- 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 QualiFor 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
- 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 WirkstofFür 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
- 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 doOn 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, SwitzerlFor 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
- 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: JaÜberFür 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
- 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.FournNous 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
- 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 – 31/05/2025On 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
- 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 rôPour 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
- Für unseren Kunden, ein führendes internationales Pharmaunternehmen, suchen wir eine/n Laboratory Worker. Allgemeine Informationen:Startdatum: 12.05.2025Spätestmögliches Startdatum: 01.07.2025Geplante Dauer der Anstellung: bis 31.12.2025, mit Möglichkeit auf VerlängerungArbeitsplatz: BaselWorkload: 100%Team: 12 PersonenDepartment: BBK QC (MMQIAB)Arbeitszeiten: StandardÜber die Stelle:Die Abteilung QC Product Analytical Testing (PAT) ist Teil der QualitätskFür unseren Kunden, ein führendes internationales Pharmaunternehmen, suchen wir eine/n Laboratory Worker. Allgemeine Informationen:Startdatum: 12.05.2025Spätestmögliches Startdatum: 01.07.2025Geplante Dauer der Anstellung: bis 31.12.2025, mit Möglichkeit auf VerlängerungArbeitsplatz: BaselWorkload: 100%Team: 12 PersonenDepartment: BBK QC (MMQIAB)Arbeitszeiten: StandardÜber die Stelle:Die Abteilung QC Product Analytical Testing (PAT) ist Teil der Qualitätsk
- On behalf of our client, we are looking for a Trade Compliance Specialist who will be responsible for Sanctioned Country due diligence, Denied Party Screening, import/export tariff code determination, and supporting the team and manager to ensure compliance with customs and other government agency regulations. The role will also support trade-sanctioned country management and acquisition-related projects. The selected candidate will contribute to compliancOn behalf of our client, we are looking for a Trade Compliance Specialist who will be responsible for Sanctioned Country due diligence, Denied Party Screening, import/export tariff code determination, and supporting the team and manager to ensure compliance with customs and other government agency regulations. The role will also support trade-sanctioned country management and acquisition-related projects. The selected candidate will contribute to complianc
- 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 ConforWe 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
