Cardinal Health

Ingeniero Junior de Proyectos (BB-28CD1)

Encontrado en: Neuvoo CR


What Engineering Prgrm/Project Mgmt contributes to Cardinal Health

Provide advanced engineering expertise in support of a broad scope of activities in a medical device manufacturing environment.

  • Function as technical lead and adviser for developing, implementing, and improving production systems related to different type of materials processing and assembly.
  • Interface with R&D on product introductions and improvements, from concept to launch.
  • Recommend, plan, and execute projects requiring extensive manufacturing or specific technical expertise.
  • Act as Influential Leader throughout cross-functional teams on key site initiatives.
  • Accountabilities

  • Develop, perform and summarize qualification and validation protocols per internal procedures, regulatory expectations, industry standards and product/process requirements.
  • Support other engineers in equipment and product qualification process.
  • Execute and document process characterization studies and designed experiments.
  • Interact cooperatively with co-workers, supervisors and engineers of other departments and receive direction from superiors.
  • Support other Engineers in investigations related to Validations and the Product Manufacturing Process.
  • Develop and update documentation such as BOM’s, SWI, Procedures, Forms and others.
  • Keep track of documentation stages to ensure its timely release.
  • Create Change Orders.
  • Asses documentation to determine gaps and needs of new documentation.
  • Obtain necessary information to create new documents.
  • Comply with Good Manufacturing Practices.
  • Qualifications

  • Bachelor's degree in Engineering, Chemistry, or related field, preferred.
  • 1+ year of experience in a Manufacturing, Process Development Environment, Chemical and/or Pharmaceutical Plant is preferred.
  • Advanced English skills (written and spoken) required.
  • Good Manufacturing Practices.
  • Previous experience with Equipment and Process Validation.
  • Excellent written and oral communication skills.
  • Proficient with MS Office (Power Point, Excel, Project, and Word).
  • Driven by results, shown significant accomplishments.
  • Self-directed with the ability to develop, facilitate and gain consensus in a team environment.
  • Ability to adapt to evolving projects requirements.
  • Problem solving skills.
  • Proficient with MS Office.
  • Demonstrate flexibility, adaptability and integrity when making decisions.
  • Dealing with ambiguity, creativity, customer focus, timely decision making, decision quality, function/technical skills, innovation management, learning on the fly, listening, managing and measuring work, organizing, perseverance, planning, presentation skills, priority setting, managing through systems, technical learning.
  • Preferred qualifications

  • Medical device manufacturing or similar experience in highly regulated industry.
  • PMP certification.
  • Black Belt certification.
  • What is expected of you and others at this level

  • Create, modify and approve production procedures and other documentation within the appropriate change control system.
  • Formulate and execute experiments, test plans, and validation activities. Collect and analyze data.
  • Generate protocols and reports.
  • Communicate and coordinate project activities with multiple functional groups.
  • Assist with selection and qualification of new materials and suppliers.
  • calendar_todayhace 4 días


    info Full time - Regular

    location_on Alajuela, Costa Rica

    work Cardinal Health

    Autorizo expresamente a Términos y condiciones

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