Quality Management Jobs in Puerto Rico

The CAPA / Complaints Technical Writer is responsible for authoring reviewing and maintaining high-quality documentation associated with Corrective and Preventive Actions (CAPA) customer complaints investigations non conformances and Quality Management System (QMS) remediation activities within a re...

SummaryThe Senior Supplier Quality Engineer supports the Supplier and Distribution Quality organization by managing supplier quality activities ensuring compliance with quality standards and maintaining approved supplier relationships. This role is responsible for supplier qualification auditing per...

Knowledge in: Environmental Monitoring Microbial Identification (Micro ID) Critical Utilities (CU) monitoring Sampling monitoring: equipment and techniques Data trending and evaluation Microbiological testing methods and standards for clean rooms and controlled environments Aseptic behavior in manuf...

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...

Key ResponsibilitiesLead and oversee all quality assurance activities to ensure compliance and continuous improvementDevelop implement and maintain ISO 9001:2015 quality management systems and documentationManage internal and customer audit processes including corrective actions and follow-upMonitor...

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...