Responsibilities:Lead the implementation of EHS standards and practices throughout the project lifecycle.Collaborate with design teams to ensure safety, environmental, and sustainability aspects are embedded into project designs.Participate in risk assessments, including HAZOP, ATEX, containment, and fire safety evaluations during different project phases (from feasibility to detailed design).Maintain accurate records of basic container data to facilitate
Responsibilities:Lead the implementation of EHS standards and practices throughout the project lifecycle.Collaborate with design teams to ensure safety, environmental, and sustainability aspects are embedded into project designs.Participate in risk assessments, including HAZOP, ATEX, containment, and fire safety evaluations during different project phases (from feasibility to detailed design).Maintain accurate records of basic container data to facilitate
For our client, a pharmaceutical company based in Lucerne, we are looking for a Quality Assurance Specialist. In this role you will be responsible for the oversight and support of certain quality assurance activities in the space of Quality Operations and Compliance.General Information: Start Date: ASAPDuration: 6 months contractExtension: unlikely (maternity cover)Workload: 100%Workplace: Schachen, LuzernHome office: possible in exceptional cases upon dis
For our client, a pharmaceutical company based in Lucerne, we are looking for a Quality Assurance Specialist. In this role you will be responsible for the oversight and support of certain quality assurance activities in the space of Quality Operations and Compliance.General Information: Start Date: ASAPDuration: 6 months contractExtension: unlikely (maternity cover)Workload: 100%Workplace: Schachen, LuzernHome office: possible in exceptional cases upon dis
S'assurez d'être compliant par rapport aux documentations cGMP. Assurez la libération des lots à temps en respectant les indicateurs qualité. Coordonnez le processus de libération des produits avec les différents départements et Contrôle Qualité. Vous serez en charge d'évaluer et clôturer les déviations et identifier les récurrences, donner les requis pour les enquêtes/investigation associées. Définir les actions correctives et préventives (CAPA), propose
S'assurez d'être compliant par rapport aux documentations cGMP. Assurez la libération des lots à temps en respectant les indicateurs qualité. Coordonnez le processus de libération des produits avec les différents départements et Contrôle Qualité. Vous serez en charge d'évaluer et clôturer les déviations et identifier les récurrences, donner les requis pour les enquêtes/investigation associées. Définir les actions correctives et préventives (CAPA), propose
Location: Bulle, SwitzerlandActivity rate : 100%Type of contract: Temporary contractStart Date: 01.02.2025End Date: 31.12.2025 (with a potential extension) Are you passionate about ensuring the reliability and compliance of equipment in the pharmaceutical industry? We're looking for a meticulous Qualification Specialist to take the lead in qualifying GMP installations, equipment, and utilities. Key responsibilities:Define the global qualification strategyL
Location: Bulle, SwitzerlandActivity rate : 100%Type of contract: Temporary contractStart Date: 01.02.2025End Date: 31.12.2025 (with a potential extension) Are you passionate about ensuring the reliability and compliance of equipment in the pharmaceutical industry? We're looking for a meticulous Qualification Specialist to take the lead in qualifying GMP installations, equipment, and utilities. Key responsibilities:Define the global qualification strategyL
Exportspecialist m/f/d (100%)Für ab Sofort suchen wir für einen Exportspecialist für ein internationales Energieunternehemen für Sitz in Turgi, AG das weltweit für seine innovativen und qualitativ hochwertigen Produkte bekannt ist.Aufgaben:Organisation und Überwachung weltweiter Transporte (Luft, See, Straße, Kurier)Versand von Reparatur- und Austauschlieferungen sowie Gefahrgut und MessematerialEinholen und Bewerten von Transportofferten, Auswahl der Sped
Exportspecialist m/f/d (100%)Für ab Sofort suchen wir für einen Exportspecialist für ein internationales Energieunternehemen für Sitz in Turgi, AG das weltweit für seine innovativen und qualitativ hochwertigen Produkte bekannt ist.Aufgaben:Organisation und Überwachung weltweiter Transporte (Luft, See, Straße, Kurier)Versand von Reparatur- und Austauschlieferungen sowie Gefahrgut und MessematerialEinholen und Bewerten von Transportofferten, Auswahl der Sped
Nous recherchons pour notre client Merck un.e Compliance Production Specialist, pour une mission d'une durée de 12 mois. Vos Missions: Assurer la gestion des déviations, CAPA, Change Control liés à l'activité aseptique.Prend en charge la rédaction de l'ensemble de la documentation liée aux activités aseptiques.Prend en charge les observations en chambre liées au comportement aseptique des opérateurs de production.Support production de l'ensemble du départe
