QA Jobs at Pfizer Vizag | MSc Chemistry Graduates Apply Now
Are you looking for rewarding QA Jobs in the pharmaceutical industry? Pfizer is hiring an Associate Quality Assurance – MQA Downstream in Vizag. This role ensures compliance with cGMP standards in Terminal Sterilization, Visual Inspection, and Packaging operations. It is perfect for candidates seeking Chemistry Jobs and hands-on experience in pharmaceutical quality systems. Joining Pfizer offers exposure to global standards, regulatory compliance, and opportunities to advance your career through prestigious Pfizer Careers in manufacturing, quality monitoring, and process optimization.
About Pfizer:
Pfizer is a global pharmaceutical leader dedicated to developing innovative medicines and vaccines that improve patient lives worldwide. With a strong focus on quality, research, and manufacturing excellence, Pfizer provides numerous QA Jobs and Chemistry Jobs across its global operations. The company fosters a collaborative and inclusive work environment, offering employees opportunities to grow their skills, advance in their careers, and contribute to cutting-edge healthcare solutions. By joining Pfizer, professionals can pursue rewarding Pfizer Careers in manufacturing, quality assurance, research, and development, making a tangible impact on health and science globally.
Job Details
- Job Post: Associate Quality Assurance – MQA Downstream
- Locations: India – Vizag
- Job Requisition ID: 4945660
Role Summary:
The MQ TS Downstream Associate is responsible for primary contact of quality on the floor, particularly in the Terminal sterilization, Visual Inspection, and Packing areas of production, and monitors processes for compliance with cGMP standards.
Job Responsibilities:
- Responsible for ensuring the 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. Associate or Sr. Team Leader.
- Review of Batch reports and Equipment audit trails.
- Perform Acceptable Quality level sampling, Inspection in VIDT, and Batch record review and release.
- 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 with respect to Product Quality and patient safety with technical support/inputs from Sr. Associate or Sr. Team Leader.
- Review and assessment of equipment alarms and review of quarterly alarm trends.
- Report any non-compliance to the Sr. Associate or Sr. Team Leader.
- Should have troubleshooting abilities in the manufacturing area, which helps the organization to develop, implement, and achieve its mission, vision, and values.
- Identify gaps and participate in Process and Procedure Simplification to reduce downtime and increase efficiency.
Requirements:
- B. Pharm, M. Pharm, MSc.
- 2-6 years of experience in Manufacturing Quality Assurance / Quality Assurance / Production of a pharmaceutical manufacturing facility.
- Experience in the pharmaceutical industry and Quality administration systems.
- Sound knowledge of current Good Manufacturing Practices (part of GxP).
- Ability to work effectively in a team environment, both within one’s own team and interdepartmental teams.
- Practical written and oral communication skills.
