Offer summary
Qualifications:
Advanced degree in Pharmaceutical Sciences, Chemistry, or related field, 5+ years in process development and manufacturing of peptide and oligonucleotide APIs, Experience in cGMP environment required, Familiarity with solid phase peptide/oligo synthesis preferred, Available to travel if needed.
Key responsabilities:
- Lead drug substance team in development and manufacturing
- Oversee preclinical and clinical material production
- Manage DS strategy and long-term development plans
- Collaborate with internal CMC team and external partners
- Approve development protocols, production records, and testing results