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- ...responsibilities inherent to the position. Minimum requirements of the position : High School Diploma. Bilingual (English / Spanish). Valid Puerto Rico driver’s license. Computer proficiency (Word, Excel, Access, Outlook). Ability to drive both manual and automatic...SugeridoTiempo completoInicio inmediatoTurno de mañanaTurno de nocheHorario flexibleFin de semana
- ...requirements of the position : High School Diploma. Knowledge of basic repair skills (plumbing, electricity, painting, etc.). Valid Puerto Rico driver's license. Ability to work seated for extended periods, bend, lift objects up to 50 lbs, walk continuously,...SugeridoTiempo completoInicio inmediato
- ...day and night shifts, holidays, and weekends).** Proficiency in both English and Spanish. Preferably 6 months of experience. Valid Puerto Rico driver's license.** Must be able to stand, walk, or bend. Must be able to lift a minimum of 50 pounds. Problem-...SugeridoTiempo completoInicio inmediatoTurno de mañanaTurno de nocheFin de semana
- ...as required by the role. Minimum requirements of the position : ~ High school diploma and/or related studies preferred. ~ Valid Puerto Rico driver’s license. ~1 year of experience in hospitality or a related field. ~ Flexible schedule (available to work...SugeridoTiempo completoInicio inmediatoTurno de mañanaTurno de nocheHorario flexibleFin de semana
- ...Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America. Responsibilities: Plan, coordinate, and execute validation activities for parenteral and aseptic manufacturing processes. Prepare, review, and approve validation protocols, reports, and...SugeridoTiempo completo
- ...Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America. Responsibilities: Support process development and validation activities in commercial biopharmaceutical manufacturing, with emphasis on formulation and aseptic filling operations. Apply...SugeridoTiempo completo
- ...English & Spanish). Project Management skills. Shift: Administrative, and according to business needs. Experience in: CQV Validation Expert: Risk-based qualification methods (ASTM E 2500) for pharmaceutical manufacturing equipment and utilities Sterilization...SugeridoContratoTrabajo por turnos
- ...or technicians. * Lead efforts with research, manufacturing, process development, utilities, facilities, quality assurance and validation departments in developing requirements and recommendations for large and/or highly complex system/facility or process...SugeridoDe duración determinadaTiempo completoTrabajar en la oficinaTurno de nocheTrabajo por turnosFin de semana
- ...troubleshooting mentorship. Work with manufacturing, maintenance, process development, utilities, facilities, quality assurance and/or validation departments in developing requirements and recommendations for process and/or system modifications. Support the execution of...SugeridoContratoTrabajo por turnos
- ...complexity. Work with research, manufacturing, maintenance, process development, utilities, facilities, quality assurance, and/or validation departments. Work under the direct supervision of project managers to complete design, engineering, and construction projects...SugeridoContratoTrabajo por turnos
- ...troubleshooting mentorship. Work with manufacturing, maintenance, process development, utilities, facilities, quality assurance and/or validation departments in developing requirements and recommendations for process and/or system modifications. Support the execution of...SugeridoContratoTrabajo por turnos
- ...QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields. Log on now to our website qrcgroup.com / to learn more about our services and solutions! Job Description...SugeridoContrato
- ...QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields. Log on now to our website qrcgroup.com / to learn more about our services and solutions! Job Description...SugeridoContrato
- ...Description: With minimal supervision, support the execution of manufacturing/quality systems such as non-conformances, process validation, procedures, training, and new product introductions. Apply process, operational, scientific expertise, basic compliance...SugeridoTiempo completoTrabajo por turnos
- ...QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields. Log on now to our website qrcgroup.com / to learn more about our services and solutions! Job Description...SugeridoContrato
- ...and apply standard engineering techniques and procedures. Assistance given for unusual problems. Comprehensive understanding of validation protocol execution requirements. Education: ~ Master degree or Bachelor degree in Engineering & 2 years of Engineering...Tiempo completoTrabajo por turnos
- ...Chemical Engineering. Skills: Scientific Data Analysis Project Management Knowledge in Computer System and Method Validation (Experience preferable) Strong knowledge and experience with quality process management Knowledge on equipment validation and...Contrato
- ...maintenance with a working knowledge of crane and rigging requirements. Demonstrated teamwork, initiative and positive attitude. Valid driver's license and acceptable driving record. Weight must not exceed 285lbs excluding equipment/gear worn when performing job...Fin de semana
- ...For Data Analytics and Validation services WHAT MAKES YOU A FIT: The Technical Part: ~ Bachelor’s Degree in Computer Science, Computer Engineering, Electrical Engineering or related technical discipline. ~5+ years of experience in CSV in regulated environments...ContratoTrabajo por turnos
- ...~ MES platforms (Emerson Syncade, including development and maintenance of BI solutions). ~Computer systems integration and validation experience. ~ Authoring and executing validation documentation (test scripts, protocols, reports). The Personality Part:...ContratoTrabajar en la oficinaTrabajo por turnos
- ...cGMPs, SOPs, job plans, and company policies. Develop, revise, and review SOPs, job plans, and work instructions. Support validation activities for mechanical and utility equipment. Assist in optimizing maintenance procedures and continuous improvement initiatives...TemporalTurno rotativo
- ...QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields. Log on now to our website qrcgroup.com / to learn more about our services and solutions! Job Description...ContratoTrabajo por turnos
- ...start-up of new equipment to ensure it meets all mechanical design specifications. Assist with the development and execution of validation documents for mechanical equipment. WHO WE ARE: We are a Service Provider company different from the rest. We pride...ContratoTrabajo por turnos
- ...industry in Puerto Rico & USA. Responsibilities: Support the execution of manufacturing such as non-conformances, process validation, procedures, training, and new product introductions. Apply process, operational, scientific expertise, basic compliance knowledge...ContratoTrabajo por turnos
- ...Documentation platforms (e.g., CDOCS), Maximo, TrackWise, LIMS, MES/electronic batch record systems, and SAP. Computer systems validation (CSV) or computer systems quality assurance. Validation of GxP applications, including Validation Master Plans, GxP risk...ContratoTurno de nocheTrabajo por turnos
- ...QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields. Log on now to our website qrcgroup.com / to learn more about our services and solutions! Job Description...ContratoTrabajo por turnos
- ...of TECHSUPPORT on engineering, regulatory, and compliance. ~ Calibration, quality, microbial/environmental, technical cleaning, validation, electrical, and process automation issues. ~ Assist in the evaluation and implementation of engineering improvements, policy...Trabajo por turnos
- ...QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields. Log on now to our website qrcgroup.com / to learn more about our services and solutions! Job Description...Contrato
- ...Data Analysis ~ Strong knowledge in Microsoft Excel as a Tool for Data Analysis. ~ Knowledge in Computer System and Method Validation (Experience preferable). ~ Strong knowledge and experience with quality process management. ~ Experience on Equipment Validation...ContratoTrabajo por turnos
- ...For Sterilization/Validation services in the Quality area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Science (preferred Microbiology or Biology) and three (3) years of exposure within the Medical Devices Industry. Bilingual: Spanish and...ContratoTrabajo por turnos