FDA Green List API & Peptide Consultant – Importation, Forwarding & Qualification

Peptide Test is a leading independent analytical peptide testing laboratory in the United States. In addition to our analytical testing operations, we are developing lyophilization capabilities and work closely with a 503A sterile compounding pharmacy and sterile manufacturing group. We are looking to connect with individuals who have direct experience sourcing, importing, forwarding, and qualifying raw pharmaceutical APIs and peptide APIs from FDA green-listed manufacturers. We are specifically interested in speaking with professionals who have hands-on experience with: FDA green-listed API manufacturers Raw pharmaceutical API sourcing and procurement Peptide API sourcing and procurement Importation and customs logistics Supplier qualification and auditing Pharmaceutical ingredient forwarding and distribution U.S. regulatory and documentation requirements This is not a beginner-level role. We are looking for someone who has actually worked in this space and can provide practical guidance, introductions, sourcing support, supplier qualification assistance, or supply chain expertise. Potential areas of interest include: GLP-1 related peptide APIs Therapeutic peptide APIs Sterile manufacturing supply chains Pharmaceutical-grade raw materials International supplier identification and qualification If this describes your background, please send a brief summary of: Your relevant experience Manufacturers, regions, or supply chains you have worked with Pharmaceutical, compounding, CDMO, peptide, or API industry experience How you believe you could assist our organization This will begin as a consulting engagement, with the potential for ongoing work if there is a strong fit. We are interested in speaking with knowledgeable professionals who understand the realities of pharmaceutical API sourcing, qualification, and importation—not just the theory.