Elan Personal AG

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    "title": "Senior Organizational Change Lead, Global MES",
    "description": "Rejoignez Elan Personal AG en tant que Senior Organizational Change Lead, Global MES a Basel.\n\nRoche Switzerland bridges the gap between pharmaceuticals and diagnostics. Important research and development functions are located here. For our long-term client, F. Hoffmann-La Roche AG in Basel, we are looking for a\nSenior Organizational Change Lead, Global MES\nBackground:\nThe global MES program is accountable for developing MES business strategies and the implementation of harmonized Manufacturing Execution Systems (MES) within the entire PT network covering clinical and commercial manufacturing operations. You will develop the overarching change strategy to establish our solutions as global tools and ensure their effective use organization-wide. You will partner with OCM functional leads to drive the necessary mindset shift, creating a consistent and valuable user background across functions. Additionally, you will track OCM performance, manage OCM risks transparently, and demonstrate exceptional people leadership in an agile and dynamic environment. You will lead a network of change experts and change agents across our implementation projects.\nTo achieve this, you will work closely with the program’s core team and stakeholders from different functional areas across the organization You are reporting directly to the global MES Program lead, and you are part of the global MES core leadership team.\nTasks & Responsibilities:\nStrategic Leadership\n•\nFormulate and execute tailored global OCM strategies to support MES harmonization and the digital journey, aligning with overall PT goals\n•\nLead and mentor the OCM teams, embedding best change management practices across all program/project activities.\nStakeholder Engagement\n•\nEngage key stakeholders to address specific needs, fostering trust and buy-in for transformation activities\n•\nDevelop and maintain strong relationships to support seamless implementation.\nChange Management Execution\n•\nOversee change management plans, including communication, training, and support strategies, to ensure smooth adoption.\n•\nManage end-to-end transformation activities, ensuring alignment with program’s timelines and objectives.\nProgram Monitoring and Continuous Improvement\n•\nTrack change management progress, adapting strategies as needed for maximum effectiveness. Benchmark against industry best practices, especially in pharmaceutical and\n•\nGxP-compliant environments, for ongoing enhancement.\nRisk Management and Advisory\n•\nAct as a trusted advisor, assessing change-related risks and identifying opportunities to optimize outcomes.\n•\nAddress challenges proactively, ensuring resources, timelines, and objectives align across global workstreams.\nAdoption and Transformation Leadership\n•\nDrive the adoption of new systems, processes, and behaviours, championing change readiness and impact management.\n•\nCommunicate transparently about progress and challenges, fostering organizational alignment and agile responsiveness to evolving needs.\nMust Haves:\n•\nBachelor’s or Master’s degree in a related field such as Business Administration, Organizational Development, or Change Management\n•\nProven experience in Change Management within MES environments required\n•\nBackground leading and mentoring program and project teams, particularly within pharmaceutical manufacturing, production, or GxP environments\n•\nDemonstrated success managing large-scale programs and projects, including system deployments, with a strong focus on Change Management\n•\nStrong teamwork and leadership capabilities in global transformation and change initiatives\n•\nExcellent problem-solving skills with the ability to apply sound judgment and make mature decisions\n•\nOutstanding interpersonal and communication skills, with the ability to collaborate effectively across all organizational levels\n•\nExperience in consulting or client-facing environments, with a proven ability to manage stakeholder expectations in large corporate organizations\n•\nStrong written and verbal communication skills in English; German language skills are considered a strong advantage\n•\nGood understanding of project management methodologies, tools, and project lifecycle phases\n•\nPositive, proactive personality with a hands-on, solution-oriented mindset\n•\nAbility to work independently and manage multiple assignments with minimal supervision\n•\nStrong intercultural awareness and ability to work effectively within multicultural teams\n•\nAbility to inspire enthusiasm and foster commitment to excellence\nWhat you will be offered:\n•\nAn opportunity to work in one of the world's most important pharmaceutical companies\n•\nModern campus with plenty of green spaces and meeting areas\n•\nCentral location in Basel\n•\nVaried job profile\n•\nFurther training opportunities through temptraining\n•\nWorking in a dynamic and motivated team\nIf you are interested please send your application documents addressed to Ms Marianne Bus",
    "datePosted": "2026-05-30",
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    "title": "MSAT Process Engineer",
