healthcare solutions. Strong project management skills, including planning, estimation, prioritization, dependency management, risk management, and progress tracking. Ability to define UX work packages, delivery milestones, staffing needs, and effort estimates. Experience working with Product Management, Engineering, Regulatory, Quality, Research, and business stakeholders. Strong facilitation, storytelling, communication, presentation, and stakeholder management skills. Ability to manage ambiguity, structure complex problems, and translate insights into practical design direction. Experience working in agile product development environments. Experience with SAFe, Agile Release Trains, PI Planning, Lean UX, or scaled agile delivery is a strong plus. Experience in healthcare, diagnostics, medical devices, life sciences, laboratory workflows, or regulated industries is highly desirable. Experience managing UX work across distributed, global, or matrixed teams. Strong command of English; additional languages such as German are a plus. Nice to Have: Experience with regulated product development, usability engineering, human factors validation, or risk management. Experience contributing to design systems or solution-level UX governance.     ​ Please apply with a copy of your CV

​ For our Global Pharmaceutical client based in Baar, Zug we are looking for a Senior Pharmacovigilance Scientist for a 12 months contract with extension possibilities.  ​ The Senior PV Scientist is responsible for overseeing and leading the process for safety signal management activities, aggregate reports (PSURs, DSURs, Line Listings, RMPs), responding to safety questions from internal and external stakeholders, reviewing medical and scientific literature for safety information, and supporting Clinical Trial PV medical activities. The Senior PV Scientist also serves as a Subject Matter Expert for Safety and cross-functional teams on relevant global safety regulations and guidelines; data output and analyses; and product specific information. In this capacity, the Sr. PV Scientist is critical to ensure products in clinical trials continue to maintain good standing with countries where studies are ongoing to ensure clinical studies are completed, and for marketed products, ensures the marketing authorization remains in good standing. Key Responsibilities: - Leads the signal management process (i.e., signal detection, signal tracking, signal documentation, facilitating decisions regarding signals and safety risk, etc.) for assigned product(s) and evaluates safety data and signals as part of ongoing pharmacovigilance activities. - Includes synthesis of data from multiple sources and authoring signal evaluation reports. Leads signaling review process and product Safety Signaling Team meetings. Manages literature review for safety information. - Leads process for responding to safety questions from regulatory authorities. - Leads Aggregate Report management, including strategy, review and finalization of aggregate safety reports for assigned products, such as PSURs, DSURs, Pharmacovigilance Plans, Risk Evaluation and Mitigation Strategy Plans (REMS), and Risk Management Plans (RMPs). - Collaborates with Global Safety Officers and other Safety MDs for assigned investigational programs including clinical trial activities (protocol review, ICF review, etc.), safety committee management, data analysis, signal detection, ad hoc requests and other product activities, as assigned. Essential Skills and Qualifications Required: - Understands, interprets, analyzes, and clearly presents scientific and medical data in verbal and written format (including intermediate understanding and application of medical concepts and terminology). - Leads and conducts, independently and/or collaboratively, all aspects of substantive projects such as signaling, authoring of aggregate data reports, and responses to regulatory agency requests. - Strong Pharmacovigilance and drug development foundation, including knowledge of applicable clinical trial safety regulations and post-marketing safety regulations. Includes knowledge of case processing, expedited reporting rules, and safety database concepts.  - Basic knowledge of common data processing software (EXCEL, PowerPoint, Microsoft Word, Business - Objects). Knowledge of common safety database systems. - Demonstrates leadership and interacts collaboratively and effectively in a team environment (including - Safety, Clinical Development, Medical Affairs, Clinical Operations, and Regulatory), as well as with externa colleagues - Applies clinical judgment to interpret case information. - Strong organizational skills, including the ability to prioritize independently with minimal supervision Education and Experience Requirements for Job: - Education bachelor's degree in biologic or natural science; or health case discipline and/or advanced degree (PhD, MPH, NP, PharmD, etc.) required dependent on experience. - Experience Minimum 7 years Pharmacovigilance experience, including experience in aggregate safety reports and safety signal management. ​ If you are interested, please apply with a copy of your CV. 

