Regulatory affairs associate jobs in New Brunswick, NJ

Responsibilities and Requirements. Support daily Regulatory Affairs function eg. compliance to 21 CFR.. Provides regulatory expertise in any significant or non significant changes. Support in maintaining and..

Associate Director, Regulatory Affairs UK The Regulatory Affairs team manages a broad portfolio of.. A new opportunity has arisen in the UK Regulatory Affairs Department, at the Associate Director level..

Regulatory Affairs Manager. Permanent. Bridgewater, NJ Proclinical is seeking a Manager, Regulatory.. This role is a global regulatory position, working closely with site Quality, R&D, Operations, and..

The Regulatory Affairs Manager will create, evaluate and execute domestic and or international.. Incumbent may supervise approximately 5 to 10 team members at the Associate, Specialist or Manager..

Job Description POSITION OVERVIEW For the LVMH Beauty scope of brands, joining the Regulatory Affairs.. Identifying and actioning opportunities on operational regulatory affairs topics to drive our Beauty..

Manager Regulatory Affairs Preparation and review of various regulatory submissions to the appropriate.. Regulatory submissions, initiation review of change controls and labeling. Collect and review..

Summary Our client, a growing pharmaceutical company, has engaged GForce to provide a CMC Regulatory Affairs Manager Consultant. The role will be focused on providing CMC regulatory strategy..

Negotiable Responsibilities. Excellent employment opportunity for a Regulatory Affairs Consultant in the.. Represent Regulatory Affairs by attending project team meetings, providing regulatory strategies..

The Senior Director, Regulatory Affairs will lead and formulate the regulatory affairs strategy for.. Responsibilities Analyze FDA regulatory requirements for all pharmaceutical dosage forms, applying..

The requirement is for 3 Regulatory Affairs Specialist.Responsibilities. Identify reference documents.. Maintain information on worldwide regulatory requirements and the status of product registrations..

The Role Genmab is looking for an experienced and passionate leader to be a part of our Global Regulatory Affairs (GRA) organization. In this role, you will be primarily responsible for the..

OBJECTIVES PURPOSE OF JOB. The Senior Director of Global Regulatory Operations is responsible for.. Serve as a leadership team member for Global Regulatory Affairs Lead and grow individuals on the..

Innovating every day. Position Overview The Senior Director, Regulatory Affairs will lead and formulate.. Responsibilities Analyze FDA regulatory requirements for all pharmaceutical dosage forms, applying..

On Board Scientific is hiring a Regulatory Affairs Assistant!For immediate consideration please send.. st shiftBenefits Compensation. per hour based on previous experience The Regulatory Assistant needs to..

About the Department. The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of.. Are you ready to make a difference?. The Position The Regulatory Affairs Therapeutic Area Postdoctoral..