Quality Assurance Job at Pfizer
Searching for a high-growth Quality Assurance Job in the pharmaceutical industry? Here’s an exciting career update from Pfizer that could transform your professional journey. Pfizer Jobs in Vizag are now open for the role of Quality Assurance Associate, offering an incredible Biotech Job opportunity for candidates with pharma, biotechnology, or life science backgrounds. If you are passionate about quality systems, GMP compliance, and patient safety, this is an outstanding opportunity for life science graduates to work with one of the world’s leading pharmaceutical companies.
About Pfizer
Pfizer is one of the world’s largest pharmaceutical companies known for developing innovative medicines and healthcare products. With operations across multiple countries, Pfizer continues to lead advancements in healthcare, vaccines, biotechnology, and patient-focused pharmaceutical solutions. Pfizer Jobs are highly sought after by professionals looking for international exposure and career stability in the life sciences industry.
Job Details:
- Job Title: Quality Assurance Associate
- Location: Visakhapatnam
- Job Type: Full-Time
Overview
The Quality Assurance Associate plays a key role in ensuring the delivery of safe, effective, and high-quality pharmaceutical products. The position supports quality systems, compliance, and operational excellence across manufacturing and packaging activities while contributing to improved patient outcomes through adherence to regulatory and cGMP standards.
Key Responsibilities
- Evaluate and review clinical and commercial drug batches to ensure product quality and compliance.
- Verify that product and process documentation meets established specifications through sampling and statistical process control methods.
- Identify, investigate, and address deviations related to manufacturing and packaging processes.
- Approve investigations and oversee change control activities in line with configuration management policies.
- Support project execution by organizing tasks and ensuring milestone completion within timelines.
- Apply team collaboration and problem-solving skills to support departmental objectives.
- Ensure manufacturing and packaging records comply with company policies and current Good Manufacturing Practices (cGMP).
- Maintain inspection readiness and support regulatory and customer audits.
- Assist manufacturing and packaging teams in identifying and resolving compliance issues in real time.
- Participate in or lead Quality Risk Management assessments and continuous improvement initiatives.
Required Qualifications
- Bachelor’s Degree in Sciences with 4–5 years of experience in the Pharma/Biotech industry, or Master’s Degree in Sciences with 2–3 years of experience in the Pharma/Biotech industry.
- Experience with pharmaceutical quality systems and compliance processes.
- Strong understanding of current Good Manufacturing Practices (GxP/cGMP).
- Ability to work effectively within cross-functional and interdepartmental teams.
- Strong written and verbal communication skills.
Preferred Qualifications
- Experience working at a pharmaceutical manufacturing site.
- Hands-on experience managing and writing deviations.
- Knowledge of batch record review, ERP systems, non-conformance investigations, root cause analysis, and change control management.
- Strong analytical and problem-solving abilities.
- Ability to work independently as well as collaboratively within a team environment.
- Effective time management and multitasking skills.
- Familiarity with AI-powered tools such as ChatGPT and Microsoft Copilot to support productivity and problem-solving.
