Independently conduct routine analytical testing, method qualification, and stability in a GMP environment in at least two areas: LC (PA, SEC, RP), CE (icIEF, CGE-SDS), OD, Immunoassays (ELISA), or ddPCR.

Deliver high-quality data treatment and analytical reports in a digitally agile manner.

Interact with customers to discuss results or coordinate routine and validation activities.

Work autonomously on routine/non-routine activities requiring specialized technical expertise (e.g., stability).

Strong expertise in GMP environment; validate GMP methods including analysis and documentation (mandatory).

Actively seek, share, and re-apply knowledge in your field.

Recommend and lead analytical workflow improvements in a cross-functional setting.

Present and defend relevant topics during health authority inspections.

Abil...