Teams at SGS

Review and approve laboratory QC records, validation/transfer reports, and method development documentation to ensure GMP/GDP/SOP compliance. Identify and escalate deviations/OOS, audit logbooks, lead SOP improvements, and train staff per approved training records.

Perform finished-product analytical testing per SOPs and cGMP, record results in the Laboratory Information System, maintain and calibrate instruments (HPLC, GC, dissolution, ovens), assist in failure investigations, prioritize daily workflow, and ensure documentation completeness for QA review.

The Analyst is responsible for complex testing and analysis of pharmaceutical products, following SOPs, conducting maintenance on lab instruments, and reporting results accurately while managing multiple projects.