Réceptionniste (H/F).
- Heute veröffentlicht
- läuft am 30. November 2024 ab
Qualifikationen
Ce que nous recherchons chez toi :
- D'excellentes compétences en communication et une capacité à gérer les priorités avec efficacité.
- Un sens de l'organisation irréprochable et une grande attention aux détails.
- Une envie de travailler en équipe et de t'adapter à un environnement dynamique.
- Une solide expérience en réception ou dans un poste similaire est un atout.
- Une bonne maîtrise des outils informatiques de base.
- Une bonne maîtrise des langues étrangères (Anglais / Allemand / Italien) est un atout.
Si tu es une personne positive, orientée vers le service et motivée à offrir une expérience exceptionnelle à nos patient·es, n'hésite plus et envoie-nous ta candidature !
kontaktiere uns.
wir sind da um deine Fragen zu beantworten.
HB
Hadrien Blanc
- +41 58 201 48 20
- Randstad Lausanne Office
der Bewerbungsprozess.
Erfahre wie der Bewerbungsprozess aussieht. Finde heraus wie wir dir helfen werden, diesen Job zu bekommen.
ähnliche jobs.
alle Jobs anzeigen- The MSAT DP within the Fill & Finish Department leads and manages all the Drug Products site technical activities within our client site in Aubonne to ensure the supply of New Biologic Entities (NBEs) and the business continuity and Product-Lifecycle activities on legacy products portfolio, in compliance with specifications, registration and GMP requirements.To evolve in this environment, we are looking for our next Process Validation Expert to ensure theThe MSAT DP within the Fill & Finish Department leads and manages all the Drug Products site technical activities within our client site in Aubonne to ensure the supply of New Biologic Entities (NBEs) and the business continuity and Product-Lifecycle activities on legacy products portfolio, in compliance with specifications, registration and GMP requirements.To evolve in this environment, we are looking for our next Process Validation Expert to ensure the
- Key Responsibilities· Contribute to CSV strategies, plans, and protocols in accordance with regulatory As a QA IT CSV Engineer, you will be responsible for ensuring compliance for computerized systems and computerized systems validation, fulfill with regulatory requirements and operate as intended.Your primary responsibilities will include:guidelines (e.g., FDA 21 CFR Part 11, EU Annex 11, GAMP 5)· Contribute to risk assessments and participate to test scrKey Responsibilities· Contribute to CSV strategies, plans, and protocols in accordance with regulatory As a QA IT CSV Engineer, you will be responsible for ensuring compliance for computerized systems and computerized systems validation, fulfill with regulatory requirements and operate as intended.Your primary responsibilities will include:guidelines (e.g., FDA 21 CFR Part 11, EU Annex 11, GAMP 5)· Contribute to risk assessments and participate to test scr
- The MSAT DP within the Fill & Finish Department leads and manages all the Drug Products site technical activities within our client site in Aubonne to ensure the supply of New Biologic Entities (NBEs) and the business continuity and Product-Lifecycle activities on legacy products portfolio, in compliance with specifications, registration and GMP requirements.To evolve in this environment, we are looking for our next Process Validation Expert. You will be rThe MSAT DP within the Fill & Finish Department leads and manages all the Drug Products site technical activities within our client site in Aubonne to ensure the supply of New Biologic Entities (NBEs) and the business continuity and Product-Lifecycle activities on legacy products portfolio, in compliance with specifications, registration and GMP requirements.To evolve in this environment, we are looking for our next Process Validation Expert. You will be r
