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​ MANPOWER AG ist spezialisiert in der Rekrutierung von qualifiziertem Mitarbeiter/innen und unterstützt Firmen in der ganzen Schweiz, dass diese ihre offenen Positionen, unter Berücksichtigung der nötigen Stellenanforderungen, erfolgreich besetzen können.    ​ Ihre Aufgaben: - Eigenverantwortliche Erstellung und kontinuierliche Weiterentwicklung von Reports und Dashboards mit Power BI - Modellierung und Integration von Daten aus Dynamics 365 Finance & Operations - Nutzung der Power Platform (PowerApps, Power Automate, Power Virtual Agents) zur Automatisierung von Geschäftsprozessen - Umsetzung fachlicher Anforderungen in effiziente, praxisnahe Reporting-Lösungen - Optional: Unterstützung im Bereich Dynamics 365 CE / Field Service Ihr Profil: - Abgeschlossenes Studium oder Ausbildung in Wirtschaftsinformatik, Informatik oder Data Science - Fundierte Erfahrung mit Power BI, DAX, Power Query und der Power Platform - Kenntnisse in Datenintegration, Schnittstellen und ETL-Prozessen - Analytisches Denkvermögen, Eigeninitiative und eine strukturierte Arbeitsweise - Sehr gute Deutsch- und gute Englischkenntnisse ​ Haben wir Sie mit diesem abwechslungsreichen Stellenangebot begeistern können, dann bewerben Sie sich noch heute über den Online Button. Jovan Radovanovic gibt Ihnen sehr gerne weitere Auskünfte. Sie können ihn unter folgender Nummer 058 307 23 20 erreichen. In wenigen Schritten können Sie sich auch direkt auf www.manpower.ch als Gast registrieren und Ihre Bewerbungsunterlagen einreichen.   

​ MANPOWER AG ? Your Career, Our Focus! Become part of our network and take advantage of countless opportunities! ManpowerGroup is the leading global company for staffing solutions. With our three brands ? Manpower, Experis, and Talent Solutions ? we assist companies across various industries with their recruitment needs. For 75 years, we've operated in over 75 countries, and throughout Switzerland, we support our clients in successfully completing their tasks and projects. We are looking for a Senior Data Scientist - Literature (m/f/d) (LSW) - BS ​ Background The position of Senior Data Scientist ? Literature sits within the Safety Analytics and Reporting (SAR) group of the Safety Risk Management (PDS) function. In this role, you support Roche's product portfolio by conducting global literature searches and extracting information from biomedical databases to address safety-related medical inquiries for both medicinal products and medical devices. Additionally, the team provides tailored literature searches for various Pharma Development (PD) groups, including Medical Affairs, to gather evidence on product efficacy for documents such as Periodic Safety Update Reports (PBRERs). As many of these deliverables are mandated by health authorities, the role requires consistent quality, adherence to timelines, and close alignment with stakeholders from Clinical Science, Safety Operations, PDMA, Regulatory Affairs and related functions. The insights generated from these analyses form a crucial component of patient-focused risk assessment. You will further contribute by supporting projects, improving processes, and participating in strategic initiatives that strengthen Roche's safety strategy. The Ideal Candidate The preferred candidate holds a university degree in medicine, pharmacy or life sciences and brings at least two years of experience in Information Science, ideally with strong exposure to pharmacovigilance and drug development. We are looking for a proactive, analytical and collaborative individual with excellent communication skills and the ability to train others. Strong organisational skills, a continuous improvement mindset and the ability to build effective cross-functional relationships are essential for success in this role. General Information - Start date: asap - Latest start date: 01 February 2026 - Planned duration: 9 months (maternity cover) - Extension: TBD - Workplace: Basel - Workload: 100% - Home Office: yes - Travel required: no - Team size: 2 people - Department: PV & Scientific Development (TLSC) - Working hours: Standard Tasks & Responsibilities - Conduct ad-hoc literature searches in biomedical databases to identify potential adverse drug reactions and safety risks associated with the company's medicinal products and devices. - Develop, test, document and maintain literature search profiles for published case reports of adverse drug reactions. - Create and maintain search strategies supporting regulatory deliverables such as Development Safety Update Reports (DSURs), Periodic Benefit-Risk Evaluation Reports (PBRERs) and signal detection activities. - Build and maintain search profiles for identifying incidents and safety risks related to medical devices (e.g., MDIR, signal detection). - Perform efficacy-focused literature searches for PDMA to support PBRER preparation. - Collaborate with internal stakeholders to define search criteria and clarify requirements. - Review search results for accuracy, plausibility and completeness. - Ensure timely, compliant and well-documented delivery