Staff Quality Engineer -Model Farm Rd - Cork - Stryker Corporation

Date de publication : 1/20/2020

Résumé de l'offre

  • Type de salarié :
    CDI / CNE
  • Lieu :
    Cork
  • Type d’offre :
  • Job ID:
    R417094

Description de l'offre



Every day in our Neurovascular manufacturing site in Cork we make products that save our patients/customers lives! This is an opportunity for you to become a key part of that of that!



If you are a natural problem solver with excellent interpersonal skills and a passion for Quality then a Staff Quality Engineer role in Stryker could be a match for what you’re looking for!

Who We Want:

  • Effective communicators. People who can interpret information clearly and accurately to concisely communicate results and recommendations to stakeholders, senior management, and their teams.
  • Dedicated achievers. People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations.
  • Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, information, use cases, and industry analyses to develop best practices.
  • Analytical problem solvers. People who go beyond just fixing to identify root causes, evaluate optimal solutions, and recommend comprehensive upgrades to prevent future issues

What You will Do:

Every day in this role represents a new and exciting challenge!

On a daily basis you will be a key player in ensuring that Stryker’s fantastic Quality performance continues to excel.

You will work on some key projects including New Product Introductions, Cost Saving Initiatives and Manufacturing Transfers.

As our site continues to grow it will be among your key responsibilities to support and ensure production levels continue to flourish with the utmost emphasis being on Quality.

What You Need:

  • Bachelor degree in Science, Engineering or equivalent/ related subject and 4 years of work experience in a quality discipline, or Masters of Science, Engineering or related subject with 2 years of experience
  • Previous experience in a regulated environment required.
  • CQE or equivalent course work / experience desirable
  • Proficient in understanding of Med Device manufacturing processes required.
  • Proficient in ISO 13485, GDP, GMP.
  • Lean Six Sigma training a distinct advantage.
  • Excellent communication skills and attention to detail.
  • Have a good understanding of engineering and quality practices & methods.
  • High level of PC skills. Must be proficient with Microsoft Word, Microsoft Excel and PowerPoint packages.
  • Exhibits strong leadership and mentoring behaviours. Self-starter with demonstrated efficient work methods, analytical & problem solving skills and ability to handle multiple tasks in a fast paced environment.
  • Must be willing to work as part of a multi-site team, with some travel required.
  • High level knowledge/experience of Risk Based and statistical techniques, in particular process risk, statistical sampling plans, Process Capability, Gauge R&Rs.
  • Highly developed problem solving and strong analytical skills.
  • Builds strong relationships by fostering open communications, respect and trust. Strong team player and acts with a customer service/stakeholder focused approach Is diplomatic, tactful and leverages excellent interpersonal keys to help achieve outcomes.
  • Presents as a change agent and adopts a continuous improvement orientation to the role Excellent English (both oral and written) .
  • Ability to be the voice of Quality when dealing cross functionally, will take the lead discussions / meetings to ensure the correct outcome.

Work From Home: Not available

Travel Percentage: 10%

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