https://www.youtube.com/watch?v=n6euQqD5bb8 Rejoignez le programme de stage en alternance de GSK : Aidez-nous à devancer la maladie ensemble. Formation requise : Vous êtes étudiant(e) en Master en alternance en Business Analyst ou en Gestion et Transformation Digitale
SHE Officer (Safety, Health & Environment) Job Purpose The SHE Officer is responsible for supporting and driving the Safety, Health and Environmental management system at site level, ensuring compliance with legal, corporate, and internal standards, while
Technicien QA Opérationnel Process En tant que Technicien QA Opérationnel, vous travaillerez en équipe et en interaction avec les différentes équipes de production et/ou supports. Vos responsabilités sont : Vous effectuez la lecture, la correction, la
The Opportunity: The Supervisor II, Onsite Lab Operations Support is responsible for leading and coordinating daily lab support operations within a pharmaceutical client environment. This role ensures high-quality service delivery aligned with operational objectives, client expectations,
Company Description AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on peoples lives
Rattaché au Safety & Culture Change Manager, vous êtes membre du SIPPT et conseiller et assister lemployeur dans le déploiement de la politique Prévention. Vous jouez un rôle clé dans létablissement et la consolidation des objectifs
As a QA GMP Compliance Support , you will act as a Person‑in‑Plan (PIP) at a Contract Manufacturing Organization (CMO) in Germany. You will provide on‑site quality oversight of clinical drug product manufacturing activities and ensure
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our
QA GMP Compliance Support , you will act as a Person‑in‑Plan (PIP) at a Contract Manufacturing Organization (CMO) in Germany. You will provide on‑site quality oversight of clinical drug product manufacturing activities and ensure compliance with