Life Sciences industry experience in the Pharmaceutical R&D regulatory affairs function to include:Experience introducing new technologies such as GenAI/AI/ML and automation for pharmaceutical regulat...

Preparation, submission, and monitoring of PLAIR activities, prior to new product launch Manage regulatory correspondence mainly to CDER, FDA, User fee staff, drug listing and Board of Pharmacies for ...

The Contractor - Senior Manager, Regulatory Affairs - Quality of Life (QOL), plays a pivotal role in supporting the Senior Director in overseeing regulatory activities related to QOL initiatives. This...

The Contractor - Senior Manager, Regulatory Affairs - Quality of Life (QOL), plays a pivotal role in supporting the Senior Director in overseeing regulatory activities related to QOL initiatives. This...

Manager, Regulatory Affairs integrates and applies knowledge of US regulatory guidelines and federal regulations governing pharmaceutical drug development to all aspects of Our Client’s drug developme...

The Global Regulatory Labeling Strategy Sr Manager/Associate Director will be responsible for leading the development and maintenance of global labeling documents (e. This role will be within Global R...

Support maintaining regulatory intelligence database regarding national and EU regulatory requirements through review of publications, attendance at seminars and direct communication with outside regu...

Works closely with Regulatory Affairs Managers to ensure business unit account remediation projects meet regulatory expectations, have effective project plans, and provide regular reporting to Bank ex...

This role will report directly to the VP of Global Regulatory Affairs. This list is not totally inclusive, and the person will be expected to complete tasks reasonably requested by the VP of Global Re...

Regulatory Affairs Senior Manager. A leading, global pharmaceutical client of ours is looking to hire a Senior Manager of Regulatory Affairs at their prescription drug specific subsidiary, based out o...

A leading, global pharmaceutical client of ours is looking to hire a Senior Manager of Regulatory Affairs at their prescription drug specific subsidiary, based out of New Jersey. Regulatory Affairs Se...

Senior Manager, Regulatory Affairs. Working closely with the Senior Director, Regulatory Affairs to support with Regulatory documents, submissions, strategy.

We are seeking a Senior Manager, Regulatory Affairs to play a key role in advancing our mission to deliver innovative healthcare solutions. Senior Manager, Regulatory Affairs'. Senior Manager, Regulat...

Develop and implement regulatory strategies, including regulatory risk management, ensuring that any RA issues are highlighted and addressed satisfactorily and in a timely fashion. Lead process for fi...

The Manager of Regulatory Affairs will lead the regulatory strategy and submission processes for Chemistry, Manufacturing, and Controls (CMC) associated with Abbreviated New Drug Applications (ANDAs) ...

Pay Range: 200- 220K The Regulatory Affairs Program Manager is responsible for a multitude of multi-year projects and programs leading mandatory and strategic regulatory change supporting multiple lin...

The Global Regulatory Affairs Manager will lead the team tasked with supporting product submissions globally. You will coordinate regulatory documents, ensuring that submissions are timely and regulat...

Senior Manager, Regulatory Affairs. Working closely with the Senior Director, Regulatory Affairs to support with Regulatory documents, submissions, strategy.

The Global Regulatory Labeling Strategy Sr Manager/Associate Director will be responsible for leading the development and maintenance of global labeling documents (e. This role will be within Global R...

The Manager, Regulatory Affairs will report to the Global Regulatory Liaison (GRL) and provides support to the GRL in all aspects of regulatory affairs related to the development of novel therapeutics...