Quality Assurance Jobs at Pfizer | M Pharma Candidates Apply Now

Pharma Quality Assurance Jobs at Pfizer | M Pharma Candidates Apply Now

Are you looking for a career in pharmaceutical quality assurance where your work directly impacts patient care? Pfizer is hiring an Executive – Quality Assurance in Goa, offering you the opportunity to ensure the highest product standards while supporting manufacturing, packaging, and compliance processes. This role is perfect for professionals passionate about cGMP, regulatory readiness, and continuous quality improvement.

About Pfizer

Pfizer is a global leader in biopharmaceutical innovation, dedicated to discovering, developing, and delivering medicines and vaccines that improve lives. With a legacy spanning over 170 years, Pfizer’s mission is to apply science and global resources to bring therapies to people that extend and significantly improve their lives. Operating in over 125 countries, Pfizer focuses on advancing wellness, prevention, treatments, and cures for challenging diseases. Our commitment to quality, safety, and scientific excellence ensures that every product meets the highest standards, benefiting millions of patients worldwide.

Job Details

Job Post: Executive-Quality Assurance

Location: India – Goa

Minimum Requirements:

• Bachelor’s degree (B.Phar./M.Pharm).

• Pharmaceutical industry experience in quality systems.

• Sound knowledge of current Good Manufacturing Practices (cGMP).

• Strong communication and teamwork skills.

Preferred Qualifications:

• Experience at a manufacturing site.

• Expertise in deviations, batch record review, ERP systems, non-conformance investigation, and change control management.

• Strong problem-solving, time management, and multitasking abilities.

About the Role

Pfizer’s commitment to quality ensures the delivery of safe and effective products to patients worldwide. As Executive – Quality Assurance, you will uphold our science-based compliance culture, ensuring every product meets the highest standards.

Key Responsibilities:

• Evaluate and review clinical and commercial drug batches for quality.

• Ensure product and process documents meet specifications via sampling and statistical process control.

• Identify and resolve deviations from manufacturing and packaging standards.

• Manage supplier quality and in-process quality checks in manufacturing areas.

• Handle quality documentation, validation, and qualification activities.

• Organize work to meet deadlines while supporting project milestones.

• Ensure manufacturing and packaging records comply with Pfizer policy and cGMP standards.

• Maintain inspection readiness, support regulatory/customer inspections, and improve QA systems.

• Assist manufacturing/packaging staff in real-time compliance error resolution.

• Lead or participate in Quality Risk Management assessments.

APPLY ONLINE HERE