Nelvik Pharma Inc. is seeking a senior regulatory advisor for a focused biologics/vaccine pathway assessment.

Note: this is a short-term advisory mandate to support internal investment decision‑making.

The mandate relates to a contemplated vaccine platform intended to support export, access, and potential technology‑transfer initiatives.

We are looking to speak with advisors who have direct experience with one or more of the following:

- Health Canada biologics/vaccine pathways
- BRDD engagement
- Experience with LATAM regulatory authorities
- NDS / CTA pathway strategy
- CMC strategy for biologics or vaccines
- GMP, lot release, stability, analytical validation, and batch-consistency expectations
- clinical immunogenicity and safety bridging considerations
- export-related regulatory questions, including DEL/GMP, CPP, or Section 37 considerations
- right-of-reference and technology-transfer diligence

Relevant backgrounds may include Health Canada, vaccine manufacturers, biologics-focused regulatory consulting, CDMOs, CROs, or senior CMC/regulatory strategy roles.

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📌 Senior Regulatory Advisor - Vaccines/Biologics (Toronto)
🏢 Nelvik Pharma
📍 Toronto