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About our client
Our client is a leading privately held pharmaceutical company with operations in over 40 countries. With marketed products, an experienced management team, and an empowering corporate culture that is focused on the professional development of its employees, this is a great opportunity for the right candidate.
Position	Location
Manager of Regulatory Affairs	New Jersey
Salary
Highly competitive package, commensurate with experience
Responsibilities
1) Oversee document management duties in the Regulatory Affairs department 2) Organize all FDA submissions 3) Coordinate FDA submissions calendar 4) Ensure reports are submitted on time 5) Manage creation of electronic copies of all FDA submissions 6) Create/maintain up-to-date computer accessible FDA files
Requirements
1) Bachelor’s or master’s degree in a scientific discipline 2) 2-5 years related experience 3) Experience in preparing/coordinating FDA submissions 4) Superb organizational and interpersonal skills 5) Excellent verbal, written and presentation skills