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Ofertas de Empleo en Medtronic

Ofertas de Empleo en Medtronic

ofertas de empleo
Recientes Relevantes

ofertas de empleo

Recientes Relevantes

Assoc analyst - us field inventory

COP

industry Medtronic

Ofertas de empleo en Medtronic.
Hace 2 semanas
$3,5 a $4 millones
Salario
Indefinido
Tipo de contrato
Remoto country
Ubicación
Remoto
Modalidad laboral
Hace 2 semanas

  • Assoc analyst - us field inventory

    COP
  • The Associate Analyst, U.S. Field Inventory plays an important role in supporting field sales teams through effective inventory management, order fulfillment, and obsolescence reduction across multiple businesses. This role partners closely with U.S. Field Inventory, Field Sales, and cross-functional stakeholders to help ensure the right product is in the right place at the right time.

    This position supports the execution of inventory strategies tied to product availability, new product launches, and inventory optimization initiatives. Success in this role requires strong analytical capability, systems proficiency, effective communication, and the ability to manage multiple priorities in a dynamic environment with limited supervision. This role will be remote for candidates located in Colombia.

    Required Knowledge and Experience:

    Bachelor’s degree
    One year of experience in customer service, inventory management or supply chain
    Fluent in English
    Intermediate proficiency in Microsoft Office, including Outlook, Excel, Word, and PowerPoint
    Experience with data analysis and reporting tools such as Excel, Access, Business Objects, or similar platforms is a plus
    Inventory, supply chain, or asset management experience; Experience in healthcare, MedTech, or other highly regulated industries and experience with SAP ERP is advantageous

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Senior cyber info assur analyst

COP

industry Medtronic

Ofertas de empleo en Medtronic.
Hace 3 semanas
$5,5 a $6 millones
Salario
Indefinido
Tipo de contrato
Bogotá country
Ubicación
Híbrido
Modalidad laboral
Hace 3 semanas

  • Senior cyber info assur analyst

    COP
  • Job Specific Summary
    We’re a mission-driven leader in medical technology and solutions with a legacy of integrity and innovation. Work with us to incentivize better patient care and partner across the industry to make healthcare more affordable and accessible. Be a part of a community of experts committed to ensuring quality, affordable healthcare worldwide.

    The Directory Services Administrator is responsible for the overall administration, management, and support of the company's directory services infrastructure. This position functions as part of the IAM delivery team, responsible for operational fitness of the system(s) through support, monitoring and response, and system lifecycle management directory services administration, strong troubleshooting skills, and a proactive approach to maintaining and improving the directory services environment and includes ensuring the reliability, security, and performance of Active Directory (AD), Entra ID, LDAP, and related directory services technologies.

    Responsibilities may include the following and other duties may be assigned:

    Administer and manage the company's Active Directory (AD) and Entra ID environments, implement and manage Group Policies (GPOs) to ensure compliance and security

    Ensure system availability, capacity, and performance for IAM technologies, including ownership for logging, monitoring, and alerting standards, processes, and systems, monitor and manage access controls, user permissions, and role-based access

    Plan and manage system upgrade and patching projects, in collaboration with local and offshore teams, and platform subject matter experts (SMEs), communicate with vendors as needed to understand and research open issues, new versions, or changes

    Explore and help build automation to enhance end-user experience, define and develop policies and procedures for system operations to ensure consistency, reduce rework, and improve quality

    Ensure directory services adhere to company

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Principal it business systems analyst

COP

industry Medtronic

Ofertas de empleo en Medtronic.
Hace 1 mes
$12,5 a $15 millones
Salario
Indefinido
Tipo de contrato
Bogotá country
Ubicación
Híbrido
Modalidad laboral
Hace 1 mes

  • Principal it business systems analyst

    COP
  • We are seeking a senior-level experienced Principal IT Business Analyst to join our IT Regulatory Systems team which supports the Regulatory Affairs functions within all operating units and regions.
    Primary focus will be on the design and configuration of our UDI platform, via which we create, manage, publish, and maintain Unique Device Identification data in compliance with global regulatory requirements in the Medical Device industry (e.g., FDA - GUDID, EU MDR - EUDAMED, etc.).
    Its core purpose is to ensure device traceability, regulatory compliance, supply chain visibility, and patient safety across the full product lifecycle.

    The ideal candidate will have a strong background in requirements gathering, writing functional specifications as input for configuration and development efforts, is experienced working in a regulated industry in which strict software validation practices apply, and has experience with communicating with business- and IT stakeholders on project status on a global level.

    Responsibilities may include the following and other duties may be assigned:
    • Consults with business stakeholders to understand and evaluate current business processes and identify complex business problems and needs, turning those needs into system requirements.
    • Writing system functional specifications and support development teams during implementation phase with testing and quality documentation.
    • Deploy new and current systems, processes, and procedures in a cost-effective manner.
    • Configure system settings, plan, and execute unit-, system- and integration tests and lead cross-functional linked teams to address business or systems enhancements for applications within the Regulatory Affairs domain.
    • Maintain relevant documentation and ensure proper validation documentation is created for all projects according MSCM (Medtronic Systems Compliance Methodology) and ensuring compliance with applicable regulations such as FDA 21CFR, ISO13485 and EU MDR.
    •

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