Quality System Jobs in Juncos

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...

QA Investigations Lead to oversee and drive the end-to-end investigation processes within a regulated environment. This role will ensure timely compliant and effective resolution of quality events while providing strong project management oversight.The selected candidate will be responsible for man...

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...

Job Board Only - No Asmts AllowedFull Steam Staffing is now hiring a Quality Control Technicion in Modesto CA. Apply now!Job Title: Quality Control TechnicianLocation: Modesto CASchedule: VariesPay Rate: $17.25/hourJob Summary:We are seeking a detail-oriented Quality Control Technician to join our t...

Quality Professional with experience in Quality System and addition some knowledge or to be familiar with in PASx/MES application MAXIMO SAP LIMS QMTS and Veeva. Available during weekends and holidays as requested always available to be on site. RequirementsDoctorate OR Masters 2 years of experien...

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...

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...