Regulatory Affairs Manager Jobs in Newark, NJ

The Regulatory Affairs Manager provides regulatory leadership to platform teams, aligns regulatory strategies with business objectives, fosters regulatory partnerships, assesses regulatory pathways, a...

The Regulatory Affairs Manager at Aptar Pharma will manage and execute US regulatory affairs across three divisions, focusing on drug delivery systems. Responsibilities include defining regulatory str...

The Regulatory Affairs Manager at Penn Medicine is responsible for maintaining compliance with standards and regulations for various regulatory bodies, collaborating with stakeholders, and driving con...

The Regulatory Affairs Senior Manager will be responsible for managing regulatory affairs activities related to FDA communication, submissions, and compliance in the generic pharmaceutical industry. T...

The Manager of Regulatory Affairs for the Wellness portfolio is responsible for overseeing regulatory activities related to dietary supplements, ensuring compliance with regulations, and developing ef...

The Regulatory Affairs Manager is responsible for overseeing regulatory compliance for ByHeart's product portfolio, particularly in the infant formula industry. This role involves ensuring compliance...

The Regulatory Affairs Manager/Sr Manager at Theradex Oncology will provide strategic regulatory input for oncology trials, manage regulatory submissions, and serve as a key liaison for regulatory res...

Manage CMC regulatory affairs for gene therapies, ensuring compliance with regulations and guidelines. Develop regulatory strategies, review filing documents, and support interactions with global regu...

Manage CMC regulatory affairs activities for gene therapies, ensuring compliance with regulations and guidelines. Develop regulatory strategies, review filing documents, and support interactions with...

Manage CMC regulatory affairs for gene therapies, ensuring compliance with regulations and guidelines. Develop regulatory strategies and support interactions with global regulatory authorities...

Manage CMC regulatory affairs for gene therapies, ensuring compliance with regulations and guidelines. Develop regulatory strategies, review filing documents, and support interactions with global regu...

Seeking a CMC Manager- Regulatory Affairs to lead global product and project regulatory strategy, manage CMC documentation, and ensure regulatory compliance for assigned products...

The Senior Manager, Regulatory Affairs-GDP - Quality of Life (QOL), plays a pivotal role in overseeing regulatory activities related to QOL initiatives, collaborating with regional regulatory authorit...

Inviting applications for the role of CMC 3 Manager- Regulatory Affairs responsible for managing CMC compliance activities, authoring regulatory reports, leading global regulatory strategies, and ensu...

The Senior Manager, Regulatory Affairs at Insmed will be responsible for formulating and implementing regulatory plans for efficient product development, providing regulatory input into cross-function...

The Manager, Regulatory Affairs at Lupin is responsible for managing existing REMS programs, developing new REMS programs, analyzing FDA requirements, working with cross-functional teams, and maintain...

Seeking a Regulatory Studio - CMC Senior Manager to develop CMC regulatory strategy for post-approval small molecule product submissions, collaborate with cross-functional teams, and maintain knowledg...

The Global Regulatory CMC Manager is responsible for developing and implementing CMC regulatory strategies for small molecules. This role involves preparing and reviewing regulatory submissions, manag...

The Global Regulatory CMC Manager is responsible for developing and implementing CMC regulatory strategies for small molecules, preparing regulatory submission documents, managing CMC activities for c...

The Global Regulatory CMC Manager is responsible for developing and implementing CMC regulatory strategies for various submissions, managing CMC activities for compounds, representing Regulatory CMC o...

The Global Regulatory CMC Manager is responsible for preparing and reviewing CMC submission documents, managing CMC activities for compounds, and developing regulatory strategies for biologics submiss...

The Global Regulatory CMC Manager is responsible for developing and implementing CMC regulatory strategies for small molecules, preparing regulatory submission documents, managing CMC activities, and...

Lead proactive global monitoring and surveillance of changes in the regulatory landscape focused on drug development lifecycle. Manage intelligence query requests and support cross-functional projects...

Lead proactive global monitoring and surveillance of changes in the regulatory landscape focused on drug development lifecycle. Manage intelligence query requests and support cross-functional projects...

Lead global monitoring and surveillance of changes in the regulatory landscape focused on drug development lifecycle. Manage intelligence query requests and support cross-functional projects in GxP co...