    "description": "Offre d'emploi : MSAT Process Engineer -- Elan Personal AG, Rotkreuz.\n\nRoche Switzerland bridges the gap between pharmaceuticals and diagnostics. Important research and development functions are located here. For our long-standing customer, Roche Diagnostics International AG in Rotkreuz, we are looking for a\nMSAT Process Engineer\nBackground:\nAs an MSAT Engineer, you will have a direct impact on and bring value to our patients and customers. Supported by your squad and chapter team, you will start with core compliance tasks—such as non- conformity, change, and document management and continuously grow in your role, taking on increased responsibility for products and processes.\nThe Perfect Candidate:\nThe perfect candidate is a proactive engineer or natural scientist with experience in a highly regulated, GxP-compliant environment and a strong command of both English and German (B2+). They possess a data-driven mindset capable of managing deviations, optimizing production processes, and utilizing SAP to handle non-conformities and quality lifecycles. Ultimately, they are a collaborative, hands-on problem solver who can independently manage stakeholder relationships, maintain technical supplier connections, and ensure complete audit readiness.\nTasks & Responsibilities:\n•\nCompliance & Quality Lifecycle:\nManage non-conformities, changes, and documentation in SAP (covering processes, methods, materials, and equipment)\n•\nManage technical relationships with external suppliers and collaborate closely with internal departments—including Logistics, Development, and Quality—to ensure a seamless product supply\n•\nRoot Cause Analysis:\nEnact structured problem-solving processes to ensure fact-based, data- driven root cause analysis and identify effective countermeasures\n•\nDeviation Management:\nSupport the investigation and processing of deviations within the S&C sensors and reagents production\n•\nProcess Optimization:\nAdopt and optimize production processes to improve quality, increase yield, and lower costs for your respective products\n•\nControl Loops:\nEstablish, maintain, and continuously improve control loops\n•\nStakeholder Management:\nIndependently communicate with and gather crucial information from various cross-functional stakeholders\n•\nRegulatory Compliance:\nEnsure strict adherence to existing frameworks, regulatory guidelines, and department-specific requirements.\n•\nAudit Readiness:\nPrepare for quality audits and successfully represent the Chapter during audit procedures\nMust Haves:\n•\nUniversity degree in Natural Sciences or Engineering (e.g., Biotechnology, Biology, Chemistry, Material Science, Mechanical/Electrical Engineering) and/or a completed apprenticeship with equivalent professional experience in a related field\n•\nExpertise & Mindset: First proven professional background within a highly regulated environment, backed by a strong quality awareness (GxP mindset)\n•\nEssential knowledge in process and product development\n•\nCollaboration: High motivation for teamwork, excellent communication skills, and the ability to work independently within and across multi-disciplinary teams\n•\nProactivity: Enthusiasm for taking on responsibility and proactively collaborating with a highly engaged team of engineers, operators, QA, and logistics\n•\nHands-on Approach: A genuine interest in learning manufacturing technologies and continuously improving diverse BG&E processes to support our in-house production efficiently\n•\nLanguages: Fluent communication skills in English and a good working knowledge of German (B2+)\nWhat you are offered:\n•\nModern campus with plenty of green spaces and meeting zones\n•\nCentral location with highway access and train station nearby\n•\nVaried job profile\n•\nHome office option up to 40%\n•\nFurther training opportunities through temptraining\n•\nWorking in a dynamic and motivated familar team of 10 peers\n•\nGood remuneration\nYou are welcome to send your complete application documents to Ms. Nadine Rutz.\nIngenieur Prozessingenieur Vollzeit Fulltime Remote Zentralschweiz Zugerland Diagnostik Pharma\n\nCe poste est a pourvoir rapidement. Candidatez sans tarder.",
    "datePosted": "2026-05-30",
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    "title": "MES Deployment Support Specialist",
    "description": "Nouvelle opportunite : MES Deployment Support Specialist chez Elan Personal AG (Basel).\n\nRoche Schweiz schlägt die Brücke zwischen Pharmazie und Diagnostik. Wichtige Forschungs- und Entwicklungsfunktionen sind hier angesiedelt. Für unsere langjährige Kundin, die F. Hoffmann - La Roche AG in\nBasel\n, suchen wir eine/n\nMES Deployment Support Specialist\nHintergrund:\nIm Rahmen des Projekts \"Synthetic Molecule Clinical and Launch Facility\" (SMF) in Basel, in dessen Rahmen ein bestehendes Produktionsgebäude umgebaut und zusätzlich ein neues erstellt werden soll, soll u.a. ein Manufacturing Execution System (MES) eingeführt werden (Rockwell PharmaSuite). SMF ist dabei auf der Reise von papierbasierten Arbeitsprozessen zu voll digitalen Arbeitsprozessen mit einer Integration mit dem Roche SAP System ASPIRE, dem lokalen Warehouse Management System sowie dem vorhandenen PLS/DCS System (Siemens PCS7) und anderen Systemen.\nDas Projekt startet aktuell in die Detailed Design Phase mit einem geplanten Business Golive in 2030.\nWir suchen eine erfahrene Person, die als MES Deployment Support Specialist fungiert, um die Site Deployment Lead bei der Implementierung des Manufacturing Execution System (MES) in den pharmazeutischen Produktionsanlagen umfassend zu unterstützen. Diese Rolle ist entscheidend für die Gewährleistung einer nahtlosen Koordination, Planung und Ausführung der MES-Implementierung über mehrere Teams und Stakeholder hinweg, um die Organisation zu einem nachhaltigen Betrieb zu befähigen.