A company is looking for a CMC Technical Manager, Peptide Development.
Key Responsibilities
Oversee peptide programs at CDMO and ensure timely completion of activities for peptide-based radiopharmaceuticals
Review and approve master batch records, method validation protocols, and specifications for clinical and commercial peptide products
Manage technical and quality aspects of clinical projects from raw materials to manufacturing and distribution
Required Qualifications
Minimum B.S. degree in Chemistry, Biochemistry, or a related field
7+ years of experience in the Pharmaceutical Industry in a similar role
Prior experience with peptide synthesis, purification, and lyophilization
Experience working with CMC peptide programs in regulatory settings with external collaborators / vendors
Familiarity with regulatory and quality assurance aspects in peptide manufacturing processes
Technical Manager • Independence, Missouri, United States