Argentina Job Openings
Merck Group
Regulatory Analyst
Buenos Aires
FULL TIME
October 22, 2024
¿Estás listo para explorar, romper barreras y descubrir mucho más? Sabemos que tienes grandes planes. Nosotros, también, innovar con la ciencia y la tecnología para enriquecer la vida de las personas con las soluciones en Healthcare, Life Science y Electronics apasiona a nuestros colegas en el mundo entero. Juntos, soñamos en grande y compartimos el entusiasmo por cuidar a una gran diversidad de personas, clientes, pacientes y al planeta. Por eso, siempre buscamos mentes curiosas que imaginen lo nunca visto con nosotros.
Your role:
As a Regulatory Affairs Analyst you will be dedicated to support one of our Life Science Division, being responsible for assigned portfolio products, planning, and executing regulatory activities supporting the implementation portfolio expansion, working in collaboration with global/ regional functions and stakeholders across country, region and the globe providing strategic and functional inputs to the LATAM Regulatory team.
General Scope of Responsibility:
- To work cross-functionally by collaborating with regulatory discussions and inputs with local, regional, and global stakeholders, as needed.
- To ensure regulatory compliance of the local portfolio:
- Control and management of the regulatory lifecycle of products subject to registration/control in Argentina by local authorities (e.g: ANMAT, SENASA);
- Provide support to regulatory and commercial projects.
- Review/ creation of local operating procedures affecting the maintenance of the local portfolio.
- Execute local regulatory surveillance and intelligence to ensure business continuity and mapping of business opportunities.
- Represent the organization at local trade associations’ meetings and discussions.
- Become an expert in specific regulatory topics impacting the local business.
- Be the co-technical responsible before specific authorities.
To enable success in this position you will have:
- A pharmacist with desired 2-3 years of experience in regulatory affairs activities preferably related to Life Science/ medical device/ pharmaceutical and food ingredients.
- Experience of interactions with Regulatory Authorities
- The ability to work independently and function well in a team-oriented environment.
- Able to communicate in English (advanced level) in both reading, speaking, writing, and listening.
Esto es lo que ofrecemos: Somos mentes curiosas con distintas procedencias, perspectivas y experiencias vitales. Celebramos la diversidad en todas sus dimensiones, porque creemos que impulsa la excelencia y la innovación, las cuales son indispensables para mejorar nuestra capacidad de liderazgo en ciencia y tecnología. Abrir puertas y oportunidades es nuestro compromiso para que todo el mundo crezca y se desarrolle a su propio ritmo. Acompáñanos a crear una cultura de inclusión y pertenencia con impacto en millones de personas y que nos empodera a aplicar la magia y abanderar el progreso humano.
Envíanos tu solicitud ahora mismo y sé parte tú también de este equipo tan diverso.
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