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 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.QualificationsMust-Have Bachelors Degree in Pharmacy or Masters in Chemistry/ Pharmacy 1-1.5 years of experience in sampling testing Demonstrated technical skills in sampling testing Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations Knowledge of Good Manufacturing Practices and its application standards, processes and policies Excellent organizational skills and strong ability to multi-task Strong written and verbal communication skillsNice-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 statisticsRole: Quality Control AnalystIndustry Type : PharmaceuticalFunctional Area: QCEmployment Type: Full Time, PermanentEducationUG : Bsc , BPharmaPG : MscJob Type: Full-timeSalary: ?10,000.00 - ?15,000.00 per monthSchedule:
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