Au sein du département Engineering & Maintenance, vous intégrerez l'équipe E&M Compliance & Qualification en tant que compliance. L'équipe, performante et dynamique, assure la compliance GMP au sein du département E&M.Vos Tâches :En tant que compliance, vous aurez principalement la charge de la gestion des déviations du départementVous avez la charge de la mise en place d'actions de corrections et de prévention efficacesVous serez point de contact privilég
Au sein du département Engineering & Maintenance, vous intégrerez l'équipe E&M Compliance & Qualification en tant que compliance. L'équipe, performante et dynamique, assure la compliance GMP au sein du département E&M.Vos Tâches :En tant que compliance, vous aurez principalement la charge de la gestion des déviations du départementVous avez la charge de la mise en place d'actions de corrections et de prévention efficacesVous serez point de contact privilég
As a MOS Compliance Expert at Merck, you will play a pivotal role in the Production department, especially in the Compliance field, by conducting critical and transversal complex investigations, ensuring data integrity, leading Corrective and Preventive Actions (CAPA), maintaining compliance with Good Manufacturing Practices (GMP), and overseeing classified environment monitoring activities. Your responsibilities will also include overseeing project qualit
As a MOS Compliance Expert at Merck, you will play a pivotal role in the Production department, especially in the Compliance field, by conducting critical and transversal complex investigations, ensuring data integrity, leading Corrective and Preventive Actions (CAPA), maintaining compliance with Good Manufacturing Practices (GMP), and overseeing classified environment monitoring activities. Your responsibilities will also include overseeing project qualit
Key Responsibilities· Contribute to CSV strategies, plans, and protocols in accordance with regulatory As a QA IT CSV Engineer, you will be responsible for ensuring compliance for computerized systems and computerized systems validation, fulfill with regulatory requirements and operate as intended.Your primary responsibilities will include:guidelines (e.g., FDA 21 CFR Part 11, EU Annex 11, GAMP 5)· Contribute to risk assessments and participate to test scr
Key Responsibilities· Contribute to CSV strategies, plans, and protocols in accordance with regulatory As a QA IT CSV Engineer, you will be responsible for ensuring compliance for computerized systems and computerized systems validation, fulfill with regulatory requirements and operate as intended.Your primary responsibilities will include:guidelines (e.g., FDA 21 CFR Part 11, EU Annex 11, GAMP 5)· Contribute to risk assessments and participate to test scr
Caring for the world, one person at a time. inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of Johnson & Johnson work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 265 operating companies in more than 60 countries employing approximatel
Caring for the world, one person at a time. inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of Johnson & Johnson work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 265 operating companies in more than 60 countries employing approximatel
Nous sommes à la recherche d’un.e Compliance Specialist Biotech pour notre client, Merck, pour une mission d’une durée de 12 mois. Votre rôle : Le/la Compliance Specialist Biotech aide à assurer la compliance au sein de l’équipe Compliance au Manufacturing Operational Support, en respectant les cGMPs, et en assurant l’exactitude de la documentation. Il contribue à maintenir les exigences qualité en participant aux Déviations, CAPAs, Change control et la re
Nous sommes à la recherche d’un.e Compliance Specialist Biotech pour notre client, Merck, pour une mission d’une durée de 12 mois. Votre rôle : Le/la Compliance Specialist Biotech aide à assurer la compliance au sein de l’équipe Compliance au Manufacturing Operational Support, en respectant les cGMPs, et en assurant l’exactitude de la documentation. Il contribue à maintenir les exigences qualité en participant aux Déviations, CAPAs, Change control et la re
For our client based in Vaud canton and specialized in biopharmaceutical area, we’re looking for a Senior Quality Assurance - CSV specialist ResponsabilityManage Quality oversight for computerized systems validation and the data integrity program & support QA activities for system introduction/upgrades, ensuring compliance with quality policies, cGMP, EU/US, and Swiss regulations.Oversee daily quality for GxP IT, CSV, and automated systems (SISA).Act as th
