Boost Your Career with a Pharma QA Job at Pfizer Careers | Pharma Graduates | Apply Now
Looking for a rewarding Pharma QA job with global exposure? Explore this exciting opportunity under Pfizer Careers for a Quality Assurance Associate role in Vizag. This role offers hands-on experience in quality systems, compliance, and manufacturing excellence, making it ideal for professionals aiming to grow in the pharmaceutical industry.
- Job Title: Quality Assurance Associate
- Locations: India – Vizag
- Job Requisition ID: 4955980
About the Company
Pfizer is a leading global pharmaceutical company known for developing innovative medicines and vaccines that improve patient health worldwide. Headquartered in the United States, Pfizer focuses on research, development, and manufacturing across areas like oncology, vaccines, cardiology, and rare diseases. With a strong commitment to quality, safety, and scientific excellence, the company plays a vital role in advancing healthcare and improving lives globally.
Job Description
- Work in a quality-focused environment ensuring safe and effective pharmaceutical products
- Be part of a culture driven by science, innovation, and compliance
- Contribute directly to improving patient care and outcomes
- Support activities like development, maintenance, compliance, and research analysis
- Help maintain high-quality standards across all products
- Play a key role in strengthening and evolving quality systems
Key Responsibilities
- Review clinical and commercial drug batches to ensure quality standards
- Check product and process documents using sampling and statistical controls
- Identify and resolve issues in manufacturing and packaging processes
- Approve investigations and manage change control activities for compliance
- Support project tasks and ensure deadlines are met
- Work effectively within the team and improve team collaboration skills
- Solve basic problems with guidance from supervisors
- Ensure all manufacturing and packaging records follow policies and cGMP standards
- Stay prepared for inspections and support audits by regulatory authorities and customers
- Help detect and fix compliance errors in real time and participate in quality risk assessments
Qualification
- Master’s in Science/Pharmacy with 2–3 years of experience
- Experience in the pharmaceutical industry and quality systems
- Good knowledge of cGMP (GxP) guidelines
- Ability to work well in team and cross-functional environments
- Strong written and verbal communication skills
