For one of our clients, a global pioneer in pharmaceuticals, we are currently looking for a Quality Control Analyst.General Information:Start date: asapDuration: 2 years with the possibility of extensionWorkplace: Kaiseraugst Workload: 100%Remote/Home Office: possible, 2 daysWorking hours: StandardDepartment: MMQIAB8R - Unit QC Master Data (MMQIAB8R)Team: 9 peopleAbout the job:The newly formed “ QC Digital Backbone - Master Data Management” team in the QC
For one of our clients, a global pioneer in pharmaceuticals, we are currently looking for a Quality Control Analyst.General Information:Start date: asapDuration: 2 years with the possibility of extensionWorkplace: Kaiseraugst Workload: 100%Remote/Home Office: possible, 2 daysWorking hours: StandardDepartment: MMQIAB8R - Unit QC Master Data (MMQIAB8R)Team: 9 peopleAbout the job:The newly formed “ QC Digital Backbone - Master Data Management” team in the QC
Nous recherchons un/e Quality Control Analyst pour un de nos clients de l’industrie pharmaceutique.Localisation: NeuchatelDémarrage: 1er DécembreContrat temporaire de 6 moisVous apportez une expérience solide de laboratoire, y compris des méthodes biochimiques telles que ELISA, activité enzymatique, Western Blot, HPLC ou autre. Nous privilégions un environnement de proximité et détendu. Le travail s’effectue au sein d'une équipe où les tâches changent
Nous recherchons un/e Quality Control Analyst pour un de nos clients de l’industrie pharmaceutique.Localisation: NeuchatelDémarrage: 1er DécembreContrat temporaire de 6 moisVous apportez une expérience solide de laboratoire, y compris des méthodes biochimiques telles que ELISA, activité enzymatique, Western Blot, HPLC ou autre. Nous privilégions un environnement de proximité et détendu. Le travail s’effectue au sein d'une équipe où les tâches changent
For one of our clients, a global pioneer in pharmaceuticals, we are currently looking for a Laboratory Technician in microbiological quality control.General Information: Start date: 01.01.2026Duration: 1 year with the possibility of extensionWorkplace: KaiseraugstWorkload: 75%Working hours: Standard during the day - flexible working hours as part of everyday laboratory workDepartment: QC Microbiology Kaiseraugst / BaselAbout the job:The “Microbiology
For one of our clients, a global pioneer in pharmaceuticals, we are currently looking for a Laboratory Technician in microbiological quality control.General Information: Start date: 01.01.2026Duration: 1 year with the possibility of extensionWorkplace: KaiseraugstWorkload: 75%Working hours: Standard during the day - flexible working hours as part of everyday laboratory workDepartment: QC Microbiology Kaiseraugst / BaselAbout the job:The “Microbiology
Do you excel at precision and possess an unwavering attention to detail? We invite you to contribute your expertise to the team, leveraging cutting-edge metrology to uphold the highest quality benchmarks for our client's products. Core ResponsibilitiesAs the Quality Specialist, you will be the gatekeeper for component excellence, ensuring strict adherence to specifications:Lead the dimensional and visual verification of incoming materials and
Do you excel at precision and possess an unwavering attention to detail? We invite you to contribute your expertise to the team, leveraging cutting-edge metrology to uphold the highest quality benchmarks for our client's products. Core ResponsibilitiesAs the Quality Specialist, you will be the gatekeeper for component excellence, ensuring strict adherence to specifications:Lead the dimensional and visual verification of incoming materials and
On behalf of our client, we are looking for a QS Analyst (Training & Document Control). Contract: Temporary unlimitedLocation: Le LocleHome office: max 1 day per weekAvailability: ASAP or with maximum 1-month noticeLanguages: French and English fluency requiredResponsibilities:Manage and maintain the electronic training system (assignment, data entry)Support the maintenance of the document control systemManage circulation of documents for approvalReview
