Explore Pfizer Hiring for Associate QA MQA Downstream role in Vizag, covering responsibilities, qualifications, cGMP compliance, and complete application process.
Pfizer, one of the world’s most trusted and innovative pharmaceutical companies, is inviting applications for the position of Associate Quality Assurance – MQA Downstream at its Vizag facility in India. This is an excellent career opportunity for experienced pharmaceutical professionals seeking to work in the area of Manufacturing Quality Assurance (MQA), terminal sterilization, visual inspection, and packaging operations. Pfizer Hiring for Associate QA MQA Downstream
This long-format post provides a detailed overview of the job role, responsibilities, required qualifications, and how to apply. It is written in an SEO-friendly structure suitable for job-oriented websites. Pfizer Hiring for Associate QA MQA Downstream
About Pfizer
Pfizer is a global biopharmaceutical company known for developing high-quality, life-saving medicines and vaccines. With decades of excellence in research, development, and manufacturing, the company continues to lead innovation that improves patient health worldwide. Pfizer’s Vizag manufacturing site plays a significant role in delivering high-quality pharmaceutical products, ensuring the highest standards of safety, quality, and compliance. Pfizer Hiring for Associate QA MQA Downstream
Pfizer’s commitment to compliance, operational excellence, and continuous improvement makes it an ideal organization for aspiring Quality Assurance professionals. As part of its strong Quality culture, Pfizer ensures adherence to global manufacturing standards, cGMP regulations, and robust quality systems across all its manufacturing units. Pfizer Hiring for Associate QA MQA Downstream
Job Title: Associate Quality Assurance – MQA Downstream
Location: India – Vizag
Job Type: Full-Time
Requisition ID: 4945660
Posted: Today
Role Summary
The MQ TS Downstream Associate will act as the primary Quality Assurance contact on the production floor, particularly focusing on Terminal Sterilization, Visual Inspection, and Packaging areas. The role requires ensuring that all processes adhere strictly to current Good Manufacturing Practices (cGMP) and Pfizer’s internal Quality standards. This position plays a crucial part in maintaining product quality, regulatory compliance, and patient safety. Pfizer Hiring for Associate QA MQA Downstream
The Associate Quality Assurance professional will monitor operations, perform checks, review documentation, assess equipment performance, and coordinate with team leaders to identify and resolve quality gaps. The role demands attention to detail, strong technical understanding, and the ability to work in a fast-paced manufacturing environment. Pfizer Hiring for Associate QA MQA Downstream
Key Job Responsibilities
Below is a detailed description of the responsibilities associated with the Associate Quality Assurance – MQA Downstream role: Pfizer Hiring for Associate QA MQA Downstream
1. Ensuring cGMP Compliance
The candidate is responsible for ensuring that Terminal Sterilization, Visual Inspection, and Packaging operations follow current Good Manufacturing Practices (cGMP) at all times. Compliance is vital to ensure product quality, safety, and consistency.
2. Maintaining Regulatory Compliance
The role involves continuous monitoring of processes to ensure they comply with internal Pfizer policies, standard operating procedures (SOPs), and global quality guidelines. The Associate will verify documentation, assess deviations, and ensure corrective actions are implemented as required. Pfizer Hiring for Associate QA MQA Downstream
3. Reviewing eBR and AMPs Exceptions
A major responsibility includes reviewing electronic Batch Records (eBR) and assessing the significance of Automated Manufacturing Process exceptions (AMPs). The Associate will obtain technical support and guidance from Senior Associates or the Sr. Team Leader wherever required.
4. Reviewing Batch Reports and Audit Trails
The candidate must review batch manufacturing reports and equipment audit trails to ensure accurate and complete documentation. This includes verifying entries, evaluating alarms, and ensuring all recorded data aligns with operational activities.
5. Performing AQL Sampling and Inspections
The Associate will perform AQL (Acceptable Quality Level) sampling, conduct inspections in VIDT (Visual Inspection and Defect Test), and execute batch record reviews for product release.
6. Executing Batch Start-Up and End Activities
Responsibilities include performing sensor challenge tests, verifying recipes, and ensuring all pre-start and post-completion processes meet required standards.
7. Conducting Random Process Checks
The role requires random in-process checks for terminal sterilization, visual inspection, and packaging processes to ensure consistent adherence to quality requirements.
8. Daily Walkthroughs & Observations
To maintain continuous oversight, the Associate must perform daily production floor walkthroughs, document observations, and report quality issues to the Sr. Team Leader.
9. Equipment Breakdown Assessment
In case of equipment malfunction, the Associate must assess its impact on product quality and patient safety, with guidance from senior QA members.
10. Alarms Review & Trends Analysis
The candidate will review equipment alarms, assess quarterly alarm trends, and recommend actions to minimize recurring issues.
11. Reporting and Troubleshooting
Reporting non-compliance, equipment issues, and process deviations to the Sr. Associate or Sr. Team Leader is critical. The Associate must have the capability to troubleshoot issues and support Pfizer’s mission of achieving high-quality, efficient production.
12. Identifying Gaps and Improving Processes
The role encourages active participation in process simplification, identifying inefficiencies, and contributing to improvements that reduce downtime and enhance operational efficiency. Pfizer Hiring for Associate QA MQA Downstream
Minimum Qualifications Required
To be eligible for the role of Associate Quality Assurance – MQA Downstream, candidates must meet the following criteria: Pfizer Hiring for Associate QA MQA Downstream
- Educational Requirement:
- B.Pharm
- M.Pharm
- M.Sc
- Experience:
- 2 to 6 years of experience in:
- Manufacturing Quality Assurance
- Quality Assurance
- Production in a pharmaceutical manufacturing facility
- 2 to 6 years of experience in:
- Technical Skills:
- Strong understanding of cGMP, GxP practices
- Experience in pharmaceutical industry quality systems
- Knowledge of batch record reviews, audit trails, and inspection processes
- Soft Skills:
- Ability to work effectively in a team environment
- Strong written and oral communication skills
- Ability to collaborate with cross-functional departments
Pfizer’s Commitment to Equality
Pfizer is an equal opportunity employer and follows all applicable employment laws. The company maintains a diverse and inclusive workplace free from discrimination based on gender, race, religion, nationality, disability, or veteran status. All qualified applicants are encouraged to apply.
How to Apply
If you are interested in applying for the Associate Quality Assurance – MQA Downstream role at Pfizer, follow the steps below:
- Visit the official Pfizer Careers website.
- Search for the Job Requisition ID: 4945660.
- Select the location: Vizag, India.
- Click the Apply button.
- Log in or create a new candidate profile.
- Fill out all required personal, educational, and professional details.
- Upload your updated resume and supporting documents.
- Review your application and submit it.
Once submitted, the Pfizer recruitment team will review your profile and contact you if shortlisted. Pfizer Hiring for Associate QA MQA Downstream
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