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Associate Quality Engineer in Carrigtohill at Stryker Corporation

掲載日付: 2/10/2019

求人のスナップショット

仕事内容

Associate Quality Engineer

Summary

Develops and implements methods and procedures for process control, process improvement, testing and inspection to ensure that the products are free of flaws and function as designed. Designs and installs sophisticated testing equipment and performs product testing and analysis to maintain quality levels and minimize defects and failure rates. Analyzes reports and defective products to determine trends and recommend corrective actions. Collaborates with supplier representatives on quality problems, ensures that effective corrective actions are implemented and contributes to supplier quality improvement programs.

This is an individual contributor role that requires the use of judgement in applying professional expertise and is expected to work independently with minimal supervision. This position requires professional mastery of a specialized field of expertise that typically requires a college degree or equivalent.   Job requires a good knowledge and comprehensive understanding of the range of processes, procedures and systems to be used in carrying out assigned tasks and a basic understanding of the underlying concepts & principles upon which the job is based. The job requires the ability to make judgements based on practice and previous experience. This job typically requires a degree in process or equivalent and no experience.

Your key responsibilities

Will work within the quality operations team, under coaching and supervision, has responsibility for quality related activities, including, but not limited to the following:

  • Approval of NC, builds proficient in problem solving and root causing activities.
  • Participate in the development and improvement of the manufacturing processes for existing and new products.
  • Review of change management activities.
  • Maintain KPIs for monitoring of process quality, perform analysis and interpret trends, take action as necessary.
  • Support execution and analysis of QATs.
  • Advocate of Human Factor practices, familiarity in the science of Human Factor identification, reduction and mitigation.
  • Develop understanding of risk management practices and concepts, ability to become proficiency in process risk.
  • Develop understanding of optimization of inspection methods and sampling. Support First Article Inspections.
  • Developing proficiency in statistical methods and application.
  • Participate and interface in internal audits providing effective narrative and description of topic of expertise, participate in external audits preparation building confidence and proficiency in interactions with same.
  • Assist in the development and review of process and equipment validation/qualification. Build proficiency in validation processes.
  • Support manufacturing transfers to other plants/facilities, execution quality activities.
  • Responsible for initiation, internal containment and support of ship and product holds for potential product escapes.

What are we looking for?

In the case where a candidate has a relevant qualification but the minimum educational requirements have not been met, and the candidate is in active education towards minimum requirements, “Associate” will be used in the title and duties outlined above will be supervised.

  • France
    • Engineering/Science licence and 2 years work experience in a quality discipline or
    • Engineering diploma (diplôme d'ingénieur)
  • Germany / Switzerland
    • In active Education to a Bachelor of Science, Engineering or related subject
    • Associate Degree (Berufsausbildung) and in active Education to a Technician degree (or similar Level 6 Education like Meister)
  • Ireland
    • Diploma or equivalent in Engineering, Science or related subject
    • In active Education to a bachelor’s degree in science, Engineering or equivalent/ related subject
  • North America
    • Associate degree in Engineering, Science or related subject 
    • In active Education to a bachelor’s Degree in engineering, Science or related subject 
  • 2 years’ experience in industry in quality or engineering function or related experience required.
  • Understanding of Med Device concepts desirable.
  • Familiarity with ISO 13485, GDP, GMP concept desirable.
  • Excellent communication skills and attention to detail.
  • Have a good understanding of engineering and quality concepts / theories.
  • High level of PC skills. Must be proficient with Microsoft Word, Microsoft Excel and PowerPoint packages.
  • Self-starter with efficient work style 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.
  • Knowledge of Risk Based and statistical concepts desirable.
  • Problem solving and 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.
  • Accepts change openly 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

Work From Home: No

Travel Percentage: None

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