Quailty & Reliability Engineer

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  • Aanbod € 60000 - € 70000
  • Functiegroep Engineering
  • Dienstverband Fulltime
  • Vacaturenummer 8381700
  • Locatie Eindhoven
  • Contract Detachering via YER
  • Branche Manufacturing, High Tech, Medical & Health

Over deze vacature

The Quality and Reliability Engineer (QE) is responsible in developing and implementing systems to ensure products are designed and produced to meet customer requirements and expectations. He/she drives the strategy and approach of the team to establish the root cause in a systematic way and coordinates the use of adequate tools and methods. Provides direction for the cross-functional team with other business and engineering disciplines to follow a structured problem solving approach. Establishes the principles of product and service quality evaluation and control for the system. Provides independent oversight and review of the project deliverables throughout the product lifecycle. Provides leadership and is responsible and accountable to the organization for own decisions and actions, while also holding others accountable for the same.

Functie

Key areas of responsibilities for this role include:

  • Provide leadership and oversight to ensure effective solving and closure with a cross-functional team;
  • Ensures that appropriate quality plans are made that include all stages of the process;
  • Validates key design inputs like: usability, reliability, performance, supportability, manufacturability, localizability, safety, security, privacy, serviceability, sustainability and costs;
  • Provides effective oversight of the execution of the quality plan, any risk management activities, and of all design related activities during the product/system lifecycle;
  • Performs independent technical assessment on product quality performance and post-market product quality analysis;
  • Uses post-market analytics and statistics to report on product quality performance in the field (provide feedback to manufacturing, suppliers or design teams) and initiates field actions when required;

Bedrijf

With a growing presence in cardiology, oncology, and women's health, Philips operates in the areas of Imaging Systems, Patient Care & Clinical Informatics, Home Healthcare and Customer Services. Philips combines its clinical expertise and human insights to create innovative solutions across the continuum of care, in partnership with clinicians and our customers, to provide better value and expand access to care for millions. Our teams are working hard every day to improve patient outcomes all the way from disease prevention and screening to diagnosis, treatment, therapy monitoring, and disease management. Irrespective of whether the care cycle takes the patient from doctor's office to hospital or hospital to home, or simply from one medical department to another, Philips Healthcare's unique medical solutions are designed to optimize the quality and flow of patient information and clinical decision making.

Aanbod

We welcome you to a challenging, innovative environment with great opportunities for you to explore. YER is preferred supplier. You will be employed by YER and seconded to Philips.

Our benefits are very competitive and designed around your preferences:

  • A competitive salary depending on experience
  • Extensive set of tools to drive your career, such as a personal development budget, training and coaching
  • Healthy work-life balance

Profiel

A person who has strong technical competencies, and demonstrates resilience in challenging, often demanding situations. We are looking for a perfectionist- a fixer who continuously strives for excellence as a way of life; not just as a job. We’re looking for someone who can inspire others to adopt this mentality of prioritizing quality above all else in a relentless pursuit to improve the quality of life billions for the billions of people Philips brand touches each year.

Specific skill requirements for this role include:

  • ASQ certified Quality Engineer or DfSS/DMAIC Black Belt (or equal by experience).
  • Engineering degree or equivalent experience in medical device industry.
  • 5+ years experience with a medical device company.
  • Have understanding of a quality system and its development, documentation, and implementation with respect to domestic and international standards or requirements.
  • Be able to develop and implement quality programs, including tracking, analyzing, reporting, and problem solving.
  • Be able to plan, control, and assure product and process quality in accordance with quality principles, which include planning processes, material control, acceptance sampling, and measurement system.
  • Use established Business Excellence methodologies such as DfSS, DMAIC, statistical engineering (shainin tools), PDCA, SPC, 8D ...
  • Provide data driven expert opinion on root cause analysis of failure modes.
  • Experience in manufacturing quality control and improvement programs is highly preferred.
  • You combine analytical and conceptual thinking, physical insight, flexibility and a hands-on mentality to deliver sustainable results and creative solutions.
  • Excellent reporting and documentation skills.
  • Experience with working with quality and reliability tools and templates, e.g. Minitab, JMP, Reliasoft, FMEA, FTA, HAZOP, …
  • Excellent consultancy skills, a team player with the ability to connect with business stakeholders.
  • Good project management skills.

Furthermore to be successful in this role you are :

  • Motivated, self-driven with a determination to succeed and the ability to manage change.
  • Analytical, you are open to new ideas and believe in continuous learning in order to develop new competencies.
  • Fluent in English.
  • Travelling will be required to US and Asia for 40% of working time!
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