Nous recherchons pour notre client Merck un.e Compliance Production Specialist, pour une mission d'une durée de 12 mois. Vos Missions: Assurer la gestion des déviations, CAPA, Change Control liés à l'activité aseptique.Prend en charge la rédaction de l'ensemble de la documentation liée aux activités aseptiques.Prend en charge les observations en chambre liées au comportement aseptique des opérateurs de production.Support production de l'ensemble du départe
For Lonza in Visp Randstad (Switzerland) AG is looking for a CQV Specialist for 8 months (July 2025) Job description:Oversee facilities, utilities, validation lifecycle, technical documentation, and processes, including GAP analysis and risk assessmentDevelop and manage validation documentation (URS, DQ, FMEA, FAT, SAT, IQ, IOQ, OQ, PQ)Execute validation protocols (IQ/OQ/PQ) for equipment, systems, and utilitiesPrepare detailed reports on validation activi
For Lonza in Visp Randstad (Switzerland) AG is looking for a CQV Specialist for 8 months (July 2025) Job description:Oversee facilities, utilities, validation lifecycle, technical documentation, and processes, including GAP analysis and risk assessmentDevelop and manage validation documentation (URS, DQ, FMEA, FAT, SAT, IQ, IOQ, OQ, PQ)Execute validation protocols (IQ/OQ/PQ) for equipment, systems, and utilitiesPrepare detailed reports on validation activi
Lieu: Bulle, SwitzerlandTaux d'activité : 100%Type de contrat: contrat temporaireDate de début: 03.02.2025Date de fin: 31.12.2025 Nous recherchons un(e) Bio DS Manufacturing Specialist, expert(e) en procédés biotechnologiques, pour accompagner nos activités de production. Votre mission : garantir la conformité qualité (GMP), améliorer la sécurité, optimiser les coûts et la fiabilité des processus, tout en respectant nos engagements (délais, satisfaction cl
Lieu: Bulle, SwitzerlandTaux d'activité : 100%Type de contrat: contrat temporaireDate de début: 03.02.2025Date de fin: 31.12.2025 Nous recherchons un(e) Bio DS Manufacturing Specialist, expert(e) en procédés biotechnologiques, pour accompagner nos activités de production. Votre mission : garantir la conformité qualité (GMP), améliorer la sécurité, optimiser les coûts et la fiabilité des processus, tout en respectant nos engagements (délais, satisfaction cl
We are seeking an enthusiastic and hands-on Junior IT Onsite Support Specialist to play an important role in the deployment and scaling of modern workplace technologies. This position is ideal for someone at the beginning of their IT career, eager to work with the latest IT hardware and conferencing solution Microsoft Teams Rooms (MTR). The ideal candidate will actively participate in modernizing user workplaces and meeting rooms, while providing support t
We are seeking an enthusiastic and hands-on Junior IT Onsite Support Specialist to play an important role in the deployment and scaling of modern workplace technologies. This position is ideal for someone at the beginning of their IT career, eager to work with the latest IT hardware and conferencing solution Microsoft Teams Rooms (MTR). The ideal candidate will actively participate in modernizing user workplaces and meeting rooms, while providing support t
TON RÔLE :En tant que membre de l'équipe QC Projet & Equipement, tu participeras à la mise en place de nouveaux équipements, en suivant les flux de qualification interne (IQ,OQ,PQ). Ces qualifications incluent une partie importante de CSV, pour garantir le respect de la data integrity.Ton rôle est de conduire notre évolution vers une automatisation accrue et un laboratoire de pointe par la qualification et la validation de nouveaux équipements et systèmes
TON RÔLE :En tant que membre de l'équipe QC Projet & Equipement, tu participeras à la mise en place de nouveaux équipements, en suivant les flux de qualification interne (IQ,OQ,PQ). Ces qualifications incluent une partie importante de CSV, pour garantir le respect de la data integrity.Ton rôle est de conduire notre évolution vers une automatisation accrue et un laboratoire de pointe par la qualification et la validation de nouveaux équipements et systèmes
• Define and implement Belimo's EPD program and build up internal knowledge/ competence in developing LCAs/EPDs, using state-of-art LCA software• Conceptualize the EPD program, define and implement the initial setup including processes, templates and LCA software, and manage operational execution with focus on region EMEA• Perform LCAs and develop EPDs according to established ISO and EN standards• Act as interface to internal LCA/EPD contributors and exte