On behalf of our client, we are looking for a QS Analyst (Training & Document Control). Contract: Temporary unlimitedLocation: Le LocleHome office: max 1 day per weekAvailability: ASAP or with maximum 1-month noticeLanguages: French and English fluency requiredResponsibilities:Manage and maintain the electronic training system (assignment, data entry)Support the maintenance of the document control systemManage circulation of documents for approvalReview
For our client, an international company based in Klingnau, Aargau, we are looking for a dedicated Quality & OpEx Engineer 80 – 100% (f/m/d). General Information: Location: Klingnau, AargauStart Date: ASAPDuration: permanentWorking Hours: 80- 100% Your Responsibilities: Oversee product and service quality, including decisions on non-conforming materialsManage customer complaints from acknowledgment to resolution and reportingEnsure compliance with
For our client, an international company based in Klingnau, Aargau, we are looking for a dedicated Quality & OpEx Engineer 80 – 100% (f/m/d). General Information: Location: Klingnau, AargauStart Date: ASAPDuration: permanentWorking Hours: 80- 100% Your Responsibilities: Oversee product and service quality, including decisions on non-conforming materialsManage customer complaints from acknowledgment to resolution and reportingEnsure compliance with
Location: Bulle, SwitzerlandActivity rate : 100%Type of contract: Temporary contractStart date: 05.01.2026End date: 30.06.2026 (potential extensions)We are looking for an experienced Electronic Data Integrity QA Specialist to join the Quality Assurance team of UCB.In this role, you will act as a QA subject matter expert in data integrity, computerized system validation (CSV), and automation within a biotech manufacturing environment. You will review and
Location: Bulle, SwitzerlandActivity rate : 100%Type of contract: Temporary contractStart date: 05.01.2026End date: 30.06.2026 (potential extensions)We are looking for an experienced Electronic Data Integrity QA Specialist to join the Quality Assurance team of UCB.In this role, you will act as a QA subject matter expert in data integrity, computerized system validation (CSV), and automation within a biotech manufacturing environment. You will review and
For our client, a pharmaceutical company committed to excellence and operating in the Greater Lausanne area, we are looking for a:Quality Assurance Specialist - GMP AuditorStart date: ASAPYour tasksReview and approve quality documents and data to ensure they follow GMP rules.Manage quality processes like deviations, CAPAs, and change controls to support continuous improvement.Bring your quality expertise to company projects and report on your
For our client, a pharmaceutical company committed to excellence and operating in the Greater Lausanne area, we are looking for a:Quality Assurance Specialist - GMP AuditorStart date: ASAPYour tasksReview and approve quality documents and data to ensure they follow GMP rules.Manage quality processes like deviations, CAPAs, and change controls to support continuous improvement.Bring your quality expertise to company projects and report on your
Pour le compte de notre client basé dans le canton de Vaud, nous recherchons un/une Expert QA Réglementaire.Poste temporaire jusqu'à fin 2026 Start ASAP Pour ce poste, vous assurez les activités d’assurance qualité réglementaire et conformité d’un site de production biopharmaceutique, en garantissant le respect des exigences GMP/GDP et des réglementations internationales. Ce poste couvre la supervision QA des activités liées aux affaires réglementaires,
Pour le compte de notre client basé dans le canton de Vaud, nous recherchons un/une Expert QA Réglementaire.Poste temporaire jusqu'à fin 2026 Start ASAP Pour ce poste, vous assurez les activités d’assurance qualité réglementaire et conformité d’un site de production biopharmaceutique, en garantissant le respect des exigences GMP/GDP et des réglementations internationales. Ce poste couvre la supervision QA des activités liées aux affaires réglementaires,
Pour le compte de notre client basé dans le canton de Vaud, nous recherchons un/une Spécialiste / Senior Spécialiste, Assurance Qualité Opérations.Poste temporaire jusqu'à fin 2026 Start ASAPLe poste consiste à assurer la supervision qualité des activités de fabrication de biomédicaments au sein d’un site de production. ResponsabilitésAssurer le suivi qualité quotidien des activités de production (USP, DSP, préparation des milieux et tampons, zones de
