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

Location