• Define and implement Belimo's EPD program and build up internal knowledge/ competence in developing LCAs/EPDs, using state-of-art LCA software• Conceptualize the EPD program, define and implement the initial setup including processes, templates and LCA software, and manage operational execution with focus on region EMEA• Perform LCAs and develop EPDs according to established ISO and EN standards• Act as interface to internal LCA/EPD contributors and exte
Wir suchen einen spezialisierten Administration Spezialist, der das Team unseres Kunden in der Region Lupfig AG verstärkt und an der Verantwortung für die gesamte Administrationsabläufe teilhaben möchte. Administration Spezialist FR 100% (m/w/d)Als Sachbearbeiter Administration werden Sie aktiv an der Unterstützung bei Abwicklungen von sämtlichen Trainings und Qualifizierungsprogramme beteiligt sein. Ihre Hauptaufgaben umfassen:Die gesamte Betreuung von St
Wir suchen einen spezialisierten Administration Spezialist, der das Team unseres Kunden in der Region Lupfig AG verstärkt und an der Verantwortung für die gesamte Administrationsabläufe teilhaben möchte. Administration Spezialist FR 100% (m/w/d)Als Sachbearbeiter Administration werden Sie aktiv an der Unterstützung bei Abwicklungen von sämtlichen Trainings und Qualifizierungsprogramme beteiligt sein. Ihre Hauptaufgaben umfassen:Die gesamte Betreuung von St
Wir suchen einen spezialisierten Administration Spezialist, der das Team unseres Kunden in der Region Lupfig AG verstärkt und an der Verantwortung für die gesamte Administrationsabläufe teilhaben möchte. Administration Spezialist IT 100% (m/w/d)Als Sachbearbeiter Administration werden Sie aktiv an der Unterstützung bei Abwicklungen von sämtlichen Trainings und Qualifizierungsprogramme beteiligt sein. Ihre Hauptaufgaben umfassen:Die gesamte Betreuung von St
Wir suchen einen spezialisierten Administration Spezialist, der das Team unseres Kunden in der Region Lupfig AG verstärkt und an der Verantwortung für die gesamte Administrationsabläufe teilhaben möchte. Administration Spezialist IT 100% (m/w/d)Als Sachbearbeiter Administration werden Sie aktiv an der Unterstützung bei Abwicklungen von sämtlichen Trainings und Qualifizierungsprogramme beteiligt sein. Ihre Hauptaufgaben umfassen:Die gesamte Betreuung von St
Location: Bulle, SwitzerlandActivity rate : 100%Type of contract: Temporary contract (6 months)Start Date: ASAP The Bio DS Local Quality Specialist works closely with both local and global teams to promote high-quality standards and ensure their integration into operations. This role involves overseeing product documentation to ensure full product knowledge and implementing improvements in response to business needs, operational excellence, quality, or reg
Location: Bulle, SwitzerlandActivity rate : 100%Type of contract: Temporary contract (6 months)Start Date: ASAP The Bio DS Local Quality Specialist works closely with both local and global teams to promote high-quality standards and ensure their integration into operations. This role involves overseeing product documentation to ensure full product knowledge and implementing improvements in response to business needs, operational excellence, quality, or reg
Für die Welt sorgen … beim Einzelnen beginnen. Dieser Leitsatz inspiriert und eint die Menschen bei Johnson & Johnson. Die Kultur der Fürsorge steht im Mittelpunkt unserer Unternehmensphilosophie, welche im Credo verankert ist.Johnson & Johnson ist ein internationales Produktionsunternehmen und stellt an seinem Produktionsstandort in Schaffhausen pharmazeutische und medizintechnische Produkte sowie chemische Wirkstoffe (APIs) für die globalen Märkte her. D
Für die Welt sorgen … beim Einzelnen beginnen. Dieser Leitsatz inspiriert und eint die Menschen bei Johnson & Johnson. Die Kultur der Fürsorge steht im Mittelpunkt unserer Unternehmensphilosophie, welche im Credo verankert ist.Johnson & Johnson ist ein internationales Produktionsunternehmen und stellt an seinem Produktionsstandort in Schaffhausen pharmazeutische und medizintechnische Produkte sowie chemische Wirkstoffe (APIs) für die globalen Märkte her. D
As part of the QC Project & Equipment team , your will be able:To coordinate QC activities related to outsourcing Technology transfer and/or routine analytical activities .To ensure that all QC testing related to Tech Transfert are performed according to the established plan, good manufacturing practices, registration product files and site quality standards.To ensure that the documentation linked to the validation is done according to defined planning to
As part of the QC Project & Equipment team , your will be able:To coordinate QC activities related to outsourcing Technology transfer and/or routine analytical activities .To ensure that all QC testing related to Tech Transfert are performed according to the established plan, good manufacturing practices, registration product files and site quality standards.To ensure that the documentation linked to the validation is done according to defined planning to
