Teams at Syner-G

Lead analytical development for oligonucleotide and peptide products across clinical phases: design, validate, and execute methods; perform characterization and stability testing; manage CDMO method transfers and comparability protocols; prepare regulatory submissions (IND/CTA); collaborate with CMC teams; mentor junior staff; and support project timelines and stakeholder communications.

General company overview and invitation to submit a general application for future roles across Syner-G. Applicants are encouraged to apply for consideration; the recruiting team will contact candidates when a suitable position opens.

Lead Syner-G's West Coast biologics practice, drive business development, and personally deliver biologics CMC consulting across upstream/downstream/analytical/formulation. Author CMC regulatory submissions (INDs, BLAs), mentor staff, build regional team, and represent the firm at industry events. Role requires deep technical ownership and frequent client travel.