Mandated by one of our client companies, we are currently seeking a dedicated and detail-oriented Quality Compliance Manager to oversee and manage quality compliance, as well as facility management and Facility Project related processes within our client's facility management (FM) organization. General Information:Start date: ASAPDuration: 1 yearExtension: not confirmedWorkplace: SchachenWorkload: 100%Home office: not possible Responsibilities: Quality Com
Mandated by one of our client companies, we are currently seeking a dedicated and detail-oriented Quality Compliance Manager to oversee and manage quality compliance, as well as facility management and Facility Project related processes within our client's facility management (FM) organization. General Information:Start date: ASAPDuration: 1 yearExtension: not confirmedWorkplace: SchachenWorkload: 100%Home office: not possible Responsibilities: Quality Com
Pour le compte de notre client basé dans le nord vaudois, nous recherchons un Technicien USP motivé pour rejoindre une équipe dynamique et opérationnelle. Type de contrat : CDD - 1 anLieu : Canton de VaudDébut : Dès que possibleVous serez en charge de piloter les équipements de production tout en garantissant le respect des bonnes pratiques de fabrication (GMP). Votre mission principale consistera à participer activement aux différentes étapes de productio
Pour le compte de notre client basé dans le nord vaudois, nous recherchons un Technicien USP motivé pour rejoindre une équipe dynamique et opérationnelle. Type de contrat : CDD - 1 anLieu : Canton de VaudDébut : Dès que possibleVous serez en charge de piloter les équipements de production tout en garantissant le respect des bonnes pratiques de fabrication (GMP). Votre mission principale consistera à participer activement aux différentes étapes de productio
For one of our clients, an international pharma company in Kaiseraugst, we are looking for a Compliance Expert.As a compliance expert, you and your colleagues ensure that the relevant GMP requirements are implemented. You are the contact person for initiating, coordinating and implementing all necessary measures to achieve and maintain GMP compliance. To this end, the compliance expert has a key technical function in GMP matters for all personnel in the va
For one of our clients, an international pharma company in Kaiseraugst, we are looking for a Compliance Expert.As a compliance expert, you and your colleagues ensure that the relevant GMP requirements are implemented. You are the contact person for initiating, coordinating and implementing all necessary measures to achieve and maintain GMP compliance. To this end, the compliance expert has a key technical function in GMP matters for all personnel in the va
On behalf of our client company in Basel, we are currently looking for an Associate in Drug Delivery and Preformulation Sciences. The perfect candidate has a professional in pharmaceutics, pharmaceutical technology or biopharmaceutics and experience in the pharmaceutical industry. A good understanding of the drug development process is required. General Information: Start date: ASAP / 06.01.2025Latest Start Date: 01.03.2025Planned duration: 1 year via Rand
On behalf of our client company in Basel, we are currently looking for an Associate in Drug Delivery and Preformulation Sciences. The perfect candidate has a professional in pharmaceutics, pharmaceutical technology or biopharmaceutics and experience in the pharmaceutical industry. A good understanding of the drug development process is required. General Information: Start date: ASAP / 06.01.2025Latest Start Date: 01.03.2025Planned duration: 1 year via Rand
We've got an exciting new opportunity for a Design Control Specialist for combination products. Location: Basel, SwitzerlandContract Duration: 6 months (01.12.2025 - 30.05.2025) Reason for Opening:The team is expanding due to increasing project demands. You will join a growing team of 8, working on multiple drug-device combination projects. Role Overview:We are seeking a highly skilled Design Control Specialist with a strong "get things done" mindset to s
We've got an exciting new opportunity for a Design Control Specialist for combination products. Location: Basel, SwitzerlandContract Duration: 6 months (01.12.2025 - 30.05.2025) Reason for Opening:The team is expanding due to increasing project demands. You will join a growing team of 8, working on multiple drug-device combination projects. Role Overview:We are seeking a highly skilled Design Control Specialist with a strong "get things done" mindset to s
For our client, an international pharma company in Basel, we are looking for a motivated Quality Assurance Manager.General Information: Start date: 01.01.2025Latest Start Date: 01.03.2025Planned duration: Project planned until up to 3 yearsWorkplace: BaselWorkload: 80-100%Home Office: up to 40% possible (Monday and Wednesday onsite days)Team: about 15 team membersWorking hours: Standard Tasks & Responsibilities: End-to-end quality oversight on the qualif
