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Quality

Analyst Global PMS Compliance

Company Description

Descripción de la empresa

En Intuitive, estamos unidos detrás de nuestra misión: creemos que la atención mínimamente invasiva es la atención que mejora la vida. Mediante la inventiva y la tecnología inteligente, ampliamos el potencial de los médicos para curar sin limitaciones.

Como pioneros y líderes del mercado en cirugía robótica, nos esforzamos por fomentar un equipo inclusivo y diverso, comprometido con marcar la diferencia. Durante más de 25 años, hemos trabajado con hospitales y equipos de atención de todo el mundo para ayudar a resolver algunos de los desafíos más difíciles de la atención médica y avanzar en lo que es posible.

Intuitive se ha construido gracias a los esfuerzos de grandes personas de diversos orígenes. Creemos que las grandes ideas pueden provenir de cualquier lugar: nos esforzamos por fomentar una cultura inclusiva basada en la diversidad de pensamientos y en el respeto mutuo. Lideramos con inclusión y capacitamos a los miembros de nuestro equipo para que trabajen de la mejor manera y manifiesten su auténtica personalidad.

Las personas apasionadas que quieren marcar la diferencia impulsan nuestra cultura: los miembros de nuestro equipo se basan en la integridad, tienen una sólida capacidad para aprender, la energía para hacer las cosas, y aportan experiencias diversas del mundo real para ayudarnos a pensar de nuevas maneras. Invertimos activamente en los miembros de nuestro equipo para apoyar su crecimiento a largo plazo y así poder continuar avanzando en nuestra misión y alcanzar su máximo potencial.

Únase a un equipo comprometido a dar grandes pasos hacia delante para una comunidad global de profesionales de atención médica y sus pacientes. Juntos, avancemos en el mundo de la atención mínimamente invasiva.

Job Description

The Analyst Global Post Market Surveillance (PMS) Compliance works with the Manager Global PMS Compliance, global PMS leadership, and cross-functional teams to ensure corporate/regional alignment and regulatory compliance.

Primary responsibilities will include continuous monitoring of the global post market surveillance regulatory landscape, and collaboration with global post market teams to implement proactive procedure/process/system improvements to ensure compliance.

In addition, this role will perform project management for PMS projects and CAPAs relevant to global compliance, ensuring the product vision, priorities, and solutions are actively serving functional and cross-functional business needs. This role will take responsibility for the delivery of the project deadlines and commitments.

Roles and Responsibilities:

  • Support management to ensure on-going compliance of Intuitive to global PMS requirements, and alignment of internal corporate/regional PMS teams.
  • Continuously evaluate Intuitive PMS against any new, emerging, or updated global PMS regulatory requirements, and proactively support implementation of procedure, process, system changes and training to address.
  • Participate in internal/external audits as necessary; provide PMS SME expertise in the front and back room when needed.
  • Author and manage global PMS regulatory responses as needed and ensure Intuitive RAQA and cross-functional alignment.
  • Lead and organize project teams to drive focused results and projects/CAPAs related to global PMS compliance.
  • Accomplish project objectives by planning and evaluating project related activities and communicating status to management on a regular basis.
  • Prepare and complete action plans to implement productivity, quality, problem resolving, identifying trends, determine system improvements, and implement change.
  • Perform other duties as directed.

Qualifications

Required Knowledge, Skills, and Experience:

  • Education: degree in engineering, life science, or equivalent.
  • Experience: 3+ years of experience in the medical device field, with specific experience in the following: project management, Quality Management System activities/implementation and/or active participation in audits/inspections.
  • In-depth knowledge and understanding of global medical device regulations, requirements and standards such as ISO 13485, MDD, EU MDR, US FDA requirements, local regulations/guidance documents, etc.
  • Ability to handle multiple tasks and to prioritize and schedule workload to meet business needs independently.
  • Demonstrate good interpersonal skills, ability to work with others in international team environment, effective interactions in cross-functional teams.
  • Organizational and planning skills, including action oriented, focused urgency, and driving for results.
  • Orientation for work result details, with emphasis on accuracy and completeness

Additional Information

Intuitive es un empleador que brinda igualdad de oportunidades de empleo. Proporcionamos igualdad de oportunidades de empleo a todos los solicitantes y empleados cualificados, y prohibimos cualquier tipo de discriminación y acoso, independientemente de su raza, sexo, condición de embarazo, orientación sexual, identidad de género, origen nacional, color, edad, religión, condición de veterano protegido o de discapacidad, información genética o cualquier otra condición protegida por las leyes federales, estatales o locales aplicables.

Shift: Day
Travel: 10% of the time

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