Senior QC Engineer - Utrecht

Vacancy information

Publication date:April 09 2021
Employment type: Permanent
Sector: Medical Devices
Function Group: Engineering

Function Group: Engineering / Design Engineer


For a rapidly growing Medical Devices company, we are looking for a Senior QC Engineer. This start-up develops and manufactures innovative and life-changing electronic Medical Devices with the goal of giving people with diabetes more time to enjoy life. This organisation is one that people can rely on. At this moment, the organisation is experiencing tremendous growth and is expected to become a global leader in its field in the near future. Currently, the organisation employs around 100 talented and ambitious professionals who believe in a work hard/play hard approach.


As a Senior QC Engineer, you will be responsible for the Quality of all operational processes and work on non-operational procedures. Together with stakeholders, you implement quality measures to ensuring processes and product(s) consistently meet established quality standards. Next to daily activities, you are part of projects and you are involved in Quality Assurance (like reviewing NC’s and execute impact assessments).

Daily activities involve but are not limited to:

  • Create and implement quality control systems, quality standards and quality control strategies
  • Identify NC’s & Bottlenecks and suggest improvements or process changes
  • Take part of audits (supplier, internal & external)
  • Support Correction and preventive actions and monitor the effectiveness
  • Lead or be involved in risk assessments.
  • Create and give Quality related training modules.
  • Participate in calibrations on-site and support external calibrations


For this challenging and varied role, we believe it is important that you meet the following requirements:

  • Bachelor’s degree in Biomedical engineering/ health sciences/ Quality/ Mechanical or equivalent experience
  • Minimum 4 years of experience in Quality
  • Excellent knowledge of quality control principles
  • Good knowledge of validation, test method validation/ gage R&R and statistical techniques
  • Excellent knowledge of ISO 13485, MDD 93/42/EEC, MDR and 21 CFR 820
  • Strong admin and IT skills, particularly Microsoft Office
  • Fluent written and spoken English. Dutch language is not required


Besides working for a rapidly growing organisation, the company offers you:

  • A competitive salary depending on your experience and expertise
  • 32 days holiday per year + 5 optional purchase days
  • A defined benefit pension scheme and disability insurance
  • 40 hours per week to be worked anytime between 07:00h to 19:00h
  • Assistance for relocation and 30% ruling
  • Team lunches and free parking spots
  • A great and relaxing atmosphere in the office
  • An informal dress code


If you are interested in this job, or in similar ones, please feel free to contact me directly.

Quintes Hamer

Associate | Medical Devices




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