Associate Director, Regulatory Affairs - Florham Park

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. · ...

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

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. · ...

+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. · ...

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 position has the primary responsibility to contribute and support the US AML & MF Lead in Medical Affairs strategy meetings, · educational meetings, advisor boards, individual KOL meetings, · US congresses among others. · This position requires a Senior Manager with advanced ...

Responsible for developing and implementing CMC regulatory strategies for assigned pharmaceutical products in accordance with global regulations and guidances. · ...

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 ...

The CMC Regulatory Affairs Specialist will be responsible for developing and implementing regulatory strategies for assigned pharmaceutical products in accordance with global regulations and guidances. · ...

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 ...

This is a six-month contract position for a Regulatory Affairs Specialist to provide regulatory advice and risk assessment to Commercial Teams. The role involves providing innovative solutions and advice on promotional materials and ensure full regulatory compliance. · Provides r ...

Job title: Global Regulatory Affairs (GRA) Chemistry, Manufacturing and Controls (CMC) CMC Lead · Location: Morristown, NJ, Framingham, MA · About The Job · Join the engine of Sanofi's mission — where deep immunoscience meets bold, AI-powered research. In R&D, you'll drive breakt ...

Job title:  Global Regulatory Affairs (GRA) Chemistry, Manufacturing and Controls (CMC) CMC Lead · Location: Morristown, NJ, Framingham, MA · About the Job · Join the engine of Sanofi's mission — where deep immunoscience meets bold, AI-powered research. In R&D, you'll drive break ...

Job title:  Global Regulatory Affairs (GRA) Chemistry, Manufacturing and Controls (CMC) CMC Lead · Location: Morristown, NJ, Framingham, MA · *This role does not offer international relocation support · About the Job · Join the engine of Sanofi's mission — where deep immunoscienc ...

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 ...

Job Title: Manager Regulatory Affairs · Location: Morristown, NJ Cambridge, MA · About the Job · Join the engine of Sanofi's mission — where deep immunoscience meets bold, AI-powered research. In R&D, you'll drive breakthroughs that could turn the impossible into possible for mil ...

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 ...

Job title: · Global Regulatory Affairs (GRA) Chemistry, Manufacturing and Controls (CMC) CMC Lead · Location: · Morristown, NJ, Framingham, MA · About The Job · Join the engine of Sanofi's mission — where deep immunoscience meets bold, AI-powered research. In R&D, you'll drive br ...