\nAufgaben & Verantwortlichkeiten:\nPlanung & Koordination\n•\nUnterstützung des SDL bei der umfassenden Projektplanung, einschliesslich der Entwicklung von Zeitplänen, der Ressourcenzuweisung und des Kapazitätsmanagements\n•\nAbbildung und Dokumentation von Projektabhängigkeiten mit anderen gleichzeitigen Initiativen, um Konflikte zu vermeiden und einen reibungslosen Arbeitsablauf zu gewährleisten\n•\nKoordination mit funktionsübergreifenden Teams, um realistische Meilensteine und Lieferpläne festzulegen\nChange Management & Stakeholder-Einbindung\n•\nUnterstützung bei der Gestaltung und Ausführung der Strategie für das Organisatorische Change Management (OCM)\n•\nUnterstützung von Kommunikationsplänen und Aktivitäten zur Stakeholder-Einbindung, um die Organisationsreife sicherzustellen\n•\nHilfe bei der Identifizierung und Minderung von veränderungsbedingten Risiken\nMobilisierung funktionsübergreifender Teams\n•\nKoordination mit unterstützenden Teams (z. B. Material Data Management, Qualitätssicherung, Betrieb, IT), um deren Beiträge mit der MES-Implementierungs-Roadmap abzustimmen\n•\nErleichterung von Planungssitzungen und Workshops, um sicherzustellen, dass alle Teams Abhängigkeiten und Ergebnisse verstehen\n•\nFungieren als Verbindungsperson zwischen dem SDL und den funktionalen Teams\nMust Haves:\n•\nAbgeschlossenes Studium im Wirtschaftlichen Bereich oder vergleichbares\n•\nMin. 8 Jahre Kenntnisse und Erfahrungen im pharmazeutischen Umfeld und deren Prozesse\n•\nMin. 8 Jahre Kenntnisse und Erfahrungen wie eine Organization zu einem nachhaltigen Betrieb geführt wird\n•\nMin. 8 Jahre Kenntnisse im Projektmanagement\n•\nAusgezeichnete Kommunikationsfähigkeiten; Fähigkeit zur Zusammenarbeit mit technischen und geschäftlichen Interessengruppen\n•\nFliessende Deutsch und Englisch Kenntnisse\nNice to Have:\n•\nFundierte Kenntnisse in einem MES System (PharmaSuite, Werum, o.a.)\n•\nPCS7 Kenntnisse\nWas Ihnen geboten wird:\n•\nEine Chance, in einem der bedeutendsten Pharmaunternehmen der Welt mitzuwirken\n•\nModerner Campus mit viel Grünflächen und Begegnungszonen\n•\nAbwechslungsreiches Tätigkeitsprofil\n•\nWeiterbildungsmöglichkeiten durch temptraining\n•\nMitarbeit in einem dynamischen und motivierten Team\nGerne können Sie Ihre vollständigen Bewerbungsunterlagen an Frau Diana Afonso senden.\nBasel Basel-Land Aargau Chemie Pharma MES PCS7 PharmaSuite SDL OCM Data Management IT\n\nNe laissez pas passer cette offre -- postulez maintenant.",
    "datePosted": "2026-05-27",
    "validThrough": "2026-06-26",
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    "title": "Process Engineer",
    "description": "Elan Personal AG recrute un(e) Process Engineer a Basel.\n\nRoche Schweiz schlägt die Brücke zwischen Pharmazie und Diagnostik. Wichtige Forschungs- und Entwicklungsfunktionen sind hier angesiedelt. Für unsere langjährige Kundin, die F. Hoffmann - La Roche AG in\nBasel\n, suchen wir eine/n\nProcess Engineer\nHintergrund:\nAls Process Engineer Downstream liefern Sie Lösungen in der B91 Manufacturing Unit SUT (Single-use Technology) bei Basel Drug Substance Manufacturing für eine sichere und qualitativ hochwertige Antikörper Produktion. Sie dienen sowohl unseren Patienten als auch unseren Mitarbeitern, indem Sie Prozessverbesserungen entwickeln und implementieren und den Dialog und die Zusammenarbeit zwischen lokalen und globalen Funktionen in den Bereichen Entwicklung, Innovation und Regulatory fördern. Innerhalb unseres RePeng-Teams (Recipe and Process Engineering) suchen wir Sie als Process Engineer zur Optimierung unserer Downstream-Prozesse.\nAufgaben & Verantwortlichkeiten:\n•\nTechnische und wissenschaftliche Unterstützung der Schichten zur Sicherstellung robuster und effizienter Herstellungsprozesse im GMP-Umfeld, sowie Bereitschaftsdienst (On-Call)\n•\nPlanung und Koordination von Troubleshooting Aktivitäten und Ursachenanalyse in enger Zusammenarbeit mit den weiteren Manufacturing Units, Quality, MSAT und weiteren Abteilungen\n•\nUmgang mit geplanten und ungeplanten Ereignissen nach GMP-Richtlinien (Planned / unplanned events)\n•\nReview und Approval von elektronischen Chargenprotokollen für kommerzielle und klinische Produkte (MES basierter Batch Record Review)\n•\nHandeln gemäss den Anforderungen des internen Qualitätssystems (PQS) und den cGMP-Vorschriften der Gesundheitsbehörden.\n•\nLeiten oder Unterstützen von Optimierungsprojekte und Einführung neuer Technologien oder Produkten\n•\nPlanung, Vorbereitung, Moderation, Durchführung, Zusammenfassung, Überprüfung und Aktualisierung neuer und bestehender Qualitäts-Risikobewertungen im Rahmen von kommerzieller Herstellung um eine systematische Identifizierung und Reduzierung/Eliminierung von GMP-Compliance-Risiken zu gewährleisten\n•\nOwner der Produktionsprozesse (Schnittstelle Bereiche Manufacturing, Science and Technology)\n•\nErstellung und Präsentation von Konzepten, Dokumenten und Assessments bei GMP-Audits und Behördeninspektionen\n•\nGgfs. Vertretung des Standorts bei Netzwerkinitiativen und in Network-Communities\nMust Haves:\n•\nAbgeschlossenes Studium im Bereich Natur- oder Ingenieurwissenschaften oder Abschluss im Bereich Biotechnologie oder Bioprozesstechnik bevorzugt\n•\nMin. 3-5 Jahre Erfahrung und entsprechend umfangreiche Kenntnisse im Bereich Downstream Processing\n•\nMin. 2 Jahre Erfahrung in der biopharmazeutischen Herstellung oder Entwicklung\n•\nErfahrung im Arbeiten in cGMP-Umgebung\n•\nHands-On Erfahrung in Large Molecules Drug Substance Herstellungsprozessen in Stahl oder Single-Use-Technologie von Vorteil\n•\nErfahrung bei technischen Transfers und im Qualitätsrisikomanagement (QRM) von Vorteil\n•\nTeamplayer mit sehr hohem Grad an Selbständigkeit in einer Self Directed Umgebung\n•\nAusgezeichnete Kommunikationsfähigkeiten bei der Interaktion im Team, lokalen und globalen Schnittstellen\n•\nFreude an der Arbeit in globalen Teams\n•\nLokale Arbeitssprache ist Deutsch daher sehr gute Deutschkenntnisse und Schreibkenntnisse erforderlich\n•\nAusgezeichnete Deutsch- und Englischkenntnisse in Wort und Schrift\nWas Ihnen geboten wird:\n•\nEine Chance, in einem der bedeutendsten Pharmaunternehmen der Welt mitzuwirken\n•\nModerner Campus mit viel Grünflächen und Begegnungszonen\n•\nAbwechslungsreiches Tätigkeitsprofil\n•\nWeiterbildungsmöglichkeiten durch temptraining\n•\nMitarbeit in einem dynamischen und motivierten Team\nGerne können Sie Ihre vollständigen Bewerbungsunterlagen an Frau Marianne Buser senden.