Empleos de fda en Valencia

We are the people who give possibilities purpose BD is one of the largest global medical technology companies in the world. Advancing the world of healthTM is our Purpose, and it's no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per...

En BETWEEN te ofrecemos las oportunidades que necesitas para alcanzar tus objetivos profesionales. Si quieres desarrollar tus capacidades en IT e Ingeniería, este es tu próximo destino. Nuestro soporte abarca una gran variedad de áreas, como Firmware, Software, BI, Diseño, Project Management y muchas más. Además, desarrollamos soluciones tecnológicas...

Cytel is seeking a Senior/Principal Statistical Programmer to work remotely on sponsor-driven clinical trials. The role focuses on conducting advanced statistical programming, generating SDTM/ADaM outputs, and delivering compliant datasets, tables, listings, and graphs across studies.You will lead programming activities, supervise CRO deliverables, and...

Cytel Inc. is seeking a Senior/Principal Statistical Programmer (SAS + R) to work remotely with a sponsor team in the pharmaceutical sector. The role involves independent work, CRO oversight, and delivering SDTM/ADaM specifications and Define.Xml across multiple studies.Responsibilities include developing SAS and R programs, supporting regulatory...

Precision Medicine Group is seeking a Senior Medical Writer/Principal Medical Writer to lead the development of high-quality clinical study documents in Spain. This role requires planning, writing, editing, and QC of documents like protocols, IBs, CSRs, and narratives with strict adherence to regulatory guidelines.You will ensure alignment with ICH, FDA,...

Mercor is seeking a Regulatory Law Expert to design and supervise regulatory compliance programs, including investigations and enforcement actions. The role covers financial services regulation, healthcare and FDA rules, antitrust and data privacy, cybersecurity, and environmental and energy regulation in a global setting.You will use regulatory tracking...

Cytel is seeking a Senior/Principal Statistical Programmer (Remote) to join a sponsor-integrated program. You will work on clinical development programs across therapeutic areas, independently guiding CRO programmers and delivering high-quality SAS and R analyses for trials.You will generate SDTM/ADaM specifications and define.Xml, create datasets and...

Precision Medicine Group is seeking a Senior Medical Writer/Principal Medical Writer to lead the development of high-quality clinical study documents in Spain. You will plan, write, edit, format, and QC protocols, IBs, CSRs and associated narratives with regulatory-compliant content and eCTD readiness.The role requires 5+ years as a Senior Medical Writer or...

Legit. Health is seeking a Clinical Affairs Manager to own clinical evaluation and regulatory documentation end-to-end, acting as the expert in the room for European and US submissions.The role requires leading CEP/CER development, post-market follow-up, and regulatory strategy with cross-functional teams. You will design and defend our clinical evidence...

Senior/Principal Statistical Programmer SAS + R (Remote)Sponsor-dedicated:Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Principal Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is...

Position: Deputy Technical Director of QualityExperience: 5+ years in leadership roles within pharmaceutical FDF manufacturingWant to know more? BioNanoPharma is a global company committed to excellence across the pharmaceutical value chain, bringing innovation, quality, and expertise in research, development, manufacturing, and distribution of...

En BETWEEN te ofrecemos las oportunidades que necesitas para alcanzar tus objetivos profesionales. Si quieres desarrollar tus capacidades en IT e Ingeniería, este es tu próximo destino. Nuestro soporte abarca una gran variedad de áreas, como Firmware, Software, BI, Diseño, Project Management y muchas más. Además, desarrollamos soluciones tecnológicas...

Senior/Principal Statistical Programmer SAS + R (Remote)Sponsor-dedicated: Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Principal Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is...

Overview In this role you lead MedTech Complaints implementations for Veeva's customers, guiding transformation of complaints management processes and configuring Vault for enterprise use. You will partner with customers and cross-functional teams to translate requirements into scalable solutions that drive quality and regulatory compliance. The position...

Senior/Principal Statistical Programmer SAS + R (Remote)Sponsor-dedicated: Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Principal Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is...

Tu día a día Buscamos incorporar un/a Especialista en Legislación de Materiales en Contacto con Alimentos (MCA) para el área de Laboratorios, dentro del clúster de Salud y Seguridad del Consumidor y del Medioambiente. Tu misión será garantizar la adecuación regulatoria y la seguridad de materiales y envases en contacto con alimentos, acompañando...

Senior/Principal Statistical Programmer SAS + R (Remote)Sponsor-dedicated: Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Principal Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is...

Senior/Principal Statistical Programmer SAS + R (Remote)Sponsor-dedicated: Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Principal Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is...

Analytical Development Scientist – Biological Methods Applications to be sent to: fcoronel@bionanopharma.com Global Responsibility Responsible for the execution, documentation, and technical integrity of analytical activities related to the development of bioanalytical methods within the organization. This includes ensuring that all analytical...

Overview In this senior role, you drive the creation of high-quality clinical study documents, from planning through QC, aligned with regulatory standards. Your expertise shapes content strategy, standards, and processes for global regulatory submissions. This is a hands-on writing leadership role with a clear focus on precision, deadlines, and impact on...