Analyst, Global Stability

Job Description Summary QC Analyst with 3–6 years of experience in pharmaceutical quality control, skilled in routine in‑process samples, and finished products. Experienced in instrumental analysis (HPLC, GC, UV, Dissolution), method execution as per approved SOPs, OOS/OOT investigations, and data integrity compliance. Well‑versed in GMP, documentation practices, and regulatory guidelines, with strong analytical and problem‑solving skills. Job Description Perform routine QC testing of raw materials, intermediates, and finished products using approved analytical methods. Conduct instrumental analysis including HPLC, GC, UV–Vis, Dissolution, and wet chemistry techniques. Execute stability studies, compile data, trend results, and prepare stability reports.…