\nBasel Basel-Land Aargau Chemie Prozessingenieur QRM Downstream Processing Prozesstechnik Engineering PQS GMP\n\nInteressé(e) ? Postulez directement sur notre site.",
    "datePosted": "2026-05-20",
    "validThrough": "2026-06-19",
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    "title": "Quality Control Project Lead",
    "description": "Nouvelle opportunite : Quality Control Project Lead chez Elan Personal AG (Basel).\n\nRoche Switzerland bridges the gap between pharmaceuticals and diagnostics. Important research and development functions are located here. For our long-term client, F. Hoffmann-La Roche AG in Basel, we are looking for a\nQuality Control Project Lead\nBackground:\nGlobal Technical Development (PTD) is an organization of over two thousand people globally that are integral for the mission of Roche to develop meaningful medicines for patients. Therefore, PTD actively collaborates and develops creative technical solutions to bridge early- stage, late-stage and commercial product needs. The mandate of the group is to reliably deliver the pipeline and supply quality products to patients. The group excels in its work through innovation, teamwork, dedication, and mutual respect and contributes every single day, continuously improving what it does. Synthetic Molecules Technical Development (PTDC) brings a broad range of experience across drug substance (DS), drug product (DP), analytical sciences and Manufacturing Science & Technology (MS&T), and collaborates closely with key partners in the departments Research and Early Development (pRED / gRED), Small and Large Molecules (PTC, PTB), PTD and MS&T across the manufacturing network. This position on offer is located in Analytical Development Synthetic Molecules within Pharma Technical Development.\nAnalytical Development is responsible for the development of resource and cost efficient analytical methods for all materials used during drug manufacturing using state of the art methodologies such as e.g. High-performance liquid chromatography (HPLC), Gas\nChromatography (GC), Ion Chromatography (IC), Mass Spectrometry (MS), and others. The ultimate goal of the work is a robust control strategy to release pharmaceutical products for clinical trials, and finally for commercial supply. The QC-Section within the Analytical Development Department is responsible for the Release of Materials based on the GMP compliant execution of Analyses of Inprocess controls, raw materials, intermediates, APIs and Drug products.\nTasks & Responsibilities:\n•\nWork in a modern quality control organization in compliance with cGMP regulations\n•\nCooperation with internal and/or external partners of Analytical Development\n•\nActive participation in shaping the working methods of the analytical group\n•\nComprehensive analytical support for supply plants for API and drug product for clinical use\n•\nCritical evaluation of own work results\n•\nSupport the analytical group by fulfilling cross-laboratory tasks and project tasks (e.g.reference standard management, CSV business process owner of analytical applications)\n•\nImplementing and fully complying with relevant Roche policies, procedures, and standards in the areas of safety, health, and environmental protection\n•\nEnsuring that laboratory employees are informed of all relevant SHE requirements and their implementation\n•\nEnsuring an appropriate GMP standard in the laboratory\n•\nScientific and regulatory documentation of the work done\nMust Haves:\n•\nBachelor’s or Master’s degree in Natural Sciences OR a Laboratory Technician with 10+ years of high-level GMP experience\n•\n3–5 years of professional industry experience with a core focus on Analytical Chemistry\n•\nPractical experience working under cGMP regulations is required\n•\nProficiency in laboratory-specific software (e.g., Waters Empower, Metrohm Tiamo, or Labware LIMS)\n•\nEnglish (Fluent/Mandatory). German language skills are considered a significant advantage\nNice to Have:\n•\nRoche Experience\n•\nExperience in roles such as Lab Head, Analytical Project Manager, or equivalent\nWhat you will be offered:\n•\nAn opportunity to work in one of the world's most important pharmaceutical companies\n•\nModern campus with plenty of green spaces and meeting areas\n•\nCentral location in Basel\n•\nVaried job profile\n•\nFurther training opportunities through temptraining\n•\nWorking in a dynamic and motivated team\nIf you are interested please send your application documents addressed to Ms Diana Afonso.\nBasel-Stadt Aargau Pharma Science GMP Quality Control QC-PL Laboratory Waters Empower Metrohm Tiamo LIMS\n\nCe poste est a pourvoir rapidement. Candidatez sans tarder.",
    "datePosted": "2026-05-17",
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    "@id": "https://ch-jobs.com/job/validation-engineer-global-external-manufacturing#jobposting",
    "title": "Validation Engineer Global External Manufacturing",