For our client based in Vaud canton and specialized in biopharmaceutical area, we’re looking for a Senior Quality Assurance - CSV specialist ResponsabilityManage Quality oversight for computerized systems validation and the data integrity program & support QA activities for system introduction/upgrades, ensuring compliance with quality policies, cGMP, EU/US, and Swiss regulations.Oversee daily quality for GxP IT, CSV, and automated systems (SISA).Act as th
No sponsorships for non-EU candidatesWe are seeking a detail-oriented and analytical IT Business Analyst to join our bank. The successful candidate will be responsible for analyzing our IT infrastructure, identifying network devices and system components within PCI scope, and following up on PCI requirements in consultation with the company's PCI Officer.Start: AsapDuration: until 30.11.2024 (option to extend)Work location: Zürich + Homeoffice (only in Swi
No sponsorships for non-EU candidatesWe are seeking a detail-oriented and analytical IT Business Analyst to join our bank. The successful candidate will be responsible for analyzing our IT infrastructure, identifying network devices and system components within PCI scope, and following up on PCI requirements in consultation with the company's PCI Officer.Start: AsapDuration: until 30.11.2024 (option to extend)Work location: Zürich + Homeoffice (only in Swi
We are seeking a highly skilled and experienced QC Support Investigation Expert to join our Quality Control team. The ideal candidate will have a strong engineering background and extensive experience in the pharmaceutical or biotech industry. The primary responsibility of the QC Support Investigation Expert will be to lead and support investigations related to quality control issues, deviations, and non-conformances in our manufacturing processes.Key Resp
We are seeking a highly skilled and experienced QC Support Investigation Expert to join our Quality Control team. The ideal candidate will have a strong engineering background and extensive experience in the pharmaceutical or biotech industry. The primary responsibility of the QC Support Investigation Expert will be to lead and support investigations related to quality control issues, deviations, and non-conformances in our manufacturing processes.Key Resp
A leading bank is looking for an Infrastructure Lead based in Zurich, Switzerland. Its a permanent position. What exactly you want to do here:Providing expert leadership to ensure the implementation, operation and compliance of infrastructure servicesKey contributor to the infrastructure technology transformation roadmap ensuring key objectives are met and timely delivery of implementationsDefining technical standards across all infrastructure areas and en
A leading bank is looking for an Infrastructure Lead based in Zurich, Switzerland. Its a permanent position. What exactly you want to do here:Providing expert leadership to ensure the implementation, operation and compliance of infrastructure servicesKey contributor to the infrastructure technology transformation roadmap ensuring key objectives are met and timely delivery of implementationsDefining technical standards across all infrastructure areas and en
Für die Firma Jabil Switzerland Manufacturing GmbH in Grenchen suchen wir Betriebsmitarbeiter (m/w/d) für den Bereich Finish.In dieser Position hast du folgendes Aufgabengebiet:Bereitstellen von Werkzeugen, Kontrollmitteln und Vorrichtungen gemäss Anweisung und/oder UnterlagenAbarbeiten von Aufträgen nach Anweisung des Vorgesetzten gemäss QSKorrektes und vollständiges Ausfüllen der Produktionsunterlagen gemäss GMPKennen und Befolgen der Richtlinien bezügli
Für die Firma Jabil Switzerland Manufacturing GmbH in Grenchen suchen wir Betriebsmitarbeiter (m/w/d) für den Bereich Finish.In dieser Position hast du folgendes Aufgabengebiet:Bereitstellen von Werkzeugen, Kontrollmitteln und Vorrichtungen gemäss Anweisung und/oder UnterlagenAbarbeiten von Aufträgen nach Anweisung des Vorgesetzten gemäss QSKorrektes und vollständiges Ausfüllen der Produktionsunterlagen gemäss GMPKennen und Befolgen der Richtlinien bezügli
Caring for the world, one person at a time. Inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of Johnson & Johnson work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 265 operating companies in more than 60 countries, employing approximate
