For one of our clients, a global manufacturing company specialized in the life sciences sector, we are looking for a Manufacturing Engineer based in the canton of Fribourg. The Manufacturing Science and Technology (MSAT) Engineer will lead technology transfer efforts, support manufacturing processes and products, and contribute to overall technical improvements. Your Impact:Contribute to technical transfer projects to establish robust and compliant manufa
For one of our clients, a global manufacturing company specialized in the life sciences sector, we are looking for a Manufacturing Engineer based in the canton of Fribourg. The Manufacturing Science and Technology (MSAT) Engineer will lead technology transfer efforts, support manufacturing processes and products, and contribute to overall technical improvements. Your Impact:Contribute to technical transfer projects to establish robust and compliant manufa
We are looking for a Complaint Engineer 100% for one of our clients in the canton of Neuchatel.If you want to work in a nice and dynamic environment in the medical devices industry then this position is made for you ! Contract type: open-ended temporary contractPlease note this position requires fluency in English and French. Your responsibilities:Manage complaint investigation: communication with intake service, decontamination process, complaint investig
We are looking for a Complaint Engineer 100% for one of our clients in the canton of Neuchatel.If you want to work in a nice and dynamic environment in the medical devices industry then this position is made for you ! Contract type: open-ended temporary contractPlease note this position requires fluency in English and French. Your responsibilities:Manage complaint investigation: communication with intake service, decontamination process, complaint investig
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
For our client in Berne we are looking for a CQV Engineer for a pharma/biotech company:Location: Berne Contract: limited contractDuration: 1 year The CQV Engineer is responsible for planning and executing Commissioning & Qualification (C&Q) activities to ensure project milestones are met. Key responsibilities include:Overseeing commissioning and qualification processes to meet project deadlines.Preparing, executing, and obtaining approval for Design Quali
For our client in Berne we are looking for a CQV Engineer for a pharma/biotech company:Location: Berne Contract: limited contractDuration: 1 year The CQV Engineer is responsible for planning and executing Commissioning & Qualification (C&Q) activities to ensure project milestones are met. Key responsibilities include:Overseeing commissioning and qualification processes to meet project deadlines.Preparing, executing, and obtaining approval for Design Quali
Du liebst Technik und Kundenkontakt? In dieser Rolle sorgst du weltweit für erstklassigen Support, erstellst wichtige technische Dokumentationen und führst Schulungen durch. Wenn du eine technische Ausbildung hast und gerne im internationalen Umfeld arbeitest, bist du hier genau richtig!AufagabenSicherstellen des globalen technischen Supports für Distributoren, Tochtergesellschaften und EndkundenBearbeiten von technischen Kundenanfragen und BeanstandungenK
Du liebst Technik und Kundenkontakt? In dieser Rolle sorgst du weltweit für erstklassigen Support, erstellst wichtige technische Dokumentationen und führst Schulungen durch. Wenn du eine technische Ausbildung hast und gerne im internationalen Umfeld arbeitest, bist du hier genau richtig!AufagabenSicherstellen des globalen technischen Supports für Distributoren, Tochtergesellschaften und EndkundenBearbeiten von technischen Kundenanfragen und BeanstandungenK
Über die PositionWir suchen einen erfahrenen Glasbläser (m/w/d) für unser Produktionsteam im Raum St. Gallen. In dieser Rolle sind Sie für die Herstellung und Montage spezialisierter Glaskomponenten für hochwertige Laborgeräte verantwortlich. Diese Position bietet eine spannende Gelegenheit für eine qualifizierte Fachkraft mit Leidenschaft für präzises Handwerk in einem High-Tech-Umfeld.Ihre AufgabenHerstellung, Formung und Montage maßgeschneiderter Glasko
Über die PositionWir suchen einen erfahrenen Glasbläser (m/w/d) für unser Produktionsteam im Raum St. Gallen. In dieser Rolle sind Sie für die Herstellung und Montage spezialisierter Glaskomponenten für hochwertige Laborgeräte verantwortlich. Diese Position bietet eine spannende Gelegenheit für eine qualifizierte Fachkraft mit Leidenschaft für präzises Handwerk in einem High-Tech-Umfeld.Ihre AufgabenHerstellung, Formung und Montage maßgeschneiderter Glasko
On behalf of our client, we are looking for a QS Analyst (Training & Document Control) for a temporary contract of 6 months (extension unlikely). Location: Le LocleContract: Temporary – 6 monthsAvailability: ASAP or with maximum 1-month noticeLanguages: French and English fluency required Responsibilities:Manage and maintain the electronic training system (assignment, data entry)Support the maintenance of the document control systemManage circulation of do
