**Sr. No.** **Job Responsibilities** **1** **Have a knowledge on Quality control function like FP/RM/PM/Stability of Solid dosage forms.** **2** **Having a good knowledge on QC Instrumentations** **3** **Having sound knowledge on trouble shooting of QC instruments like Auto titrator, HPLC, GC etc.** **4** **Expected knowledge of 21CFR part 11 compliance and Computer system validation** **5** **Must having knowledge on Investigation like OOS, OOT, events and deviation management.** **6** **Having** **knowledge on LEAN management and Good presentation skill** **7** **Having exposure on Regulatory Audit handling and management** **8** **Regular review of SOPs versus practices for gap analysis.** **9** **Trending of QC data and deriving action plan for compliance readiness** **10** **Having good exposure of review of analytical raw data** We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.