Working Student Technical Documentation

HUMAN Gesellschaft für Biochemica und Diagnostica mbH
Wiesbaden, Germany
5 days ago

Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Working hours
Regular working hours
Languages
English

Job location

Wiesbaden, Germany

Tech stack

Microsoft Windows
Clinical Data Repository
Document Management Systems

Job description

Technischer Assistent (m/w/d) Produktentwicklung Immunoassays

,

At the earliest possible date, we are looking for a

Working Student (m/f/d) Technical Documentation

Location Wiesbaden

Are you interested in gaining hands-on experience at the interface of Regulatory Affairs and Product Management? Do you have a strong eye for detail and enjoy working with structured, precise documentation? Then join our team as a Working Student in Technical Documentation and contribute your skills in the dynamic field of in vitro diagnostics (IVD).

WHAT YOU CAN EXPECT:

  • Assist in the preparation, revision, review, and maintenance of technical and scientific documentation for IVD product files in compliance with IVDR (EU 2017/746), the IVD Directive, and other applicable regulatory requirements - ensuring the creation and maintenance of the Declaration of Conformity.
  • Support the management of product documentation within the electronic document management system (eDMS), including workflow creation and coordination.
  • Actively contribute to and coordinate tasks within projects such as IVDR implementation, development initiatives, and new product launches.
  • Provide administrative and operational support in day-to-day business activities.
  • Prepare process-related documentation and collaborate closely with internal stakeholders including Regulatory Affairs, Product Management, Clinical Affairs, and International Registration.
  • Support operational workflows, including the provision of customer-relevant information to internal departments and, where applicable, external partners.
  • Contribute to corrective actions and related processes as part of the ongoing maintenance of technical documentation.
  • Review scientific reports, including the evaluation of product-specific analytical and clinical data and their interrelationships.

Requirements

  • You are currently enrolled in a technical or scientific degree program (e.g., Chemistry, Biochemistry, Biology, Biotechnology, or Medical Engineering).
  • Solid understanding of scientific principles, ideally with initial experience in analyzing and evaluating scientific or clinical data.
  • Excellent written and spoken English skills.
  • Proficiency in Microsoft 365 and other digital tools.
  • A proactive mindset, strong team spirit, willingness to learn, and a structured, detail-oriented approach to work.

Benefits & conditions

  • Flat hierarchies and the opportunity to contribute your own ideas
  • A supportive team environment that values collaboration
  • Complimentary fruit and beverages
  • Free on-site parking

Does this sound like you and the kind of challenge you're looking for? Then we look forward to receiving your application. Send us your application

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