Regulatory Affairs (FDA) SME

SyncIQ helps life sciences teams work faster and stay compliant using our product. Our platform brings together specialized product “agents” that automate routine tasks and support complex, review-heavy work in areas like Regulatory Affairs, Quality/GMP, Market Access, and Medical Affairs. We focus on quick, safe adoption and integrate with the products teams already use.

Location: Remote

Type: Full-time

We’re hiring a Regulatory Affairs SME to help design and validate how our product supports regulatory work. You will review product outputs for accuracy, design clear workflows, and make sure our products follow the right guidelines (FDA, ICH, and 21 CFR). You’ll work closely with product, engineering, data science, and quality teams.

• Validate product outputs: Review, challenge, and approve product-generated regulatory content (for examp...