Associate-Quality Control | Vizag | Pfizer

Job Description

• Ensure training records are updated and correctly filed to reflect current testing capabilities.
• 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 documentation and quality records are conducted in accordance with Good Manufacturing Practices and Good Laboratory Practices requirements and that they are filed in accordance with 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 Masters in Chemistry/ Pharmacy
• 0-3 years of experience in Packing material sampling testing
• Demonstrated technical skills in Packing material sampling testing
• 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

• Laboratory work experience with analytical techniques like IR, UV, pH
• Experience leading continuous improvement projects
• Knowledge of lean manufacturing, six sigma methodologies, and statistics