Associate Quality Control | Pfizer | Vizag

Job Description

• Perform sampling and labeling of materials as per defined procedure and verification of all the equipment/instruments.
• Interpret and evaluate data in terms of accuracy, precision, trends, and potential Good Manufacturing Practices {also cGMP} impact and recommend appropriate corrective actions.
• Ensure all documentations and quality records are conducted in accordance to Good Manufacturing Practices and Good Laboratory Practices requirements and that they are filed in accordance to existing policies.
• Review and revise Standard Operating Procedures (SOPs), analytical methods and related procedures/documents, to keep them current.
• Perform analyses on finished products, raw materials, and components including entry, review, and/or approval of data in a computerized database and generate EMS reports.
• Contribute to the completion of complex projects, manage own time to meet agreed targets and develop plans for work activities on own projects within a team.

Qualifications

Must-Have

• Bachelor’s Degree in Pharmacy or Master in science/Pharmacy
• Demonstrated technical skills in sampling and testing incoming materials.
• Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations.
• Knowledge of Good Manufacturing Practices and their application standards, processes, and policies
• Excellent organizational skills and strong ability to multi-task
• Strong written and verbal communication skills

Nice-to-Have

• 0-5 years of Laboratory work experience with sampling and analytical HPLC (High-Pressure Liquid Chromatography) technique
• Experience leading continuous improvement projects.
• Knowledge of lean manufacturing, six sigma methodologies, and statistics