**Position:** **Senior Manager- Production (Injectables)** **Block Head** **Job Title:** Senior Manager Operations **Job Grade:** **Function:** Manufacturing Formulation **Sub-function:** **Managers Job Title:** **Skip Level Managers Title:** **Function Head Title:** **Location:** **No. of Direct Reports (if any)** **Job Summary** He is responsible for Vial Filling Line, PFS Filling Line, Infusion bag line and API line Manufacturing area and Autoclave area, aseptic area, Freeze drying area, qualification / re-qualification activities in Parenteral manufacturing Area (Block-E). **Areas of Responsibility** 1. He is authorize to sign (as a doer, reviewer & Approver): 1. Parenteral GMP documents 2. Breakdown memo perform impact analysis 3. Equipment and Area cleaning/sanitization logs 1. He is responsible for overall QMS activity. 2. Involved in the equipment Qualification / Re-Qualification activity in parenteral Manufacturing area (Block-E). 3. He is responsible for activities related to parenteral Manufacturing area (Block-E). 4. He is responsible for Vial Filling Line, PFS Filling Line, Infusion bag line and API line Manufacturing area and Autoclave area, aseptic area, Freeze drying area, qualification / re-qualification activities in Parenteral manufacturing Area (Block-E). 5. Up-keeping the cGMP document of area and equipment log books. 6. Any other job assigned by Department head. **Travel Estimate** **Job Requirements** **Educational Qualification** B Pharm **Specific Certification** **Skills** **Experience** 15+ Years (with USFDA approved sites) 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.