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 a lavorare su turni   API HPAPI GMP Logbook BPR principi attivi  glovesbox

​ 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.  Solida realtà industriale svizzera, riconosciuta per qualità, innovazione e presenza consolidata sul territorio, ricerca un/una Assistente Ufficio Acquisti da inserire a tempo indeterminato all'interno di un team strutturato. ​ Responsabilità principali: ? Monitoraggio scorte e pianificazione riordini in base ai volumi produttivi ? Gestione operativa degli ordini di acquisto (materie prime, materiali e servizi) con aggiornamento delle condizioni di consegna ? Controllo e gestione delle conferme d'ordine ? Coordinamento trasporti e pratiche doganali per forniture internazionali ? Monitoraggio consegne e solleciti a fornitori ? Gestione documentazione di acquisto (DDT, entrata merce, fatture) ? Controllo fatture fornitori in coerenza con ordini e consegne ? Gestione resi e non conformità ? Raccolta, verifica e aggiornamento della documentazione qualità fornitori (schede tecniche, certificazioni, analisi, dichiarazioni) ? Gestione certificati di analisi e conformità dei materiali ? Aggiornamento anagrafiche e database fornitori ? Supporto interno per richieste tecniche e documentali legate a clienti e qualità Requisiti ? Ottima conoscenza di italiano, tedesco, inglese e francese ? Esperienza in ambito acquisti operativi e/o qualità fornitori ? Familiarità con documentazione tecnica e certificazioni di prodotto ? Conoscenza delle pratiche doganali di importazione ? Precisione, rapidità operativa e attenzione al dettaglio Offriamo: ? Inserimento in un'azienda solida e strutturata, con lunga tradizione industriale ? Ambiente dinamico e collaborativo ? Possibilità di crescita professionale ? Contratto a tempo indeterminato ​ PLEASE REGISTER YOURSELF AND UPLOAD YOUR CV AT OUR OFFICIAL WEBSITE: WWW.MANPOWER.CH, IN ORDER TO PROCESS YOUR APPLICATION.  

​ 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) ​ 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).