Pour le compte de notre client basé dans le canton de Vaud, nous recherchons un/une Spécialiste / Senior Spécialiste, Assurance Qualité Opérations.Poste temporaire jusqu'à fin 2026 Start ASAPLe poste consiste à assurer la supervision qualité des activités de fabrication de biomédicaments au sein d’un site de production. ResponsabilitésAssurer le suivi qualité quotidien des activités de production (USP, DSP, préparation des milieux et tampons, zones de
Pour le compte de notre client basé dans le canton de Vaud, nous recherchons un/une Expert QA/QC.Poste temporaire 12 mois de missionStart date - Janvier 2026 Assurer la supervision qualité des activités de contrôle qualité (QC) et de la libération des lots de substances actives/produits, en garantissant la conformité avec les politiques Qualité, les BPF (cGMP) et les exigences réglementaires suisses, européennes et FDAResponsabilitésLibération de
Pour le compte de notre client basé dans le canton de Vaud, nous recherchons un/une Expert QA/QC.Poste temporaire 12 mois de missionStart date - Janvier 2026 Assurer la supervision qualité des activités de contrôle qualité (QC) et de la libération des lots de substances actives/produits, en garantissant la conformité avec les politiques Qualité, les BPF (cGMP) et les exigences réglementaires suisses, européennes et FDAResponsabilitésLibération de
Pour le compte de notre client spécialisé dans le domaine du Life Science, nous recherchons un Opérateur Controle Visuel - Salle blanche.Lieu : Canton de Vaud Entrée en fonction : AsapContrat : Open endedHoraires : Travail en équipe 2x8 En tant qu’opérateur(trice) de production en salle blanche, vous jouez un rôle clé dans la fabrication des produits de dispositifs médicaux en garantissant la qualité, la sécurité et la conformité des produits. Vous serez
Pour le compte de notre client spécialisé dans le domaine du Life Science, nous recherchons un Opérateur Controle Visuel - Salle blanche.Lieu : Canton de Vaud Entrée en fonction : AsapContrat : Open endedHoraires : Travail en équipe 2x8 En tant qu’opérateur(trice) de production en salle blanche, vous jouez un rôle clé dans la fabrication des produits de dispositifs médicaux en garantissant la qualité, la sécurité et la conformité des produits. Vous serez
Head of Quality 100% Spritzguss (m/w/d)Für unseren Klienten, ein international aufgestelltes Industrieunternehmen im produzierenden Sektor, suchen wir eine erfahrene Führungskraft zur Besetzung der Position Leiter/in der Qualitätsabteilung (Spritzguss).Deine Kernaufgaben:Führung: Fachliche und personelle Leitung Deiner Qualitäts-Teams (Messtechnik, Kontrolle).Qualitätsmanagement: Hauptverantwortung für die Einhaltung, Aufrechterhaltung und
Head of Quality 100% Spritzguss (m/w/d)Für unseren Klienten, ein international aufgestelltes Industrieunternehmen im produzierenden Sektor, suchen wir eine erfahrene Führungskraft zur Besetzung der Position Leiter/in der Qualitätsabteilung (Spritzguss).Deine Kernaufgaben:Führung: Fachliche und personelle Leitung Deiner Qualitäts-Teams (Messtechnik, Kontrolle).Qualitätsmanagement: Hauptverantwortung für die Einhaltung, Aufrechterhaltung und
Für einen unserer Kunden, ein etabliertes und international tätiges Unternehmen im Pharmabereich mit Sitz in Winterthur, suchen wir zur Verstärkung des Teams per sofort oder nach Vereinbarung eine/nBatch Release Manager 100 %Ihre AufgabenKlassifizierung und Beurteilung von Abweichungen sowie Koordination der Aktivitäten im Rahmen der Bearbeitung von Abweichungen, inkl. Sicherstellung des rechtzeitigen Abschlusses von UntersuchungenUnterstützung bei der
Für einen unserer Kunden, ein etabliertes und international tätiges Unternehmen im Pharmabereich mit Sitz in Winterthur, suchen wir zur Verstärkung des Teams per sofort oder nach Vereinbarung eine/nBatch Release Manager 100 %Ihre AufgabenKlassifizierung und Beurteilung von Abweichungen sowie Koordination der Aktivitäten im Rahmen der Bearbeitung von Abweichungen, inkl. Sicherstellung des rechtzeitigen Abschlusses von UntersuchungenUnterstützung bei der
Per conto di nostro stimato cliente, siamo alla ricerca di un Quality & Compliance Specialist.
