Job details

Quality Control Inspector / Administrator - Utrecht





Last edited
February 7, 2020

Job contact

Leonie Barabas
0031 33 479 3095

Share this page

Quality Control Inspector / Administrator – Utrecht


Our client is an international medical company specialized in product design, manufacture and distribution of products within the medical and pharmaceutical industries. They are currently seeking a Quality Control Inspector to join their team. Our client’s offices are in the heart of Utrecht.

Main Tasks

Our client is seeking a Quality Control Inspector to join their innovative team in Utrecht and play an integral role in changing the face of their industry. Working for this company, you will have the opportunity to make a real difference to people’s lives. Our client believes that their continued success depends upon the engagement and development of their employees and they strive to provide a fun, inspiring and supportive work environment.

A key member of the Quality team, you will be responsible for ensuring the medical devices meet agreed quality standards and specifications. The diverse responsibilities for this role include:

  • Timely inspection of incoming raw materials, components and finished goods – sampling, analyzing and monitoring product quality in line with established protocols
  • Timely completion and maintenance of records associated with inspections and non- conformance
  • Investigating deviations to make an informed, substantiated decision for approval or rejection
  • Analyze customer returns and implement corrective and preventive plans/actions
  • Support the resolution of identified Quality issues related to suppliers’ quality performance
  • Communicating outcomes and proposed corrective actions to the production management team
  • Support prevention of quality issues in the manufacturing line due to suppliers’ issues
  • Developing and documenting test and inspection processes
  • Investigating and testing new equipment
  • Implementing quality requirements per documented quality systems and procedure
  • Review of production records
  • Preparing quality metrics for reporting of trends to support process improvement
  • Apply for amendments to Quality Controlled Documents as required


  • Proven experience working in a similar quality/ production engineering related role
  • Affinity with technology and qualification in Electrical / Mechanical engineering
  • Strong documentation skills
  • Excellent communication skills
  • Exceptional attention to detail
  • Be comfortable communicating in English. Dutch language is not required
  • Self-motivated, flexible and cooperative
  • Demonstrated decision making skills and effective problem-solving abilities
  • Strong organizational and interpersonal skills
  • An excellent work ethic
  • Knowledge of the ISO 13485 medical quality standard
  • Quality control qualifications