    "description": "Offre d'emploi : Validation Engineer Global External Manufacturing -- Elan Personal AG, Rotkreuz.\n\nRoche Schweiz bridges the gap between pharmacy and diagnostics. Important research and development functions are located here. For our longstanding client, Roche Diagnostics International AG in Rotkreuz, we are looking for a\nValidation Engineer Global External Manufacturing (GEM)\nBackground:\nThis is more than just a validation engineer position. You act as a reliable quality partner, auditor, supplier developer, technical expert, and diplomat. As an expert in validation, you will work together with our suppliers in qualification and validation projects. With your sound knowledge about quality regulations (e.g., IVDR / MDR, ISO 13485, 21 CFR 820), qualification and validation, and various production technologies, you will ensure that our high-quality products are manufactured in compliance with our standards and external regulations. Your main task is the supervision of qualification and validation activities with our suppliers. This encompasses process risk analyses, qualification and validation documentation, and the corresponding documented evidence.\nThe Perfect Candidate holds a Bachelor's Degree in an engineering or scientific/technical field, or equivalent experience, supplemented by at least 10 years of professional background in quality functions like Q&V or auditing within the Pharma or medical device sectors. The candidate possesses over 5 years of parcours professionnel in external manufacturing and holds a deep understanding of relevant standards and automated production technologies, such as injection and blow molding. Additionally, the individual demonstrates a consistent commitment to personal and team development, paired with professional-level communication skills in both English and German.\nTasks & Responsibilities:\n•\nReview and evaluate qualification and validation documents and process risk analyses provided by our suppliers\n•\nOversee the assessment of deviations related to qualification and validation activities, ensuring they meet our rigorous standards\n•\nMeticulously document the outcomes of your evaluations in compliance with established quality standards\n•\nActively engage in the continuous improvement of processes, providing support in technical matters, and performing statistical data analyses\n•\nOffer expert advice to suppliers on quality and compliance, ensuring adherence to all relevant quality standards and specifications\n•\nThrive in cross-departmental collaboration, working effectively within squads to achieve common goals\nMust Haves:\n•\nA Bachelor's Degree in engineering, scientific/technical field, or equivalent work experience, with at least 10 years of related background (Q&V, Auditing, or Quality functions) in Pharma or the medical device industry\n•\nAt least 5 years of expertise with external manufacturing business\n•\nProfound understanding of applicable standards and norms, along with expertise in injection molding, blow molding, or other automated production technologies\n•\nDemonstrate a continuous desire for learning and improvement both for yourself and your team members\n•\nExcellent communication skills in English and German (written and verbal)\nNice to Haves:\n•\nKnowledge of computerized systems validation and controlled environment qualification (ISO 14644)\n•\nFamiliarity with product risk management according to ISO 14971\n•\nCertified Lean Six Sigma Green Belt / Black Belt\nWhat We Offer You:\n•\nA chance to contribute to one of the world's leading pharmaceutical companies\n•\nModern campus with plenty of green spaces and meeting areas\n•\nCentral location with highway access and nearby train station\n•\nVaried job profile\n•\nHome office options\n•\nOpportunities for further training through temptraining\n•\nCollaboration in a dynamic and motivated team\n•\nCompetitive salary\nPlease send your complete application documents to Mr. Severin Räfle.\nChemistry Pharma Pharmacy Diagnostics Zug Lucerne Full-time Research Laboratory\n\nPostulez des maintenant pour ce poste de Validation Engineer Global External Manufacturing a Rotkreuz.",
    "datePosted": "2026-05-13",
    "validThrough": "2026-06-12",
    "employmentType": "FULL_TIME",
    "url": "https://ch-jobs.com/job/validation-engineer-global-external-manufacturing",
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    "@id": "https://ch-jobs.com/job/analytical-project-leader-scientist-senior-scientist#jobposting",
    "title": "Analytical Project Leader (Scientist / Senior Scientist)",
    "description": "Rejoignez Elan Personal AG en tant que Analytical Project Leader (Scientist / Senior Scientist) a Basel.\n\nRoche Switzerland bridges the gap between pharmaceuticals and diagnostics. Important research and development functions are located here. For our long-term client, F. Hoffmann-La Roche AG in Basel, we are looking for a\nAnalytical Project Leader (Scientist / Senior Scientist)\nBackground:\nThe Analytical Research & Development department is a key part of Synthetic Molecules Technical Development. It is globally responsible for advancing analytical methodologies, performing in-depth analyses of active pharmaceutical ingredients, and diverse dosage forms, as well as preparing detailed regulatory documentation for submission to health authorities.\nIn this role, you will join a motivated and experienced team of analytical scientists. You will lead the analytical development of synthetic molecule projects involving small molecules, from early development to commercialization. This role offers a unique opportunity to apply your expertise in a dynamic, fast-paced environment and contribute to the development of life-changing medicines.