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- ...environmental impact reports for new construction projects, plant processes and permit changes. ~ Reviews and analyzes environmental documentation issued by the federal EPA, state and local regulatory agencies. ~ Evaluates proposed regulations to determine financial,...SugeridoTemporalTrabajo 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
- For Product Development services in the Manufacturing area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Science and five (5) years of exposure in management within the Pharmaceutical & Medical Devices Industry. Bilingual: Spanish and English...SugeridoContratoTrabajo por turnos
- ...processes and permit changes. Reviews and analyzes environmental documentation issued by the federal EPA, state and local regulatory... ...training on matters of environmental, health, and safety. SPECIALIST CAREER STREAM: Typically an individual contributor with responsibility...SugeridoTiempo completo
- Leads or leverages cross functional teams to evaluate, develop and manage projects for new product development and ongoing lifecycle management of products, processes and therapies. Oversees and manages the operational aspects of ongoing projects and serves as liaison ...SugeridoContrato
- ...manager. Coaches, reviews and delegates work to lower level specialists. Contributes to defining the direction for new products,... ...processes and procedures are in compliance with regulations. SPECIALIST CAREER STREAM: Typically an individual contributor with responsibility...SugeridoInicio inmediato
- ...determining deliverables of assignments, with limited oversight from manager. Coaches, reviews and delegates work with lower-level specialists. Contributes to defining the direction for new products, processes, standards, or operational plans based on business strategy...SugeridoTrabajo por turnos
- ...determining deliverables of assignments, with limited oversight from manager. Coaches, reviews and delegates work to lower-level specialists. Contributes to defining the direction for new products, processes, standards, or operational plans based on business strategy...SugeridoTrabajo por turnos
- ...Inspection requirements as required and associated test method validation for all internal Medtronic Test Methods. TECHNICAL SPECIALIST CAREER STREAM: An individual contributor with responsibility in our technical functions to advance existing technology or introduce...SugeridoInicio inmediato
- ...packaging and manufacturing systems. Perform testing and analysis to validate packaging materials and manufacturing equipment. Document validation activities, including protocols, reports, and standard operating procedures. Identify and resolve non-compliance...SugeridoContratoTrabajo por turnos
- ...The day-to-day on the job) Conducts a compliant validation process for quality information technology systems, requiring formal documentation (including SOP). Coordinates activities with clients, programmers/developers, and operating personnel, domestic and, as...SugeridoContratoTrabajar en la oficinaTrabajo por turnos
- ...personnel to ensure that processes and designs are compatible. ~ May develop and conduct statistical analysis or recommend additions to document work. ~ Leads the innovation, development and/or optimization of new manufacturing concepts, processes and procedures for...SugeridoTemporalTrabajo por turnos
- ...: Conducts a compliant validation process for quality information technology systems which requires formal validation documentation (including standard operating procedures) under appropriate federal regulations. Coordinates activities with clients, programmers...SugeridoTemporalTrabajar en la oficinaTrabajo por turnosFin de semana
- ...Validation Specialist with experience in aseptic areas. Knowledege and experience validating tanks and aseptic filling equipment. Requirements Bachelor's degree in sciences and five years experience in related field. Bilingual (Spanish/English) Technical...SugeridoContrato
- ...Validation Specialist with experience in regulated industry, validating/qualifying laboratory equipment, manufacturing equipment, processes, utilities and facilities. Tasks: Execute complete validation cycle Change Control Equipment qualification (manufacturing...SugeridoContrato
- ...Applications will be accepted only electronically until July 26, 2025. Please submit a cover letter and your resume. Documentation should be saved as a single document and sent to: ****** Only qualified candidates will be interviewed. Please reference Communications Manager...Trabajo de veranoTemporalTiempo completoTrabajo por turnosFin de semana
- ...repairs on all production equipment. Trouble shoot mechanical, electrical and pneumatic problems. Fill out necessary documentation to comply with specifications and SOP'S. Perform preventive maintenance work according to established standards. Fill...Temporal
- ...enriquecedor que facilite el máximo desarrollo social y emocional. Mantener los requisitos del sistema de recopilación de datos para documentar y rastrear datos. (Child Plus, Teaching Strategies Gold) Compromiso de los padres, la familia y la comunidad: Proporcionar...AprendizTiempo completoTrabajar en la oficinaLunes a miércoles
- ...Sciences University* will support a dynamic cross-functional marketing and admissions team. This role will involve receiving official documents for evaluation purposes and communicating with new and prospective students from various locations. Also, will support the...Por horaTiempo completoTrabajar en la oficinaTrabajo por turnos
- ...y/o empacan el producto de acuerdo al Bill of Material, Blueprints, Specs y SOPs siguiendo las Buenas Prácticas de Manufactura, Documentación, Calidad, Seguridad y Ambiental. Se asegura de que el producto tenga todos sus componentes. Realiza las pruebas de fuga y...PrácticaTemporalTrabajo por turnosFin de semana12 horas
- ...realizar el movimiento al area de producción. Cumplir en todo momenta con las reglas de la compañía, con las Buenas Practicas de Documentación y regulaciones de EHS. Organizar "staging area" colocando paletas y cajas suficientes para la producción del turno....PrácticaTemporalTrabajo por turnos
- ...máquina o equipo que pudieran afectar su buen funcionamiento. Suplir materiales a las maquinas asignadas. Inspeccionar, empacar y documentar el material según los procedimientos de la Planta. Coordinar y monitorear el uso de materiales en las áreas del departamento....TemporalTrabajo por turnos
- ...Must complete validation execution on new and existing machines. Manually (ex: checker chart) and/or electronically (ex: POMs) document the required information during shift changes to comply with applicable procedures and specifications. This information includes but...TemporalTrabajo por turnosFin de semana
- ...manera segura y apropiada y que cumpla con las políticas de EHS. ~Ensure that all documents are completed complying with the GMP’s practices when required. Asegurar que todos los documentos estén completos cumpliendo con las prácticas de GMP cuando sea requerido. ~...PrácticaContratoCAS
- ...assists in equipment troubleshooting problems. Audits manufacturing areas assuring compliance with specifications, batch record documentation and procedures. Supports and assures compliance with all the Operational Excellence projects implemented in his/her area....TemporalTurno rotativoTrabajo por turnosFin de semana
- ...compliance with regulations. Execute validation activities for equipment and process changes, including IQ, OQ, PQ, and associated documentation. Design and optimize manufacturing processes, ensuring efficient production layouts, material handling, and tool fabrication....Tiempo completoContratoContratistaTurno de mañanaTrabajo por turnosLunes a viernes
- ...Technical review of site Standard Operating Procedures, requirements, specifications, regulatory filings, and/ or other controlled documents as needed. Tracks and trends relevant technical and business process metrics to ensure fill/finish platforms are performing...Contrato
- ...Process Engineer with experience in process validation among other related. Also experience with Protocols execution, IQ/OQ/PQ, Documentation and validation activities. Requirements ~ BS Engineering ~5 years of experience in the Medical Devices industry ~...Contrato
- ...Capacitar a los nuevos empleados. # Monitorear que todas las compras se realicen en tiempo y forma. # Gestionar y controlar los documentos aduanales y funcionarios relacionados con las compras. # Revisar y entregar los documentos al agente aduanal. # Participar en...Tiempo completoTrabajar en la oficinaInicio inmediato
- ...projects goals. ~ Must keep work area in the cleanest and most orderly conditions. ~ Performs visits to areas of responsibility, document findings and suggestions to improve processes. ~ Revises, implements changes and audits existing specifications and SOPs;...TemporalTrabajar en la oficinaInicio inmediato