Quality Management Jobs in Puerto Rico

Scientific Data Analysis Strong Technical Writing (English and Spanish) mainly focuses Strong knowledge in Microsoft Excel as a Tool for Data Analysis Good Communication skills Project Management Knowledge in Computer System and Method Validation (Experience preferable) Strong knowledge and experie...

Experience (manufacturing process development or quality assurance) in Biotech or pharmaceutical industry with progressively increasing responsibility and demonstrated experience in compliance problem solving critical thinking project management and quality systems. Proficient and experienced in ow...

Scientific Data Analysis Strong Technical Writing (English and Spanish) mainly focuses Strong knowledge in Microsoft Excel as a Tool for Data Analysis Good Communication skills Project Management Sample Management Knowledge in Computer System and Method Validation (Experience preferable) Strong kno...

Execute Quality disposition (approval or rejection) of bulk drug substances. Provide Quality oversight to ensure that operations for clinical and licensed pharmaceutical Drug Substance (API) are manufactured tested stored and managed according to current Good Manufacturing Practices (cGMP) Good Lab...

SummaryThe Quality Applications Specialist supports quality systems and product transfer activities by ensuring compliant validation of computerized systems and manufacturing processes. The role focuses on sterilization equipment process validation and quality system compliance in regulated environm...

Responsible for providing quality leadership governance and expertise in Quality Assurance processes related to the manufacture. Ensure compliance with regulatory requirements and West procedures. Proactively develop lead and drive the execution of the Quality Assurance strategy. Develop and impleme...

Lead and execute Computer System Validation (CSV) activities for Quality Information Technology systems in compliance with FDA GxP ISO and global regulatory requirements.Conduct and maintain formal validation documentation including Validation Plans Risk Assessments IQ OQ PQ protocols and reports an...

Description:Perform one or more of the following duties and responsibilities in support of site Quality Assurance program under minimal supervision. Review and approve product MPs. Approve process validation protocols and reports for manufacturing processes. Request Quality on incident triage team....