AssociateManager-MQA

**Role Summary** The MQ TS Downstream Associate Manager is responsible for primary contact of quality on the floor, particularly in the Terminal sterilization, Visual Inspection and Packing areas of production and monitor processes for compliance to cGMP standards. **Responsibilities** Responsible for ensuring operating state of cGMP compliance in Terminal Sterilization, Visual Inspection and Packaging operations. Maintain regulatory compliance in accordance with cGMP practices Ensure manufacturing policies and procedures conform to Pfizer standards Knowledge and hands on experience in reviewing eBR and assessing the impact of AMPs exceptions with technical support/inputs from Sr. Team leader. Review of Batch reports, and Equipment audit trails Perform Acceptable Quality level sampling, Inspection and record the results in Batch records for all products Perform batch start-up and end activities viz. sensor challenge tests, recipe review etc. Perform random process checks for Terminal Sterilization, Visual Inspection and Packaging Perform Daily walkthroughs and report observations to the Sr. Team leader. Perform Equipment breakdown assessments w.r.t to Product Quality and patient safety with technical support/inputs from Sr. Team Leader. Review and assessment of equipment alarms and review of quarterly alarm trends. Report any non-compliance to the Sr. Team Leader Should have trouble shooting abilities in manufacturing area, which helps the organization to develop, implement and achieve its mission, vision and values. Identify gaps and involve in Process and Procedure Simplification, thereby reduce downtime, and increase the Efficiency. AMPS Recipe review and validation of recipe. Experience in handling regulatory, corporate and internal auditors/ inspectors **Here Is What You Need**(Minimum Requirements) Candidate must have B. Pharm, M. Pharm, MSc. with 6-8 years of experience in Manufacturing Quality Assurance / Quality Assurance / Production of a pharmaceutical ma