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- ...Date: Mar 16, **** Location: San Juan, PR Company: Popular Workplace Type: Hybrid Quality Assurance Specialist General Description Perform ongoing quality assurance while monitoring and enhancing account opening procedures and guidelines to ensure Branches...SugeridoPrácticaInicio inmediatoTrabajo híbrido
- ...Specialist Quality Control with experience in: Laboratory Equipment Validation Periodic Monitoring Periodic Review Equipment Data Integrity Equipment Procurement Decommissioning process New equipment Introduction and Maintenance Others:...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
- ...fields. Log on now to our website qrcgroup.com / to learn more about our services and solutions! Job Description Specialist Quality Control with experience in: Scientific Data Analysis Strong Technical Writing (English and Spanish) mainly focuses...SugeridoContrato
- ...advance patient outcomes and set new standards of care. The QA Specialist will perform Lab equipment troubleshooting as required and... ...implement and monitor procedures and policies that ensure that the Quality Control unit are following corporate policies, U.S. Food and...SugeridoTemporal
- ...Description Under general direction, functions as the technical specialist for testing and development in areas of molecular biology and... ...Experience preferable) Strong knowledge and experience with quality process management Basic Knowledge on equipment preventive...SugeridoTiempo completoTrabajo por turnos
- ...QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented... ...in Puerto Rico & USA. Responsibilities: Technical specialist for testing and development in areas of molecular biology and...SugeridoContratoTurno 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
- 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 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...SugeridoTemporal
- ...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...SugeridoContratoTrabajo 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...SugeridoContrato
- ...For Engineer services in the Quality area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Engineering and three (3) years of exposure within the Pharmaceutical & Medical Devices Industry. Bilingual: Spanish and English Soft Skills: Excellent...SugeridoPrácticaContratoTrabajo por turnos
- ...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...SugeridoContratoTrabajo por turnos
- ...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
- ...advance patient outcomes and set new standards of care. The Lead, Quality Inspector tests and inspects raw materials, work in process,... ...or in production process, and tests products for variety of qualities, such as dimensions, performance, appearance, correct assembly,...Temporal
- ...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...TemporalTrabajar en la oficinaTrabajo híbridoTrabajo por turnosLunes a viernes1 día a la semana2 días a la semana
- ...Procurement & Logistics Manager Job Summary As a Procurement Specialist within the Electrification Smart Power division in Arecibo,... ..., managing supplier relationships, and ensuring cost, quality, and delivery targets are met. You will play a key role in supporting...Tiempo completoLunes a viernes
- ...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
- ...website qrcgroup.com / to learn more about our services and solutions! Job Description Specialist QA with experience in regulated industry. • Execute Quality disposition (approval or rejection) of bulk drug substances. • Provide Quality oversight to...Contrato
- ...Job Title : Quality Inspector Location : Aguadilla, Puerto Rico Hire Type : Contingent Pay Range : $ ***** - $*****/hour Work Type : Full-time Work Model : Onsite Work Schedule : Monday – Friday, 6 am – 2:30 pm / 7a – 3:30pm plus OT as needed Recruiter...Tiempo completoTrabajar en la oficinaLunes a viernes
- ...Qualification area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Science or Engineering and previous exposure in Quality activities within the pharmaceutical or medical devices industry. Bilingual (Spanish and English) Shift: Administrative &...ContratoTrabajo por turnos
- ...service pro is one your (many) talents. Being the Piece means you're full of bright ideas and eager to innovate, always bringing top-quality results to the table. Are you ready to Be The Piece? AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job) Supporting...ContratoTrabajo por turnos
- ...QUALIFICATIONS Serco Inc. is seeking a motivated Senior Part Time On-Call Specialist to join our team. Represent and support various Directorates... ...to continuous improvement, and a focus on delivering high-quality solutions round out the core skill set for this role. * U.S...Tiempo completoContratoInicio inmediatoVisa de trabajoHorario flexible
- ...re also a skilled multitasker with an incredible ability to set priorities. Add to this a commitment to serving customers with high-quality research and products, to embracing a diverse work culture, and even to the environment, and you might just be what we’re looking...ContratoRemotoTrabajo por turnos
- ...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...ContratoTrabajo por turnos
- ...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...Temporal
- ...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...TemporalTrabajar en la oficinaTrabajo híbridoTurno de mañanaLunes a viernes1 día a la semana2 días a la semana
- ...For Validation support services in the Quality area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Science with four (4) years of experience and exposure within the Pharmaceutical or Medical Devices industry . Bilingual (Spanish and English...ContratoTrabajo por turnos
- ...services and solutions! Job Description Investigation Specialist for Solid Dosage will be responsible for performing thorough, detailed and timely investigations and generation of high quality and timely investigation reports. Responsibilities: •...Contrato
