QA DS Operations Expert.
- veröffentlicht vor 4 Tagen
- läuft am 22. November 2024 ab
Qualifikationen
- Doté.e d'une formation et d'une expérience de minimum 5 ans dans l'industrie pharmaceutique / biotechnologie.
- Vous avez une bonne connaissance des différents processus qualité.
- Vous avez une expérience significative dans la gestion de déviations et la mise en place d'actions correctives et préventives (CAPA)
- L'organisation, la rigueur et la précision sont vos principaux atouts.
kontaktiere uns.
wir sind da um deine Fragen zu beantworten.
NB
Nils Bellieres
- Randstad Merck Aubonne
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. 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
- 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
