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La persona ideal tendrá al menos 2 años de experiencia en roles similares dentro de entornos industriales y trabajará estrechamente con el equipo financiero para garantizar una contabilidad rigurosa y oportuna, con foco en /p #J-18808-Ljbffr.

pRoche Spain is seeking a Safety and Reporting Senior Specialist in Post Market Quality to ensure safety and regulatory compliance after market release, with autonomy and global collaboration. /ppYou will manage safety and PMS cases, interface with authorities and affiliates, drive PMS activities, and contribute to process improvements while mentoring colleagues. /ppFluent English is required; German is a plus; laboratory or IT experience is encouraged; join a patient-centric team. /p #J-18808-Ljbffr

pRoche in Spain seeks a Safety and Reporting Senior Specialist of Post Market Quality to join our quality and regulatory team. You will work with autonomy to ensure products meet safety and compliance after market release, diving into complex cases and collaborating with global experts. /ppResponsibilities include managing safety, vigilance, and PMS cases per ISO and country rules; engaging Regulatory Authorities and affiliates; planning PMS activities; improving data monitoring systems; conducting /p #J-18808-Ljbffr

pRoche seeks a Safety and Reporting Senior Specialist of Post Market Quality to lead post-market safety, vigilance, and PMS activities. You will collaborate globally with Regulatory Authorities and affiliates, ensuring ISO-compliant case handling and continuous process improvement in a patient-centric setting. /ppYou will drive data generation, lead PMS activities, and mentor junior colleagues while contributing to agile squads and risk assessments. /p #J-18808-Ljbffr

pNovartis Farmacéutica, S.A. in Barcelona is seeking Associate Director, Aggregate Reports Risk Management to lead AR RM operations across the product portfolio, ensuring compliance and cross-functional collaboration. /ppYou will develop and maintain the global aggregate reporting schedule, monitor KPIs, and drive investigations and CAPA; act as a key operational interface with Country Organisations and partners. Hybrid work model in Barcelona; fluent English required. /p #J-18808-Ljbffr

ppAt Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. /p h3The Position /h3 pAt Roche, we are passionate about transforming patients’ lives and we are fearless in both decision and action - we believe that good business means a better world. That is why we come to work each day. We commit ourselves to scientific rigor, unassailable ethics, and access to medical innovations for all. We do this today to build a better tomorrow. /p pbSafety and Reporting Senior Specialist /b of Post Market Quality, you will be a key player within our Quality and Regulatory organization. Working with a high degree of autonomy and minimal supervision, you will ensure our products maintain the highest standards of safety and compliance after they reach the market. You will dive into complex cases, collaborate globally, and contribute to continuous improvement in a dynamic, patient-centric environment. /p h3Your Main Responsibilities /h3 ul liCase Report Management: Take accountability for the timely and compliant handling of safety, vigilance, and Post-Market Surveillance (PMS) cases/reports, strictly adhering to ISO Quality System requirements and country-specific regulations /li liRegulatory Affiliate Collaboration: Interface directly with Regulatory Authorities (e.g., FDA, Notified Bodies) and Affiliate Organizations. Coordinate, prepare, and deliver precise responses by collaborating with global subject matter experts /li liPost-Market Surveillance (PMS): Maintain and facilitate the schedule of PMS reports, drive data generation, and lead the planning, completion, and evaluation of PMS activities for various product families /li liQuality System Process Improvement: Develop advanced monitoring systems for data and PMS reports to boost efficiency. Review case quality and customer feedback to optimize our internal processes /li liCompliance Risk Management: Ensure all records meet established quality processes, and take ownership of completing thorough risk assessments for product quality issues /li liTraining, Mentoring Squad Support: Participate in developing and delivering training on vigilance/safety/PMS topics. Onboard and coach less experienced colleagues, lead or contribute to agile projects (e.g., SQUADs), and act as a proxy for the Principal Specialist when needed /li /ul h3What’s in your toolbox? (Qualifications Experience) /h3 ul liEducation: Bachelor’s degree in Sciences and/or vocational training with equivalent related experience /li liExperience: 3+ years of experience working in a regulated environment (preferred experience in Quality Systems, Vigilance, and/or Safety) /li liLanguages: Fluent professional knowledge of English is required. Knowledge of German is a strong asset /li liTechnical Savvy: Laboratory experience and/or strong IT skills are highly preferred /li liGlobal Mindset: Proven experience working successfully in virtual, cross-functional, and intercultural teams /li /ul h3Leadership Soft Skills that will make you thrive /h3 ul liCritical Thinking Problem Solving: Ability to make sound decisions even when dealing with limited or ambiguous information /li liResilience Confident Manner: A strong sense of quality, a solution-oriented mindset, and the ability to adapt to changing environments /li liCommunication Technical Writing: Excellent negotiation skills and the ability to author technical documentation tailored for regulatory authorities /li /ul h3Who we are /h3 pA healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. /p pLet’s build a healthier future, together. /p pRoche is an Equal Opportunity Employer. /p /p #J-18808-Ljbffr

