Senior Regulatory CMC Consultant
- Type
- Job
- Organization
- Excelya
- Location
- Saclay, France
- Deadline
- Rolling or not stated
- Who can apply
- On-site in Saclay, France
- Posted
- 24 September 2026
About this Opportunity
Join Excelya, a dynamic and innovative company committed to excellence and collaboration in the field of translational research.Our global team of experts are the powerful force behind our success. When you work at Excelya, you become part of an international network that nurtures your talent, builds your skills and recognizes your value.The selected consultant will play a critical role in leading the global Regulatory CMC strategy for a small molecule product, with a particular focus on Module 3 preparation, Marketing Authorization Applications, global health authority interactions, and regul
Eligibility
- Solid experience in Regulatory CMC within the pharmaceutical industry, strong expertise in small molecules, proven experience with Module 3 and global Marketing Authorization Applications / NDA submissions.
- Skills : Strong knowledge of FDA, EMA and ICH requirements.
- Experience with international markets such as China, Japan, Brazil and Canada is a plus.
Documents you may need
- Updated CV / Resume
- Cover Letter (tailored to this role)
How to apply
- Click the "Apply — via Arbeitnow" button to go to the source page.
- Read the full description and confirm you meet the requirements.
- Prepare your CV and cover letter tailored to this role.
- Submit your application through the official portal.
- Follow up within 1–2 weeks if you do not hear back.
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