Trabajo Regulatory Affairs Manager

The Plant Manager's responsibility is to provide leadership to all departments for overall vision and direction of the plant by way of guidance, direction, encouragement, training, and development. The Plant Manager is also responsible for developing and coaching managers and supervisors to excel to...

Product Manager with MedTech Experience with English Barcelona, Spain (hybrid) Employee Product Management Leader and innovative biomedical company is looking for someone ready to proactively bring new ideas to the team, push boundaries, and constantly look for innovation. The company believes on sh...

Descripción del puesto:At (COMPANY NAME), we're not just about treating diseases - we're about defeating them. We're on a mission to turn innovative science into life-changing medicines, and we need your help. As a Reg Affairs Manager in our Oncology R&D department, you'll play a crucial role in gai...

Dar soporte a la marca en la coordinación de nuevos diseños o modificación de los existentes vinculados con aspectos regulatorios o de innovaciónCoordinar estos cambios con los agentes involucrados : Regulatory Affairs, R&D, Marketing Internacional, Filiales..Todos estos cambios serán gestionados ju...

The person in this role will be responsible for submitting Medical Affairs scientific publications developed by the North America and International Medical Directors for medical and regulatory review and approval in top 12 countries and as required other nominated markets. These include new publicat...

Descripción del puesto:DescriptionYour RoleAs Regulatory Affairs Specialist, reporting to Regulatory Affairs Manager, you will join the Affinity's Quality team to oversee and navigate the complex landscape of regulatory compliance in the petfood industry.What will you do?* Be part of the product dev...

Do you have experience in supervising, preparing, and implementing protocols/reports for technology transfers? Are you looking for a new professional challenge?At Grupo Crit, we're looking for you!Global responsabilitiesMonitor, prepare and implement protocols/reports for technology transfers, manuf...

Descripción del puesto:DescriptionFor more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo. We know that the...

Descripción del puesto:Why do we need you ?As Product Manager VIE, you won't just be working on product development; you'll get a 360º view of the business. This includes delving into marketing strategies, liaising with manufacturers, and collaborating closely with the sales team to deliver comprehe...

¿Dónde vas a trabajar? International diagnostic company (analysis, image and pathology) with more than 30 years in the market, is looking for a Group Quality Management System Manager located in Barcelona. ¿Qué harás en tu nuevo puesto? The Group QMS Manager will have the following responsibili...

Descripción del puesto:Job Description:About this roleThe main purpose of this position is meeting patients' individual needs, through the following activities and responsibilities, to be carried out in his/her country: * Provide field-based medical / scientific expertise ensuring understanding of t...

- Collaborates with North America and International Medical Directors to submit new and/or repurposed medical affairs assets for review and approval for all regions and ensures accurate submission details are captured for medical and regulatory approvals.- Collaborates with cross-functional colleagu...

Desde Grupo Crit buscamos un/a responsable del departamento de Asuntos Regulatorios Europeos en relación con nuevos productos, nuevos registros, nuevos territorios y proyectos de BD. para una empresa dedicada al suministro de productos farmacéuticos genéricos sobre todo para hospitales ubicada en Al...

¿Dónde vas a trabajar? Multinational Pharmaceutical Company. ¿Qué harás en tu nuevo puesto? Ensuring high quality contents for regulatory CMC documentation in line with applicable guidelines for new and approved Drug Products and/or Drug Substances in Europe, USA and other countries. To lead the...

Acerca de nuestro cliente Important multinational energy company is looking for a Commercial Regulatory Affairs Manager focused on the Gas and Hydrogen Spanish market. Descripción As a Commercial and Regulatory Affairs Adviser for gas, biomethane and hydrogen for the Spanish market, you are going to...