Pharma QA Jobs at Pfizer | M Pharm Candidates Apply Now
Are you looking for a rewarding career in pharmaceutical quality assurance? Pfizer is hiring an Executive – Quality Assurance in Goa, India. In this role, you’ll play a vital part in ensuring product quality, compliance with cGMP standards, and regulatory readiness—directly impacting patient care worldwide.
About Pfizer
Pfizer is one of the world’s leading biopharmaceutical companies, dedicated to discovering, developing, and delivering innovative medicines and vaccines that improve health and well-being. With a strong commitment to quality, compliance, and scientific excellence, Pfizer’s products serve millions of patients across the globe every day. The company combines cutting-edge research with a purpose-driven approach to address some of the world’s most pressing health challenges. Guided by values of integrity, innovation, equity, and patient focus, Pfizer continues to set benchmarks in healthcare, making essential medicines more accessible while driving advancements that shape the future of global health.
Job Details
- Job Post: Executive – Quality Assurance
- Location: India – Goa
- Type: Full-time
- Job Requisition ID: 4939223
Minimum Requirements
- Bachelor’s degree (B.Pharm/M.Pharm).
- Experience in the pharmaceutical industry and quality systems.
- Strong knowledge of cGMP (part of GxP).
- Effective communication skills and the ability to collaborate across teams.
Bonus Points If You Have (Preferred Requirements)
- Experience at a pharmaceutical manufacturing site.
- Knowledge in managing deviations, root cause analysis, and change control.
- Proficiency in production batch record review and ERP systems.
- Strong problem-solving, time management, and multitasking skills.
What You Will Achieve
As an Executive – Quality Assurance, you will:
- Evaluate and review clinical and commercial drug batches for quality assurance.
- Ensure product and process compliance through rigorous sampling and statistical process control.
- Identify, investigate, and resolve deviations in manufacturing and packaging.
- Manage supplier quality and documentation systems.
- Conduct in-process quality checks in the manufacturing area.
- Handle validation, qualification, and compliance activities.
- Maintain inspection readiness, supporting regulatory and customer audits.
- Lead or participate in Quality Risk Management assessments.
- Assist staff in real-time compliance error detection and resolution.
- Contribute to project milestones while managing documentation and timelines.
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