Key Responsibilities:Develop and implement regulatory strategies for global medical device clearances and approvalsManage regulatory submissions and communications with FDA and EU notified bodiesProvide regulatory guidance to cross-functional teams throughout the product lifecycleRequired Qualificat...
An international medical devices manufacturer is seeking a Senior Regulatory Affairs Specialist to join their US team. Keep abreast of legislation, guidelines, and regulations relating to regulatory affairs in the US; inform and advise the team in Japan. Participate in medical, industrial activities...
A company is looking for an Associate Director, Regulatory Affairs and Submissions. ...
Oversight responsibility for all regulatory body surveys, such as, JCAHO, State Licensing Review, HCFA (CMS) Validation surveys. Create a Job Alert for Similar Jobs About Kindred Hospitals Connections working at Kindred Hospitals More Jobs from This Employer https://regulatorycareers. ...
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Strong project management skills, with the ability to manage multiple concurrent projects and priorities. Strong project management skills, with the ability to manage multiple concurrent projects and priorities. Managing the logistics, resources, and operational support needed to execute critical pr...
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