Senior Vice President, Regulatory Affairs - Parsippany, NJ

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 ...

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 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 ...

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 · . For h ...

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

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

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

Under general direction responsible for successfully filing original Abbreviated New Drug Application submissions and for managing post approval changes requiring regulatory submissions. Can be primary contact with regulatory authorities for assigned projects and products. · ...

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. · ...

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

We seek a · Regulatory Site Quality Specialist · to support a leading CPG company's OTC drug listing portfolio. · ...

We are seeking a Regulatory Site Quality Specialist to support a leading CPG company's OTC drug listing portfolio. · This role will manage the drug listing process for skincare and cosmetic products, ensuring compliance with FDA regulations and GMP standards. · ...

This position reports to the Myeloid Medical Promotional Review lead and is a key member of the US Medical Affairs Myeloid Team.The primary responsibility is to support the strategic review of promotional materials from a medical lens for Client products. · Advanced Degree · , Cl ...

This is a rare, · CEO-facing executive leadership · role with broad influence across the organization. · The Senior Vice President, Regulatory Affairs, will own and shape global regulatory strategy across commercial products, lifecycle management, · pipeline development and serve ...

This is a rare opportunity to step into a Chief Executive facing role and shape global regulatory strategy for a commercial-stage biopharmaceutical organization with a growing pipeline. · ...

The Senior Vice President, Regulatory Affairs will own and shape global regulatory strategy across commercial products, lifecycle management, and pipeline development serving as a trusted advisor to the CEO, Executive Leadership Team, and Board of Directors on regulatory risk opp ...

This position reports to the Franchise Cell Therapy Lead and is a key member of the US Medical Cell Therapy Team. · The primary responsibility is to work across the Medical matrix teams, driving strategy and overall Medical excellence across the Cell Therapy Franchise. · Contribu ...