QC Jobs at Pfizer | Associate Quality Control Jobs in Vizag
QC Jobs at Pfizer | Associate Quality Control Jobs in Vizag. Pfizer, a global leader in pharmaceuticals, is hiring an Associate – CQ (Quality Control) at its Vizag facility. This full-time, on-site role offers an opportunity to work in a dynamic, compliance-driven laboratory environment, ensuring that every product meets the highest quality standards. Ideal for chemistry or pharmacy graduates, this role involves analytical testing, method validation, and contributing to continuous improvement initiatives that directly impact patient care.
Associate – CQ (Quality Control) – Pfizer, Vizag
At Pfizer, quality is at the heart of everything we do. Our science-driven, risk-based compliance culture ensures that every product delivered is safe and effective. By joining our Quality Control team, you contribute directly to patient care and help maintain a culture of continuous improvement, innovation, and excellence.
Key Responsibilities:
- Perform various analytical tests, including water analysis, Limit Test, and instrumental testing using HPLC and GC.
- Conduct analyses of finished products, raw materials, and components, including data entry, review, approval, and EMS report generation.
- Ensure training records are current and reflect testing capabilities.
- Perform sampling, labeling, and verification of materials and equipment per established procedures.
- Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending corrective actions where necessary.
- Maintain documentation and quality records in compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
- Review and revise SOPs, analytical methods, and related documentation to ensure currency.
- Contribute to complex projects, manage time efficiently, and collaborate within a team under supervision while exercising judgment.
Minimum Requirements:
- Bachelor’s or Master’s degree in Chemistry or Pharmacy.
- 1–5 years of relevant experience in Quality Control.
- Strong technical skills in method validation and analytical testing.
- Understanding of compendial methods, SOPs, technical procedures, and regulations.
- Knowledge of GMP standards, processes, and policies.
- Excellent organizational, multitasking, and communication skills.
- Proficiency with QC instruments for accurate sample handling and analysis.
Preferred Requirements (Bonus Points):
- Experience with HPLC analytical techniques.
- Track record in continuous improvement projects.
- Knowledge of lean manufacturing, Six Sigma, and statistical analysis.
- Strong problem-solving skills, attention to detail, and ability to handle multiple priorities.
- Excellent interpersonal skills and adaptability to learn new techniques.
Work Location: On Premise, Vizag