Per conto di nostro stimato cliente, siamo alla ricerca di un Quality & Compliance Specialist.
For one of our clients, a leading global pharmaceutical company, we are currently looking for a Qualification and Validation Manager.General Information:Start date: 05.01.2026Duration: until 30.09.2026Workplace: BaselWorkload: 100%Remote/Home Office: possible, max 20%Working hours: StandardDepartment: MSAT (MMNGF)Team: 10 peopleAbout the job:The Qualification Manager is responsible for the CSV and qualification program at Basel DS Manufacturing, as well
For one of our clients, a leading global pharmaceutical company, we are currently looking for a Qualification and Validation Manager.General Information:Start date: 05.01.2026Duration: until 30.09.2026Workplace: BaselWorkload: 100%Remote/Home Office: possible, max 20%Working hours: StandardDepartment: MSAT (MMNGF)Team: 10 peopleAbout the job:The Qualification Manager is responsible for the CSV and qualification program at Basel DS Manufacturing, as well
Tasks:Drive the development of embedded software solutions in C/C++ and RTOS environments, ensuring code quality, performance, and compliance with project requirementsGuide and mentor embedded software engineers in day-to-day development tasks, quality control, effort estimation, and technical decision-makingSupport or lead the adoption of model-based development approaches (e.g. Simulink), including automated code generation for embedded targetsTranslate
Tasks:Drive the development of embedded software solutions in C/C++ and RTOS environments, ensuring code quality, performance, and compliance with project requirementsGuide and mentor embedded software engineers in day-to-day development tasks, quality control, effort estimation, and technical decision-makingSupport or lead the adoption of model-based development approaches (e.g. Simulink), including automated code generation for embedded targetsTranslate
For one of our clients, a global pioneer in pharmaceuticals, we are currently looking for a GMP Process Expert.General Information: Start date: 01.01.2026 Latest possible start date: 01.03.2026Duration: 12 months, with the possibility of extensionWorkplace: Kaiseraugst Workload: 100%Remote/Home Office: possible, max 1 day per weekWorking hours: Standard, on-call dutyDepartment: Manufacturing Unit Solids (MMMCB)Team: 10-20 peopleAbout the job:Manufacturing
For one of our clients, a global pioneer in pharmaceuticals, we are currently looking for a GMP Process Expert.General Information: Start date: 01.01.2026 Latest possible start date: 01.03.2026Duration: 12 months, with the possibility of extensionWorkplace: Kaiseraugst Workload: 100%Remote/Home Office: possible, max 1 day per weekWorking hours: Standard, on-call dutyDepartment: Manufacturing Unit Solids (MMMCB)Team: 10-20 peopleAbout the job:Manufacturing
We are looking for a Senior Java Technical-Functional Expert to join our customdevelopment team. This role combines strong technical expertise in Java development with the ability to understand and support business processes in a complex environment.You will contribute to the design, development, and maintenance of applications, ensuring highstandards of quality, security, and performance. You will also play a key role in continuousimprovement
We are looking for a Senior Java Technical-Functional Expert to join our customdevelopment team. This role combines strong technical expertise in Java development with the ability to understand and support business processes in a complex environment.You will contribute to the design, development, and maintenance of applications, ensuring highstandards of quality, security, and performance. You will also play a key role in continuousimprovement
Location: Switzerland (100% on-site)Contract type: Full-timeLanguage: German (mandatory); English a strong plusThe roleJoin a growing pharmaceutical site as a CQV Engineer owning validation activities for equipment, systems and facilities. You’ll coordinate installations, author and execute IQ/OQ/PQ protocols, and deliver audit-ready documentation in line with cGMP/GxP and internal procedures.What you’ll doPlan and coordinate CQV for facilities &
