Vice President Regulatory Affairs Quality Assurance
... 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, ...
... quality products while maintaining full regulatory compliance. They will be responsible ... and Africa.Experience with drafting regulatory submissions.Demonstrated knowledge of QMS, ...
... development and growth.RoleAs a Regulatory Science and Strategy Senior Principal ... of quality added value: Specifically:Advisor on the strategy to deliver EMEA regulatory services to customers concerning PASS, ...
... and, biological portfolios.Regulatory focal point and advisor for country business management team. ... Work with Commercial Team Leader to develop sustainable regulatory team resourcing plans ...
... 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 ...
... Insurance. Role Summary Purpose: · The Regulatory Affairs Leader - Pharma may be ... ensures accurate & optimal submission of regulatory medical product clearance files & postmarket ... Act as liaison with external regulatory reviewers to gain rapid approval ...
... (minimum 8-10 years) in regulatory affairs within the pharmaceutical, biotechnology, ... . In-depth knowledge of European regulatory requirements and guidelines governing clinical ... environment. If youre passionate about regulatory affairs and driven to make ...
... 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 ...