Quality Process Engineer Manufacturing – Brunel – Drachten


Over deze functie

The processes include the introduction/validation of new/changed manufacturing processes and their associated Q systems, the trend analysis and monitoring of manufacturing processes and their environment, the remediation to non-conformances, and the development and improvement of Q systems. You are having the ability to switch very easily between your hard en soft skills from engineering till operator level. Your main task is to ensure the quality and performance level of our existing processes. With this, your self-esteem and self-respect should be relatively high.

  • Responsible for performing timely quality engineering and quality assurance tasks.
  • Accountable for ensuring Manufacturing quality systems are established, maintained and documented according to needs of the business, customers and applicable quality system standards ®ulations at manufacturing line level and as individual contributor.
  • Provide oversight of Q&R supported Manufacturing NPI projects ensuring timely completion of project deliverables, correcting issues delaying completion and reporting on status of projects at project level.
  • Developing professional expertise, applies company policies and procedures to resolve a variety of issues.
  • Qualified expert who is developing beyond entry level knowledge of the quality assurance and quality engineering field.
  • Has working knowledge of manufacturing systems products and services. Frequently interacts with supervisors and functional peer groups. Interaction normally requires the ability to gain cooperation of others, conducting presentations of technical information concerning specific projects or schedules. Works on issues where analysis of situation or data requires review of relevant factors.
  • Exercises judgment within defined procedures and policies to determine appropriate action.
  • Over jou

  • Bachelor’s Engineering degree, or equivalent experience.
  • Basic understanding of global medical device regulations, requirements, and standards, such as ISO13485, and ISO9001.
  • Preference 3+ years of experience in a medical device or non-regulated industry.
  • Wat wij je bieden

    We offer you the opportunity to work in a dynamic environment and you will also be part of an enthusiastic and motivated team. You get plenty of room for initiatives and there are plenty of opportunities for growth. Being mediated by Brunel means that you have a contract with Brunel. Not only do you have a contract, you are also guaranteed a great career!

    Our primary and secondary terms of employment are excellent. Some examples are:

  • Price reductions with CZ health insurance.
  • Bonus opportunities.
  • Standard 26 vacation days.
  • 8% vacation pay.
  • Salary ranges €3800 – €5000 depending on experience.
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