Key Responsibilities · Serve as Regulatory Team Lead on complex global studies, including oversight of technical writing and submission publishing. · Draft, review, and quality-check clinical trial regulatory core study documentation at global and country level
Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It
Description Dot Compliance is a leading provider of cloud Quality and Compliance management solutions for the life science industry. Dot’s SaaS solutions are based on the world’s most innovative cloud technology provider, Salesforce.com. We are a
En Catalent estamos buscando un Coordinador/a de Validaciones para nuestra planta productiva de Loma Hermosa, Buenos Aires. Principales Responsabilidades: Liderar y desarrollar al equipo de Validaciones, promoviendo una cultura de aprendizaje, responsabilidad y mejora continua. Coordinar
En Catalent estamos buscandoun Operario de Encapsulado para nuestra planta productiva de Buenos Aires. Principales Responsabilidades: Preparar las máquinas de encapsulado y elaborar capsulas de gelatina a partir de la gelatina y el contenido elaborado en
Who We Are: We are a tech-enabled growth firm–at the intersection of marketing, consulting & data intelligence–igniting revenue and brand recognition for leading and emerging companies around the world. As a people-first firm, we value diversity
Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It
Description Medison is a rapidly growing global biotech with a strong global presence, operating in 4 continents and over 24 countries. Our mission is to provide access to highly innovative therapies to patients who suffers mainly
At 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,
En Catalent estamos buscandounAnalista de Cumplimiento de la Calidad para nuestra planta productiva de Loma Hermosa, Buenos Aires. Principales Responsabilidades: Alineación normativa y requerimientos regulatorios: Realizar el monitoreo y análisis de cambios en farmacopeas, regulaciones FDA
This is us At Avenga, we believe that human creativity empowers technology that matters. Operating globally, our 6000+ specialists provide a full spectrum of services, including business and tech advisory, enterprise solutions, CX, UX and Ul
Company Description At Turner & Townsend we’re passionate about making the difference. That means delivering better outcomes for our clients, helping our people to realize their potential, and doing our part to create a prosperous society.
Solution Design Manager, Pharma Drug Launch/Commercial Strategy The Solution Design Manager - Pharma Drug Launch role within the Full-Service Commercial team is responsible for driving the development of select pitches, engaging with business unit (BU) partners to collect
Omega CRM is a Merkle & Dentsu company, a leader in the development of Customer Experience services with +20 years of experience in the use of technology applied to marketing. Focused mainly on innovation, we provide
Omega CRM is a Merkle & Dentsu company, leader in development of Customer Experience services, with +20 years of experience in the use of Technology applied to Marketing and providing a unique Customer Relationship with mainly
The Position As a Portfolio Lead Molecular, you will be fully empowered to design and implement the business, marketing, and portfolio strategies for the Molecular customer area. In this role, you will act as the single
En Catalent estamos buscandounAnalista de Cumplimiento de la Calidad para nuestra planta productiva de Loma Hermosa, Buenos Aires. Principales Responsabilidades: Alineación normativa y requerimientos regulatorios: Realizar el monitoreo y análisis de cambios en farmacopeas, regulaciones FDA
Buenos Aires, Argentina Mexico City, Mexico São Paulo, Brazil Full time R Key Responsibilities · Serve as Regulatory Team Lead on complex global studies, including oversight of technical writing and submission publishing. · Draft, review, and
About the role As a SAP Quality Management (QM) Consultant, you will make an impact by supporting end-to-end SAP QM implementations, rollouts, and enhancements that help improve quality control and compliance across the organization. You will
Buenos Aires, Argentina São Paulo, Brazil Full time R Key Responsibilities · Serve as Regulatory Team Lead on complex global studies, including oversight of technical writing and submission publishing. · Draft, review, and quality-check clinical trial