22.03.24 | Vollzeit | Luzern | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
Später ansehen18.04.24 | Vollzeit | Luzern | Michael Page InternationalIT Data Analysis 1 - IT Project & Programme Management 1 - Networks 1 - Technology consultancy 1 - Healthcare & Life Sciences 15 - Biotechnology 8 - Regulatory Affairs 3 - Medical devices 2 - Medical Affairs 1 - Pharmaceutical 1 - Logistics, Procurement & Supply Chain 14 - Contract & Vendor Management 2
Später ansehen18.04.24 | Vollzeit | Luzern | Randstad Schweiz AGAnd coordination with Quality and Safety Standards - Be knowledgeable and a subject matter expert in both MSD’s internal engineering standards and in country regulatory requirements. Project Management - Project execution and oversight to ensure compliance with procurement policies and engineering standards
Später ansehen15.04.24 | Vollzeit | Luzern | Randstad Schweiz AGFor a clinical packaging job. - Reviewing county-specific label text on accuracy and regulatory requirements. - Handling of randomization schedules for clinical studies. - Reviewing and release of label batch record documents. - Ensuring activities are completed within given timelines and timely escalation when
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