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Paid Internship
Work Mode
Time Spent
Required Degree
Duration

21Open Positions

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Quality Management Systems Trainee

ZEISS Group
Found 1 month ago
Location
Lisboa, Portugal
Time
Not disclosed
Work Mode
Not disclosed
Salary
Not disclosed
Visa Help
Not disclosed
Last Verified
1 month ago

Education

  • Bachelor
  • Master

Skills & Qualifications

Technical Skills

  • ISO 13485
  • QMS
  • DMS
  • Microsoft Office suite (Word, Excel, Power Point)

Soft Skills

  • Project Management
  • Administration
  • Global collaboration

Job Description

The role focuses on assisting in development, implementing and maintaining the Quality Management System (QMS) and Document Management System (DMS) in compliance with ISO 13485 standards. The trainee will contribute to generating controlled documentation, execution support, process progress monitoring, and support the Global XRX Team in Global Quality initiatives. Working within an international environment, the trainee will collaborate with the quality team to help stream-line processes, improve system reliability, and support document management. The trainee will take part and support in organizing and conducting internal audits as well as preparing quality reports for management review, highlighting key performance indicators (KPIs) and audit findings. The position offers hands-on experience with ISO13485 in a regulated environment, exposure to QMS and DMS strategies and execution and global collaboration. Additional QMS/DMS project initiatives may be developed over time, and the trainee will have the opportunity to contribute to new solutions aligned with the organization’s roadmap. The role of Quality Management Systems Trainee will involve: Support in Coordinating and Developing QMS Assistance in DMS and Documents and Records Generation and Maintenance Global Project Process Monitoring and Reporting Audit Preparation and Assistance

Requirements

  • Bachelor or Master student in: Engineering (e.g., Biomedical, Mechanical, or Industrial Engineering) or Life Sciences (e.g., Biology, Biotechnology, or Chemistry) Quality Management or a related discipline
  • Academic or project-based experience in Quality Management, Project Management, Administration, working within regulations and guidelines in a medical technology or technical environment.
  • Experience with university or personal quality management/ document management projects is considered valuable.
  • Good proficiency in Microsoft Office suite (Word, Excel, Power Point)
  • Fluent English

Related Field

  • Engineering Management

Related Subfield

  • Quality Assurance Management

Languages

  • English
▶Apply Now

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