Regulatory Affairs Associate (Labeling & FDA) - Hybrid

Scorpion Therapeutics; Barrington (IL); Hybrid; USD 85,000 - 110,000; Full time

Job summary

Eton is seeking a Regulatory Affairs Support Specialist to assist labeling, submissions, and compliance for its pharmaceutical products. You will collaborate with Marketing, Medical Affairs, QA, R&D, and Legal to ensure regulatory adherence and maintain organized documentation.

The role requires a Bachelor’s degree in Life Sciences or Chemistry and 2–4 years of regulatory affairs experience, with emphasis on labeling and FDA submissions. Hybrid onsite work in Deer Park, IL is available.

Qualifications

• Bachelor's degree in Life Sciences, Chemistry, or related field.
• 2-4 years of regulatory affairs experience in pharma/biotech.
• Experience with regulatory labeling and FDA submissions.

Responsibilities

• Assist with regulatory labeling updates and prepare FDA submissions.
• Maintain regulatory documentation and contribute to lifecycle management.
• Collaborate with Marketing, Medical Affairs, QA, R&D, and Legal to ensure regulatory adherence.
• Track submission deadlines and maintain organized records.

Skills

Regulatory affairs

FDA submissions

Cross-functional collaboration

Education

Bachelor's degree in Life Sciences/Chemistry

Tools

FDA Form 2253

Job description

Eton is seeking a Regulatory Affairs Support Specialist to assist labeling, submissions, and compliance for its pharmaceutical products. You will collaborate with Marketing, Medical Affairs, QA, R&D, and Legal to ensure regulatory adherence and maintain organized documentation.

The role requires a Bachelor’s degree in Life Sciences or Chemistry and 2–4 years of regulatory affairs experience, with emphasis on labeling and FDA submissions. Hybrid onsite work in Deer Park, IL is available.