For our client, an international pharma company in Basel, we are looking for a motivated Quality Assurance Manager.General Information: Start date: 01.01.2025Latest Start Date: 01.03.2025Planned duration: Project planned until up to 3 yearsWorkplace: BaselWorkload: 80-100%Home Office: up to 40% possible (Monday and Wednesday onsite days)Team: about 15 team membersWorking hours: Standard Tasks & Responsibilities: End-to-end quality oversight on the qualif
For our client company in Luzern, we are currently looking for a Process Engineer, a highly motivated individual to fill an open position to support drug substance tech transfer and commercial manufacture within their External Manufacturing Network. This is an exciting opportunity to work with key strategic external partners, grow technical experience in biologics or vaccines manufacturing, and work on high visibility network initiatives. Our client's team
For our client company in Luzern, we are currently looking for a Process Engineer, a highly motivated individual to fill an open position to support drug substance tech transfer and commercial manufacture within their External Manufacturing Network. This is an exciting opportunity to work with key strategic external partners, grow technical experience in biologics or vaccines manufacturing, and work on high visibility network initiatives. Our client's team
For our client Merck in Aubonne, we are looking for a QA Specialist for QC (m/f/d) for a period of 12 months.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 activities including ne
For our client Merck in Aubonne, we are looking for a QA Specialist for QC (m/f/d) for a period of 12 months.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 activities including ne
For our client Merck in Aubonne, we are looking for a Quality Assurance – Documentation and Training Specialist (all genders) for a period of 12 months.Your role : As member of the Quality System & Compliance group, you will be responsible for the daily operational activities relating to training, documentation and archiving processes:Documentation and archiving:Manage the distribution and life cycle of GxP documentation.Administration of operational activ
For our client Merck in Aubonne, we are looking for a Quality Assurance – Documentation and Training Specialist (all genders) for a period of 12 months.Your role : As member of the Quality System & Compliance group, you will be responsible for the daily operational activities relating to training, documentation and archiving processes:Documentation and archiving:Manage the distribution and life cycle of GxP documentation.Administration of operational activ
For our client Merck in Aubonne, we are looking for a Cleaning Validation Expert (m/f/d) for a period of 12 months. Your Role : Coordinate cleaning validation and monitoring activities in line with the life cycle of a manufacturing process for biotech manufacturing equipmentEstablish and execute validation protocols and reports for cleaning validationEnsure reliability and conformity of validation and control activities in line with internal and regulatory
For our client Merck in Aubonne, we are looking for a Cleaning Validation Expert (m/f/d) for a period of 12 months. Your Role : Coordinate cleaning validation and monitoring activities in line with the life cycle of a manufacturing process for biotech manufacturing equipmentEstablish and execute validation protocols and reports for cleaning validationEnsure reliability and conformity of validation and control activities in line with internal and regulatory
Nous recherchons un Technicien de laboratoire QC orienté sur la partie administrative.Pour le poste. vous soutenez les activités du département de Contrôle Qualité avec des missions liées à des tâches administratives telles que la gestion de la documentation et des rapprochements, l'achat de réactifs/consommables de laboratoire, la réception de marchandises, l'organisation de l'expédition d'échantillons/matériaux, le rapprochement des factures, la réceptio
Nous recherchons un Technicien de laboratoire QC orienté sur la partie administrative.Pour le poste. vous soutenez les activités du département de Contrôle Qualité avec des missions liées à des tâches administratives telles que la gestion de la documentation et des rapprochements, l'achat de réactifs/consommables de laboratoire, la réception de marchandises, l'organisation de l'expédition d'échantillons/matériaux, le rapprochement des factures, la réceptio