​ 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 someone with a technical background, ideally in system engineering , software engineering or medical engineering who brings experience in software and hardware requirement engineering - and eventually testing - for diagnostic instruments. The Perfect Candidate: The perfect candidate brings over 5 years of experience driving the full product development lifecycle, with a sharp focus on requirements engineering within highly regulated environments, ideally in In Vitro Diagnostics (IVD) or medical device development. They possess a deep understanding of the V-model and extensive hands-on expertise in requirement analysis, structuring, and breakdown using advanced ALM tools. General Information: - Start Date: asap - Latest Possible Start Date: 31.08.2026 - Planned Duration of Employment: 12 months - Extension (for temporary contracts): possible - Workplace: Rotkreuz - Workload: 100% - Home Office: onsite presence preferred. Tasks & Responsibilities:  - Definition of technical requirements for diagnostic instruments based on business and customer inputs, risk ratings and context according to internal guidelines - Knowledge in definition of requirements using EARS (Easy Approach to Requirements Syntax) - Contribution to the development of requirement engineering concepts and strategies for software and hardware on different levels - Review of requirements and specifications - Collaboration within the interdisciplinary development team - Status reporting to respective project or product leader Must Haves: - 5+ years of experience working across full product development lifecycles with focus on requirements engineering - Background in regulated environments, ideally within IVD or medical device development  - Strong requirements engineering experience, including ALM tools and requirement breakdown/structuring - Certifications such as CPRE/IREB, CCBA/IIBA, or INCOSE are advantageous - Experience with requirement analysis, test case creation, test execution, and defect lifecycle management  - Understanding of the V-model - Strong analytical thinking, problem-solving, and ability to balance big-picture and detail-oriented work - Experience moderating and collaborating with multidisciplinary stakeholders and teams - Strong communication skills, autonomous working style, and pragmatic mindset  - Fluent English and German are required ​ Please apply 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. ​ Background: We are looking for a Project Manager who also serves as Scrum Master for three delivery teams within a strategic programme that applies agentic AI and rule-based automation to clinical trial data review. The programme is in active build with a fixed MVP deadline, a distributed team of approximately 50 people across 5 delivery teams, and GxP regulatory requirements. At the programme level, you own delivery execution - planning, tracking, risk management, dependency resolution, and stakeholder communication. At the team level, you facilitate agile ceremonies, coach teams on effective ways of working, and remove impediments for cross-functional delivery teams. You will work alongside a Product Manager (who owns vision and prioritisation) and a Solution Architect (who owns technical decisions). The perfect candidate: The perfect candidate is a pragmatic, hands-on servant leader who thrives in ambiguity and leads by enabling the team rather than controlling them. He maintains a high-trust, psychologically safe environment while remaining firm on scope and commitments. Balancing a sharp eye for detail with a broad program-level perspective, he leads by example?equally comfortable shaping high-level strategy or diving into the trenches to update a RAID log or fix a broken Jira filter. General Information: ? Start date: asap ? latest Start Date: 01.07.2026 ? Planned duration: 30.11.2027 ? Extension: not planned ? Workplace: Basel ? Workload: 100% ? Home Office: 50% Tasks & Responsibilities: ? Programme Delivery Management - Own the delivery plan across multiple parallel teams from current state through MVP and subsequent releases - Drive PI-level planning, manage cross-team dependencies, and resolve blockers before they hit the critical path - Maintain the RAID log with clear owners, deadlines, and recommendations - Enforce scope discipline through a structured requirements intake and triage process - Release management: develop and maintain a release calendar and schedule, coordinating with development, QA, and operations teams on timelines. Lead post-implementation reviews to identify release cycle process improvements. ? Scrum Master for Three Delivery Teams - Facilitate sprint planning, daily standups, reviews, and retrospectives for the teams - Shield teams from external disruptions and remove impediments quickly - Coach team members on agile practices and continuous improvement - Track sprint health (velocity, burndown, blocked items) and surface concerns early - Support Product Owners with backlog refinement, story breakdown, and Definition of Done compliance ? Cross-Team Coordination - Facilitate Scrum of Scrums, PO Sync, and dependency resolution sessions across all 5 delivery teams - Manage the Jira ALM project structure as the single source of truth for programme status - Ensure consistent Jira hygiene across all teams (issue types, labels, linking, workflows) - Enable effective collaboration between co-located (Basel) and virtual (US, India) team members ? Stakeholder Communication - Provide transparent program status reporting to leadership - Manage stakeholder expectations around MVP scope and post-MVP deferrals - Coordinate with adjacent programmes and platform teams on integration dependencies Must Haves: - 7+ years of project management experience in software delivery, including 3+ years managing programmes with multiple parallel teams  - Demonstrated Scrum Master experience - you have facilitated agile teams, not just observed them. You know how to run an effective retro and how to coach without directing - Pharmaceutical or Life Sciences industry experience with understanding of GxP requirements and what inspection readiness means in practice  - Hands-on Jira experience - you have configured and managed Jira projects, not just consumed reports. Xray test management experience preferred  - Experience with scaled agile delivery (SAFe or similar) and the pragmatism to know when to adapt the framework to the situation - Strong risk and dependency management skills with a bias toward action - Experience managing distributed hybrid teams across multiple time zones  - Fluent English communication - written and verbal Nice to haves: - Clinical data management domain familiarity - you understand CRFs, EDC systems, data queries, and the data review process at a working level - Experience with AI/ML product delivery, particularly the challenges of validating non-deterministic systems - GxP validation experience for AI/ML or software systems in pharma - Experience with clinical data systems (Medidata Rave, CDMS, RBQM tools) - CSM, PSM, SAFe SM/RTE, PMP, or equivalent certification ​ Please apply with a copy of your CV. 

