Senior QA Officer - Shape a Global Medical Device Niche

ROM Utrecht Region

Utrecht

On-site

EUR 65,000 - 90,000

Full time

48 hours ago
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Benefits offered by this job

Pension plan
25 days annual leave
Team activities

Job summary

Vitestro is pioneering autonomous blood collection with the Aletta ARPD. We seek a Senior Quality Assurance Officer to drive continuous improvement of quality systems and support change control in a cutting-edge medical device environment.

You will review processes, identify improvements, and guide colleagues to ensure changes are completed correctly and on time. The role demands 3–5 years of QA/quality systems experience in medical devices, a pragmatic mindset, and a Bachelor's degree in a

Qualifications

  • Analytical thinking, strong problem-solving in regulated contexts.
  • Experience in regulated environments and quality systems.
  • Understanding of quality systems and change control processes.
  • Systematic, process-oriented working approach.

Responsibilities

  • Focus on the continuous improvement of quality systems.
  • Review existing quality processes and identify improvements.
  • Guide colleagues through change control and ensure timely completion.
  • Identify problems and develop workable solutions.
  • Adapt and think creatively to find compliant ways forward.
  • Develop practical solutions to improve quality processes.
  • Support the company through the change control process.
  • Work with a high-skilled team and participate in team activities.
  • Be a key shaper of a new global industry niche.

Skills

Analytical thinking
Regulated environments
Quality systems
Process-oriented
Problem solving
Pragmatic mindset
Guiding colleagues

Education

Bachelor's degree in relevant field

Job description

Vitestro is pioneering autonomous blood collection with the Aletta ARPD. We seek a Senior Quality Assurance Officer to drive continuous improvement of quality systems and support change control in a cutting-edge medical device environment.

You will review processes, identify improvements, and guide colleagues to ensure changes are completed correctly and on time. The role demands 3–5 years of QA/quality systems experience in medical devices, a pragmatic mindset, and a Bachelor's degree in a

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