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- ...patient outcomes and set new standards of care. The Lead, Quality Inspector tests and inspects raw materials, work in process, and... ...or in production process, and tests products for variety of qualities, such as dimensions, performance, appearance, correct assembly...SugeridoTemporal
- ...implement and monitor procedures and policies that ensure that the Quality Control unit are following corporate policies, U.S. Food and... ...interface with technical and non-technical personnel such as inspectors, designers, buyers, vendors, manufacturing personnel and...SugeridoTemporal
- ...Housekeeping Coordinator/Inspector Full-Time / Hourly Job Summary The Housekeeping Coordinator/Inspector is responsible for... ...ensuring that guest rooms and public areas meet the company’s quality and satisfaction standards. Main responsibilities : Responsible...SugeridoTiempo completoInicio inmediatoTrabajo por turnos
- ...Responsible for developing, applying, revising, and maintaining quality standards for processing raw materials and/or components into... ...May coordinate the activities of one or more Quality Control Inspectors and/or Technicians. May evaluate the performance of one or...SugeridoTemporal
- ...Se busca Inspector(a) de Calidad para empresa del sector de dispositivos médicos. Esta posición requiere una persona responsable, organizada y con gran atención al detalle, que pueda ejecutar inspecciones en todas las etapas de producción, documentar no conformidades,...SugeridoTurno de mañanaTurno de tarde
- ...Summary The 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...SugeridoContrato
- ...The Quality Application Specialist supports product transfer activities with a primary focus on process validation, sterilization processes, and commercial release readiness. This role ensures compliant execution of validation activities and quality system requirements...SugeridoContrato
- ...Quality Evaluator Senior Location: Puerto Rico. This role requires associates to be in-office 1 - 2 days per week, fostering collaboration and connectivity, while providing flexibility to support productivity and work-life balance. This approach combines structured office...SugeridoTemporalTrabajar en la oficinaTrabajo híbridoTrabajo por turnosLunes a viernes1 día a la semana2 días a la semana
- ...Date: Mar 5, **** Location: San Juan, PR Company: Popular Workplace Type: Hybrid Quality Assurance Specialist General Description The Quality Assurance Specialist position requires expert knowledge and experience with consumer credit bureau reporting,...SugeridoPrácticaTrabajar en la oficinaInicio inmediatoTrabajo híbrido
- ...Experienced Quality Supervisor with a strong background in regulated industry. Proven ability to lead and execute commissioning and qualification activities in compliance with regulatory and quality standards. Skilled in conducting thorough investigations to identify root...SugeridoTrabajar en la oficina
- ...s possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care. The Quality Documentation Coordinator will be responsible for: * Maintaining NC/CAPA/Training systems documentation, corresponding logs, and...SugeridoTemporal
- ...Performance Quality Analyst I Location: Puerto Rico. This role requires associates to be in-office 1 - 2 days per week, fostering collaboration and connectivity, while providing flexibility to support productivity and work-life balance. This approach combines structured...SugeridoTemporalTrabajar en la oficinaTrabajo híbridoTurno de mañanaLunes a viernes1 día a la semana2 días a la semana
- ...Proficient in Microsoft Excel data migration and Microsoft Word and PowerPoint. Product Transfer, Injection molding, and New Tooling. Quality Systems (CAPA’s, FMEA’s, Risk Assessments, Supplier Qualifications, Quality Audit, and Non-Conformance Reports). The...SugeridoContratoTrabajo por turnos
- ...For Quality services in the Manufacturing area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Engineering and two (2) years of exposure within the Pharmaceutical & Medical Devices Industry. Bilingual: Spanish and English Soft Skills: Excellent...SugeridoContratoTrabajo por turnos
- QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world...SugeridoTemporalTrabajo por turnos
- ...Quality Auditor Lead Location: Puerto Rico.This role requires associates to be in-office 3 days per week, fostering collaboration and connectivity, while providing flexibility to support productivity and work-life balance. This approach combines structured office engagement...TemporalTrabajar en la oficinaTrabajo híbridoTurno de mañanaLunes a viernes3 días a la semana
- ...t always be easy, growing takes grit. But at ABB, you'll never run alone. Run what runs the world. This Position reports to: Quality Specialist En ABB, ayudamos a las industrias a avanzar más rápido, de forma más eficiente y sostenible. Aquí, el progreso es una...PrácticaTiempo completoInicio inmediatoLunes a viernes
ABB
Arecibo23 días atrás $12,5 por hora
...Perform checks on HACCP, SSOP, and GMP Policies and on product to assure that the final product meets with all food safety and quality standards. DAILY- TASKS DONE ON A DAILY BASIS/QUANTITATIVE TASKS ~Perform all regulatory procedures, which include HACCP, SSOP’s...TemporalTurno de nocheTrabajo por turnos- ...EOSOL is seeking two Quality Supervisors for a photovoltaic plant + substation + transmission line project. The selected candidates will be responsible for ensuring compliance with technical specifications, quality standards, and project procedures during construction...ContratistaTiempo completo
- ...For Engineer services in the Quality area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Engineering and... ...and inspection findings and liaises with auditing groups and inspectors through all stages. Coordinates legal requests in support of...PrácticaContratoTrabajo por turnos
- ...For Quality services in the Engineering area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree and or an equivalent of two (2) years of experience in regulated industries. Bilingual (Spanish and English). Good organizational and problem-solving...ContratoTrabajo por turnos
- ...QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world...Temporal
- ...needs. Experience in: IT systems, including integrations with manufacturing equipment Computer System Validation (CSV) Quality and Compliance The Personality Part: ~ Our Next Piece is someone who treats everyone they meet like family, especially our...ContratoTrabajo por turnos
- QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world...TemporalTrabajo por turnos
- Mentor Technical Group (MTG) provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering and technical solutions, MTG ensures compliance with pharmaceutical, biotechnology, and medical...Tiempo completoTrabajar en la oficina
- ...For Remediation services in the Quality Assurance area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Engineering and 5 years of experience in the review and approval of life cycle validation documentation in the regulated industry. Bilingual...ContratoTrabajo por turnos
- ...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...Contrato
- ...Quality role to support product transfer activities. focused on process validation. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree in Engineering with at least three (3) years of experience within the regulated industry. Bilingual (English & Spanish...ContratoTrabajo por turnos
- ...equipment's, gauges, etc. 5. Re-works rejected lots from Q.A. Inspectors. 6. Assists group peers to complete assigned tasks. 7.... ...schedules. 14. Achieve established productivity levels and quality standards. 15. Follows Clean Room Rules an Gowning Practices...Temporal
- ...drive company van to transport products or materials when required. 16. Verifies stock transfer information provided by Incoming Inspectors and locates products in the corresponding areas of warehouse when required. 17. When required, coordinates, and participates in...Temporal
