Senior Regulatory Affairs Scientist

Venesco, LLC; Washington (District of Columbia); On-site; USD 170,000 - 210,000; Full time

Job summary

Venesco, LLC is seeking a Senior Regulatory Affairs Scientist to serve as a senior regulatory subject matter expert responsible for developing regulatory strategies, leading FDA interactions, managing submissions, and ensuring compliance throughout the medical product lifecycle. The role emphasizes mentoring, review of development documentation, and leadership in SOP improvements.

A Master’s degree plus RAC and extensive FDA experience are required, with the opportunity to influence regulatory

Qualifications

• Master’s degree or higher in Life Sciences, Pharmacy, Regulatory Affairs, or related field.
• Regulatory Affairs Certification (RAC) required.
• Minimum 12 years of FDA regulatory affairs experience.

Responsibilities

• Develop regulatory pathways and approval strategies.
• Lead preparation and review of FDA submissions.
• Serve as regulatory lead for assigned programs.
• Provide regulatory risk assessments and mitigation strategies.
• Support FDA meetings and agency interactions.
• Create and maintain Target Product Profiles.
• Monitor regulatory intelligence and emerging requirements.
• Review product development documentation.
• Mentor junior regulatory personnel.
• Lead SOP and process improvement initiatives.

Skills

FDA submissions

Regulatory strategy

Regulatory leadership

Regulatory risk assessment

FDA interactions

Mentoring

SOP improvement

Education

Master's degree in Life Sciences / Pharmacy / Regulatory Affairs

Regulatory Affairs Certification (RAC)

Job description

Description

Senior Regulatory Affairs Scientist

Venesco LLC is seeking a Senior Regulatory Affairs Scientist to serve as a senior regulatory subject matter expert responsible for developing regulatory strategies, leading FDA interactions, managing submissions, and ensuring compliance throughout the medical product lifecycle.

Requirements

Duties and Responsibilities

• Develop regulatory pathways and approval strategies.
• Lead preparation and review of FDA submissions.
• Serve as regulatory lead for assigned programs.
• Provide regulatory risk assessments and mitigation strategies.
• Support FDA meetings and agency interactions.
• Create and maintain Target Product Profiles.
• Monitor regulatory intelligence and emerging requirements.
• Review product development documentation.
• Mentor junior regulatory personnel.
• Lead SOP and process improvement initiatives.

Minimum Qualifications

• Master's degree or higher in Life Sciences, Pharmacy, Regulatory Affairs, or related field.
• Regulatory Affairs Certification (RAC) required.
• Minimum 12 years of FDA regulatory affairs experience.
• Extensive experience preparing INDs, NDAs, BLAs, IDEs, and 510(k) submissions.
• Experience interacting directly with FDA review divisions.
• Strong leadership and mentoring experience.

Venesco, LLC, is an equal opportunity and affirmative action employer. Venesco is committed to administering all employment and personnel actions on the basis of merit and free of discrimination based on race, ethnicity, religious affiliation, gender, gender identity or expression, sexual orientation, national origin, protected veteran status, or status as an individual with a disability. Consistent with this commitment, we are dedicated to the employment and advancement of qualified minorities, women, individuals with disabilities, protected veterans, persons of all ethnic backgrounds and religions according to their abilities.

For more information on Venesco, LLC., visit https://venesco.com.