Regulatory affairs jobs in Kenner, LA

A company is looking for a Regulatory Affairs Manager to facilitate product development and global.. Key Responsibilities Assist in regional regulatory activities, including IMPD development and submission..

Sharing your scientific, technical, regulatory and or commercial expertise with them, so that they can.. 5. years experience with expert level industry or regulatory knowledge experience in Clinical..

Has an outstanding opportunity for a Medical Director (Medical Affairs).The Medical Affairs department.. with a solid understanding of medical statistics, regulatory agencies, and analytic programsUnrestricted..

The position requires collaboration with other state and US government affairs team members and 3M's government affairs team globally, as well as the company's regulatory, legal, compliance..

Director, Academic Affairs to support and execute the strategy and priorities for Graduate Medical.. good clinical practices and regulatory compliance.Proficient with Microsoft Word, PowerPoint and Excel..

The ability to develop a strong understanding of a state's regulatory environment and the needs.. and regulatory affairs and or an advanced education degree in public policy, finance, economics, public..

Accreditation requirements from the Regulatory Guidance team. Translate and communicate compliance.. accreditation requirements across multiple jurisdictions, including assessments of the regulatory impact..

Job Purpose and ImpactThe Product Safety and Regulatory Specialist supports the 3rd party locations of CBI (Cargill Bio Industrial) products in providing specialized knowledge of specific..

Come make a difference at Ochsner Health and discover your future today! Associate Medical Director & Vice President of Medical Affairs (AMD VPMA)Under the direction of the Regional Medical..

Role. You will supervise and prepare, edit, refine, and modify regulatory medical writing documents of.. Duties. Regulatory Medical writing. Regulatory, Clinical trial related documents, including clinical..

Medical Device Equipment (Remote with travel) Your tasks As the Quality and Regulatory Manager you will be responsible for quality control, quality assurance and regulatory affairs for the U.S..