Location: Switzerland (100% on-site)Contract type: Full-timeLanguage: German (mandatory); English a strong plusThe roleJoin a growing pharmaceutical site as a CQV Engineer owning validation activities for equipment, systems and facilities. You’ll coordinate installations, author and execute IQ/OQ/PQ protocols, and deliver audit-ready documentation in line with cGMP/GxP and internal procedures.What you’ll doPlan and coordinate CQV for facilities &
About the roleWe’re looking for a CQV Engineer to drive the validation of equipment, systems, and facilities in a regulated pharmaceutical environment. You will coordinate installations, author and execute IQ/OQ/PQ protocols, and document results in compliance with cGMP/GxP requirements—ensuring our operations are safe, compliant, and inspection-ready.What you’ll doPlan and coordinate CQV activities for facilities & utilities (e.g., HVAC, cleanrooms, WFI,
About the roleWe’re looking for a CQV Engineer to drive the validation of equipment, systems, and facilities in a regulated pharmaceutical environment. You will coordinate installations, author and execute IQ/OQ/PQ protocols, and document results in compliance with cGMP/GxP requirements—ensuring our operations are safe, compliant, and inspection-ready.What you’ll doPlan and coordinate CQV activities for facilities & utilities (e.g., HVAC, cleanrooms, WFI,
CQ EngineerFor our Client a biopharmaceutical company in the Aargau we are currently seeking a number of CQ engineers.The C & Q Execution Engineer is primarily responsible for the execution of the CQV activities corresponding to their project area’s equipment and processes. Key Responsibilities:System Boundary development + approvalDesign Qualification preparation, execution and approval. Includes release for IQ.Good Manufacturing Practice (GMP) Rapid
CQ EngineerFor our Client a biopharmaceutical company in the Aargau we are currently seeking a number of CQ engineers.The C & Q Execution Engineer is primarily responsible for the execution of the CQV activities corresponding to their project area’s equipment and processes. Key Responsibilities:System Boundary development + approvalDesign Qualification preparation, execution and approval. Includes release for IQ.Good Manufacturing Practice (GMP) Rapid
Pour le compte d'un de nos clients situé à Morat spécialisé dans la fabrication de pièces pour le domaine automobile, nous sommes à la recherche de plusieurs : Spécialiste galvanoplastie· En tant que spécialiste en galvanisation, vous assurez la production des traitements de surface en aval sur les pièces embouties.Vos responsabilités :Direction technique et personnelle des employés sous votre responsabilité, en charge de leur développement et
Pour le compte d'un de nos clients situé à Morat spécialisé dans la fabrication de pièces pour le domaine automobile, nous sommes à la recherche de plusieurs : Spécialiste galvanoplastie· En tant que spécialiste en galvanisation, vous assurez la production des traitements de surface en aval sur les pièces embouties.Vos responsabilités :Direction technique et personnelle des employés sous votre responsabilité, en charge de leur développement et
For our client, an international company based in Elsau, we are looking for a dedicated Process/System Engineer (f/m/d). We represent a global leader in manufacturing exhaust aftertreatment systems for high-horsepower engines in both mobile and stationary operations. Their applications span a wide range, from marine engines with an output of 200kW up to massive power plant engines generating 20MW. In addition, our client is at the forefront of developing
For our client, an international company based in Elsau, we are looking for a dedicated Process/System Engineer (f/m/d). We represent a global leader in manufacturing exhaust aftertreatment systems for high-horsepower engines in both mobile and stationary operations. Their applications span a wide range, from marine engines with an output of 200kW up to massive power plant engines generating 20MW. In addition, our client is at the forefront of developing