Nous recherchons un(e) Expert(e) GMAO, pour notre client, une société pharmaceutique internationale. Lieu: NeuchâtelPossibilité de télétravail mais pas à temps pleinContrat temporaire de début mai à novembre 2025 Vos responsabilités:Gestion des données GMAO :Création Equipements/ Instruments de mesure / TAGsCréation et codification des pièces détachéesCréation / Modification / Suppression des listes de pièces d'équipementCréation / Modification / Suppressi
Nous recherchons un(e) Expert(e) GMAO, pour notre client, une société pharmaceutique internationale. Lieu: NeuchâtelPossibilité de télétravail mais pas à temps pleinContrat temporaire de début mai à novembre 2025 Vos responsabilités:Gestion des données GMAO :Création Equipements/ Instruments de mesure / TAGsCréation et codification des pièces détachéesCréation / Modification / Suppression des listes de pièces d'équipementCréation / Modification / Suppressi
We are currently seeking a Microbiologist for one of our clients in Le Locle, 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 via Randstad.Please note this vacancy requires fluency in French and English.Start: ASAP (max 1 month of notice period)Location: Le Locle, on site Your responsibilities:Ensures that adequ
We are currently seeking a Microbiologist for one of our clients in Le Locle, 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 via Randstad.Please note this vacancy requires fluency in French and English.Start: ASAP (max 1 month of notice period)Location: Le Locle, on site Your responsibilities:Ensures that adequ
Pour le compte de l’un de nos clients du secteur des dispositifs médicaux, nous recherchons un·e technicien·ne de laboratoire dans un environnement GMP stimulant et dynamique. Le poste inclut un horaires d’équipe (2x8). Contrat temporaire unlimitè via RandstadLieu : Le LocleDémarrage : ASAPHoraires: passage en horaires d’équipe (2x8) prevu en SeptembreTaux d’activité : 100% Vos responsabilitésRéaliser des échantillonnages en zones contrôlées et non contrô
Pour le compte de l’un de nos clients du secteur des dispositifs médicaux, nous recherchons un·e technicien·ne de laboratoire dans un environnement GMP stimulant et dynamique. Le poste inclut un horaires d’équipe (2x8). Contrat temporaire unlimitè via RandstadLieu : Le LocleDémarrage : ASAPHoraires: passage en horaires d’équipe (2x8) prevu en SeptembreTaux d’activité : 100% Vos responsabilitésRéaliser des échantillonnages en zones contrôlées et non contrô
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 complianc
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 complianc
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
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 el
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 el
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
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