ppAs a Safety and Reporting Senior Specialist of Post Market Quality, you will be a key player within our Quality and Regulatory organization. Working with a high degree of autonomy and minimal supervision, you will ensure our products maintain the highest standards of safety and compliance after they reach the market. You will dive into complex cases, collaborate globally, and contribute to continuous improvement in a dynamic, patient‑centric environment. /ph3Responsibilities /h3ulliCase Report Management – Take accountability for the timely and compliant handling of safety, vigilance, and Post‑Market Surveillance (PMS) cases/reports, strictly adhering to ISO Quality System requirements and country‑specific regulations. /liliRegulatory Affiliate Collaboration – Interface directly with Regulatory Authorities (e.g., FDA, Notified Bodies) and Affiliate Organizations. Coordinate, prepare, and deliver precise responses by collaborating with global subject matter experts. /liliPost‑Market Surveillance (PMS) – Maintain and facilitate the schedule of PMS reports, drive data generation, and lead the planning, completion, and evaluation of PMS activities for various product families. /liliQuality System Process Improvement – Develop advanced monitoring systems for data and PMS reports to boost efficiency. Review case quality and customer feedback to optimize internal processes. /liliCompliance Risk Management – Ensure all records meet established quality processes and complete thorough risk assessments for product quality issues. /liliTraining, Mentoring Squad Support – Develop and deliver training on vigilance/safety/PMS topics. Onboard and coach less experienced colleagues, contribute to agile projects, and act as a proxy for the Principal Specialist when needed. /li /ulh3Qualifications Experience /h3ulliEducation – Bachelor’s degree in Sciences and/or vocational training with equivalent related experience. /liliExperience – 3+ years in a regulated environment; preferred experience in Quality Systems, Vigilance, and/or Safety. /liliLanguages – Fluent professional knowledge of English required; knowledge of German is a strong asset. /liliTechnical Savvy – Laboratory experience and/or strong IT skills highly preferred. /liliGlobal Mindset – Proven success working in virtual, cross‑functional, and intercultural teams. /liliLeadership Soft Skills – Demonstrated critical thinking and problem‑solving, resilience, confidence, excellent communication and technical writing, and negotiation skills. /li /ulpRoche is an Equal Opportunity Employer. /p /p #J-18808-Ljbffr

Un laboratorio farmacéutico busca un Contable para garantizar la gestión contable y el cumplimiento normativo. Las responsabilidades incluyen el registro de asientos contables, ejecución de cierres, y colaboración con auditorías.

En Banco Sabadell, #QueremosQueSeasTú, porque sabemos que el talento único de cada persona es lo que nos hace #SerSabadell. Compartes estos valores? Únete a Banco Sabadell y haz que tu talento marque la diferencia.

Buscamos Traductor/a jurado en Santa Coloma de Gramenet y alrededores. Gracias a nuestra plataforma de gestión de clientes, podrás aceptar o descartar solicitudes de trabajos en tu área, enviando presupuestos solo a los clientes que más te interesen. Pertenecer a la red de profesionales de Crono

Take accountability for the timely and compliant handling of safety, vigilance, and Post‑Market Surveillance (PMS) cases/reports, strictly adhering to ISO Quality System requirements and country‑specific regulations. As a Safety and Reporting Senior Specialist of Post Market Quality, you will be

Banco Sabadell, cuarto grupo bancario de España, busca un Técnico/Técnica Especialista Reporting para liderar la calidad y evolución de procesos de Reporting Regulatorio.

Associate Director, Aggregate Reports & Risk Management – you will lead AR & RM operations, ensuring compliance, operational excellence, and cross-functional collaboration across the product portfolio.

Una importante empresa del sector industrial busca incorporar un/a Administrativo/a Contable en Santa Perpètua de Mogoda.

Buscamos Redactor/a web en Barcelona y alrededores. Conocimientos previos para desarrollar funciones de Redactor/a web. Solicitudes de nuevos trabajos y clientes en tu zona, que necesitan Redactor/a web.

Una empresa de consultoría e ingeniería busca un/a Ingeniero/a de Caminos, Canales y Puertos con al menos 8 años de experiencia en redacción de proyectos ferroviarios.La persona seleccionada se encargará de la redacción técnica, control de proyectos, y coordinación de equipos.Se espera auton

Desde El Diario Hoy, líder de la información impresa y digital tanto en la provincia de Cáceres como la de Badajoz, nos encontramos en la búsqueda de un perfil Redactor especializado en información económica y de mercados financieros para incorporar al equipo de redacción de forma inmediata.