A company is looking for a Director/Senior Director, Regulatory Affairs Advertising and Promotion. Collaborate with cross-functional teams to incorporate regulatory considerations into materialsServe as primary liaison to FDA Office of Product and Drug Promotion (OPDP)Required Qualifications:Minimum...
If the answers to these questions were yes; then this Director Quality Assurance and Regulatory Affairs opportunity with an outstanding Medical Device organisation in Illinois might be the change you need. Ensures compliance with regulatory standards and readiness for inspections. Independently revi...
A company is looking for a Regulatory Affairs Director - Global Regulatory Leader in General Medicine/Cardiovascular. ...
This role will provide CMC regulatory support and guidance for assigned projects and interfaces with R&D, Project Management, Manufacturing, Quality, and Regulatory colleagues to ensure a robust CMC regulatory strategy is developed and implemented to have on time submissions with the highest quality...
Key Responsibilities:Focus on clinical regulatory filings and providing strategic and operational leadership on project teamsContribute to IND/CTA and BLA submissions activities for products in developmentDevelop regulatory strategies for assigned programs and communicate with regulatory agenciesReq...
Job Description - Director of Quality, Regulatory Affairs and Accreditation (00134192). Coordinates efforts to assure regulatory compliance with standards established by our managed care partners. Develops and leads a regulatory survey readiness program in support of the organization's mission, valu...
Coordinates efforts to assure regulatory compliance with standards established by our managed care partners. Develops and leads a regulatory survey readiness program in support of the organization's mission, values and business objectives. Develops and maintains plans to assure compliance with regul...
Director Regulatory Affairs Global Regulatory Lead, Global Regulatory Strategy, responsible for developing and implementing global strategies to secure and maintain market approval for product(s) in the assigned therapeutic area. May lead the Labeling Regulatory Strategy Team (LRST), and serve as th...
Associate Director, Regulatory Affairs Project Manager. Director, Regulatory Affairs and Program Management Team Lead. The Associate Director, Regulatory Affairs Project Management will be responsible for supporting the development and implementation of program strategy. The individual will be a key...
Director, Information Services. NM, adheres to the organization’s Code of Ethics and Corporate Compliance Program, and complies with all relevant policies, procedures, guidelines and all other regulatory and accreditation standards. The Director, Information Services will serve as the IS leader for ...
The Senior Director of Regulatory Affairs, Specialty Pharma, will be responsible for leading regulatory strategy for specialty pharma products, especially combination products in development and life cycle management, including A/NDA products and biosimilars. Over 10 years related experience in prod...
Director, Information Services. NM, adheres to the organization’s Code of Ethics and Corporate Compliance Program, and complies with all relevant policies, procedures, guidelines and all other regulatory and accreditation standards. The Director, Information Services will serve as the IS leader for ...
Director, Information Services. NM, adheres to the organization’s Code of Ethics and Corporate Compliance Program, and complies with all relevant policies, procedures, guidelines and all other regulatory and accreditation standards. The Director, Information Services will serve as the IS leade...
Coordinates efforts to assure regulatory compliance with standards established by our managed care partners. Develops and leads a regulatory survey readiness program in support of the organization's mission, values and business objectives. Develops and maintains plans to assure compliance with regul...
This role will provide CMC regulatory support and guidance for assigned projects and interfaces with R&D, Project Management, Manufacturing, Quality, and Regulatory colleagues to ensure a robust CMC regulatory strategy is developed and implemented to have on time submissions with the highest quality...
Corporate Scientific & Regulatory Affairs Director, Additives & Ingredients. Corporate Scientific & Regulatory Affairs Director, Additives & Ingredients leads cross-segment SRA initiatives related to additives, ingredients, and regulated undesirable substances. Demonstrated understanding of human an...
The Director, Regulatory Affairs will represent Invenergy before and manage relationships with state economic and environmental regulators, transmission system operators, and regional trade associations in Texas on behalf of Invenergy's existing assets as well as its pipeline of development projects...
As the Senior Director Regulatory Affairs, Advanced Surgery you will be responsible for global strategic direction and performance (strategy and execution) of the Regulatory Affairs (RA) function within the division including development, implementation and management of global regulatory strategies...
This role will provide CMC regulatory support and guidance for assigned projects and interfaces with R&D, Project Management, Manufacturing, Quality, and Regulatory colleagues to ensure a robust CMC regulatory strategy is developed and implemented to have on time submissions with the highest qua...
The Director of Regulatory Affairs & Quality will lead the Philips RespirTech InCourage Vest Therapy Regulatory Affairs and Quality teams in the development and execution of compliant regulatory strategies and quality team/QMS responsibilities. Leading Regulatory Affairs strategy end-to-end executio...
This role will provide CMC regulatory support and guidance for assigned projects and interfaces with R&D, Project Management, Manufacturing, Quality, and Regulatory colleagues to ensure a robust CMC regulatory strategy is developed and implemented to have on time submissions with the highest quality...