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- ...For Validation services in the Quality/Validation area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s degree in Engineering and at least two (2) years of previous experience in Validation activities within the Pharmaceutical & Medical Devices Industry...SugeridoContratoTrabajo por turnos
- ...For Validation services in the Project Engineeirng/Medical Device Packaging area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Engineering and at least four (4) years of exposure to Validation Engineering activities within the Pharmaceutical...SugeridoContratoTrabajo por turnosFin de semana
- ...For Validation services . WHAT MAKES YOU A FIT: The Technical Part: Bachelor's in Engineering or Sciences with three (3) years of experience in Validation activities within the Medical Devices Industry. Bilingual: English and Spanish Soft Skills: Great...SugeridoTrabajo 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
- ...The Validation Specialist is responsible for supporting qualification and validation activities for manufacturing equipment and processes. The role focuses on the execution of IQ, OQ, and PQ protocols, development and maintenance of SOPs, risk management activities such...Sugerido
- ...We are seeking Validation Engineer professionals to support validation activities for sterile manufacturing, plant operations, facilities, equipment, systems, room requalification, and project-based validation initiatives. Assignment may include one or more active site...SugeridoContrato
- ...electronic document management systems. ~Support Data Integrity and ALCOA+ principles throughout qualification activities. ~Prepare validation summary reports. Risk Management & Change Control ~Lead risk assessments supporting system qualification. ~Evaluate...SugeridoContratistaContrato
- ...For Validation Engineering services in the Manufacturing area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Engineering and at least four (4) years of exposure to Validation Engineering activities within the Pharmaceutical or Medical Devices...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
- ...Title: Validation Specialist I - ***** (Añasco) Job Type: Professional services contract. Duration: Depends on project schedule (long term) Where: Añasco, On-Site Hour Rate: Depends on the expertise. Negotiable MINIMUM QUALIFICATIONS Education and/or experience...SugeridoPor horaPrácticaTiempo completoContratoTrabajar en la oficinaTrabajo por turnosFin de semana
- ...please visit us at . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description The Senior Validation Engineer/Analyst functions as the lead for maintenance, engineering, and validation activities within the assigned site/area of...SugeridoTemporalTiempo completo
- ...For Project Validation services in the Manufacturing area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Engineering or Science and at least five (5) years of exposure to Validation Engineering activities within the Pharmaceutical or Medical...SugeridoContratoTrabajo por turnos
- ...For Validation & Qualification services in the Manufacturing and Engineering area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Life Sciences or Engineering and previous exposure to Validation and/or Qualification activities within the pharmaceutical...SugeridoContratoTrabajo por turnos
- ...States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America. Responsibilities: Performed assigned validation and documentation activities under supervision, ensuring accuracy and compliance with established procedures. Executed documentation...SugeridoTiempo completoTrabajar en la oficina
- ...and FAT planning/execution. Coordinate equipment design integration with the Design Interface Manager and BIM Coordinator. Validate Design and CMs logistics: shipping, receiving, rigging, set-in-place, and protection during construction. Support equipment installation...SugeridoContratistaContratoTrabajo por turnos
- ...and attach to PMs/WOs. Obtains necessary approvals for all types of documents. Support any method transfer, verification and validation protocols. Works with document owner to make appropriate revision. Contributes to the team; supports everyone's efforts to...ContratoTrabajo por turnos
$13,69 - $19,02 por hora
...para resolver incidencias Diagnosticar problemas técnicos y documentar causas raíz y acciones correctivas Apoyar instalación, validación, mantenimiento y limpieza de equipos Participar en iniciativas de mejora continua aprobadas por la gerencia ¿Qué necesitas...PrácticaTemporalTiempo completo- ...readiness, support manufacturing investigations, lead quality improvement initiatives, manage change control activities, participate in validation efforts, and ensure compliance with Quality Management System (QMS) requirements and applicable regulatory standards....Tiempo completo
$17 - $20 por hora
...inventory control. We will consider employment of qualified applicants with arrest and conviction records. Obtains and maintains valid PTCB certification or pharmacy license as required by state. An Equal Opportunity Employer, including disability/veterans. The...Trabajo de temporadaTrabajo por turnos- ...Advanced English proficiency Commissions available Excellent customer service skills Sense of urgency and ability to work under pressure Valid Puerto Rico driver's license Own vehicle in good condition, Car Allowance provided Previous B2B collections experience Advanced...Lunes a viernes
- ...requirements. Support clean-room, sterile, aseptic, Grade C/D, environmental monitoring, bioburden, contamination-control, and cleaning-validation activities as applicable. Support equipment relocation, facility qualification, remediation activities, and quality-system...Contrato
- ...Bring it on! AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job) Review and approve product MPs. Approve process validation protocols and reports for manufacturing processes. Request Quality on incident triage team. Approve Environmental Characterization...ContratoTrabajo por turnos
- ...candidate will provide technical leadership, execute engineering projects, drive process improvements, and support manufacturing validations while working with minimal supervision. This role requires strong analytical and problem-solving skills, the ability to manage...ContratistaTemporal
- ...We are seeking a highly motivated and experienced Senior Engineer to support engineering initiatives, equipment development, validation activities, and project execution within a regulated manufacturing environment. The successful candidate will play a key role in driving...Contrato
- ...Air Systems & Building Automation Systems (BAS/BMS) ~ Generating and executing: URS, FRS, SDS, FAT/SAT, IQ, OQ, PQ Protocols, Validation Plans and Reports, & Traceability Matrices. ~ Computer System Validation (CSV) experience required ~ FDA, GMP, ISO, OSHA, EPA...ContratoTrabajo 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
- ...Engineers with at least three (3) years of experience in Medical Device or Pharmaceutical industries. The role will focus on executing validation protocols (IQ, OQ, PQ), troubleshooting, and optimizing manufacturing processes. Responsibilities: Develop and execute...ContratistaTiempo completoRemotoTrabajo híbrido
- ...efficiency. Actively support readiness for Regulatory audits and meeting commitments from such audits. Develops and executes Validation Strategies for new packaging processes and configurations. Completion on time of action items for Packaging Tech Transfer of...ContratoTrabajo por turnos
- ...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
- ...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