Caring for the world, one person at a time. Inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of Johnson & Johnson work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 265 operating companies in more than 60 countries, employing approximate
Für die Firma Jabil Manufacturing GmbH suchen wir in Grenchen per sofort einen CNC-Operateur 100% (m/w/d):Deine täglichen Hauptaufgaben:Einrichten, Bedienen und Überwachen von CNC Kurz- und/oder LangdrehmaschinenBereitstellen von Werkzeugen, Kontrollmitteln und Vorrichtungen gemäss Anweisungen Termin- und sachgerechte Abarbeitung nach Fertigungsaufträgen, Prüfanweisungen, Verfahrensanweisungen und ZeichnungenReinigen von Maschinen und Ausführen einfacher W
Für die Firma Jabil Manufacturing GmbH suchen wir in Grenchen per sofort einen CNC-Operateur 100% (m/w/d):Deine täglichen Hauptaufgaben:Einrichten, Bedienen und Überwachen von CNC Kurz- und/oder LangdrehmaschinenBereitstellen von Werkzeugen, Kontrollmitteln und Vorrichtungen gemäss Anweisungen Termin- und sachgerechte Abarbeitung nach Fertigungsaufträgen, Prüfanweisungen, Verfahrensanweisungen und ZeichnungenReinigen von Maschinen und Ausführen einfacher W
Are you looking for a challenging job as an Automation Engineer?Do you have experience working with MES Syncade? Would you like to work in the pharmaceutical sector? Our client is looking for an Automation Engineer, who would be a part of a disciplinary team. This role plays a key part in designing, testing, and troubleshooting recipes in Syncade, ensuring compliance with regulatory standards during the design, start-up, qualification, and production phase
Are you looking for a challenging job as an Automation Engineer?Do you have experience working with MES Syncade? Would you like to work in the pharmaceutical sector? Our client is looking for an Automation Engineer, who would be a part of a disciplinary team. This role plays a key part in designing, testing, and troubleshooting recipes in Syncade, ensuring compliance with regulatory standards during the design, start-up, qualification, and production phase
For our client Merck in Aubonne, we are looking for a QA Specialist for QC (m/f/d) for a period of 12 months from 1st September 2024.Your role: To ensure the quality oversight and compliance of QC activities and the data integrity of QC analytical data in timely manner. QA Oversight on QC analytical data:To perform the QA review on QC analytical data, on QC documentation. Manage QC deviation, CCP and CAPA as QA.Compliance of QC activities:QA support for QC
For our client Merck in Aubonne, we are looking for a QA Specialist for QC (m/f/d) for a period of 12 months from 1st September 2024.Your role: To ensure the quality oversight and compliance of QC activities and the data integrity of QC analytical data in timely manner. QA Oversight on QC analytical data:To perform the QA review on QC analytical data, on QC documentation. Manage QC deviation, CCP and CAPA as QA.Compliance of QC activities:QA support for QC
Are you ready to bring your mechanical skills to a large healthcare manufacturing services company in Switzerland? If so, we have the perfect opportunity for you.For Jabil Manufacturing GmbH we are urgently seeking for CNC Machinists (100%) (m/f/d) for long term temporary missions (crossborder talents from neighbouring countries are welcome).Your main daily responsibilities include:Setting up, operating, and monitoring CNC short and/or long turning machine
Are you ready to bring your mechanical skills to a large healthcare manufacturing services company in Switzerland? If so, we have the perfect opportunity for you.For Jabil Manufacturing GmbH we are urgently seeking for CNC Machinists (100%) (m/f/d) for long term temporary missions (crossborder talents from neighbouring countries are welcome).Your main daily responsibilities include:Setting up, operating, and monitoring CNC short and/or long turning machine
Project Overview:We are seeking a talented individual to build a comprehensive single-entry data site for the Server Platform. This site will include market data and segmentation, with a focus on assessing value creation for customers across various quality dimensions such as efficiency, reliability, productivity, and compliance.Key Responsibilities:Requirement Collection: Gather requirements for the data site and identify key metrics of interest for the t
