Quality Systems 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...

Educational background in Mechanical Electrical Industrial and/or Chemical Engineering Experience with equipment and/or process troubleshooting in a regulated environment. Knowledge of pharmaceutical/biotech processes and GMP production operations. Organizational & technical writing skills.Proficie...

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...

Experience with automated inspection systems development and implementation. Hands-on experience developing AI/ML models for image analysis defect detection classification or process optimization. Experience with Computer Vision technologies and industrial camera systems. Knowledge of Machine Learn...

Responsibilities:Analyze and design sequences of operations and workflow to improve production efficiency and resource utilizationDevelop and optimize manufacturing line layouts using tools such as AutoCADConduct capacity analysis throughput evaluation and bottleneck identification to improve produc...

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...

SummaryResponsible for coordinating projects inventory activities and operational initiatives to support business continuity and manufacturing operations. The Project Coordinator collaborates with cross-functional teams to monitor timelines manage documentation track project progress and support spa...

IntroductionWerfen Werfen is a growing family-owned innovative company founded in 1966 in Barcelona Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis Acute Care Diagnostics Transfusion Autoimmunity and Transplant. Through our Original Equipment Manufacturing (OEM...

Responsibilities may include the following and other duties may be assigned:Provide production support engineering for testing methods procedures device specifications and yield issues.Analyze customer returns supplier-related engineering changes and implement cost optimization strategies.Support mi...

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...