Senior RA CMC Manager, Drug Product

Must be based in Central France
4 days on site / 1 day remote
Bi-monthly travel to Switzerland
1 direct report
Salary range: €60K–90K

Responsibilities:

• Take ownership of Drug Product (DP) CMC strategy, with strong focus on Fill/Finish activities, formulation, and stability programs.

• Draft clinical and commercial dossiers from scratch (IMPDs, INDs, BLAs/MAAs), ensuring compliance with EU/FDA expectations.

• Outline development pathways and fast-track options to accelerate timelines.

• Review and approve validation protocols (analytical/stability) and source documents provided by development and QC teams.

• Partner closely with process development, manufacturing, and QA to ensure alignment between tech ops and regulatory deliverables.

• Act as a regulatory point of contact for internal teams and external collaborators.

• Mentor and lead 1 direct report, supporting their professional development.

Ideal Background:

• Strong technical CMC foundation, ideally coming from a DP/formulation or Fill/Finish environment.

• Experience with bioconjugates or small molecules.

• Regulatory writing experience, with the ability to translate technical knowledge into regulatory language.
  
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