\nTasks & Responsibilities:\n•\nDeveloping a phase-appropriate control strategy for drug substances and drug products\n•\nCollaborating effectively with stakeholders across various departments\n•\nCoordinating comprehensive analytical activities, which involves generating physical and chemical data for materials, developing/improving and validating analytical test methods or other analytical controls and ensuring thorough documentation, timely delivery and adherence to quality standards\n•\nCoaching technicians and junior scientists on project work and serving as a central point of contact for project-related information\n•\nConduct work in compliance with cGMP where applicable, safety, and regulatory requirements\n•\nSupervise internal laboratory activities and / or testing activities at CLOs/CDMOs\n•\nPlan and document experiments/results independently and prepare for regulatory submissions such as IND and NDA\nMust Haves:\n•\nA Master’s or Ph.D. in chemistry, pharmacy, or a related field, with at least three years of professional parcours professionnel in analytical development of drug substances or drug products for small molecules\n•\nIn-depth knowledge of chemistry, including synthesis, purification, and characterization\n•\nExpertise in key analytical techniques such as High-Performance Liquid Chromatography (HPLC), Ultra-Performance Liquid Chromatography (UPLC)\n•\nProven experience in developing and validating ICH-compliant analytical methods\n•\nProficiency in degradation and stability studies for small molecules, including forced degradation and impurity profiling\n•\nUnderstanding of key requirements for drug substances and drug product specifications\n•\nExcellent command of the English language\n•\nA strong quality mindset and excellent attention to detail\n•\nDigital savviness to support digital transformation initiatives; familiarity with statistical analysis of analytical data is also advantageous\n•\nOpen-minded, goal-oriented, and able to work in a fast-developing environment\n•\nTakes challenges as opportunities and is able to respectfully collaborate with team members, customers and stakeholders, even in stressful situations\nNice to Have:\n•\nProficiency in German\nWhat you will be offered:\n•\nAn opportunity to work in one of the world's most important pharmaceutical companies\n•\nModern campus with plenty of green spaces and meeting areas\n•\nCentral location in Basel\n•\nVaried job profile\n•\nFurther training opportunities through temptraining\n•\nWorking in a dynamic and motivated team\nIf you are interested please send your application documents addressed to Ms Diana Afonso.\nBasel-Stadt Aargau Pharma Science Senior Scientist Project Leader Chemistry HPLC UPLC GMP\n\nRejoignez Elan Personal AG et donnez un nouvel elan a votre carriere.",
    "datePosted": "2026-05-13",
    "validThrough": "2026-06-12",
    "employmentType": "FULL_TIME",
    "url": "https://ch-jobs.com/job/analytical-project-leader-scientist-senior-scientist",
    "identifier": {
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        "value": "job-38873"
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    "@id": "https://ch-jobs.com/job/construction-manager-verfahrenstechnik#jobposting",
    "title": "Construction Manager Verfahrenstechnik",
    "description": "Vous cherchez un emploi de Construction Manager Verfahrenstechnik a Kaiseraugst ? Elan Personal AG recrute.\n\nRoche Schweiz schlägt die Brücke zwischen Pharmazie und Diagnostik. Wichtige Forschungs- und Entwicklungsfunktionen sind hier angesiedelt. Für unsere langjährige Kundin, die F. Hoffmann - La Roche AG in Kaiseraugst, suchen wir eine/n\nConstruction Manager Verfahrenstechnik\nHintergrund:\nDer Bereich «Operate and Maintain Assets» der Roche Pharma am Standort Basel/ Kaiseraugst hat den Sinn und Zweck “We do asset care - für einen reibungslosen Betrieb von Areal, Gebäuden und Anlagen”. Als Mitarbeiter im Kreis Construction Site Services arbeiten Sie in einem Team von 12Kollegen. Sie sind die Schnittstelle zwischen dem Projekt und den ausführenden Firmen auf der Baustelle. Das Aufgabengebiet umfasst\ndie Planung, Führung und Organisation von Baustellen, das Betreuen der ausführenden Firmen sowie die Qualitäts- und Kostenkontrolle der ausgeführten Arbeiten. Als wichtiger Teil in den Projekten stellen sie die Ausführung und die Übergabe der von Ihnen betreuten Projekten zum Anlagenbetreiber sicher und sorgen so für einen hohen Standard unserer Produkte und Dienstleistungen. Im streng regulierten Pharmaumfeld sorgen Sie mit ihrer Erfahrung auch dafür, dass im GMP-Umfeld die geforderten Qualitätsstandards auf der Baustelle sowie bei der Dokumentation eingehalten werden.\nAufgaben & Verantwortlichkeiten:\n•\nBaustellenplanung & Organisation, Führung und Koordination der Baustelle\n•\nBetreuung von Fremdfirmenmitarbeitern\n•\nQualitätskontrolle im Fachgewerk Rohrleitungsbau und Versorgungstechnik sowie auch fachübergreifend\n•\nRapportwesen in Abstimmung mit dem lokalen Engineering\n•\nUmsetzung der Baustellensicherheit gemäß Roche Vorgaben\n•\nInbetriebnahme und Begleitung der Fremdfirmen bis zur Mängelbehebung\n•\nHand-Over des fertigen Gewerks in Zusammenarbeit mit dem lokalen Engineering\n•\nInput bei der gewerksspezifischen Planung (Z. B. Hersteller, Materialien etc.)