Regulatory Labeling Fellow — Postdoc (Pharma)

Boehringer Ingelheim GmbH; Ridgefield (CT); On-site; USD 65,000 - 90,000; Full time

Job summary

Boehringer Ingelheim US headquarters in Ridgefield, CT invites a Postdoctoral Regulatory Affairs Fellow – Product Labeling Content to join our Regulatory Affairs team. The program provides exposure to US product labeling and rotations across therapeutic areas to build regulatory expertise for pharmacists.

The Fellow will develop competencies in regulatory labeling strategies, CCDS updates, and cross-functional collaboration, contributing to US market labeling and global alignment initiatives.

Qualifications

• Doctor of Pharmacy degree from ACPE-accredited school or PharmD OR PhD in related discipline.
• Strong communication and teamwork skills for a regulatory environment.
• Ability to work independently and adapt to rotating responsibilities across therapeutic areas.

Responsibilities

• Chair Product Label Review Teams (PLRT) meetings and prepare minutes.
• Draft/revise product labeling and ensure CCDS alignment with regulations.
• Coordinate labeling documents for regulatory submissions with cross-functional teams.
• Assist with FDA interactions and ensure US labeling consistency with global labeling.

Skills

Regulatory analysis

Team collaboration

Communication skills

Problem solving

Pharmacy knowledge

Education

Doctor of Pharmacy (PharmD)

PhD in related discipline

Tools

Outlook

Word

PowerPoint

Excel

Job description

Boehringer Ingelheim US headquarters in Ridgefield, CT invites a Postdoctoral Regulatory Affairs Fellow – Product Labeling Content to join our Regulatory Affairs team. The program provides exposure to US product labeling and rotations across therapeutic areas to build regulatory expertise for pharmacists.

The Fellow will develop competencies in regulatory labeling strategies, CCDS updates, and cross-functional collaboration, contributing to US market labeling and global alignment initiatives.