Für einen von unseren Kunden suchen wir eine*n motivierte*n Customer Service Center Specialist.Der oder die perfekte Kandidat:in: haben eine abgeschlossene Ausbildung als Biomedizinische Laborant*in sind oder als Medizinische Praxisassistent*in mit zusätzlich 2-3 Jahren Berufserfahrung in der Diagnostik, sind technisch mit IT Tools als auch mit Geräten affin, sprechen Deutsch fliessend und zusätzlich entweder Französisch oder Italienisch.Allgemeine Informa
Für einen von unseren Kunden suchen wir eine*n motivierte*n Customer Service Center Specialist.Der oder die perfekte Kandidat:in: haben eine abgeschlossene Ausbildung als Biomedizinische Laborant*in sind oder als Medizinische Praxisassistent*in mit zusätzlich 2-3 Jahren Berufserfahrung in der Diagnostik, sind technisch mit IT Tools als auch mit Geräten affin, sprechen Deutsch fliessend und zusätzlich entweder Französisch oder Italienisch.Allgemeine Informa
We are currently seeking a Supplier 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:Provides quality assurance leadership to select contract manufacturing sites and raw material suppliers engaged
We are currently seeking a Supplier 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:Provides quality assurance leadership to select contract manufacturing sites and raw material suppliers engaged
Nous recherchons un/e Ingénieur Project Operations Notre client est une société internationale travaillant dans les dispositifs médicaux. Le poste est situé dans le canton de Neuchâtel.Il s’agit d’un contrat temporaire à durée indéterminée.Pour supporter le département Continuous Improvement & PMO, nous recherchonsun Ingénieur Project Operations avec une expérience Technique et Process pourdiagnostiquer, proposer et implémenter des solutions novatrices sur
Nous recherchons un/e Ingénieur Project Operations Notre client est une société internationale travaillant dans les dispositifs médicaux. Le poste est situé dans le canton de Neuchâtel.Il s’agit d’un contrat temporaire à durée indéterminée.Pour supporter le département Continuous Improvement & PMO, nous recherchonsun Ingénieur Project Operations avec une expérience Technique et Process pourdiagnostiquer, proposer et implémenter des solutions novatrices sur
For our client Merck in Aubonne, we are currently looking for a ‘Cleaning Validation Expert’ until the end of 2025.The Cleaning validation within the Fill & Finish Department leads and manages all the cleaning validation activities within our site to ensure new production equipment and product implementation, the business continuity and Product-Lifecycle activities on legacy products portfolio, in compliance with specifications, registration and GMP requir
For our client Merck in Aubonne, we are currently looking for a ‘Cleaning Validation Expert’ until the end of 2025.The Cleaning validation within the Fill & Finish Department leads and manages all the cleaning validation activities within our site to ensure new production equipment and product implementation, the business continuity and Product-Lifecycle activities on legacy products portfolio, in compliance with specifications, registration and GMP requir
Envie de rejoindre une équipe passionnée et de jouer un rôle clé dans notre chaîne de production?Nous recherchons un Technicien DSP qui travaillera au cœur des opérations GMP pour notre client spécialisé dans le domaine de la bio-pharmaceutique. Poste : TemporaireDurée : 8 moisStart date : immédiatement ResponsabilitésPiloter les équipements de production et réaliser les IPC selon les normes GMP.Exécuter les tâches de production en suivant le planning déf
Envie de rejoindre une équipe passionnée et de jouer un rôle clé dans notre chaîne de production?Nous recherchons un Technicien DSP qui travaillera au cœur des opérations GMP pour notre client spécialisé dans le domaine de la bio-pharmaceutique. Poste : TemporaireDurée : 8 moisStart date : immédiatement ResponsabilitésPiloter les équipements de production et réaliser les IPC selon les normes GMP.Exécuter les tâches de production en suivant le planning déf
We are currently seeking an Associate scientist spectroscopy for one of our clients in Canton of Aargau. This is a temporary contract for one year. The successful candidate will bring enthusiasm for working in a R&D environment and sound experience in developing, optimizing, performing, and evaluating applied optical spectroscopy experiments. Main field of application will be in chemical process development. Responsibilities include maintaining and trouble
We are currently seeking an Associate scientist spectroscopy for one of our clients in Canton of Aargau. This is a temporary contract for one year. The successful candidate will bring enthusiasm for working in a R&D environment and sound experience in developing, optimizing, performing, and evaluating applied optical spectroscopy experiments. Main field of application will be in chemical process development. Responsibilities include maintaining and trouble