... our motivated team in Global Regulatory Affairs and grow with exciting challenges. As Global Regulatory Lead (GRL) you are the ... accordance with the respective national regulatory requirements (e.g. local studies) ...
... years’ experience in Drug development, Regulatory, Clinical Operation and Medical Devices. ... Vault, PARAXEL LIQUENT InSight, CSC Regulatory Tracker, ArisGlobal Register, OpenText, SharePoint, ...
... of pharmaceutical industry experience in Regulatory Affairs in Human Pharma; any ... RA would be highly desirable Regulatory affairs hands on experience in ...
... monitored and fulfilled Oversees validated regulatory document management system and maintains ... your experience in Quality CMC, regulatory submissions and or Regulatory Information Management (RIM) systems. Sound ...
... team is looking for a Regulatory Affairs Specialist with a strong ... the global Head of Compliance & Regulatory Affairs.ResponsibilitiesIdentifying and tracking legislation ...
... initiatives within the Regulatory Affairs department. Act as the main regulatory liaison for stakeholders to ensure ... a Masters in Drug Regulatory Affairs. Minimum of 5 years of experience in Drug Regulatory Affairs. Demonstrated experience in team ...
... ? Then join Merz Aesthetics As Regulatory Affairs Manager Medical Devices ROW ( ... as well as maintain the regulatory databases to ensure they are ... of experience in the international regulatory affairs field for medical devices. ...
... clinical trials and the regulatory approval process.Our focus is ... will be acting as a regulatory expert coaching your team and aligning regulatory strategies with experts from various ... years work experience in Regulatory CMC area including experience with ...
... Germany. A Director, in Global Regulatory Medical Writing, reports into Head of Global Regulatory Medical Writing, will primarily work ... quality, fit-for-use clinical regulatory documents for various regulatory and reporting purposes in an ...
... , with 5–7 years of regulatory affairs experience in the medical ... in SaMD.- Extensive experience with regulatory requirements for Software as a ... cross-functional teams on SaMD regulatory strategy, even without direct managerial ...