QA Job at Pfizer | Apply Now for the Chemistry Job
Are you looking for a promising QA job or chemistry job within a global pharmaceutical leader? The Associate Quality Assurance – MQA Downstream role at Pfizer Careers offers a rewarding opportunity to support quality excellence, ensure compliance with cGMP standards, and contribute directly to safe and efficient manufacturing processes.
About Pfizer:
Pfizer is a global biopharmaceutical leader committed to discovering and delivering innovative medicines and vaccines that improve health worldwide. With a strong focus on scientific excellence, advanced manufacturing, and quality compliance, Pfizer offers a dynamic environment for professionals seeking a QA job or chemistry job within the pharmaceutical industry. As part of Pfizer Careers, employees benefit from a culture that values integrity, diversity, growth, and collaboration. Operating in more than 125 countries, Pfizer provides meaningful career opportunities where individuals can contribute to patient safety, product quality, and the company’s mission to advance global health.
Job Details
- Job Title: Associate Quality Assurance – MQA Downstream
- Location: India – Vizag
- Job Requisition ID: 4945660
Role Summary:
Are you looking for a promising QA job or chemistry job within a global pharmaceutical leader? The Associate Quality Assurance – MQA Downstream role
at Pfizer Careers offers a rewarding opportunity to support quality excellence, ensure compliance with cGMP standards, and contribute directly to safe and efficient manufacturing processes.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 Inspectio,n 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 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.