\n•\nInput bei der Planung hinsichtlich Termine und Bauablauf während der Phase CC\n•\nKontrolle und Auswertung von Angeboten und Pflichtenheften\n•\nEinholen von Angeboten und Richtpreisofferten\n•\nMitarbeit bei der Vergabe an ausführende Firmen\n•\nSichten / Prüfen von Revisionsunterlagen\nMust Haves:\n•\nAbgeschlossene Berufsausbildung idealerweise als Anlagen & Apparatebauer, evtl. Weiterbildung zum Meister, Techniker oder vergleichbares\n•\nMindestens 5-10 Jahre Berufserfahrung im Projektmanagement von Rohrleitungsinstallationen /Versorgungstechnischen Anlagen\n•\nGrundkenntnisse GMP\n•\nGute Kenntnisse mit Google Suite und MS Office, verfahrenstechnische Kenntnisse und SAP-Kenntnisse sind wünschenswert\n•\nSehr gute Deutschkenntnisse in Wort und Schrift werden vorausgesetzt, Englisch- und Französischkenntnisse sind von Vorteil\n•\nKenntnisse in Baustellen- und Arbeitssicherheit (SiGeKo oder Sicherheitsassistent o.ä. sind wünschenswert).\nNice to Have:\n•\nGrundkenntnisse in Brandschutz, evtl. Kurse Lüftungsanlagen etc.\n•\nKenntnisse in Baustellenlogistik\n•\nGrundkenntnisse in Anlagenautomation, Automationssysteme etc.\n•\nSehr gute Kenntnisse in VT-Installationen, Rohrklassen, Normen etc.\n•\nGrundkenntnisse Roche Dokumentation, Elvis, SAP, techn. Plätze etc.\nWas Ihnen geboten wird:\n•\nAttraktive Entlohnung\n•\nKleines, eingespieltes und fachlich starkes Team mit\n•\nEine Chance, in einem der bedeutendsten Pharmaunternehmen der Welt mitzuwirken\n•\nModerner Campus mit viel Grünflächen und Begegnungszonen\n•\nGleitzeit-Arbeitszeit mit viel verantwortungsvollen und hochinteressanten Projekten\nGerne können Sie Ihre vollständigen Bewerbungsunterlagen an Frau Nadine Rutz senden.\nFricktal Pharmacy Konstruktion HLKKS Führung Leader Verantwortung Vollzeit Fulltime\n\nNe laissez pas passer cette offre -- postulez maintenant.",
    "datePosted": "2026-05-06",
    "validThrough": "2026-06-05",
    "employmentType": "FULL_TIME",
    "url": "https://ch-jobs.com/job/construction-manager-verfahrenstechnik",
    "identifier": {
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        "name": "Elan Personal AG",
        "value": "job-33437"
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        "name": "Elan Personal AG",
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        "logo": "https://media.jobs.ch/media/226b73cf-f1a2-4600-bba7-412ac60e2977"
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        "address": {
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            "streetAddress": "Kaiseraugst",
            "addressLocality": "BS",
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    "@context": "https://schema.org",
    "@type": "JobPosting",
    "@id": "https://ch-jobs.com/job/produktionsexperte-in-im-team-inspektion#jobposting",
    "title": "Produktionsexperte/in im Team Inspektion",
    "description": "Roche Schweiz schlägt die Brücke zwischen Pharmazie und Diagnostik. Wichtige Forschungs- und Entwicklungsfunktionen sind hier angesiedelt. Für unsere langjährige Kundin, die F. Hoffmann - La Roche AG in Kaiseraugst, suchen wir eine/n  Produktionsexperte/in im Team Inspektion   Hintergrund: Bei Roche arbeiten 100’000 Menschen in über 100 Ländern an der Zukunft der Gesundheitsversorgung. Gemeinsam wurden wir eines der führenden forschenden Pharmaunternehmen. Unser Erfolg basiert auf Innovation, Neugier und Diversität. Mit seinen 1’400 Mitarbeitenden stellt das Produktionszentrum Kaiseraugst die ununterbrochene Patientenversorgung mit qualitativ hochwertigen Medikamenten sicher. Im Team “Inspection Processes” innerhalb des Wertstroms \"Vials Volume\" sind wir für die visuelle Kontrolle von diversen Produkten, die an der AFL, FSP und GEF Produkte sowie APS zuständig sind. Wir arbeiten gemeinsam mit unseren Schnittstellen aus diversen Wertströmen zusammen (Logistik, QC, Verpackung und Abfülllinien). Damit unsere Produkte mit höchster Qualität und zeitgerecht produziert werden können, stehen verschiedene Technologien zur Verfügung.  Aufgaben & Verantwortlichkeiten:   Durchführung von manueller visueller Inspektion Visuelle Inspektion von Flüssigvials, Fertigspritzen und Lyo-Vials GMP-konforme Dokumentation Automatische Inspektionsbetreuung der Inspektionsmaschin   Must Haves:   Abgeschlossene Berufsausbildung  Mind. 6 Monate Erfahrung in der visuellen Kontrolle Gute EDV-Kenntnisse  Sehr gute Deutschkenntnisse in Wort und Schrift Bestandener Sehtest (Roche)  Bereitschaft zur Schichtarbeit (keine Nachtschicht) Kommunikationsfähig und mit hohem Engagement für die Stelle und den Arbeitgeber Bewusstsein der hohen Anforderung und Bedeutung der Tätigkeit Bereitschaft für offene Kommunikation (inkl. Fehlerkultur) Belastbarkeit und flexibel Aufgeschlossenheit gegenüber Neuem Lösungsorientierte und kreative Denkweise Bereitschaft zur Teamarbeit und gegenseitigem Coaching Bereitschaft zu anlagen- und bereichsübergreifendem Arbeiten (Polyvalenz) Gewissenhaftes, systematisches und präzises Arbeiten Langes konzentriertes Arbeiten Gute Auffassungsgabe   Nice to Have:   Pharma Erfahrung GMP Erfahrung   Was Ihnen geboten wird:   Eine Chance, in einem der bedeutendsten Pharmaunternehmen der Welt mitzuwirken Moderner Campus mit viel Grünflächen und Begegnungszonen Abwechslungsreiches Tätigkeitsprofil Weiterbildungsmöglichkeiten durch temptraining  Mitarbeit in einem dynamischen und motivierten Team  Gerne können Sie Ihre vollständigen Bewerbungsunterlagen an Frau Marianne Buser senden. Basel Basel-Land Aargau Chemie Produktion GMP Pharma Qualitätssicherung Visuelle Kontrolle Prozessoptimierung Optische Kontrolle  ",
    "datePosted": "2026-04-23",
    "validThrough": "2026-07-22",
    "employmentType": "FULL_TIME",
    "url": "https://ch-jobs.com/job/produktionsexperte-in-im-team-inspektion",
    "identifier": {
