21.09.2022 00:52
Regulatory Affairs Expert Pharma / Эксперт по регистрации лекарственных средств
По договоренности
21.09.2022 00:52
компания "johnson & johnson" key responsibilities: new products registration; regulatory product life cycle management (variations submissions and approval incl. new indications, new manuf. sites etc.); tracking of variations is regulatory database (insight); regulatory compliance: ccdss timely submissions and tracking; trackwise for change control implementation for russia; tracking of labelling updates in lift database; insignt database maintaining for russia; nd remediation project support; regulatory support of cvt: promotional and educational materials approval in imedical review system key requirements: from 2 years’ of relevant experience in a pharmaceutical company; higher education (pharmacy sphere) in depth knowledge of regulations/legislation; english – upper intermediate.
Адрес
Москва