Quality Assurance Specialist

Job description

Are you interested in the field of medical devices? Would you like to join an international company and develop their quality standards in the European region? We are offering a great opportunity in QA where you will have a lot of freedom to work out your schedule and strive together with the business to obtain ISO 13485 certification. You will be offered an exciting and challenging role in Leiden office, where you will become a subject matter expert on quality matters for the global market and partner in a team of two to manage quality control systems designed to ensure continuous production.

Your daily responsibilities will be to:

  • Investigate necessary documents and processes for the company to obtain ISO 13485 certification
  • Stay responsible for the timely implementation of required milestones in quality management
  • Ensure due diligence is respected and compliance matters are under control
  • Support ad hoc external audit with requested documentation
  • Provide required reporting to the headquarters

Job requirements

What you will be offered:

  • direct contract with the company for a year to start with
  • fun & close-knit team
  • 25 holidays
  • 100% travel allowance
  • well located Leiden office

What the company asks for:

  • Excellent written and verbal English language skills
  • Affinity with ISO 13485 and understanding of Medical Devices industry
  • Ability to work in a multicultural team
  • Strong skills in Microsoft Office

Company profile

International producer of medical devices with offices in the Netherlands and Russia. Dynamic, proactive, professional environment. Young-minded enthusiastic team!

Additional information Quality Assurance Specialist

Please, call me with questions on 06 52 66 7440 or drop an email on alexandra@adamsrecruitment.com.



Quality Assurance Specialist