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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
- ...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
- ...Sr. Validation Specialist support of manufacturing process and equipment upgrades, replacements, and modifications in the manufacturing, or manufacturing support environment. Experience in: Manufacturing Process Methasys Validation Life Cycle Validation...SugeridoContrato
- ...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
- ...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
- ...Jr Validation Specialist with experience in regulated industries to c ollaborate with cross-functional teams to draft project schedules and plans. Knowledge of Validation Life Cycle, Regulations and Project Management Good technical writing skills Requirements...SugeridoContrato
- ...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: Support process development and validation activities in commercial biopharmaceutical manufacturing, with emphasis on formulation and aseptic filling operations. Apply...SugeridoTiempo completo
- ...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
- ...WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s degree in Engineering and at least two (2) years of experience in validation activities within the Medical Device or Pharmaceutical industry. Bilingual: Spanish and English (verbal/ written) Shift: Administrative...SugeridoContratoTrabajo 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. *...SugeridoDe duración determinadaTiempo completoTrabajo por turnos
- ...from Bulk, Stability and/or In-Process areas by following analytical methods, SOP's and Pharmacopoeias. Support any required method validation activity, equipment qualification and/or method transfer. Basic Requirements: Bachelor's degree in chemistry, required....SugeridoTiempo completoVisa de trabajo
- ...Plan and execute configuration migrations between environments (e.g., dev/test/staging/prod) using established tools and processes, validating completeness, dependencies, and version alignment. Integration confidence * Partner with integration teams and vendors to...SugeridoPrácticaTiempo completoTrabajo híbridoTurno de nocheHorario flexibleFin de semana
- ...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
- ...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...Sugerido
- ...responsibilities in support of site Quality Assurance program under minimal supervision. Review and approve product MPs. Approve process validation protocols and reports for manufacturing processes. Request Quality on incident triage team. Approve Environmental...Tiempo completo
- ...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...ContratoFin de semana
- ...and according to business needs. Experience in: Change cControl, nonconformance, corrective and preventative actions, and validation practices. Technial Writing and cGMP procedures and engineering. Maximo and Purshase Orders (PO). The Personality Part...ContratoTrabajo por turnos
- ...internal stakeholders and external suppliers. Works closely with Project Managers, Project Engineers, Procurement, Maintenance, Validation, and Quality to support the successful execution of engineering projects in a regulated (FDA, cGMP) environment. Key...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...Visa de trabajo
- ...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
- ...capital projects environment 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
- ...established by our customers, in order to perform and provide a highly effective service. We are seeking a Quality Engineer to support validation activities within a regulated manufacturing environment, with strong involvement in process validation, equipment qualification,...ContratistaTiempo completo
- ...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
- ...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
- ...compensation range for this opportunity is accurate and reasonable at the time of posting. The Acosta Group utilizes E-Verify for validating the ability to work in the United States for all job candidates. If you want more information on what this entails and your...Por horaTiempo parcialTrabajo por turnos
- ...Partner with sites, functional stakeholders, data teams, and implementation partners to define standards, transformation rules, validation requirements, and issue resolution pathways. Identify data risks and dependencies that may affect implementation quality, compliance...Contrato
- For Validation services in the Manufacturing area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s degree in Engineering (preferred Mechanical or Electrical) & two (2) years of relevant experience within the Medical Devices or Pharmaceutical industry....ContratoTrabajo por turnos
- ...processes, facilities, and equipment. Experience with QRAES, Change cControl, non conformance, corrective and preventative actions, and validation practices. Experience with Maximo Capable of working and/or submitting Purchase Orders (PO). Experience working and escorting...Contrato
- ...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...ContratoTrabajo por turnos