On behalf of our client, we are looking for a QS Analyst (Training & Document Control) for a temporary contract of 6 months (extension unlikely). Location: Le LocleContract: Temporary – 6 monthsAvailability: ASAP or with maximum 1-month noticeLanguages: French and English fluency required Responsibilities:Manage and maintain the electronic training system (assignment, data entry)Support the maintenance of the document control systemManage circulation of do
For our client, we are looking for a Lead Counsel – Divestments & CMB to support the Global Manufacturing, Supply & Global Quality Legal (GMSGQ) team, with a focus on Divestments and Contract Manufacturing Business (CMB). This role involves providing strategic legal advice, leading M&A transactions, managing high-value and complex contracts, and contributing to global legal initiatives within the manufacturing and quality sector. Location: Zurich, Switzerl
For our client, we are looking for a Lead Counsel – Divestments & CMB to support the Global Manufacturing, Supply & Global Quality Legal (GMSGQ) team, with a focus on Divestments and Contract Manufacturing Business (CMB). This role involves providing strategic legal advice, leading M&A transactions, managing high-value and complex contracts, and contributing to global legal initiatives within the manufacturing and quality sector. Location: Zurich, Switzerl
Lieu : Orbe, SuisseEntité : Nestlé Product & Technology Center ? CoffeeTaux d'activité : 50%Type de contrat : Contrat temporaire, 1 anEntrée en fonction souhaitée : dès que possibleEn tant que Panel Leader & Technicien·ne Analyse Sensorielle R&D, vous serez responsable d'assister le spécialiste de l'expérience sensorielle dans tous les aspects pratiques des tests sensoriels, en veillant au respect des meilleures pratiques du laboratoire sensoriel. Cela com
Lieu : Orbe, SuisseEntité : Nestlé Product & Technology Center ? CoffeeTaux d'activité : 50%Type de contrat : Contrat temporaire, 1 anEntrée en fonction souhaitée : dès que possibleEn tant que Panel Leader & Technicien·ne Analyse Sensorielle R&D, vous serez responsable d'assister le spécialiste de l'expérience sensorielle dans tous les aspects pratiques des tests sensoriels, en veillant au respect des meilleures pratiques du laboratoire sensoriel. Cela com
Pour notre client basé dans le canton de Vaud, nous recherchons un ou une Laborant(e) chimie LC-MSMS.Poste : PermanentLocalisation : LausanneTaux d'activité : 100% Responsabilités Préparation d’échantillons pour analyses chromatographiques (SPE, dérivatisation, purification...)Analyses instrumentales de routine par LC-MSMS en suivant les protocoles validésMaintenance des instruments, spécifiquement AgilentProfil CFC ou équivalence en chimie analytiqueExpér
Pour notre client basé dans le canton de Vaud, nous recherchons un ou une Laborant(e) chimie LC-MSMS.Poste : PermanentLocalisation : LausanneTaux d'activité : 100% Responsabilités Préparation d’échantillons pour analyses chromatographiques (SPE, dérivatisation, purification...)Analyses instrumentales de routine par LC-MSMS en suivant les protocoles validésMaintenance des instruments, spécifiquement AgilentProfil CFC ou équivalence en chimie analytiqueExpér
Unser Kunde ist ein modernes und innovatives pharmazeutisches Dienstleistungsunternehmen, welches sich in der Arzneimittel-Versorgung spezialisiert hat. Zur Unterstützung des mikrobiologischen Labors suchen wir eine/n:Laborant/in Mikrobiologie - 80% (m/w/d)Aufgaben: Bestimmung von Keimzahlen, Sterilitätsprüfungen und Test auf BakterienendotoxineBeprobung von Reinräumen (Wasser, Oberflächen, Luft) und Durchführung der zugehörigen PrüfungenÜberprüfung von Nä
Unser Kunde ist ein modernes und innovatives pharmazeutisches Dienstleistungsunternehmen, welches sich in der Arzneimittel-Versorgung spezialisiert hat. Zur Unterstützung des mikrobiologischen Labors suchen wir eine/n:Laborant/in Mikrobiologie - 80% (m/w/d)Aufgaben: Bestimmung von Keimzahlen, Sterilitätsprüfungen und Test auf BakterienendotoxineBeprobung von Reinräumen (Wasser, Oberflächen, Luft) und Durchführung der zugehörigen PrüfungenÜberprüfung von Nä
Lieu: Vers-chez-les-BlancTaux d'activité: 50%Durée de mission: jusqu'au 31.12.25Responsabilités : Préparer les réactifs, les tubes, les étiquettes, les échantillons et autres pour les expériences. Apprendre sur la réalisation des essais d'acidification des aliments et de digestion statique in vitro auprès des membres de l'équipe senior et réaliser les essais de manière autonome. Traiter la fraction digérée pour l'analyse en aval Documenter et rapporter les
Lieu: Vers-chez-les-BlancTaux d'activité: 50%Durée de mission: jusqu'au 31.12.25Responsabilités : Préparer les réactifs, les tubes, les étiquettes, les échantillons et autres pour les expériences. Apprendre sur la réalisation des essais d'acidification des aliments et de digestion statique in vitro auprès des membres de l'équipe senior et réaliser les essais de manière autonome. Traiter la fraction digérée pour l'analyse en aval Documenter et rapporter les