of literature search outputs. - Actively contribute to the Safety Literature Group and support knowledge-sharing activities. - Develop training materials on literature retrieval and reporting topics and deliver training sessions to colleagues and stakeholders. - Identify improvement opportunities related to processes, methods and tools and share best practices within the team. - Establish and maintain strong working relationships with other Roche functions and departments. - Ensure that issues related to literature searches are addressed promptly and escalated when necessary. Must Haves - University degree (medicine, pharmacy or natural sciences). - Minimum 2 years of experience in Information Science with solid experience in pharmaceutical research, development or research informatics, including pharmacovigilance. - Strong understanding of medicine and drug development. - Excellent knowledge of internal and external biomedical and drug literature databases including search languages and retrieval systems. - Ability to interpret, evaluate and synthesise scientific information. - Excellent written and verbal communication skills, including the ability to present and critically discuss scientific data. - Strong proficiency in classical text search methodologies. - Expertise in literature sources and databases (e.g., Competitor Information Access Platform; DIALOG). - Ability to build and maintain effective cross-functional relationships. - Strong communication skills in an international environment, including the ability to explain search strategies clearly. - Team-oriented mindset with the ability to work in a multidisciplinary environment. - High level of self-motivation and effective prioritisation skills. - Strong attention to detail. - Fluent in English (written and spoken). ​ Dissatisfied, unchallenged, or eager to discover something new? What are you waiting for? Apply now, unlock your potential, and aim for greater satisfaction in your career. I'm here to support you with my expertise and guide you through the entire application process. I look forward to meeting you and am excited to hear your story! MANPOWER AG ? Together, we shape your future!

​ We are looking for a motivated QA Batch Record Reviewer for one of our clients based in Visp.    ​ Description: Making sure the batch was made properly, according to procedure and regulatory requirements. Reviewers should have great attention to detail, be able to work independently, and have a thorough knowledge of the manufacturing process they are reviewing What you'll do:  Review of the Executed Batch Records (e.g. production documentation review, raw data etc) Support batch release by ensuring the completeness of the documentation package Review comments added to the Executed Batch Records, clarify with the operations team and evaluate with the responsible QA Manager Support the initiation of deviations and investigations for Batch Record review related observations What we're looking for:  Academic degree OR relevant work experience in Biology/ Chemistry/ Biotechnology or other related field Previous experience in GMP regulated pharmaceutical / API industry is an advantage Ability to identify non-compliance and gaps from quality standards Structured, precise and well-organized working attitude; open-minded for new ideas and suggestions; agile, highly motivated and dynamic drive Fluent English (written and verbal) is required, German language skills preferred ​ Do not hesitate to contact me directly if you are interested and believe you can be a good fit:  Alba Jansa alba.jansa(at)experis.ch +41 61 282 22 13

​ MANPOWER AG ist spezialisiert auf Temporär- und Dauerstellen und bietet umfassende Personaldienstleistungen an. Mit Standorten in der ganzen Schweiz unterstützen wir unsere Kunden, um deren Aufträge und Projekte erfolgreich zu realisieren.  Für unseren Kunden in der Region Nordwestschweiz suchen wir eine/n Operator (a) ​ Ihre Aufgaben: - Tätigkeit als Operator und Steuerung der Prozesse in der Produktion, inklusive Protokollierung und Prozessdatenerfassung - Einhaltung aller GMP-, ISO- und Q-Vorgaben - Strikte Beachtung der SHE-Standards sowie sorgfältige Übergabe des Arbeitsplatzes bei Schichtwechsel - Herstellen von Verfahrenshilfsstoffen für den Prozess sowie aktive Unterstützung des Teams bei Wartungs- und Reparaturarbeiten - Reinigung von Anlagen und Arbeitsumgebung - Anlagenteile für AVOR (Reparatur/Wartung/Kontrolle) bereitstellen, übergeben und übernehmen Ihr Profil: - Abgeschlossene Lehre als Chemie- und Pharmatechnologe/in bzw. Chemikant oder langjährige Erfahrung im chemischen Umfeld - Bereitschaft zur Arbeit im 5-Schichtmodell - Sicherer Umgang mit dem Deichselstapler - Sehr gute Deutschkenntnisse - Teamplayer mit einer sorgfältigen und exakten Arbeitsweise - Ausgeprägtes Verantwortungsbewusstsein mit guten PC Kenntnissen ​ Sehen Sie sich in den oben genannten Punkten wieder? Dann wollen wir Sie unbedingt kennenlernen! Wir freuen uns auf Ihre kompletten Bewerbungsunterlagen, welche Sie über unsere Bewerbungsplattform hochladen können. Vielen Dank für Ihre Bewerbung.