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        "name": "Elan Personal AG",
        "value": "job-26369"
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{
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    "@type": "JobPosting",
    "@id": "https://ch-jobs.com/job/senior-procurement-manager#jobposting",
    "title": "Senior Procurement Manager",
    "description": "Roche Switzerland bridges the gap between pharmaceuticals and diagnostics. Important research and development functions are located here. For our long-term client, F. Hoffmann-La Roche AG in Basel, we are looking for a  Senior Procurement Manager   Background:  As a Senior Procurement Manager in External Manufacturing (CDMO Procurement), you will bring analytical thinking, planning, execution, and focus to the procurement sourcing and delivery capability area. Using your specialized knowledge, very good communication skills, and in-depth expertise in a specific category or spend areas and procurement overall, you will proactively identify and drive strategies and approaches for managing and sourcing third party spend requirements. You can also play the role of Category strategy owner in charge of driving, coordinating and signing the category strategy. Reporting directly to the Global Head of EMS, you will act as the \"Process Hub\" for the global 17+ member team. Your mission is to ensure operational excellence by driving adherence to their global standards, maintaining total portfolio transparency, and serving as the key interface with critical stakeholder functions. This role offers an unparalleled 360-degree view of Roche’s external manufacturing business, providing a unique vantage point for a professional looking to master the complexities of global pharma outsourcing.  Tasks & Responsibilities:   Design, execute, and analyze diverse in vivo experiments, including intravenous injections, blood and plasma collection, bleeding and thrombosis models, and related procedures Characterize efficacy and safety of novel gene therapy assets using molecular and biochemical assays (e.g., ELISA, thrombin generation assay, chromogenic assays) in murine and human samples Prepare, handle, and test patient-derived material (blood and plasma) in in vitro and ex vivo settings Perform data analysis and present results within the team Maintain thorough documentation and contribute to general lab organization, safety, and inventory management   Must Haves:   You are a Category and sourcing subject matter expert in External Manufacturing of pharmaceutical products. Conducting market and internal analysis to develop strategies, best practices, and guidance on tactical plans for how Roche should source and negotiate for third party goods and services in order to satisfy stakeholder requirements and maximize the value for Roche You have an expert understanding of the CDMO market for Drug Product and Finished Goods Manufacturing You have a good understanding about the GMP and regulatory requirements and their impact on CDMO Procurement Strategies You are a Procurement delivery practitioner delivering and executing sourcing strategies and major initiatives by leveraging spend, category know-how, robust sourcing, negotiation, contracting, supplier management methodologies and project management skills, and/or supporting team members by coaching them and enhancing their skills and knowledge You develop content and automation, translating sourcing strategy into content and automated buying channels guidelines, best practices and communication materials that improve business adoption, satisfaction, and overall efficiency You have very good communication skills, especially in English and you are an expert in pro-active stakeholder management, being used to work in a remote environment   Must Haves:   Deep expertise in CDMO sourcing for Drug Product and Finished Goods Manufacturing, with strong understanding of global market dynamics and cost drivers Proven experience in strategic sourcing and complex contract negotiations, including long-term CDMO agreements and capacity models Strong knowledge of GMP and regulatory requirements (e.g., FDA, EMA) and their impact on supplier selection and contracting Demonstrated ability to develop and execute category strategies aligned with business needs, supply security, and value delivery Experience in cross-functional stakeholder management, effectively collaborating with Quality, Regulatory, and Technical Operations in a global environment Solid track record in supplier relationship and performance management, driving continuous improvement and risk mitigation Proficiency in procurement tools (e.g., SAP Ariba) and data-driven decision making, including translating strategies into automation and buying channel guidance  Excellent communication and influencing skills in English, with the ability to simplify complex topics and support team capability building   Nice to Haves:   Previous Roche experience would be a big plus   What you will be offered:   An opportunity to work in one of the world's most important pharmaceutical companies Modern campus with plenty of green spaces and meeting areas Central location in Basel Remote work possible Varied job profile Further training opportunities through temptraining Working in a dynamic and motivated team  If you are interested please send your",
    "datePosted": "2026-04-23",
    "validThrough": "2026-07-22",
    "employmentType": "FULL_TIME",
    "url": "https://ch-jobs.com/job/senior-procurement-manager",
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        "value": "job-25972"
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