The Clinical Trial Manager is accountable for achieving the final clinical deliverable (usually clean data from evaluable patients as specified in the study……
Ciena is seeking an Import Global Trade Analyst to play a vital role in supporting the organization’s import operations and ensuring compliance with North……
5–7 years of communications experience. Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over……
The Project Coordinator II provides coordination and operational support for site activation and maintenance activities across all study phases.…
The Clinical Trial Manager is accountable for achieving the final clinical deliverable (usually clean data from evaluable patients as specified in the study……
The Clinical Trial Manager is accountable for achieving the final clinical deliverable (usually clean data from evaluable patients as specified in the study……
Document Review Specialist I is responsible for reviewing Investigator Packages, Informed Consent Forms and Advertisements following project and country……
Ensure all submissions are prepared in high-quality, compliant formats. Perform related activities as needed and provide support to both internal and external……
The Statistical Programmer will be responsible for the development, maintenance, and validation of annotated Case Report Forms (aCRFs) as well as of……
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and……
2–5 years of hands-on experience in automation engineering. Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA……
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and……
The Project Manager ensures the successful initiation, planning, execution, monitoring, controlling and closure of assigned clinical research projects.…
The Biostatistician will act as support or Lead Biostatistician on multiple phase 1 to 4 clinical trials, providing input into the statistical sections of……
The position is responsible for oversight of the entire document lifecycle, ensuring proper execution at every stage. Due dates to maintain project timelines.…
At least 5 years of clinical research experience in biotechnology, pharmaceutical or Contract Research Organization (CRO) industry, including 4 years of……
5–7 years of communications experience. Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over……
Ability to travel if necessary preferred (approximately 5%). Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA……
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and……
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and……
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and……
Type of contract: Contractor - Full Time. As a Regulatory Affairs Manager, you will be the primary point of contact for clients navigating the FDA regulatory……
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and……
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and……
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and……
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and……
Poseer sólido conocimiento en buenas prácticas de desarrollo: SOLID, Clean Architecture, TDD, design patterns y experiencia en testing: unitario, funcional,……
En Laboratorios Richmond nos encontramos en la búsqueda de un Analista de Downstream para integrarse a nuestro equipo en Planta Pilar .
Responsabilidades de la posición: Ejecutar procesos de purificación: Filtración (carcasas, fibra hueca, cassettes), precipitación, centrifugación, ultrafiltración y diafiltración.
Implementar, optimizar y escalar proyectos de Downstream
Soporte técnico para la puesta a punto de la planta productiva
Operación de equipos de cromatografía: AKTA y software Unicorn, empaque de columnas, cálculos de asimetría/HTP, siembra y elución.
Formulación y llenado de API , asegurando el plan productivo y los estándares de calidad.
Acondicionamiento y sanitización de equipos y áreas bajo normativa farmacéutica.
Instrumental y soporte técnico: Operación de equipos de TFF, cromatógrafos, bombas peristálticas, pHmetro, conductímetro, balanza analítica, centrífugas y manómetro.
Confección de SOP, protocolos e informes de desarrollo bajo normas GMP; participación en investigaciones de desvíos (Causa Raíz) y auditorías.
Gestión de stock de insumos (Carga de SOLPEDs) y manejo de SAP.
Somos una empresa farmacéutica regional con base en Argentina comprometida con la excelencia y la mejora continua: desarrollamos y producimos medicamentos de calidad con valor humano agregado.
Compartimos la visión de un mundo donde la salud no sea un privilegio. Por eso, deseamos contribuir a mejorar, proteger y cuidar la salud de las personas.
¡Ayudamos a vivir más y mejor!
Requisitos
Formación: universitaria en Biotecnología, Biología, Bioquímica, Farmacia o afines.
Idioma: Inglés técnico avanzado oral y escrito.
Experiencia: Mínima de tres años, en mejora de procesos, desarrollo o producción de la industria farmacéutica o biofarmacéutica bajo normativas GMP.
Conocimientos Técnicos : Experiencia comprobable en técnicas de purificación de proteínas, Biotecnología industrial y producción de vacunas/anticuerpos
Calidad y Normativa: Normas GMP (ANMAT/FDA/EMA), Farmacopeas e ISO (14644/17025).
Gestión: Procesos de validación, calificación de equipos y sistemas de calidad (OOS/CAPA).
Herramientas: Interpretación de planos (P&IDs), Paquete Office y sistemas de gestión (SAP/Loyal).
Beneficios
Cuponera virtual de descuentos para que puedas conseguir las mejores oportunidades en distintas categorías.
Beneficio por comedor
Semana adicional de descanso (Semana Richmond) para recargues energías y comiences el año con todo.
Si viajas a nuestra planta en Pilar, brindamos traslado
Y la posibilidad de formar parte de un equipo en constante crecimiento y expansión.
¡Esperamos tu postulación!