Regulatory Affair-Lead/Sr/Jr - Bridgewater, NJ

Jr. Publisher – Regulatory Affairs · (Bridgewater) · ...

Preparar, rastrear, compilar y publicar suministros regulatorios para asignados. · Diploma/ Bachelor degree in Pharmacy. · ...

Sr. Publisher – Regulatory Affairs at Net2Source, Inc. · Responsible for global regulatory submission / dossier publisher day-to-day activities and deliverables. · ...

Jr. Publisher – Regulatory Affairs · Location: · Bridgewater,NJ,, · Global Submission/Publishing of all submissions from a Global perspective and dispatches to worldwide Health Authorities (FDA, EMA,LATAM,RW).Accountable for all Publishing,verification,dispatch.Working in close c ...

+h2>Job Summary · Develops and mentors associates by providing expertise in all clinical electronic publishing submission types applicable to their region of responsibility. Leads team of publishers , manages people. · +Diploma/ Bachelor degree in Pharmacy, Life-Science · Minimu ...

This is a Team Lead – Regulatory Affairs job in Bridgewater. It involves developing and mentoring associates by providing expertise in all submission types applicable to their region of responsibility. · ...

Necesita experiencia de más de cinco años en publicación de presentaciones electrónicas y mantenimiento rutinario de IND. · Tener buena comprensión del ciclo de vida del medicamento. · ...

The job description states that Net2Source, Inc. is one of the fastest growing IT Consulting company across USA. The role of Delivery Lead - Regulatory Affairs involves being the first point of contact for client regional lead and for hub related queries, working in close collabo ...

The company Net2Source is an employer-of-choice for over 1000 consultants across the globe. They recruit top-notch talent for over 40 Fortune and Government clients coast-to-coast across the U.S. · ...

+p>Opella es un challenger global líder en salud personal con una cartera diversa. Buscando talentos apasionados por desarrollar marcas de consumo. · Se busca Lead, responsable regulatorio para Pain portfolio (OTC) - USA. · ​​Responsabilidades:Crea estrategia regulatoria para lan ...

Opella is the self-care challenger with the purest and third-largest portfolio in the Over-The-Counter (OTC) & Vitamins, Minerals & Supplements (VMS) market globally. Our mission is to bring health in people's hands by making self-care as simple as it should be. · ...

We are seeking a Regulatory Affairs Lead to provide oversight for the Pain portfolio in the US.As a globally certified B Corp company, · we are active players in the journey towards healthier people and planet. · The role is expected to be able to prioritize/balance activities ac ...

The Regulatory Affairs Lead provides Regulatory Affairs oversight for the Pain portfolio in the US. Key accountabilities include representing US Regulatory Affairs on innovation project teams and in advertising/promotion reviews. · ...

We are looking for a Sr. Manager, Regulatory Affairs Strategy to support submissions for various developmental, life cycle, and post-approval projects in the US, EU, Canada and beyond. The incumbent will work closely with colleagues from the US;EU and Japan gaining valuable globa ...

We have an opening in our Monmouth Junction NJ facility for an experienced Lead Reviewer Regulatory Affairs Advertising & Promotion to join our Regulatory Affairs team.The incumbent leads regulatory review efforts supporting advertising and promotional activities across the busin ...

We have an opening in our Monmouth Junction facility for an experienced Lead Reviewer to join our Regulatory Affairs team.The incumbent partners closely with cross-functional teams to ensure compliance with regulatory requirements while driving strategic promotional initiatives. ...

We have an opening in our Monmouth Junction, NJ facility for an experienced Lead Reviewer, Regulatory Affairs – Advertising & Promotion to join our Regulatory Affairs team. · ...

The Global Regulatory Affairs Device team is a globally diverse team supporting medical device products within the Sanofi portfolio. The GRA Device organization serves as a critical strategic partner providing expert guidance on regulatory requirements across the product lifecycl ...

We have an opening in our Monmouth Junction, NJ facility for an experienced Lead Reviewer, Regulatory Affairs – Advertising & Promotion to join our Regulatory Affairs team. · Incumbent leads regulatory review efforts supporting advertising and promotional activities across the bu ...

Shape the future of medicine by accelerating drug discovery and development to find answers for patients and their families. · Serve as GRA Device Lead on assigned project teams. · Provide regulatory guidance and advice to Global Regulatory Team (GRT) and cross-functional teams. ...