MQA Downstream Associate Manager

Department Icon Audit & Control
Posted: 3 months ago
6-8 years
Visakhapatnam, Andhra Pradesh
Audit & Control
work from office
Full Time

Posted: 3 months ago
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Job Description

Use Your Power for Purpose

Every day, Pfizers 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

Skills

AuditAssuranceAudit TrailsCgmpManufacturing QualityQuality OperationsSafetyQuality Assurance

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About Company

Pfizer, a global biopharmaceutical company, pioneers breakthroughs that change patients' lives. With a legacy spanning over 170 years, Pfizer is committed to advancing science and healthcare. Focusing on research, development, and manufacturing, it offers a wide range of medicines, vaccines, and consumer healthcare products. Pfizer's dedication to innovation and collaboration drives its mission to bring therapies to people that significantly improve their lives. Pfizer Careers offers diverse opportunities for professionals worldwide to contribute to transformative healthcare solutions, fostering growth and development in a supportive environment. Join Pfizer in shaping the future of healthcare and making a meaningful impact on global health.

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