A company is looking for a Director of Regulatory Affairs, Lifecycle.Key ResponsibilitiesOversee the Lifecycle Regulatory team and manage personnel activitiesDevelop and execute global regulatory strategies for commercialized productsEnsure compliance with regulatory Conditions of Approval and oversee advertising and promotion reviewsRequired Qualifications and EducationBachelor's Degree in physical or life sciences;
Master's Degree preferredMinimum 10 years of experience in regulatory affairs within the medical device industryExperience with US, EU, and international submissions and registrationsPrior team leadership experience requiredRegulatory Affairs Certification (RAC) preferred
Director of Regulatory Affairs
Director, Regulatory Affairs, Immunology. A company is looking for a Director / Sr. ...
Associate Director, Regulatory Affairs: Job ID - 1435
Must have an extensive knowledge of regulatory requirements, including ICH and regional requirements, and have an understanding of current global and regional trends in regulatory affairs and ability to assess the impact of these requirements to the business. The Associate Director, Regulatory Affai...
Director of Lifecycle Marketing
A company is looking for a Vice President of Growth Marketing to lead its Lifecycle and Cross-functional customer journey strategy. ...
Associate Director of Regulatory Medical Writing
Aramis Frost is partnering with a leading Biotech specializing in Oncology to find an Associate Director of Regulatory Medical Writing. In this pivotal role, you will oversee the regulatory writing strategy and contribute significantly to the development of cutting-edge oncology therapies. Lead the ...
Director of Regulatory Affairs, Imaging Agent Drug Development
The purpose of the Director of Regulatory Affairs, Imaging Agent Drug Development is to lead cross functional teams in major regulatory submissions to the Center for Drug Evaluation and Research (CDER), inclusive of New Drug Applications (NDA), End of Phase (EOP) Type B meetings, health authority in...
Director of Regulatory Affairs, Imaging Agent Drug Development
The purpose of the Director of Regulatory Affairs, Imaging Agent Drug Development is to lead cross functional teams in major regulatory submissions to the Center for Drug Evaluation and Research (CDER), inclusive of New Drug Applications (NDA), End of Phase (EOP) Type B meetings, health authority in...
Director, Regulatory Affairs
Requires Minimum of 12 years of progressive' experience working in a regulatory affairs role, specifically with Class II or Class III medical device experience, with previous management/leadership experience with a Bachelor's degree in a Life Sciences, Regulatory Affairs, or related field; or 10 yea...
Associate Director CMC Regulatory Affairs - Vacaville, CA
Internal regulatory support for operation and control eg:Review and approval of Lonza Regulatory Intelligence Bulletin, Interpretation of EU, US and other global regulatory requirements to support compliance in all phases of contract manufacturing of biological products and maintain transparency of ...
Director, Home States Rates Regulatory Affairs
The Director of Home States Rates & Regulatory Affairs (“Director”) is responsible for all regulatory filings, primarily General Rate Cases (GRC), with the company’s economic regulators in Hawaii, New Mexico and Washington, with future regulatory responsibilities in Texas. Liaison to officer group, ...
Associate Director of Regulatory Medical Writing
Aramis Frost is partnering with a leading Biotech specializing in Oncology to find an Associate Director of Regulatory Medical Writing. In this pivotal role, you will oversee the regulatory writing strategy and contribute significantly to the development of cutting-edge oncology therapies. Lead the ...