​ As the process owner for Signal Management, the Associate Director Global Signal Management is responsible for managing and leading a team of external partners who identify and analyze all safety signals in the Safety Signal Management tool for all products and products from partners for which an agreement is in place. Ensures compliance and efficiency of Safety Signal Management activities for all products. Responsible for training safety employees and acting as subject matter expert for MedDRA queries. Supports the development, customization, and maintenance of the signal management tool to ensure it supports all signal detection and management activities in an efficient and effective way. As the global process and business owner for Signal Management, this role has to: - Support the integration of local signal detection and management requirements into the global process. - Define and oversee the long-term strategy to ensure the organization maintains its leading position in automated signal detection and evaluation. - Lead and manage a team of external service providers who are accountable for detecting and analyzing technical signals from post-marketing surveillance in the signal management tool for all products, group companies, or partners (for which an agreement is in place) where the organization is the global safety database holder. - Oversee and ensure maintenance of all MedDRA Queries used by Patient Safety. - Drive the development and implementation of efficient workflow processes for the Safety Management Team (SMT). This includes the timely update of Business Guidance Documents and SOPs accordingly. - Provide strategic leadership and oversight for all signal detection and management activities conducted by the ESP, leveraging internal and external databases. Ensure practices are aligned with regulatory guidance and industry standards, while continuously tailoring signal management processes according to the risk profile of the product portfolio. Proactively monitor the evolving regulatory landscape to maintain compliance and drive innovation in signal management. - Ensure that all new relevant medical safety signals originating from signal review or analyses from external Health Authority databases are adequately communicated to the respective Safety Lead for further escalation to the SMT. - Partner with Safety Leads who present safety signals to various internal and external boards. - Review Safety Signal sections of license partner agreements. - Ensure timely and accurate communications of signals to license partners as per PVA and to PS countries. - Support the development and customization of signal detection and management software to ensure compliance with all applicable regulatory requirements. If required, contribute to linking the tool with appropriate regulatory information so that its outputs can be used for downstream activities (e.g., addendum to clinical overview, presentations at Signal Review Team (SRT), SMT, Medical Safety Review Board (MSRB), and Portfolio Stewardship Board (PSB) meetings, aggregate reports). - Develop new approaches (including policy, methodology, and process improvements) for signal detection in Safety Signal software. Contribute to the development and customization of the tool with a view to integrating AI solutions in the signal management process. - Provide expert guidance in the development of all relevant aspects of signal detection strategy using post-marketing safety databases. - Ensure the signal management tools support the required KPIs for signal detection and management. - Have an overall understanding of the processes and software related to signal management to ensure processes are interconnected and streamlined according to lean principles. - Develop metrics for and ensure compliance with business rules of signal review and provide a periodic compliance report to Patient Safety leadership. - Represent the organization on external working groups related to Safety Signal Management. - Lead talent-pipeline, onboarding, training, and mentoring activities for new members. - Lead audits and inspections as a Subject Matter Expert (SME) for Safety Signal Management. ​ Ideal Background Education: Bachelor of Science in Pharmacy /Bachelor of Science in Nursing / PharmD/PhD in relevant field or Medical Degree (MBBS or MD) required. Languages: Fluency in English. Knowledge of other languages desirable. Experience and Skills: At least 6 years' experience in pharmacovigilance operations, including some hands-on experience in performing signal detection and management. Additional hands-on experience in the preparation of aggregate reports, case processing, and risk management plans is a plus. ? Excellent understanding ICH GCP, GVP guidelines, local pharmacovigilance regulations and medical terminology ? Excellent understanding of signal detection process; understanding on upstream and downstream processes is a plus. ? Attention to detail, quality focused and ability to identify process interdependencies ? Strong organizational and project management skills ? Ability to motivate, direct and foster teamwork, strong negotiation and conflict management. ? Ability to develop and maintain effective working relationships with superiors and peers. ? Ability to operate effectively in an international and matrix environment. ? Understanding of signal detection statistical methodology ? Excellent communication (written and verbal) and presentation skills ? Strong computer skills including, but not limited to, creation of spreadsheets, templates, presentations and working with and development of safety databases/applications/software. ? Ability to work independently, under pressure, demonstratingn initiative and flexibility through effective innovative leadership ability. ? Experience with PV audits and inspections and writing and implementation of CAPA ? Problem solving and strong negotiation and conflict management skills. ? Some understanding of how large language models work, knowledge of regulations on the use of AI in healthcare and, more specifically, in pharmacovigilance (e.g. CIOMS XIV, EU AI act). ​ Kontakt: Alba Jansa alba.jansa(at)experis.ch