Associate Jobs at Pfizer | Chemistry Graduates Apply Now
Are you looking for Associate Jobs with a global pharmaceutical leader? Pfizer is hiring for the role of Associate MQA Downstream at its Vizag facility in India. This full-time opportunity under Pfizer Careers is ideal for professionals passionate about quality assurance, cGMP compliance, and patient safety. Join Pfizer Jobs and contribute to delivering safe, effective, and high-quality medicines to patients worldwide.
About Pfizer
Pfizer is one of the world’s leading biopharmaceutical companies, driven by science and innovation to improve patient lives globally. With a strong presence in India, Pfizer Careers offers professionals the opportunity to work in a culture focused on quality, compliance, and continuous improvement. By choosing Pfizer Jobs, you become part of a purpose-driven organization committed to delivering breakthrough medicines and maintaining the highest standards of manufacturing excellence.
- Job Title: Associate MQA Downstream
- Locations: India – Vizag
- Time Type: Full-time
- Job Requisition ID: 4949895
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 w.r.t 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, thereby reducing downtime and increasing efficiency.
Minimum Requirements
- M. Pharma / Msc with more than 1 year 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
- Effective written and oral communication skills.
