Principal Scientist, CMC Regulatory Affairs - Combination Products

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Discovery & Pre-Clinical/Clinical Development

Regulatory Science

Scientific/Technology

Horsham, Pennsylvania, United States of America, Raritan, New Jersey, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

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Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):

• United States
  - Requisition Number: R-093413

• Belgium, Poland
  - Requisition Number: R-094873

• Switzerland
  - Requisition Number: R-094883

Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.

Johnson & Johnson Innovative Medicine R&D is recruiting for a Principal Scientist, CMC Regulatory Affairs
- Combination Products. This position is a hybrid role and can be located in Raritan, NJ;
Titusville, NJ;
Spring House, PA; or Horsham, PA.

The Principal Scientist, CMC Regulatory Affairs
- Combination Products role will provide CMC (Chemistry, Manufacturing, and Controls) regulatory subject matter expertise for drug-device combination products and related device constituent parts involved in the preparation or administration of drugs. This role may support pre‑approval and post‑approval programs, synthetic or biologic products, and products in any therapeutic area.

The Principal Scientist will develop and execute regulatory strategies for assigned combination product programs, submissions, Health Authority interactions, and lifecycle management activities. This individual may serve as a core member of the combination product development team and may serve as an ad hoc member of the CMC team (or Value Chain team for post‑approval programs), and Global Regulatory Team. This role will also support successful development, registration, and lifecycle management of combination products globally.

This individual will provide subject matter expertise regarding global combination product and global medical device regulatory requirements and is expected to consult with other medical device regulatory experts within Johnson & Johnson Innovative Medicine or Johnson & Johnson Med Tech, as needed. The role will apply in-depth regulatory and scientific knowledge to address complex issues involving…