For one of our clients, a global leading contract manufacturer for medical devices, we are looking for a Microelectronics Business Development Manager - DACH region. (Need to be fluent in German & English, French is a plus) Your Tasks: As Microelectronics Business Development Manager - DACH region, you will play a key role in developing strategic partnerships and establishing relationships with appropriate Customers. Your main tasks will include: Act as t
For one of our clients, a global leading contract manufacturer for medical devices, we are looking for a Microelectronics Business Development Manager - DACH region. (Need to be fluent in German & English, French is a plus) Your Tasks: As Microelectronics Business Development Manager - DACH region, you will play a key role in developing strategic partnerships and establishing relationships with appropriate Customers. Your main tasks will include: Act as t
Nous recherchons un/e Manufacturing engineer pour un de nos clients sur le canton de Neuchâtel.Si vous souhaitez travailler dans une atmosphère agréable et dynamique dans le domaine des dispositifs médicaux ce poste est pour vous. Il s’agit d’un contrat temporaire à durée illimitée. Vos responsabilités: Participe aux cellules de production en tant que responsable Manufacturing engineering et supporte le business pour toute contribution technique clé.Fourn
Nous recherchons un/e Manufacturing engineer pour un de nos clients sur le canton de Neuchâtel.Si vous souhaitez travailler dans une atmosphère agréable et dynamique dans le domaine des dispositifs médicaux ce poste est pour vous. Il s’agit d’un contrat temporaire à durée illimitée. Vos responsabilités: Participe aux cellules de production en tant que responsable Manufacturing engineering et supporte le business pour toute contribution technique clé.Fourn
Für unseren Kunden, ein führendes internationales Pharmaunternehmen, suchen wir eine/n engagierte/n Laborspezialist/-in in der biotechnologischen Wirkstoffproduktion.Allgemeine Informationen:Startdatum: 15.04.2025Spätestmögliches Startdatum: 01.05.2025Geplante Dauer der Anstellung: 10 Monate, mit Möglichkeit auf VerlängerungArbeitsplatz: BaselWorkload: 80%Team: ca. 20 PersonenDepartment: Manufacturing Technology & Support (MMMGM)Fixe Arbeitszeiten: JaÜber
Für unseren Kunden, ein führendes internationales Pharmaunternehmen, suchen wir eine/n engagierte/n Laborspezialist/-in in der biotechnologischen Wirkstoffproduktion.Allgemeine Informationen:Startdatum: 15.04.2025Spätestmögliches Startdatum: 01.05.2025Geplante Dauer der Anstellung: 10 Monate, mit Möglichkeit auf VerlängerungArbeitsplatz: BaselWorkload: 80%Team: ca. 20 PersonenDepartment: Manufacturing Technology & Support (MMMGM)Fixe Arbeitszeiten: JaÜber
Title: Quality SpecialistLocation: Visp, Valais, Switzerland (On-site)We are looking for a Quality Specialist with experience in deviation investigations and CAPA management within a GMP-regulated environment – ideally with strong knowledge of processes related to monoclonal antibodies.This role is critical to ensuring regulatory compliance, preventing recurring issues, and strengthening the quality system through effective corrective and preventive action
Title: Quality SpecialistLocation: Visp, Valais, Switzerland (On-site)We are looking for a Quality Specialist with experience in deviation investigations and CAPA management within a GMP-regulated environment – ideally with strong knowledge of processes related to monoclonal antibodies.This role is critical to ensuring regulatory compliance, preventing recurring issues, and strengthening the quality system through effective corrective and preventive action
On behalf of our client, we are looking for a QA Validation Expert to support validation activities in a GMP-compliant pharmaceutical environment. The selected candidate will play a key role in ensuring regulatory compliance and quality oversight of processes and equipment, working in close collaboration with technical departments to support ongoing and upcoming validation projects. Location: Neuchâtel, SwitzerlandContract Duration: 07/04/2025 – 31/05/2025
On behalf of our client, we are looking for a QA Validation Expert to support validation activities in a GMP-compliant pharmaceutical environment. The selected candidate will play a key role in ensuring regulatory compliance and quality oversight of processes and equipment, working in close collaboration with technical departments to support ongoing and upcoming validation projects. Location: Neuchâtel, SwitzerlandContract Duration: 07/04/2025 – 31/05/2025
