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Regulatory Affairs Specialist

Cronus Pharma
East Brunswick, NJ Full Time
POSTED ON 3/21/2026
AVAILABLE BEFORE 4/19/2026
Regulatory Affairs Specialist needed w/ Master’s degree or Foreign Equivalent in Pharmaceutics or Drug Regulatory Affairs or Pharmacy and one (1) year experience as a Regulatory Affairs Specialist or Regulatory Affairs Associate performing following job duties: Prepare, compile, review and finalize post-approval supplements (PAS, CBE30, CBE0 and Labeling supplements), deficiency responses/amendments and Annual Reports.

Manage Self-identification, establishment registration, drug listings. Review and file submission documents for adverse event reports. Prepare and publish the regulatory submissions as per FDA/ICH requirement.

Interact with other functional departments during the entire R&D development process (review / submission / approval) to coordinate and facilitate quality and timely submissions.

Create, revise and review labeling per current FDA requirements.

Assist in FDA inspections.Salary: $80600.00 Per Year.Benefits: PTO, Health, Dental, Vision, Basic life and AD&D, short term disability, long term disability, accidental death, Cancer & specified illness.Job Location: East Brunswick, NJ

Mail resumes to: Cronus Pharma LLC2 Tower Center Boulevard, Suite 1101A, East Brunswick, NJ 08816

Salary : $80,600

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