Senior Vice President, Regulatory Affairs - Parsippany

This position is responsible for developing and applying basic knowledge and understanding of regulatory and legal frameworks, · Support international product submissions (new registrations, re-registrations, and renewals) and tender responses by compiling required product docume ...

The position of Regulatory Affairs Analyst is responsible for developing and applying basic knowledge and understanding of the regulatory and legal frameworks. · Su responsabilidad es apoyar al equipo de asuntos regulatorios con la coordinación de solicitudes internacionales de r ...

The Associate, Regulatory Affairs Submission Management manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. · Manages low to medium impact (with respect to internal visibility, risk, complexity and criticality) submiss ...

The Associate, Regulatory Affairs Submission Management manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. This individual establishes and maintains submission content planners and associated timelines , prepares cont ...

+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 ...

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 Associate, Regulatory Affairs Submission Management manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams.This individual establishes and maintains submission content planners and associated timelines, facilitates tac ...

The Associate Regulatory Affairs Submission Management manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. ...

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. · ...

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. · ...

The Associate is responsible for managing low to medium impact submission projects and ensuring the timely delivery of high-quality dossiers. The role involves establishing and maintaining submission content planners and timelines, · facilitating tactical team meetings, · prepari ...

The Associate, Regulatory Affairs Submission Management manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. · ...

The Regulatory Affairs Associate supports regulatory submission management activities for development marketing and post-marketing applications. This role manages low to medium complexity submission projects coordinates cross-functional teams and ensures timely delivery of high-q ...

The Associate, Regulatory Affairs Submission Management, manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. · Manages low to medium impact (with respect to internal visibility, risk, complexity and criticality) submis ...

The Regulatory Affairs Supervisor will be the key contact for regulatory support for customers and sales/customer service/QA teams. · ...

The Regulatory Affairs Associate manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. · ...

Join a dynamic team dedicated to seamless execution of global regulatory submissions. · ...

The Associate, Regulatory Affairs Submission Management, manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams.This individual establishes and maintains submission content planners and associated timelines, facilitates ta ...

The Regulatory Affairs Associate manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. · ...

+Under general direction, responsible for successfully filing original Abbreviated New Drug Application submissions and for managing post approval changes requiring regulatory submissions. · ...

The position will require a basic understanding and application of US Food and Drug Administration labeling regulations to ensure the accuracy and regulatory compliance of ingredient statements, nutrition facts, allergen declarations, and claims. · ...