Project Overview:We are seeking a talented individual to build a comprehensive single-entry data site for the Server Platform. This site will include market data and segmentation, with a focus on assessing value creation for customers across various quality dimensions such as efficiency, reliability, productivity, and compliance.Key Responsibilities:Requirement Collection: Gather requirements for the data site and identify key metrics of interest for the t
"Die Arbeit, die du heute machst, könnte morgen Leben retten."Möchtest auch du deine mechanischen Fähigkeiten im weltweit grössten Unternehmen für Healthcare-Design und Herstellungsdienstleistungen einbringen? Dann haben wir genau die richtige Stelle für dich.Für die Firma Jabil Manufacturing GmbH suchen wir in Grenchen per sofort einen CNC-Mechaniker 100% (m/w/d):Zu deinen täglichen Hauptaufgaben gehören:Einrichten, Bedienen und Überwachen von CNC Kurz- u
"Die Arbeit, die du heute machst, könnte morgen Leben retten."Möchtest auch du deine mechanischen Fähigkeiten im weltweit grössten Unternehmen für Healthcare-Design und Herstellungsdienstleistungen einbringen? Dann haben wir genau die richtige Stelle für dich.Für die Firma Jabil Manufacturing GmbH suchen wir in Grenchen per sofort einen CNC-Mechaniker 100% (m/w/d):Zu deinen täglichen Hauptaufgaben gehören:Einrichten, Bedienen und Überwachen von CNC Kurz- u
For our client based in Basel and specialized in pharma area, we're looking for a QA Manager - Responsible PersonResponsibilitiesSupport Quality activities in LATAM and MMG operational areas, acting as the Responsible Person for LATAM GmbH and Medical GmbH.Execute Quality Management system activities on behalf of IACs to ensure compliance with GxP legislation.Provide oversight of Quality Assurance activities for third-party manufacturers, packaging operati
For our client based in Basel and specialized in pharma area, we're looking for a QA Manager - Responsible PersonResponsibilitiesSupport Quality activities in LATAM and MMG operational areas, acting as the Responsible Person for LATAM GmbH and Medical GmbH.Execute Quality Management system activities on behalf of IACs to ensure compliance with GxP legislation.Provide oversight of Quality Assurance activities for third-party manufacturers, packaging operati
We are seeking a detail-oriented and proactive Commissioning and Qualification (C&Q) Engineer to join our team and support the successful execution of equipment and utility system commissioning. In this role, you will play a pivotal role in ensuring that all systems operate to specifications and compliance standards while working in close collaboration with our engineering and project teams. As a Commissioning Engineer, for support and align product and pr
We are seeking a detail-oriented and proactive Commissioning and Qualification (C&Q) Engineer to join our team and support the successful execution of equipment and utility system commissioning. In this role, you will play a pivotal role in ensuring that all systems operate to specifications and compliance standards while working in close collaboration with our engineering and project teams. As a Commissioning Engineer, for support and align product and pr
Für die Welt sorgen … beim Einzelnen beginnen. Dieser Leitsatz inspiriert und vereint die Menschen bei Johnson & Johnson. Die Kultur der Fürsorge steht im Mittelpunkt unserer Unternehmensphilosophie, welche im Credo verankert ist.DePuy Synthes Companies of Johnson & Johnson ist das größte und umfassendste Orthopädie- und Neurologieunternehmen der Welt. DePuy Synthes bietet eine beispiellose Breite und Tiefe unterschiedlicher Technologien, Produkte, Dienstl
Für die Welt sorgen … beim Einzelnen beginnen. Dieser Leitsatz inspiriert und vereint die Menschen bei Johnson & Johnson. Die Kultur der Fürsorge steht im Mittelpunkt unserer Unternehmensphilosophie, welche im Credo verankert ist.DePuy Synthes Companies of Johnson & Johnson ist das größte und umfassendste Orthopädie- und Neurologieunternehmen der Welt. DePuy Synthes bietet eine beispiellose Breite und Tiefe unterschiedlicher Technologien, Produkte, Dienstl
Joining our Manufacturing Department, you will be part of a team of technicians, engineers and scientists specialized in the production and purification of recombinant proteins produced from animal cells.As Support Technician, you will take part in this exciting adventure by supporting the Manufacturing Shared Services in our development and clinical suites.Your role: Support Operational Activities:Be the expert in the processes under our responsibility (r
