Regulatory affairs manager jobs in Union City, NJ

JOB SUMMARY. The Regulatory Affairs Manager will be responsible for independently compiling and.. from initial development to product termination, ensuring on time completion of regulatory milestone..

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..

Works with project management, development, and commercial teams and leads regulatory activities.. ORGANIZATION STRUCTURE The Manager, Regulatory Affairs reports into the Director Regulatory Affairs or..

CMC Regulatory Affairs Manager Company. Clinical Resource Network (CRN) Considering applying for this.. Bachelor's degree in science Minimum 5 years of Regulatory Affairs experience in the industry SAP and..

JOB SUMMARY. The Regulatory Affairs Manager will be responsible for independently compiling and.. from initial development to product termination, ensuring on time completion of regulatory milestone..

Responsibilities. Oversee the day to day functions of the regulatory initiatives for Hassen Implants.. Manage the day to day activities of less senior Regulatory Affairs professionals, including mentoring..

FDA EMA) guidelines for NDA MAA IND or CTA interactions. Manage the regulatory activities for multiple.. Support the development of regulatory strategy and update strategy based upon regulatory changes..

Regulatory Affairs Associate located in Clark, NJ. Details for the position are as follows. Pay Rate. 25.. It is not a lab based role, but rather a corporate 'desk job' supporting regulatory registration for..

Months with the possibility of extension Intake Call Notes. This is an entry level position within R&I. It is not a lab based role, but rather a corporate 'desk job' supporting regulatory..

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..

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..

Position requires a Bachelor's degree in a science or chemistry related field, coursework or certification in Cosmetic or Drug Regulatory Affairs Experience in drug or cosmetic industry..

We are proud to offer an opportunity to work as a Sr Scientist, Regulatory Affairs located in Clark, NJ.. 0 60 hr Purpose of the Role. Administer regulatory affairs over the product lifecycle from pre market..

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..

Supplements and Annual Reports) with the support and oversight of the Senior Manager Associate Director.. Primary Duties & Responsibilities CMC Regulatory Affairs Act as the Regulatory Affairs lead on assigned..

Overview. The Contractor. Senior Manager, Regulatory Affairs. Quality of Life (QOL), plays a pivotal.. This role involves actively contributing to the development and execution of regulatory strategies..

Our client is looking to fill the role of CMC Regulatory Affairs. This position will be hybrid and based.. Bachelor's degree in science Minimum 5 years of Regulatory Affairs experience in the industry SAP and..