Overview

Quality Assurance Officer Jobs in Brabantine City Row at Unity Partners

Title: Quality Assurance Officer

Company: Unity Partners

Location: Brabantine City Row

Unity Partners on behalf of our MedTech partner

Our partner is an innovative healthcare technology company developing advanced medical solutions that help improve access to high-quality diagnostics and healthcare worldwide. Combining medical hardware and software, they support healthcare providers in diverse markets.

To strengthen their QA/RA Affairs team, we are looking for a QA Officer who will play a key role in maintaining and improving the Quality Management System while ensuring compliance within a highly regulated medical device environment.

Role Overview

As a QA Officer, you will be responsible for supporting quality, compliance, and product safety activities across the organization. You will work closely with cross-functional teams to ensure processes, products, and systems comply with applicable regulations and quality standards.

This role offers a broad range of responsibilities, including audits, supplier quality management, CAPA activities, and continuous improvement initiatives, while serving as an important point of contact for external regulatory and certification bodies.

Key Responsibilities

  • Ensure compliance with ISO13485, MDR, ISO14971, IEC62304, and other standards.
  • Plan, execute, and follow up on internal and external audits.
  • Maintain and continuously improve the QMS.
  • Manage supplier approvals, supplier reviews, CAPA processes, and non-conformities.
  • Support communication and documentation activities with Notified Bodies.
  • Act as a quality representative within the organization.
  • Drive continuous improvement initiatives across quality and compliance processes.

Your Profile

  • At least a Bachelor’s degree in Engineering, Life Sciences, Quality Management, or a related field.
  • 3+ years of experience within Quality Assurance in the medical device industry.
  • Strong knowledge of ISO 13485, MDR, and medical device risk management principles.
  • Experience supporting audits and certification activities.
  • Excellent communication skills and strong attention to detail.
  • Experience working with digital quality and documentation systems.
  • Able to work independently while also thriving in a collaborative team environment.

Organization & Offer

You will join an international and rapidly growing healthcare technology organization where innovation, quality, and global impact are at the heart of everything they do.

What you can expect:

  • Direct impact on product quality, compliance, and patient safety.
  • An international and multicultural working environment.
  • Opportunities for training, professional development, and career growth.
  • Excellent pension scheme.
  • High level of autonomy, ownership, and flexibility.
  • Regular team events and informal company gatherings.

Interested?

Contact Christian Steenkamp via [email protected] or +31 (0)20 8938 606.

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