Location: Bulle, SwitzerlandActivity rate : 100%Type of contract: Temporary contract (12 months)Start Date: ASAP The Quality Specialist is responsible for ensuring product delivery compliance with national and international regulations, while supporting operational excellence and quality improvements. This role involves managing quality processes, including deviations, CAPAs, change controls, and validations, to meet UCB's high standards in Security, Quali
Location: Bulle, SwitzerlandActivity rate : 100%Type of contract: Temporary contract (12 months)Start Date: ASAP The Quality Specialist is responsible for ensuring product delivery compliance with national and international regulations, while supporting operational excellence and quality improvements. This role involves managing quality processes, including deviations, CAPAs, change controls, and validations, to meet UCB's high standards in Security, Quali
No sponsorships for non-EU candidatesBist Du bereit für eine neue Herausforderung? In dieser interessanten Position arbeitest Du bei einem führenden IT-Beratungsunternehmen. Einsatz: ab sofortDauer: 12 Monate (mit Option auf Verlängerung)Arbeitsort: Zürich, Aargau oder Bern Dein Profil:Joblevel auf Senior Fachlevel oder ExpertAusgewiesene Fachkraft im Bereich Weiterentwicklung von ITSM und ITFM Lösungen und weiteren Modulen mit mehr als 5 Jahren Erfahrung
No sponsorships for non-EU candidatesBist Du bereit für eine neue Herausforderung? In dieser interessanten Position arbeitest Du bei einem führenden IT-Beratungsunternehmen. Einsatz: ab sofortDauer: 12 Monate (mit Option auf Verlängerung)Arbeitsort: Zürich, Aargau oder Bern Dein Profil:Joblevel auf Senior Fachlevel oder ExpertAusgewiesene Fachkraft im Bereich Weiterentwicklung von ITSM und ITFM Lösungen und weiteren Modulen mit mehr als 5 Jahren Erfahrung
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 the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 260 operating companies in more than 60 countr
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 the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 260 operating companies in more than 60 countr
For one of our clients, we are looking for a Quality Control Specialist with expertise in risk analysis and GxP environments. Background:The Quality Control team focuses on testing direct materials delivered by manufacturers, including primary and secondary packaging materials and medical devices. This role ensures that packaging materials such as folding cartons, syringes, and auto-injectors meet the highest standards before being used in packaging, devel
For one of our clients, we are looking for a Quality Control Specialist with expertise in risk analysis and GxP environments. Background:The Quality Control team focuses on testing direct materials delivered by manufacturers, including primary and secondary packaging materials and medical devices. This role ensures that packaging materials such as folding cartons, syringes, and auto-injectors meet the highest standards before being used in packaging, devel
For our client Merck in Corsier-sur-Vevey, we are looking for an MSAT Process Specialist for a period of 6 months.Your role:Within the MSAT (Manufacturing Sciences And Technology) team, you support our GMP manufacturing USP and DSP processes in order to increase productivity and quality thanks to the continuous monitoring of our products, troubleshooting, investigations, process and cleaning validation. You foster a strong and positive collaboration with t
For our client Merck in Corsier-sur-Vevey, we are looking for an MSAT Process Specialist for a period of 6 months.Your role:Within the MSAT (Manufacturing Sciences And Technology) team, you support our GMP manufacturing USP and DSP processes in order to increase productivity and quality thanks to the continuous monitoring of our products, troubleshooting, investigations, process and cleaning validation. You foster a strong and positive collaboration with t
For one of our Clients, a medical diagnostics company, we are looking for a motivated Product Quality Engineer to join the PQE Production Engineering Team.The team focuses on all aspects of product quality from the supplier through assembly to the testing process. This includes, among other things, the creation of the test concept, derivation of the test procedures, coordination of the test methods and the definition of test-relevant parameters. Our PQEs a
For one of our Clients, a medical diagnostics company, we are looking for a motivated Product Quality Engineer to join the PQE Production Engineering Team.The team focuses on all aspects of product quality from the supplier through assembly to the testing process. This includes, among other things, the creation of the test concept, derivation of the test procedures, coordination of the test methods and the definition of test-relevant parameters. Our PQEs a