... quality products while maintaining full regulatory compliance. They will be responsible ... and Africa.Experience with drafting regulatory submissions.Demonstrated knowledge of QMS, ...
... quality products while maintaining full regulatory compliance. They will be responsible ... and Africa.Experience with drafting regulatory submissions.Demonstrated knowledge of QMS, ...
... and growth.RoleAs a Regulatory Science and Strategy Senior Principal ... with those experienced in regulatory affairs, clinical development and real- ... .Remain current on emerging regulatory frameworks, pivotal regulatory decisions, and industry trends in ...
... development of wider EMEA regulatory team. Techno Regulatory expectations Partner with RAS and ... science advocacy efforts with regulatory agencies or other influencers, decision, ... and engage. Experience in regulatory team leadership is essential. Experience ...
... will provide regulatory leadership, guidance, project management and ... to ensure smooth regulatory applications of clinical trials and regulatory clinical trial compliance in the ... EU) and major regulatory submissions and supplemental amendments major ...
... and in collaboration with the Regulatory Operations. Ensure regulatory compliance and maintenance of all ... Collaborate in regional and global regulatory projects and act as a ... of the network of regulatory consultants, including coordination with procurement ...
... and in collaboration with the Regulatory Operations. Ensure regulatory compliance and maintenance of all ... Collaborate in regional and global regulatory projects and act as a ... of the network of regulatory consultants, including coordination with procurement ...
... -10 years of experience in regulatory affairs, including a minimum of ... knowledge of IVD medical device regulatory requirements and submission processes for ... clinical IVD products, implementation of regulatory systems, and assuring compliance to ...
... increase efficiency and effectiveness of regulatory processes.- Lead QIAGEN Global International ... (10+) years of experience in regulatory affairs, with at least 5 ... (IVD) companies.- Deep knowledge of regulatory requirements for IVD products. Extensive ...
... or to be published in regulatory or clinical medical journal (example, ... )KEY WORKING RELATIONSHIPS CHC Global Regulatory Affairs, CHC Science Hub Regions ... and or experience5-10 years’ regulatory experience desirableIn depth understanding of ...