Senior Regulatory Affairs Specialist

EPM Scientific; Summit (NJ); On-site; USD 120,000 - 170,000; Full time

Job summary

EPM Scientific is recruiting a Senior Regulatory Affairs Specialist in Summit, New Jersey. The candidate will lead regulatory strategy, interact with FDA/other health authorities, and manage global submissions for both development and marketed products.

The role partners with cross-functional teams to ensure lifecycle regulatory compliance, staying current with evolving guidelines and industry trends in a fast-paced biotech environment.

Qualifications

• Bachelor's degree with 7+ years or Master's degree with 5+ years of regulatory affairs experience in pharma/biotech.
• Experience supporting regulatory submissions and health authority interactions.
• Strong knowledge of FDA, ICH, and global regulatory requirements.

Responsibilities

• Serve as a Regulatory Affairs subject matter expert across the organization.
• Prepare, review, and approve CTDs and other regulatory submissions for compliance and technical accuracy.
• Support U.S. and global regulatory strategies for development and commercial products.
• Coordinate responses to health authority requests and inquiries.
• Monitor regulatory guidance, requirements, and industry trends.
• Author and review Regulatory Affairs SOPs and related documentation.
• Collaborate with cross-functional teams to ensure regulatory compliance throughout the product lifecycle.

Skills

Regulatory affairs

Health authority interactions

FDA knowledge

ICH guidelines

Project management

Cross-functional collaboration

Regulatory submissions

Education

Bachelor's degree

Master's degree

Job description

Senior Regulatory Affairs Specialist (PR/613523) Summit, New Jersey

An innovative commercial-stage biotechnology company is seeking a Senior Regulatory Affairs Specialist to support regulatory compliance and submission activities across both marketed products and development-stage programs. This individual will contribute to regulatory strategy, health authority interactions, and global submission activities while partnering closely with cross-functional teams in a fast-paced environment.

Responsibilities:

• Serve as a Regulatory Affairs subject matter expert across the organization.
• Prepare, review, and approve CTDs and other regulatory submissions for compliance and technical accuracy.
• Support U.S. and global regulatory strategies for development and commercial products.
• Coordinate responses to health authority requests and inquiries.
• Monitor regulatory guidance, requirements, and industry trends.
• Author and review Regulatory Affairs SOPs and related documentation.
• Collaborate with cross-functional teams to ensure regulatory compliance throughout the product lifecycle.

Qualifications:

• Bachelor's degree with 7+ years or Master's degree with 5+ years of regulatory affairs experience in the pharmaceutical or biotechnology industry.
• Experience supporting regulatory submissions and health authority interactions.
• Strong knowledge of FDA, ICH, and global regulatory requirements.
• Experience preparing responses to regulatory agency questions and requests.
• Excellent project management, communication, and organizational skills.
• Ability to manage multiple priorities and work effectively in a collaborative environment.