The Analytical Associate would report directly to the Supervisor. The individual supports the QC/AR Supervisor in all quality control and analytical activities.
Duties and responsibilities include, but are not limited to, the following:
- Coordinating contract service projects – method transfer, method validation, and reports.
- SOP preparation in compliance with cGMP operations and FDA regulations.
- PLC assay development for pharmaceutical products and raw materials.
- Perform laboratory analytical tests including HPLC, FIR, dissolution, cleaning validation, and regular stability testing.