For one of our client, a global pharmaceutical company, based in Canton of Vaud, we are looking for a Medical Science Liaison - Oncology (MSL). (Fluency in English & French, B2 German required) Your Tasks: As Medical Science Liaison, you will act as a scientific expert, engaging with healthcare professionals and key opinion leaders (KOLs) to exchange insights, support medical strategy.You will play a critical role in bridging scientific expertise with clin
For one of our client, a global pharmaceutical company, based in Canton of Vaud, we are looking for a Medical Science Liaison - Oncology (MSL). (Fluency in English & French, B2 German required) Your Tasks: As Medical Science Liaison, you will act as a scientific expert, engaging with healthcare professionals and key opinion leaders (KOLs) to exchange insights, support medical strategy.You will play a critical role in bridging scientific expertise with clin
We are currently seeking a Quality engineer for one of our clients in Canton of Neuchatel.If you are looking to work in a dynamic and very friendly working environment and in the medical devices sector then this is for you.This is an open ended temporary contract.Please note this vacancy requires fluency in French. Your responsibilities:Ensures that adequate Quality support is provided to productions and to open projects /initiativesEnsures that Non Confor
We are currently seeking a Quality engineer for one of our clients in Canton of Neuchatel.If you are looking to work in a dynamic and very friendly working environment and in the medical devices sector then this is for you.This is an open ended temporary contract.Please note this vacancy requires fluency in French. Your responsibilities:Ensures that adequate Quality support is provided to productions and to open projects /initiativesEnsures that Non Confor
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.Die Cilag AG ist ein internationales Produktionsunternehmen der Pharmasparte des Johnson & Johnson Konzerns und stellt an ihrem Produktionsstandort in Schaffhausen pharmazeutische und medizintechnische Produkte sowie chemische Wirkstof
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.Die Cilag AG ist ein internationales Produktionsunternehmen der Pharmasparte des Johnson & Johnson Konzerns und stellt an ihrem Produktionsstandort in Schaffhausen pharmazeutische und medizintechnische Produkte sowie chemische Wirkstof
Strategic Account Manager – Switzerland – Substitution Therapy2 permanents positions openBased in : Switzerland Department: SalesReports to: Country Lead SwitzerlandLanguages : German or French (native) + English (mandatory) About the RoleAs a Strategic Account Manager, you will be responsible for developing long-term partnerships with key stakeholders in the field of substitution therapy in Switzerland. Your role will be to build strong networks, engage w
Strategic Account Manager – Switzerland – Substitution Therapy2 permanents positions openBased in : Switzerland Department: SalesReports to: Country Lead SwitzerlandLanguages : German or French (native) + English (mandatory) About the RoleAs a Strategic Account Manager, you will be responsible for developing long-term partnerships with key stakeholders in the field of substitution therapy in Switzerland. Your role will be to build strong networks, engage w
Randstad is looking, for an Analytical Chemistry Specialist with experience in peptides and drug substance analytics. If you have a strong technical background in this area and want to work for a leading company in the sector, this opportunity is for you. Responsibilities: Conduct analysis and characterization of peptides using various analytical techniques.Ensure that all critical analytical parameters for peptides — such as purity, identity, and content
Randstad is looking, for an Analytical Chemistry Specialist with experience in peptides and drug substance analytics. If you have a strong technical background in this area and want to work for a leading company in the sector, this opportunity is for you. Responsibilities: Conduct analysis and characterization of peptides using various analytical techniques.Ensure that all critical analytical parameters for peptides — such as purity, identity, and content
Pour notre client Merck à Aubonne, nous sommes actuellement à la recherche d'un/une Compliance Specialist pour une durée de 12 mois.Le specialist compliance assure la compliance au sein de l’équipe compliance MOS, en respectant les cGMPs, et en s’assurant de la conformité des productions. Ce rôle est un poste clé dans l’équipe pour maintenir les exigences qualité en participant à la revue des dossier de production et aux déviations, CAPAs associés.Votre rô
Pour notre client Merck à Aubonne, nous sommes actuellement à la recherche d'un/une Compliance Specialist pour une durée de 12 mois.Le specialist compliance assure la compliance au sein de l’équipe compliance MOS, en respectant les cGMPs, et en s’assurant de la conformité des productions. Ce rôle est un poste clé dans l’équipe pour maintenir les exigences qualité en participant à la revue des dossier de production et aux déviations, CAPAs associés.Votre rô