Joining our Manufacturing Department, you will be part of a team of technicians, engineers and scientists specialized in the production and purification of recombinant proteins produced from animal cells.As Support Technician, you will take part in this exciting adventure by supporting the Manufacturing Shared Services in our development and clinical suites.Your role: Support Operational Activities:Be the expert in the processes under our responsibility (r
An exciting new opportunity has arisen to join us as Quality Assurance Qualification & Validation Engineer for our Biotech drug substance plant in Corsier-sur-Vevey.As an integral member of the Quality Unit, you provide QA expertise for Process Validation and Analytical Validation: You elaborate the qualification/validation strategies, review and approval of protocols and reports, participates to risk analysis, identifies gap and purposes remediation plan
An exciting new opportunity has arisen to join us as Quality Assurance Qualification & Validation Engineer for our Biotech drug substance plant in Corsier-sur-Vevey.As an integral member of the Quality Unit, you provide QA expertise for Process Validation and Analytical Validation: You elaborate the qualification/validation strategies, review and approval of protocols and reports, participates to risk analysis, identifies gap and purposes remediation plan
Für die Welt sorgen … beim Einzelnen beginnen. Dieser Leitsatz inspiriert und vereint die Menschen bei Johnson & Johnson. Die Kultur der Fürsorge steht im Mittelpunkt unserer Unternehmensphilosophie, welche im Credo verankert ist.DePuy Synthes Companies of Johnson & Johnson ist das größte und umfassendste Orthopädie- und Neurologieunternehmen der Welt. DePuy Synthes bietet eine beispiellose Breite und Tiefe unterschiedlicher Technologien, Produkte, Dienstl
Für die Welt sorgen … beim Einzelnen beginnen. Dieser Leitsatz inspiriert und vereint die Menschen bei Johnson & Johnson. Die Kultur der Fürsorge steht im Mittelpunkt unserer Unternehmensphilosophie, welche im Credo verankert ist.DePuy Synthes Companies of Johnson & Johnson ist das größte und umfassendste Orthopädie- und Neurologieunternehmen der Welt. DePuy Synthes bietet eine beispiellose Breite und Tiefe unterschiedlicher Technologien, Produkte, Dienstl
Tasks:Lead and execute medium-sized customer projects and internal projects, ensuring complianceProject planning and technical detailing of gas-insulated switchgear, including preparation of all necessary documents for orders, fabrication, assembly, and customers.Discuss and align technical solutions with customers and internal stakeholders.Manage all technical communication channels, both internally and externally.Oversee project execution and material pr
Tasks:Lead and execute medium-sized customer projects and internal projects, ensuring complianceProject planning and technical detailing of gas-insulated switchgear, including preparation of all necessary documents for orders, fabrication, assembly, and customers.Discuss and align technical solutions with customers and internal stakeholders.Manage all technical communication channels, both internally and externally.Oversee project execution and material pr
We are seeking a motivated and experienced Specialist in HSE Engineering Support to join our team within the industrial production sector. This role is crucial for ensuring safety and compliance in various engineering projects.The Specialist will manage LOTOTO procedures, conduct safety walk-downs and audits, and oversee training management within the HSE Engineering Support team. This is a key position to help us maintain a safe and efficient working envi
We are seeking a motivated and experienced Specialist in HSE Engineering Support to join our team within the industrial production sector. This role is crucial for ensuring safety and compliance in various engineering projects.The Specialist will manage LOTOTO procedures, conduct safety walk-downs and audits, and oversee training management within the HSE Engineering Support team. This is a key position to help us maintain a safe and efficient working envi
