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Quality Intern – Medical Devices
Quality Intern – Medical DevicesMD Skin Solutions • Menningen, DE
Quality Intern – Medical Devices

Quality Intern – Medical Devices

MD Skin Solutions • Menningen, DE
Vor 30+ Tagen
Stellenbeschreibung

About Us | Our Company


Located in the heart of Luxembourg, MD Skin Solutions (MDSS) is a European family-owned company specialized in medical devices and medical aesthetic solutions. For over 15 years, we have been designing, developing, and distributing high-quality products that comply with the most stringent international regulatory and quality standards, including those applicable to medical devices.

Managed by four passionate siblings, MDSS has grown into a global player, with products distributed in over 70 countries worldwide. Our expertise lies at the intersection of innovation, patient safety, regulatory compliance, and performance, placing quality at the core of everything we do.

At MDSS, continuous improvement and regulatory excellence are key drivers of our growth. Our philosophy, “Your most beautiful age is now,” reflects our commitment to developing safe, effective, and compliant medical solutions. With several medical device projects currently under development, this is an ideal time to join our Quality team.

About You | The Role


We are looking for a Quality Intern – Medical Devices to join our Quality Department in Luxembourg for a 6-month internship. This role offers a valuable opportunity to gain hands-on experience in quality systems, documentation, and regulatory compliance within a medical device environment.

Under the supervision of the Quality Manager, you will support the Quality Department’s administrative and documentation activities, contributing to the proper maintenance of the Quality Management System (QMS) in line with applicable regulations.

Position: Quality Intern – Medical Devices

Department: Quality

Location: Luxembourg

Duration: 6 months

Reporting to: Quality Manager


Your Main Responsibilities


Quality Documentation & QMS Support

  • Assist in the organisation, updating, monitoring, and archiving of quality documentation related to medical devices (procedures, SOPs, work instructions, records).
  • Support document control activities, including version management and traceability.
  • Update quality databases and ensure data accuracy and consistency.
  • Provide administrative support for quality-related internal requests.

Regulatory & Compliance Support

  • Assist in the preparation and updating of quality and regulatory documents in compliance with medical device regulations and standards.
  • Support the monitoring of quality actions, corrective and preventive actions (CAPA), and follow-up activities.
  • Contribute to ensuring alignment with internal procedures and regulatory requirements.

Operational Support to the Quality Department

  • Prepare and organise quality meetings (documentation, agendas, minutes).
  • Support cross-functional teams by ensuring the availability and proper management of quality documents.

Quality Communication & Awareness

  • Assist in the creation of training and awareness materials related to quality and regulatory best practices.
  • Support the deployment and communication of quality procedures across relevant departments.

Desired Profile

  • Current student or recent graduate in Quality Management, Life Sciences, Biomedical Sciences, Medical Devices, or a related field.
  • Strong interest in medical devices and regulated environments.
  • Excellent organisational and administrative skills, with strong attention to detail.
  • Very good written and verbal communication skills in French and English (mandatory).
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, SharePoint).
  • Ability to work independently, follow procedures, and respect deadlines.
  • Previous experience in administration, quality, or regulated industries is a plus.

What We Offer


  • Hands-on experience within a medical device Quality Department in an international company.
  • Exposure to Quality Management Systems and regulatory requirements applicable to medical devices.
  • Close coaching and mentoring by an experienced Quality team.
  • Development of strong documentation, compliance, and organisational skills in a highly regulated environment.
  • A collaborative, professional, and supportive work atmosphere.

If you are detail-oriented, structured, and motivated to discover the Quality function in the medical device industry, we would be delighted to hear from you.

Apply now and join MD Skin Solutions (MDSS) for a meaningful and formative professional experience.

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Quality Intern – Medical Devices • Menningen, DE

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