15 Empleos en Florida
Coordinador(A) Call Center - Manatí
Publicado hace 9 días
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Descripción Del Trabajo
*Job description*
Planifica, organiza, dirige y coordina todas las actividades del Departamento de Call Center.
*Requisitos Mínimos:*
* Experiencia en supervisión
* Bachillerato o Grado Asociado
Conocimiento y Manejo de MS Office (Word, Excel, Power Point, Outlook). Disponibilidad inmediata.
Si reúnes todos los requisitos favor de enviar tu Resume a: ***. Equal Employment Opportunity.
Job Type: Full-time
Benefits:
* Health insurance
* Life insurance
Work Location: In person
Buscamos Promotores
Publicado hace 12 días
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Descripción Del Trabajo
? ¡Estamos contratando promotores! ? ¿Buscas una oportunidad inmediata y bien remunerada?
¡Únete a nuestro equipo y comienza a crecer con nosotros!
? Ofrecemos:
• Ingredos comienzan desde $2,400 mensuales ?
• Plazas híbridas: 2 días presenciales y el resto remoto
• Comienzo inmediato
• Adiestramiento completo y continuo (¡no necesitas experiencia previa!)
• Oportunidades de crecimiento dentro de la empresa
Requisitos:
? Requisitos básicos: • Ser mayor de 18 años
• Compromiso, responsabilidad y actitud positiva
• Disponibilidad para trabajar modalidad híbrida
• Ganas de aprender y superarse
? Interesados:
Envíanos tu resumé a: ***
¡Da el primer paso hacia tu futuro profesional!
Laboratory Commissioning & Decommissioning Engineer
Hoy
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Descripción Del Trabajo
Validation Specialist
Publicado hace 4 días
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Descripción Del Trabajo
Quality Systems Specialist
Publicado hace 4 días
Trabajo visto
Descripción Del Trabajo
In-depth knowledge of GMP, FDA regulations, 21 CFR Part 11, Data Integrity (including Risk Assessment, Data Mapping), and EU regulatory requirements, with the ability to interpret and apply them effectively.
Proficient in computer systems and data collection tools, including Microsoft Office Suite, SAP, and Infinity.
Skilled in data analysis, identifying deviations and inconsistencies, and interpreting sampling and test results.
Experienced in problem solving and root cause analysis methodologies, including Kepner-Tregoe.
RequirementsBachelor’s degree in science (Chemical, Engineering, Biology, Pharmacy or Microbiology)Six (6) years of experience in project management, investigations or relevant roles and responsibilitiesin the pharmaceutical industry.Fully bilingual (Spanish/English) communication skills, both written and verbal.Technical and scientific capability to make firm decisions and recommendations.Microsoft Office, SAP, InfinityCSV Specialist
Publicado hace 4 días
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Descripción Del Trabajo
CSV Specialist with experience in Bioprocess Validations.
Technical Skills:
Tech Transfer, Process Design, Commissioning & Qualification.Vision system technologies (Strong).Inspection/packaging Concepts.Development and Execution of Processes/Equipment CharacterizationDuties:
Provides data analysis/interpretation and assesses the impact of the data on the project.Establish Testing Strategies.Technical Reports Development.Validations, and technical reports- To support SATs executions, document generation and challenge validations strategies.RequirementsBS or higher in Chemistry/ Biology/ Microbiology/ Computer Science/ Information Systems/Engineering or related discipline.Background in pharmaceutical products manufacturing environment and in manufacturing and laboratories areasMore than five (5) years of experience working with process validation life cycle, experience in commissioning and validating laboratory and manufacturing computerized systems in a manufacturing environment, and training in validation methodologies, technologies, and process control computer systems.Knowledge on computerized system with data collection software (database).Strong knowledge of cGMP, GAMP, SAT, FDA, 21 CFR Part 11 and Data Integrity Regulations.Experience in Automation process and/or Vision Inspection systems development.Knowledge in statistics using Mini-tab, JMP or other statistical software, project management skills and knowledge in development documentation protocols and reports.Knowledge in MS Project Management and MS Vision programs.Advanced scientific analysis and troubleshooting skills.Experienced in Instrument Performance qualification, and method configurationExcellent skills writing commissioning/ validation, and technical documentation in English and using MS Office applications.Bilingual (both English/Spanish)Validation Engineer
Publicado hace 14 días
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Descripción Del Trabajo
Technical Skills
IQ/OQ/PQ protocol development and execution FAT/SAT testing and documentation Validation Master Plan (VMP) creation MES/SCADA system qualification Injection molding and automated assembly validation Metrology equipment calibration and Gage R&R Traceability Matrix development Experience with KNEAT software (highly desirable)Regulatory Knowledge
FDA 21 CFR Part 820 EU MDR 2017/745 ISO 13485 & ISO 14971 GMP complianceCertifications
ISO 13485 Quality Management ISO 14971 Risk Management GMP Training Six Sigma (Green or Black Belt)Soft Skills
Strong documentation and report writing Cross-functional collaboration Ability to train personnel Analytical thinking and problem-solvingLocation: SouthEast, United States (Travel Required)Sé el primero en saberlo
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CSV Specialist
Publicado hace 15 días
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Descripción Del Trabajo
CSV Specialist to support the installation of several manufacturing solid dosage equipment such as but not limited to:
Encapsulator CheckweigherCompression machineHardness testerEncapsulation machineAuxiliary equipmentMain activities should include:
Verification of the equipment installed and configured at the vendor site (FAT).Implement the progression from FAT through IOQ in accordance with the CC strategy.Installation at the manufacturing room for qualification activities.Qualification activities in the manufacturing room areas.Development of Standard Operating Procedures.Generation and routing of calibration and preventive maintenance forms.Development and approval of GxP and automation impact assessments.Provide alternatives to resolve documentation situations.Establish project communication and documentation controls.Assure consistent quality of activities that meets or exceeds the requirements.RequirementsBachelor in Science or related field 2-3 years of experience as CSV consultant in regulated industry.Experience with MS Office applications (Word, Excel and MS Project)Excellent technical writing skills.Bilingual: English and Spanish, speaking and writing.Validation Specialist
Publicado hace 24 días
Trabajo visto
Descripción Del Trabajo
Validation Specialist with hands-on experience in executing validation and qualification activities across diverse areas, including:
Process
Packaging
Manufacturing
Laboratory
Computer System Validation (CSV)
Software
Facilities and Utilities
Site Acceptance Testing (SAT) & Factory Acceptance Testing (FAT)
Commissioning and Decommissioning of Systems and Equipment
Core Competencies:
Skilled in drafting protocols, technical reports, and validation documentation in alignment with regulatory and industry standards (e.g., FDA, GMP).
Proven ability to collaborate effectively with cross-functional teams—including Engineering, Quality, and Production—to ensure compliance, optimize processes, and support operational readiness.
Requirements Bachelor Degree in Science, or related fieldMinimum 5 years of experience in validations within a regulated industry.In-depth knowledge of GMP, FDA, and international standards.Hands-on experience in IQ/OQ/PQ, SAT/FAT, and commissioning.Ability to write clear and precise technical documentation.Excellent communication and teamwork skills.Bilingual (English/Spanish - understand, write and speak).