Leiter Finanzen mit HR Aufgaben 80 -100% (m/w/d)Berichtslinie: Direkte Berichtslinie an die GeschäftsführungDeine Aufgaben:1. Finanzmanagement:Verantwortung für die gesamte Finanzbuchhaltung, einschließlich Debitoren- und Kreditorenbuchhaltung, Hauptbuch und Anlagenbuchhaltung.Erstellung von Monats-, Quartals- und Jahresabschlüssen gemäß den gesetzlichen und internen Anforderungen.Budgetplanung, -überwachung und -steuerung in enger Abstimmung mit der Gesch
Leiter Finanzen mit HR Aufgaben 80 -100% (m/w/d)Berichtslinie: Direkte Berichtslinie an die GeschäftsführungDeine Aufgaben:1. Finanzmanagement:Verantwortung für die gesamte Finanzbuchhaltung, einschließlich Debitoren- und Kreditorenbuchhaltung, Hauptbuch und Anlagenbuchhaltung.Erstellung von Monats-, Quartals- und Jahresabschlüssen gemäß den gesetzlichen und internen Anforderungen.Budgetplanung, -überwachung und -steuerung in enger Abstimmung mit der Gesch
For our client, a pharmaceutical company based in canton Lucerne, we are looking for a Labelling Coordinator. General Information: Start Date: ASAPDuration: 1 yearExtension: possibleWorkload: 100%Workplace: canton LucerneHome office: up to 2 days/week, but mainly onsite The primary activities include, but are not limited to: Creation of label text translations using a translation database and approval of the translations regarding study-specific, company-i
For our client, a pharmaceutical company based in canton Lucerne, we are looking for a Labelling Coordinator. General Information: Start Date: ASAPDuration: 1 yearExtension: possibleWorkload: 100%Workplace: canton LucerneHome office: up to 2 days/week, but mainly onsite The primary activities include, but are not limited to: Creation of label text translations using a translation database and approval of the translations regarding study-specific, company-i
A leading pharmaceutical company based in Basel is looking for a Senior Software Engineer, with proficiency in at least one programming language (Java or Python preferred).Its a 100% remote position but you have to be based in Switzerland.Tasks & Responsibilities:Create and maintain software for orchestrating cloud infrastructure.Identifying use cases and writing tests (unit tests, integration tests).Deploying cloud infrastructure using terraform.Prepare d
A leading pharmaceutical company based in Basel is looking for a Senior Software Engineer, with proficiency in at least one programming language (Java or Python preferred).Its a 100% remote position but you have to be based in Switzerland.Tasks & Responsibilities:Create and maintain software for orchestrating cloud infrastructure.Identifying use cases and writing tests (unit tests, integration tests).Deploying cloud infrastructure using terraform.Prepare d
For our client, an international biotech company based in Baar, we are looking for a Regulatory Affairs Senior Manager to join the Biosimilars Business Unit. The person will be responsible for leading regulatory affairs activities for assigned projects and programs and for leading affiliate RA to identify and complete national regulatory requirements for assigned projects and programs, to support commercialisation.General Information: Start date: ASAP / 02
For our client, an international biotech company based in Baar, we are looking for a Regulatory Affairs Senior Manager to join the Biosimilars Business Unit. The person will be responsible for leading regulatory affairs activities for assigned projects and programs and for leading affiliate RA to identify and complete national regulatory requirements for assigned projects and programs, to support commercialisation.General Information: Start date: ASAP / 02
We are currently seeking a Validation engineer for one of our clients in Canton of Neuchatel.If you are looking to work in a dynamic and very friendly working environment then this is for you.This is an open-ended temporary contractPlease note this vacancy requires fluency in French. Your responsibilities:Generation and execution of qualification/validation protocols including the generation, routing and approval of summary documentation.Work with project
We are currently seeking a Validation engineer for one of our clients in Canton of Neuchatel.If you are looking to work in a dynamic and very friendly working environment then this is for you.This is an open-ended temporary contractPlease note this vacancy requires fluency in French. Your responsibilities:Generation and execution of qualification/validation protocols including the generation, routing and approval of summary documentation.Work with project