**Job Description** **Position:** Officer **Department:** Quality Control **Education Qualifications:** B. Pharma **Total Work Experience:** 1-3 Years **Job Role:** Finish Product section **Responsibilities:** 1. Analysis of Finished Product samples /Process Validation samples /Stability samples/ RM. Samples /Cleaning validation samples and Beta-lactam containment monitoring samples as per SAP Request /Process Validation Protocol /Stability Protocol /and Cleaning validation protocol and STPs. 2. Documentation of analytical activity performed. 3. Document analytical data and calculate results. 4. To assist in investigation of OOS /OOT/Deviation /Lab Events. 5. Management of Finished Product /Process Validation samples as per respective SOPs. 6. Ensure integrity, accuracy and adequacy of the analysis performed. 7. Document data accurately and maintain neat/concise/organized Finished Product /Process Validation records. 8. Ensure compliance to cGMP requirements and laboratory procedures. 9. Preparation of RAPS (Record of analysis) of FP/PV Whenever required. 10. To participate in analytical method transfer and analytical method Validation activity (Like analysis, Documentation & reporting of results). 11. Timely Place the indents & Procurements of Laboratory chemical & Consumables. 12. Recording of results in SAP system. 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.