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- ...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
- ...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
- ...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-solving...SugeridoTiempo completoInicio inmediatoTurno de mañanaTurno de nocheFin de semana
- ...Job Summary: The Validation Specialists team will support process validation and cleaning validation activities for a technology transfer project in a pharmaceutical manufacturing environment. This role involves developing technical documentation for change...SugeridoContratoTrabajo por turnosLunes a viernes
- ...required by the position. Minimum requirements of the position : University degree. Proficiency in English and Spanish. Valid navigation license is required. Minimum 2 years of experience in supervising staff. Experience in a hotel or related field,...SugeridoTiempo completoTrabajar en la oficinaInicio inmediatoTurno de mañanaTurno de nocheHorario flexibleFin 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
- ...Validation Engineer with a strong knowledge of injection molding processes to support the development, execution, and documentation of validation activities (Protocols, Tests, Reports). E xperience with Minitab, including capacity analysis and Gage R&R studies....SugeridoContrato
- ...markets: United States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America. Responsibilities: # Develop Validation Process (IQ, PQ, OQ) Education & Qualifications: # Bachelor's degree in Science or Engineering and 3 years of experience...SugeridoTiempo completo
- ...Studies Responsible for the Aseptic Process Simulation Media Fill (MF) Participate in project meetings, as applicable Generate Validation Plan establishing lean strategies, as required. Develop and execute EM PQ, AVS and APS protocols for applicable systems...SugeridoTiempo completoDe duración determinadaInicio inmediatoTurno de tardeTrabajo 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
- ...complexity. Work with research, manufacturing, maintenance, process development, utilities, facilities, quality assurance and/or validation departments in developing requirements and recommendations for system modifications. Work under the direct supervision of...SugeridoContratoTrabajo por turnos
- ...equipment to ensure it meets all instrumentation design specifications. Assist with the development and lead in the execution of validation documents for instrumentation equipment. BEING A FITS PIECE COMES WITH PERKS: ~ One of these is the excellent, unmatched,...SugeridoContratoTrabajo por turnos
- ...YOU A FIT: The Technical Part: Bachelor’s degree in Engineering and at least eight (8) years of experience in Automation and Validation activities within the Medical Device or Pharmaceutical industry. Bilingual: Spanish and English (verbal/ written) Shift:...SugeridoContratoTrabajo por turnos
- ...precision compared against established specifications and recommends and implements corrective action where necessary. Develops, validates, and implements controlled environment methods. Applies existing techniques and procedures with recommendations and...SugeridoPrácticaTemporalTiempo completoTrabajar en la oficina
- ...regulatory issues, compliance issues, calibration issues, quality issues, microbial/environmental issues, technical cleaning issues, validation issues, electrical issues and process maintenance issues. Provide technical support for the maintenance team during FDA and...SugeridoTiempo completoDe duración determinadaTrabajo por turnos
- ...substance manufacturing/technical support. Skills: Experience in bulk Biological Process Technical support Process validation Fill & Finish Requirements Master’s degree OR Bachelor’s degree in Engineering & 2 years of Engineering experience (...Contrato
- ...complexity. Work with research, manufacturing, maintenance, process development, utilities, facilities, quality assurance and/or validation departments in developing requirements and recommendations for system modifications. Work under the direct supervision of...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...Contrato
- ...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
- ...ingenuity and creativity. Work 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 modifications. Work...ContratoTrabajo 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...ContratoTurno de mañanaTrabajo por turnos
- ...Supports operations in evaluation and implementation of action plans to eliminate root causes of non-conformances. Support validations as required. Provides support to Plant wide initiatives. Actively supports other Plant functions in the implementation of company...Tiempo completoTurno de tardeTrabajo por turnos
- ...ingenuity and creativity. 2. Work 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 modifications. 3....Contratista
- mirus Consulting Group is a local company based in Humacao, Puerto Rico that provides computer system validation and information technology consulting services to pharmaceutical companies and other organizations across the Island and parts of the United States. Its services...
- ...Nonconforming product, Yield, Pareto defect, Bounding. ~ Basic knowledge in Statistical Process Control. ~ Basic knowledge in Process Validation. ~Could work remote some days but preferred on site. ~ Available for Saturday and Sunday – 6 am to 6 pm, Monday and Tuesday...TemporalRemotoDomingoSábadoFin de semana
- ...mirus Consulting Group is a local company based in Humacao, Puerto Rico that provides computer system validation and information technology consulting services to pharmaceutical companies and other organizations across the Island and parts of the United States. Its services...Trabajo por turnos
- ...ingenuity and creativity. # Work 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 modifications. #...ContratoContratistaTrabajo por turnosFin de semana
- ...support #Provide solutions to a variety of technical problems of moderate scope and complexity (troubleshooting) #Familiarity with validation processes and documentation in a highly regulated environment #Complete activities as per project objectives and perform...Tiempo completoTrabajo por turnos
- ...provide troubleshooting. Work with manufacturing, maintenance, process development, utilities, facilities, quality assurance and/or validation departments. recommendations for process and/or system modifications. Analyze key performance indicators (KPIs) and utilize...ContratoTrabajo por turnos
- ...and biotechnology manufacturing facilities including C&Q & start up activities for Manufacturing facilities. ~ Familiarity with validation processes. ~ Familiarity with documentation in a highly regulated environment. ~ Ability to interpret and apply GLPs and GMPs...ContratoContratista