JOB DETAILS

MQA Downstream Associate Manager

CompanyPfizer
LocationIndia
Work ModeOn Site
PostedJune 18, 2026
About The Company
We’re celebrating over 175 years of daring scientific innovation—and we’re not done yet. Let’s outdo yesterday. Protect your health at PfizerForAll.com For additional information on our guidelines, please visit http://www.pfizer.com/community-guidelines
About the Role

Use Your Power for Purpose

Every day, Pfizer’s unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is both flexible and innovative, always putting the patient first. Whether you are involved in development, maintenance, compliance, or research analysis, your contribution directly impacts patients. 

Role Summary for Associate Manager:

The MQA 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.

Responsible for ensuring operating state of cGMP compliance in Terminal Sterilization, Visual Inspection and Packaging operations.

Responsibilities:

MES quality 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. 

Experience:

B. Pharm, M. Pharm, MSc.

6-8 years of experience in Manufacturing Quality Assurance / Quality Assurance / Production of a pharmaceutical manufacturing facility.

Shall able to work in the shifts.

  
Work Location Assignment: On Premise

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers.

Quality Assurance and Control

Key Skills
cGMP ComplianceManufacturing Quality AssuranceMES Quality OperationsBatch Record ReviewTerminal SterilizationVisual InspectionPackaging OperationsAQL SamplingEquipment Audit TrailsRisk Assessment
Categories
ManufacturingHealthcareScience & ResearchManagement & Leadership
Job Information
📋Core Responsibilities
The Associate Manager serves as the primary quality contact on the production floor, specifically for terminal sterilization, visual inspection, and packaging. They are responsible for monitoring processes to ensure strict adherence to cGMP standards and Pfizer quality policies.
📋Job Type
full time
📊Experience Level
5-10
💼Company Size
102848
📊Visa Sponsorship
No
💼Language
English
🏢Working Hours
40 hours
Apply Now →

You'll be redirected to
the company's application page