​ Description: Ferienjob / Studentenjob im technischen Bereich (m/w/d). Standort: Stein (AG) Für unseren Pharmakunden mit Sitz in Stein suchen wir motivierte Studierende oder Schüler für einen Ferien- oder befristeten Studentenjob im technischen Bereich im Zeitraum vom 1. Juli bis 31. August 2026. Ihre Aufgaben Unterstützung bei technischen Tätigkeiten gemäß Vorgaben Mitarbeit bei einfachen Wartungs-, Kontroll- und unterstützenden Produktionsarbeiten Durchführung von Hilfsarbeiten im Anlagen- oder Instandhaltungsbereich Dokumentation der ausgeführten Arbeiten nach Anleitung Einhaltung von Sicherheits- und Qualitätsvorschriften (GMP)   ​ Ihr Profil Student/in oder Schüler/in (vorzugsweise mit technischem Hintergrund) Grundlegendes technisches Interesse und Verständnis Zuverlässige, sorgfältige und strukturierte Arbeitsweise Teamfähigkeit und Lernbereitschaft Gute Deutschkenntnisse von Vorteil ​ Bist du interessiert? Dann kontaktiere mich gerne direkt unter: alba.jansa@experis.ch Alba Jansa

Per azienda cliente attiva nel settore farmaceutico selezioniamo:   OPERATORE/TRICE DI PRODUZIONE SETTORE FARMACEUTICO   Mansioni: - Controllo qualità pezzi con strumenti di misura (calibro, micrometro) - Montaggio e assemblaggio pezzi - Compilazione documentazione    Requisiti: - Disponibilità immediata - Pregressa minima esperienza nel settore meccanico, orologiero o elettronico nell'assemblaggio di pezzi  - Disponibilità al lavoro su 2/3 turni   Tipologia contratto: temporaneo

​ 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:  ​ Responsabilità principali - Coordinare gli interventi di manutenzione preventiva e correttiva - Gestire fornitori, tecnici esterni e squadre operative - Monitorare il corretto funzionamento di impianti e attrezzature - Pianificare le attività nel rispetto di tempi, costi e standard di sicurezza - Redigere report tecnici e gestire la documentazione manutentiva - Assicurare il rispetto delle normative vigenti in materia di sicurezza Requisiti - Esperienza pregressa nel ruolo o in ambito manutentivo/impiantistico - Competenze tecniche elettriche e/o meccaniche - Capacità organizzative e di coordinamento - Problem solving e autonomia operativa - Buona conoscenza degli strumenti informatici ​ VI PREGHIAMO DI ISCRIVERVI SUL NOSTRO SITO UFFICIALE: WWW.MANPOWER.CH, ALLEGANDO IL VOSTRO CURRICULUM VITAE PER POTER ESAMINARE LA VOSTRA CANDIDATURA.

Per azienda farmaceutica del Luganese selezioniamo urgentemente un   RESPONSABILE DI LABORATORIO CONTROLLO QUALITA' farma   Mansioni:  - Analisi chimico/fisiche di materie prime, intermedi, bulk e prodotti finiti - Gestione  team (10U) e  attrezzature di laboratorio - gestione e controllo dei dati nel laboratorio di controllo qualità, conformità alle cGMP e ai requisiti di buona documentazione (integrità dei dati). - Supervisione dei test di stabilità - Gestione della documentazione relativa a OOS, deviazioni, controllo delle modifiche, reclami e SOP. - gestione dei problemi di qualità insieme alla persona qualificata e al responsabile della garanzia della qualità in caso di reclami - Gestione piano CAPA e relativo follow-up con la persona qualificata e il responsabile dell'assicurazione qualità - follow-up degli audit dei clienti e delle autorità sanitarie federali e/o cantonali. Requisiti: - Disponibilità immediata per impiego inizialmente temporaneo scopo assunzione  - Formazione: Laurea in chimica, biologia, farmacia o titolo equivalente - Ottima conoscenza delle principali tecniche analitiche strumentali di laboratorio: HPLC, HSGC, Karl-Fischer, spettrofotometria UV/Vis, IR ... - Inglese: buono (parlato e scritto)  - Autonomia, precisione e flessibilità   - Controllo qualità chimico - HPLC Karl Fischer IR - inglese - GMP - responsabile