7 publicaciones de empleo destacadas de data scientist en cuauhtémoc cdmx (¡Están contratando!)

Regulatory Intelligence Specialist / Medical Devices
Abbott Laboratories —Ciudad de México, CDMX
- Tiempo completo
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
4d
Senior Software Development Engineer
Amazon.com —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Informática
- Java
Senior Software Development Engineer
Servicios Comerciales Amazon Mexico S. de R.L. de C.V. - D44 —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Informática
- Java
AI Presales
SDG Group —Ciudad de México, CDMX
- Trabajo híbrido
- Español
- Azure
- Doctorado
Postulación rápida
Senior Data Scientist, DTC
Levi Strauss & Co. —Centro (Área 1), CDMX
- Tiempo completo
- Doctorado
- Informática
- Maestría
Postulación rápida
7d
Assistant Scientist
Colgate-Palmolive —Ciudad de México, CDMX
- Administración de personal
- Inglés
- Licenciatura
1d
Data Engineer
Urban Science Applications, Inc. —Colonia Polanco, CDMX
- Tiempo completo
- Administración de personal
- Informática
- Experiencia en bases de datos
6h

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Regulatory Intelligence Specialist / Medical Devices

Abbott Laboratories -
Ciudad de México, CDMX

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Información del empleo

Tiempo completo
Hace 4 días

Cualificaciones

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Microsoft Outlook
Administración de personal
Microsoft Office
Licenciatura
Mejora continua
Habilidades de organización

Descripción completa del empleo

Regulatory Intelligence Specialist (RIS) – Medical Devices Division

Mexico City

About Abbott

Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will have access to:

Career development with an international company where you can grow the career you dream of .
A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

WHO WE WANT

Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, data, and insights to drive continuous improvement with processes.
Dedicated achievers. People who thrive in a fast-paced environment and will stop at nothing to ensure deliverables are complete in meeting regulations and expectations.
Self-directed initiators. People who take ownership of their work and need no prompting to drive productivity, change, and outcomes.

WHAT YOU’LL DO

Global Regulatory Operations is seeking a Regulatory Intelligence Specialist to join our team

This position is focused on new and changing regulations that enable global market access for new and innovative medical devices and supports compliance continuity for marketed devices. Assisting in the process to evaluate proposed regulatory changes in major markets within the CALA Region, the Regulatory Affairs Intelligence Specialist:

Monitors and fact-checks new or changing global regulations
Tracks and documents regulations within the regulatory intelligence systems
Supports the communication of emerging regulations, documents for comment, and regulations in implementation
Performs regulatory investigations to assess medical device regulatory changes within a specific country or region
Supports the maintenance of, or continuous improvement of quality system procedures, and documents
May train others on systems and processes
Facilitates the collection and reporting of data in support of key performance indicators
Gathers additional data to support interpretation, and aid businesses in determining impact
Support all company initiatives as identified by management and in support of Quality Management Systems (QMS) and other regulatory requirements
Complies with regulations, international regulations and other regulatory requirements, company policies, operating procedures, processes, and task assignments.
Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, etc.
Performs other related duties and responsibilities, on occasion, as assigned

EDUCATION AND EXPERIENCE YOU’LL BRING

Required

Bachelor’s degree (or equivalent)

Advanced english

3 years’ experience in Medical Devices, or a regulated industry (e.g., nutritional, pharma) preferred. Experience in a Regulatory or Quality role, a plus.
Ability to work within a fast-paced and matrixed team environment
Strong verbal and written communication skills · Strong attention to detail and organizational skills
Proficient in Excel, and all programs with MS Office suite (Word, PowerPoint, Outlook)
Experience in program management a plus
Experience with document management systems a plus

Apply Now

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal.

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