- Method development and validation — execute against ICH Q2 or USP guidelines on a defined product line.
- Synthesis at the gram scale — plan, run, and characterize routinely in an R&D lab.
- NMR, MS, and chromatography data — interpret independently on standard substrate classes.
- Out-of-specification investigations — lead under a senior chemist's review with documented root cause.
- Process chemistry transfers — support from R&D to pilot under a GMP framework.
- Junior analysts and interns — train on routine analyses in a QC environment.
