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Alajuela

    Production Supervisor III - Alajuela, Costa Rica - Abbott

    Abbott
    Abbott Alajuela, Costa Rica

    hace 12 horas

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    Descripción

    The Opportunity

    This position works out of our Alajuela, Coyol location in the Vascular division that provides innovative, minimally invasive, and cost-effective products for the treatment of vascular disease.

    What You'll Do

  • Implements and manages a staffing plan by identifying resource requirements, writing justifications for additional personnel, obtaining approval for changes, and coordinating the selection process with Human Resources.
  • Develops direct reports by securing appropriate training, assigning progressively challenging tasks, rewarding positive behavior, and applying disciplinary action as appropriate.
  • Trains and certifies to all critical assembly operations and understands all line PFM ́s.
  • Monitors daily metrics and provides direction and guidance to lower–level supervisors, or skilled nonexempt staff to achieve unit or Project goals.
  • Retains responsibility for the product from initial assembly to final distribution. Schedules and organizes assigned manufacturing lines to achieve 100% product availability and maintain target levels of inventories.
  • Communicates to line personnel daily while maintaining a constant line presence.
  • Maintains regular communication with exempt-level staff to ensure alignment in running operations and achieving objectives.
  • Maintains a safe environment with 100% training and compliance with applicable procedures.
  • Responsible for achieving dept. attendance targets including immediate feedback to employees by instance.
  • Coordinates activities related to shift starts and changes.
  • Communicate with other departments and functions as needed in support of meeting operational objectives.
  • Helps develop, interpret and execute policies that affect work processes and personnel within the assigned organizational unit.
  • Oversees personnel and processes to ensure full compliance with internal and external regulations.
  • Monitors and communicates internal and external indicators that impact the business and or industry by reviewing reports and newsletters, reading organizational literature, meeting with peers, and reading development reports.
  • Shift

    Shift: A (Monday - Friday from 5:50 am to 3:15 pm)

    On-Site position

    Required Qualifications

  • Bachelor's degree in engineering or related STEM field
  • 4 years of related experience
  • Influence and Leadership.
  • Knowledge of applicable regulations and standards affecting the manufacture of Medical Devices (i.e., cGMPs and CFRs).
  • Fully Bilingual (English and Spanish)
  • Preferred Qualifications

  • Industry / supervisory experience and direct exposure to Operations desired.
  • Ability to direct activities of employees. Ability to train and motivate assigned personnel.
  • Ability to continuously improve upon safety, quality, and performance.
  • Has an understanding of operations standards and documentation.
  • Has an understanding of safety, quality, and performance goals and can execute on goals.


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